BACKGROUND INFORMATION The process of discovering new therapeutically active compounds for a given indication involves the screening of all compounds from available compound collections. From the compounds tested one. or more structure (s) is selected as a promising lead. A large number of related analogs are then synthesized in order to develop a structure-activity relationship and select one or more optimal compounds. With traditional one-at-a-time synthesis and biological testing of analogs, this optimization process is long and labor intensive. Adding significant numbers of new structures to the compound collections used in the initial screening step of the discovery and optimization process cannot be accomplished with traditional one-at-a-time synthesis methods, except over a time frame of months or even years. Faster methods are needed that allow for the preparation of up to thousands of related compounds in a matter of days or a few weeks. This need is particularly evident when it comes to synthesizing more complex compounds, such as isoquinolines.

Thus, improved methods for generating therapeutically useful heterocyclic compounds, such as isoquinoline derivatives, are desired. This invention satisfies these needs and provides related advantages as well. The present invention overcomes the known limitations to classical organic synthesis of isoquinolines as well as the shortcomings of combinatorial chemistry with heterocycles. The present invention combines the techniques of solid-phase synthesis of heterocycles and the general techniques of synthesis of combinatorial libraries to prepare new isoquinoline compounds.

SUMMARY OF THE INVENTION The present invention relates to novel isoquinoline compounds, as well as libraries containing such compounds, of the following formula:

wherein R'to R', X and Y have the meanings provided below.

BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 shows the assembly of building blocks for preparing the isoquinoline derivative compounds of the present invention. It should be noted that, in Figure 1, R1 corresponds with R1l of the subject invention; R2 corresponds with R2 of the subject invention; and R3 corresponds with X of the subject invention.

DETAILED DESCRIPTION OF THE INVENTION The present invention provides novel derivatives and libraries of novel derivatives of isoquinoline compounds of the following formula: In the above formula: R1 is the structure or the structure

wherein R10 is attached to each of the four carbon ring atoms and is, independently, a hydrogen atom, C1 to C6 alkyl, Cl to C6 substituted alkyl, Cl to C12 phenylalkyl or C7 to C12 substituted phenylalkyl; and R11 is a hydrogen atom, C1 to C6 alkyl, Ci to C6 substituted alkyl, C2 to C7 alkenyl, C2 to C7 substituted alkenyl, C2 to C7 alkynyl, C2 to C7 substituted alkynyl, C3 to C7 cycloalkyl, C3 to C7 substituted cycloalkyl, Cs to C7 cycloalkenyl, C5 to C7 substituted cycloalkenyl, phenyl, substituted phenyl, naphthyl, substituted naphthyl, C, to C12 phenylalkyl, C7 to C12 substituted phenylalkyl, heterocyclic ring or substituted heterocyclic ring; R2 is a hydrogen atom, C1 to C6 alkyl, Ci to C6 substituted alkyl, C2 to C7 alkenyl, C2 to C7 substituted alkenyl, C2 to C7 alkynyl, C2 to C'substituted alkynyl, phenyl, <BR> <BR> <BR> substituted phenyl, naphthyl, substituted naphthyl, C3 to<BR> <BR> <BR> <BR> <BR> C7 cycloalkyl, C3 to C7 substituted cycloalkyl, C7 to C12 phenylalkyl, Cs to C7 cylcoalkenyl, Cs to C7 substituted

cycloalkenyl, C7 to C12 substituted phenylalkyl or a heterocyclic ring; R3 R4, R5 and R6 are, independently, a hydrogen atom, halo, hydroxy, protected hydroxy, cyano, nitro, C1 to C6 alkyl, C2 to C7 alkenyl, C2 to C7 alkynyl, C1 to C6 substituted alkyl, C2 to C7 substituted alkenyl, C2 to C7 substituted alkynyl, C1 to C7 alkoxy, Ci to C7 acyloxy, Ci to C7 acyl, C3 to C7 cycloalkyl, C3 to C7 substituted cycloalkyl, C5 to C7 cycloalkenyl, C5 to C7 substituted cycloalkenyl, a heterocyclic ring, C7 to C12 phenylalkyl, C7 to C12 substituted phenylalkyl, phenyl, substituted phenyl, naphthyl, substituted naphthyl, cyclic C2 to C7 alkylene, substituted cyclic C2 to C7 alkylene, cyclic C2 to C7 heteroalkylene, substituted cyclic C2 to C7 heteroalkylene, carboxy, protected carboxy, hydroxymethyl, protected hydroxymethyl, amino, protected amino, (monosubstituted) amino, protected (monosubstituted) amino, (disubstituted) amino, <BR> <BR> <BR> <BR> carboxamide, protected carboxamide, C1 to C4 alkylthio, Ci<BR> <BR> <BR> <BR> <BR> to C4 alkylsulfonyl, C1 to C4 alkylsulfoxide, phenylthio, substituted phenylthio, phenylsulfoxide, substituted phenylsulfoxide, phenylsulfonyl or substituted phenylsulfonyl; R7 and R9 are, independently, absent or present and, if present, are Ci to C6 alkylene or C1 to C6 substituted alkylene; R8 is absent or present and, if present, is Cl to C6 alkylene, Ci to C6 substituted alkylene, C2 to C7 alkenylene, C2 to C7 substituted alkenylene, C2 to C7 alkynylene, C2 to C7 substituted alkynylene, C3 to C7 <BR> <BR> <BR> cycloalkylene, C3 to C7 substituted cycloalkylene, Cs to Cl cycloalkenylene, Cs to C7 substituted cycloalkenylene,

phenylene, substituted phenylene, naphthylene, substituted naphthylene, heterocyclene or substituted heterocyclene; X is hydroxy, protected carboxy, amino, protected amino, (monosubstituted) amino, (disubstituted) amino, an amino acid, aniline, substituted aniline or an amino- substituted heterocyclic ring; Y is CO2H, CH2OH, SH, CH2NHR12, C (O) NHR12, or CH2NHR12, wherein R12 is a hydrogen atom, Ci to C6 alkyl, Ci to C6 substituted alkyl or a functionalized resin; and Z orH2.=O In a preferred embodiment of the above isoquinoline derivative compounds and combinatorial libraries: R1 is the structure or the structure wherein:

R10is attached to each of the four carbon ring atoms and is, independently, a hydrogen atom or C1 to C6 alkyl ; and R"is a hydrogen atom, Cl to C6 alkyl, Ci to C6 substituted alkyl, C2 to C7 alkenyl, C2 to C7 substituted alkenyl, C3 <BR> <BR> <BR> <BR> to C7 cycloalkyl, C3 to C7 substituted cycloalkyl, C5 to C7<BR> <BR> <BR> <BR> <BR> cycloalkenyl, C5 to C7 substituted cycloalkenyl, phenyl,<BR> <BR> <BR> <BR> <BR> substituted phenyl, C7 to C12 phenylalkyl, Cl to C12 substituted phenylalkyl, heterocyclic ring or substituted heterocyclic ring ; R2 is a hydrogen atom, Cl to C6 alkyl, Ci to C6 substituted alkyl, phenyl, substituted phenyl, naphthyl, substituted naphthyl, C7 to C12 phenylalkyl, C7 to C12 substituted phenylalkyl or a heterocyclic ring; R3R4, RS and R6 are, independently, a hydrogen atom, halo, hydroxy, protected hydroxy, cyano, nitro, Ci to C6 alkyl, Ci to C6 substituted alkyl, Ci to C7 alkoxy, C1 to C7 acyl, a heterocyclic ring, C7 to C12 phenylalkyl, C7 to C12 substituted phenylalkyl, phenyl, substituted phenyl, cyclic C2 to C7 alkylene, substituted cyclic C2 to C7 alkylene, cyclic C2 to C7 heteroalkylene, substituted cyclic C2 to C7 heteroalkylene, carboxy, protected carboxy, hydroxymethyl, protected hydroxymethyl, amino, protected amino, (monosubstituted) amino, protected (monosubstituted) amino, (disubstituted) amino, carboxamide or protected carboxamide; X is hydroxy, amino, protected amino, (monosubstituted) amino, (disubstituted) amino, an amino acid, aniline, substituted aniline or an amino- substituted heterocyclic ring;

Y is CO2H, CH2NHR12 or C (O) NHR12, wherein Riz is a hydrogen atom or C1 to C6 alkyl; and Z is =0.

In another preferred embodiment of the invention, the isoquinoline derivatives are wherein: R1 is the structure or the structure

wherein Rlois attached to each of the four carbon ring atoms and is a hydrogen atom ; and R11 is (2-piperidinyl) ethyl, 3- (imidazoyl) propyl, 2,3-dimethoxyphenylmethyl, 2,4-dichlorophenethyl, 2- (2-pyridinyl) ethyl, 2- (4-methoxyphenyl) ethyl, 2 (1-ethyl-2-pyrrolidinyl) methyl, 2-thiophenyl methyl, (3-pyridinyl) methyl, 3- (trifluoromethyl) phenylmethyl, 3-ethoxypropyl, 3-methoxyphenylmethyl, 2- (4-morpholinyl) ethyl, n-acetylamino, allyl, phenylmethyl, cyclopropyl, carbomethyoxyamino,

2- (N, N-di-N-butylamino) ethyl, 2- (N, N-dimethylamino) ethyl, propyl, tyramine, 2-methoxyethyl, 4-chlorophenylmethyl or 3- (N, N-diethylamino) propyl; R2 is 1-naphthyl, 2-chloro-5-nitrophenyl, 2-chloro-6-fluorophenyl, 2-cyanophenyl, 2-imidazolyl, 2-naphthyl, 2-pyridinyl, 2-quinolinyl, 3,4,5-trimethoxyphenyl, 3,4- (methylenedioxy) phenyl, 3,5-bis (trifluoromethyl) phenyl, 3-methylphenyl, 3-nitrophenyl, 3-phenoxyphenyl, 4- (3-dimethylaminopropoxy) phenyl, 4- (methylthio) phenyl, 4- (trifluoromethyl) phenyl, 4-biphenylyl, 4-bromophenyl, 4-dimethylaminophenyl, 4-ethylphenyl, 4-hydroxyphenyl, 4-propoxyphenyl, 5-nitrovanillin, 6-methyl-2-pyridinyl, phenyl, 2-methoxyphenyl or 4-methylphenyl; R3 R4, Rs and R6 are each a hydrogen atom; R7 and R9 are each absent; R8 is absent or present and, if present, is 1,2-ethylenyl, 1,4-cyclohexylenyl or 1,4-phenylenyl; X is (r)- (-)-l-cyclohexylethylamino, 1,2,3,4-tetrahydroisoquinolyl, 2- (n-pyrrolidyl)-ethylamino, 4- (2-furoyl) piperazyl, 3- (2-pipecolyl) propylamino, 3- (n-imidazoyl) propylamino, 4-benzylpiperazyl, 4-bis (4-fluorophenyl) methyl piperazyl, 4-methylpiperazyl, 5-diethylamino-2-pentylamino, 2-chlorobenzylamino, 2-methoxyethylamino, 3,3'-dipicolylamino, (3-pyridyl) methylamino, 3-butoxypropylamino, 3-dimethylaminopropylamino, 3-ethoxypropylamino, 3-methylbenzylamino, 4- (1-pyrrolidinyl) piperidyl, 4- (aminomethyl) pyridyl, n-ethyl- (4-pyridyl) methylamino,

4- (trifluoromethyl) benzylamino, 4-amino-2,2,6,6-tetramethylpiperidine, 4-bromopiperidinyl, 4-tert-butylcyclohexylamino, allylamino, benzylamino, 2-carboethoxy-1-ethylamino, cyclohexylamino, dodecylamino, 4-carboethoxypiperazinyl, 3-amino-ethylbutyrate, isoamylamino, 4-carboxamidopiperidinyl, 1-leucine methyl ester hydrochloride, methyl isobutylamino, morpholinyl, N, N, N', N'-tetraethyldiethylenetriamino, N, N, N'-triethylethylenediamino, N,N-diethyl-N'-methylethylenediamino, N, N-dimethylethylenediamino, 2- (N-ethyl-N- (2-methylphenyl) ethylamino, 3- (N-morpholinyl) propylamino, neopentylamino, pyrrolidinyl, tetrahydrofurfurylamino or thiomorpholyl; Y is C (O) NHR12, wherein R12 is a hydrogen atom; and Z is =0.

In another preferred embodiment of the invention, the isoquinoline derivatives are wherein: R2is 1,4-benzodioxan-6-yl, 1-methylindol-3-yl, 2,3- difluorophenyl, 2-bromophenyl, 2-chloro-5-nitrophenyl, 2- furyl, 2-imidazolyl, 2-naphthyl, 2-pyridinyl, 2- thiophenyl, 3,4-dichlorophenyl, 3,5- bis (trifluoromethyl) phenyl, 3,5-dihydroxyphenyl, 3,5- dimethoxyphenyl, 3,5-dimethyl-4-hydroxyphenyl, 3- (4- methoxyphenoxy) phenyl, 3-furyl, 3-hydroxyphenyl, 3- methyl-4-methoxyphenyl, 3-methylphenyl, 3-nitrophenyl, 3- pyridinyl, 3-thiophenyl, 4- (3-dimethylaminoprop-l- oxy) phenyl, 4- (dimethylamino) phenyl, 4- (methylthio) phenyl, 4- (trifluoromethyl) phenyl, 4- biphenyl, 4-bromo-2-thiophenyl, 4-cyanophenyl, 4-methoxy-

1-naphthyl, 4-nitrophenyl, 4-pyridinyl, 5- (4'- methoxybenzyl)-furan-2-yl, 5-bromo-4-hydroxy-3- methoxyphenyl, 5-nitro-2-furyl, 6-methyl-2-pyridinyl or phenyl, and, more preferably is 5- (4'-methoxybenzyl)- furan-2-yl; R3, R4, R5, R6 are each a hydrogen atom; X is aminocyclopropyl, aminoisopropyl, 3-aminopropyl, aminoethanolyl, (aminomethyl) cyclopropyl, pyrrolidilyl, aminodiethyl, amino-2-methoxyethyl, aminocyclopentyl, piperidinyl, 1- (pyrrolidin-3-ol), aminoamyl, amino- (2- (N, N-dimethyl)) ethyl, azetidinyl, aminofurfuryl, aminodiallyl, 2-aminothiazolyl, 1-aminopiperidinyl, 1-methylpiperazinyl, 4-aminomorpholinyl, aminodiethanol, 2- (aminomethyl) pyridinyl, histaminyl, 1- (2-aminoethyl) pyrrolidinyl, (+)-3-hydroxy piperidine, (s)-l-amino-2- (methoxymethyl) pyrrolidine, 1-amino-4- methylpiperazinyl, tris (hydroxymethyl) aminomethyl, 1- aminopyrrolidinyl, 1- (3-aminopropyl) imidazolyl, 1- (2- hydroxyethyl) piperazinyl, 1-amino-4- (2- hydroxyethyl) piperazinyl, trans-aminocyclohexan-2-olyl, tryptaminyl, 1-aminomethyladamantanyl, amino-2- (trimethylammonium) ethyl chloride, a-N-glycinyl, a-N- lysinyl, a-N-aspartyl, a-N-tyrosinyl, a-N-serinyl, (+)-3- aminopropyl-1,2-diol, (-)-3-amino-propyl-1,2-diol, (+)- aminotetrahydrofurfuryl, (-)-aminotetrahydrofurfuryl, (+)-exo-2-aminonorbornanyl, (-)-exo-2-aminonorbornanyl, cis-decahydroquinolinyl, trans-decahydroquinolinyl, (+)- 3-aminoquinuclidinyl and (-)-3-aminoquinuclidinyl and, more preferably, is 1-aminomethyladamantanyl or (aminomethyl) cyclohexyl; and Y is C (O) NH2.

In yet another preferred embodiment: R'is 1,4-benzodioxan-6-yl, 1-methylindole-3-yl, 2,3- difluorophenyl, 2-bromophenyl, 2-chloro-5-nitrophenyl, 2- furyl, 2-imidazolyl, 2-naphthyl, 2-pyridinyl, 2- thiophenyl, 3,4-dichlorophenyl, 3,5- bis (trifluoromethyl) phenyl, 3,5-dihydroxyphenyl, 3,5- dimethoxyphenyl, 3,5-dimethyl-4-hydroxyphenyl, 3- (4- methoxyphenoxy) phenyl, 3-furyl, 3-hydroxyphenyl, 3- methyl-4-methoxyphenyl, 3-methylphenyl, 3-nitrophenyl, 3- pyridinyl, 3-thiophenyl, 4- (3- dimethylaminopropoxy) phenyl, 4- (dimethylamino) phenyl, 4- (methylthio) phenyl, 4- (trifluoromethyl) phenyl, 4- biphenyl, 4-bromo-2-thiophenyl, 4-cyanophenyl, 4-methoxy- 1-naphthyl, 4-nitrophenyl, 4-pyridinyl, 5- (4'- methoxybenzyl)-furan-2-yl, 5-bromo-4-hydroxy-3- methoxyphenyl, 5-nitro-2-furyl, 6-methyl-2-pyridinyl or phenyl; R3, R4, R5, R6 are each a hydrogen atom; X is anilinyl, 2-fluoroanilinyl, 3-fluoroanilinyl, 4- fluoroanilinyl, 2-chloroanilinyl, 3-chloroanilinyl, 4- chloroanilinyl, 2-bromoanilinyl, 3-bromoanilinyl, 4- bromoanilinyl, 2-methoxyanilinyl, 3-methoxyanilinyl, 4- methoxyanilinyl, 2-hydroxyanilinyl, 3-hydroxyanilinyl, 4- hydroxyanilinyl, 2-carboethoxyanilinyl, 3- carboethoxyanilinyl, 4-carboethoxyanilinyl, 2- trifluoromethylanilinyl, 3-trifluoromethylanilinyl, 4- trifluoromethylanilinyl, 2-dimethylaminoanilinyl, 3- dimethylaminoanilinyl, 4-dimethylaminoanilinyl, 2- phenoxyanilinyl, 3-phenoxyanilinyl, 4-phenoxyanilinyl, 3,4-methylenedioxyanilinyl, 2,3-methylenedioxyanilinyl, 2,3-difluoroanilinyl, 2,3-dibromoanilinyl, 3,4- dibromoanilinyl, 2,3-dimethoxyanilinyl, 3,4-

dimethoxyanilinyl, 1-amino-5,6,7,8-tetrahydronaphthyl, 2- hydroxy-3-amino-5,6,7,8-tetrahydronaphthyl, 2- aminonaphthyl, 1-amino-4-chloronaphthyl, 1-amino-4- bromonaphthyl, 5-amino-l-hydroxynaphthyl, 1-amino-2- hydroxynaphthyl, 5-aminoindanyl, 1-aminofluorenyl, 2- aminofluorenyl or N-methylanilinyl ; and Y is C (O) NH2.

In still another preferred embodiment: R2is phenyl, 2-bromophenyl, 2-cyanophenyl, 2- fluorophenyl, 2-hydroxyphenyl, 2-methoxyphenyl, 3- bromophenyl, 3-carboxyphenyl, 3-cyanophenyl, 3- fluorophenyl, 3-hydroxyphenyl, 3-methoxyphenyl, 3- methylphenyl, 3-nitrophenyl, 3- (trifluoromethyl) phenyl, 4-acetamidophenyl, 4-bromophenyl, 4-carboxyphenyl, 4- cyanophenyl, 4- (3-dimethylaminopropoxy) phenyl, 4- fluorophenyl, 4- (dimethylamino) phenyl, 4-hydroxyphenyl, 4-isopropylphenyl, 4-methoxyphenyl, 4-methylphenyl, 4- (methylcarboxylate) phenyl, 4-methylsulphonylphenyl, 4- (methylthio) phenyl, 4-nitrophenyl, 4-propoxyphenyl, 4- (trifluoromethyl) phenyl, 3,5-bis (trifluoromethyl) phenyl, 3,5-dimethoxyphenyl, 3,5-dihydroxyphenyl, 3,5- dichlorophenyl, 2,3-difluorophenyl, 2,4-dichlorophenyl, 2-chloro-5-nitrophenyl, 2-chloro-6-fluorophenyl, 2,6- difluorophenyl, 3-bromo-4-fluorophenyl, 3,4- dihydroxyphenyl, 3,4-dichlorophenyl, 3,4-difluorophenyl, 3-fluoro-4-methoxyphenyl, 3-nitro-4-chlorophenyl, 3- hydroxy-4-methoxyphenyl, 3-hydroxy-4-nitrophenyl, 4- methoxy-3- (sulfonyl) phenyl, 3-methyl-4-methoxyphenyl, 2,3,4-trifluorophenyl, 2,3,5-trichlorophenyl, 3,5- dimethyl-4-hydroxyphenyl, 3-methoxy-4-hydroxy-5- bromophenyl, 3-methoxy-4-hydroxy-5-nitrophenyl, 1,4- benzodioxan-6-yl, 2,3- (methylenedioxy) phenyl, 3,4-

(methylenedioxy) phenyl, 3,4- (methylenedioxy)-6- nitrophenyl, 8-hydroxyjulolidin-9-yl, 3- (3,4- dichlorophenoxy) phenyl, 3- (4-methoxyphenoxy) phenyl, 3- phenoxyphenyl, 4-phenoxyphenyl, 4-biphenyl, 1-naphthyl, 2-naphthyl, 4-methoxy-l-naphthyl, 2-quinolinyl, 3- quinolinyl, 4-quinolinyl, 8-hydroxyquinoline-2-yl, 9- ethyl-3-carbazolyl, 2-thiophenyl, 3-thiophenyl, 5-methyl- 2-thiophenyl, 2-furyl, 3-furyl, 5-methylfur-2-yl, 2- pyridinyl, 3-pyridinyl, 4-pyridinyl, 6-methyl-2- pyridinyl, pyrrol-2-yl, 1-methyl-2-pyrrolyl, 2- imidazolyl, 2-thiazolyl, 5- (4'-methoxybenzyl)-2-fur-2-yl or 5-nitro-2-fur-2-yl; R3, R, R5, R6 are each a hydrogen atom; X is pyridoxamino, 4- (dimethylamino) benzylamino, 2- chloro-4-fluoroanilino, 3-pyridylmethylamino, 4- (dimethylamino) aniline, 1-adamantanemethylamino, 4- isopropylanilino, 3,4-dichlorobenzylamino, N- benzylethanolamino, 4- (a, a, a-trifluoro-m- tolyl) piperazino, 4-nitrobenzylamino, 5-indanylamino, cyclohexylamino, 4- (2-pyridyl) piperazino, 4- methoxyphenethylamino, 1-naphthalenemethylamino, 2,4- dimethoxybenzylamino, (+/-)-exo-2-norbornaneamino, 2- (2- chlorophenyl) ethylamino, 2- (4-methoxyphenyl)-2- phenylethylamino, 1,4-benzodioxan-6-amino, 5-bromo-2- fluorobenzylamino, 4-pyridylmethylamino, 4- phenylpiperazino, 2-fluoreneamino, 3,4- dimethoxybenzylamino, 2- (4-chlorophenyl) ethylamino, diphenylmethylamino, phenethylamino, N-benzylmethylamino, 4-iodoanilino, 3-nitrobenzylamino, (+/-)-endo-2- norbornaneamino, 2- (3-chlorophenyl) ethylamino, 3-phenyl- 1-propylamino, 3,5-dimethylanilino, 1,2,3,4- tetrahydroisoquinolino, 1,3,3-trimethyl-6- azabicyclo [3.2.1] octyl, 2-chloro-5-methylanilino, 3-

chloro-4-methoxyanilino, 4- (4-methoxyphenyl)-4- phenylpiperidino, 5-fluoro-2-methylanilino, 4- phenoxyanilino, tryptamino, cycloheptylamino, 2,4- difluorobenzylamino, 2-fluoro-5-methylanilino, 3,4- difluorobenzylamino, 1-methyl-3-phenylpropylamino, 2,4- dichlorophenethylamino, 2-indanamino, 3,4,5- trimethoxybenzylamino, 2-bromobenzylamino, 2-bromo-4- methylanilino, trans-2-phenylcyclopropylamino, 3-amino- 2,6-dimethoxypyridino, 5-chloro-2-methoxyanilino, 2- iodoanilino, 2,3-dimethoxybenzylamino, 2,6- difluorobenzylamino, 2,4-dimethoxyanilino, 4-chloro-2- methoxy-5-methylanilino, 1-amino-4-bromonaphthalene, 3- trifluoromethylbenzylamino, 3-chloro-2-methylanilino, 3- carboxamidoanilino, 2-fluorophenethylamino, 3- bromobenzylamino, 3-iodoanilino, 3-phenoxyanilino, 3,4- dimethoxyphenethylamino, 4-morpholinoanilino, 2- ethoxyanilino, tyramino, 2-trifluoromethylbenzylamino, 4- bromobenzylamino, 4-pentylanilino, 6,7-dimethoxy- 1,2,3,4-tetrahydroisoquinolino, 3- (l- (4-methoxyphenyl) ethyl) anilino, 1-adamantanamino, 2- thiazoleamino, 3-hydroxyanilino, 2- (4-aminophenyl)-6- methylbenzothiazolo, 3-methylsulphonylanilino, 4- propylanilino, 2-fluoro-4-methylanilino, 4- chlorobenzylamino, 3-fluorobenzylamino, 4-bromo-3- methylanilino, ()-a- (methylaminomethyl) benzyl alcohol, 5,6,7,8-tetrahydronaphthalene-1-amino, 3- methylbenzylamino, 4- (methylmercapto) anilino, 5-chloro-2- methylanilino, 4- (diethylamino) anilino, ()-a- methylbenzylamino, 2-chlorobenzylamino, 4- fluorobenzylamino, 2-methoxybenzylamino, 2- methylbenzylamino, 3-bromo-4-methylanilino, 4- fluorophenethylamino, 4-ethoxyanilino, 2,5- difluorobenzylamino, 2,3-dimethylanilino, benzylamino, 4- aminopyridino, 4-chloroanilino, 3-fluorophenethylamino, 4-bromoanilino, 4-hydroxyanilino, 4-bromo-2-

methylanilino, benzothiazol-2-amino, 6- methoxybenzothiazol-2-amino, 4-methylbenzylamino, 2,4- dimethylanilino, 6-fluorobenzothiazol-2-amino, 3- (methylmercapto) anilino, 2-methylanilino, 4-picolin-2- amino, 3-chloro-4-fluoroanilino, 4-fluoroanilino, 4- methoxybenzylamino, 3-ethoxyanilino, 4-methoxy-2- methylanilino, 4-methylanilino, 2,5-dimethylanilino, 2- methoxyanilino, 2-fluoroanilino, 3,5-dimethoxyanilino, 2- methoxy-5-methylanilino, 2-methoxy-5-nitroanilino, 2- (methylmercapto) anilino, cytosino, 3- trifluoromethylanilino, anilino, 3,4-dimethylanilino, 3,4,5-trimethoxyanilino, 2,5-dimethoxyanilino, 3- fluoroanilino, 3,4-dimethoxyanilino, 4- carboxamidoanilino, 2,4-difluoroanilino, 3- methoxyanilino, or 4-methoxyanilino; and Y is C (O) NH2.

In the above formula, the stereochemistry of chiral centers associated with the attached groups can independently be in the R or S configuration, or a mixture of the two.

In the above formula, the term''C1 to C6 alkyl" denotes such radicals as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, amyl, tert- amyl, hexyl and the like. A preferred''C1 to C6 alkyl" group is methyl.

The term"C2 to C alkenyl"denotes such radicals as vinyl, allyl, 2-butenyl, 3-butenyl, 2- pentenyl, 3-pentenyl, 4-pentenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 2-heptenyl, 3-heptenyl, 4-heptenyl, 5-heptenyl, 6-heptenyl, as well as dienes and trienes of straight and branched chains.

The term"C2 to C7 alkynyl"denotes such radicals as ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl, as well as di-and tri-ynes of straight and branched chains.

The term''C1 to C6 substituted alkyl,""C2 to Cl substituted alkenyl,"and"C2 to C7 substituted alkynyl," <BR> <BR> <BR> <BR> denotes that the above Ci to C6 alkyl groups and C2 to C7 alkenyl and alkynyl groups are substituted by one or more, and preferably one or two, halogen, hydroxy, protected hydroxy, oxo, protected oxo, cyclohexyl, naphthyl, amino, protected amino, (monosubstituted) amino, protected (monosubstituted) amino, (disubstituted) amino, guanidino, heterocyclic ring, substituted heterocyclic <BR> <BR> <BR> <BR> ring, imidazolyl, indolyl, pyrrolidinyl, C1 to C alkoxy,<BR> <BR> <BR> <BR> <BR> <BR> Ci to C7 acyl, C1 to C7 acyloxy, nitro, C1 to C7 alkyl ester, carboxy, protected carboxy, carbamoyl, carboxamide, protected carboxamide, N- (Ci to C6 alkyl) carboxamide, protected N- (Ci to C6 alkyl) carboxamide, N, N-di (C1 to C6alkyl) carboxamide, cyano, methylsulfonylamino, thio, Cl to C4 alkylthio or C, to C4 alkyl sulfonyl groups. The substituted alkyl, alkenyl and alkynyl groups may be substituted once or more and, preferably, once or twice, with the same or with different substituents.

Examples of the above substituted alkyl groups include the 2-oxo-prop-1-yl, 3-oxo-but-1-yl, cyanomethyl, nitromethyl, chloromethyl, hydroxymethyl, tetrahydropyranyloxymethyl, trityloxymethyl, propionyloxymethyl, amino, methylamino, aminomethyl, dimethylamino, carboxymethyl, allyloxycarbonylmethyl, allyloxycarbonylaminomethyl, methoxymethyl, ethoxymethyl, t-butoxymethyl, acetoxymethyl, chloromethyl, bromomethyl, iodomethyl, trifluoromethyl, 6-hydroxyhexyl, 2,4-

dichloro (n-butyl), 2-aminopropyl, chloroethyl, bromoethyl, fluoroethyl, iodoethyl, chloropropyl, bromopropyl, fluoropropyl, iodopropyl and the like.

Examples of the above substituted alkenyl groups include styrenyl, 3-chloro-propen-1-yl, 3-chloro- buten-1-yl, 3-methoxy-propen-2-yl, 3-phenyl-buten-2-yl, 1-cyano-buten-3-yl and the like. The geometrical isomerism is not critical, and all geometrical isomers for a given substituted alkenyl can be used.

Examples of the above substituted alkynyl groups include phenylacetylen-1-yl, 1-phenyl-2-propyn-1- yl and the like.

The term"oxo"denotes a carbon atom bonded to two additional carbon atoms substituted with an oxygen atom doubly bonded to the carbon atom, thereby forming a ketone moiety.

The term"protected oxo"denotes a carbon atom bonded to two additional carbon atoms substituted with two alkoxy groups or twice bonded to a substituted diol moiety, thereby forming an acyclic or cyclic ketal moiety.

The term''C1 to C, alkoxy"denotes groups such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, t- butoxy and like groups. A preferred alkoxy is methoxy.

The term''C1 to C acyloxy"denotes groups such as formyloxy, acetoxy, propionyloxy, butyryloxy, pentanoyloxy, hexanoyloxy, heptanoyloxy and the like.

Similarly, the term''C1 to C acyl"encompasses groups such as formyl, acetyl, propionyl, butyryl, pentanoyl, pivaloyl, hexanoyl, heptanoyl, benzoyl and the like. Preferred acyl groups are acetyl and benzoyl.

The term"C3 to C7 cycloalkyl"includes the cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl rings. The term"C3 to C7 substituted cycloalkyl"indicates the above cycloalkyl rings are substituted by one or two halogen, hydroxy, protected hydroxy, Ci to CE alkyl, C1 to C7 alkoxy, oxo, protected oxo, (monosubstituted) amino, (disubstituted) amino, trifluoromethyl, carboxy, protected carboxy, phenyl, substituted phenyl, amino, or protected amino groups.

The term tßCs to C7 cycloalkenyl"indicates a 1,2, or 3-cyclopentenyl ring, a 1,2,3 or 4-cyclohexenyl ring or a 1,2,3,4 or 5-cycloheptenyl ring, while the term "substituted Cs to C7 cycloalkenyl"denotes the above C5 to C, cycloalkenyl ring is substituted by a Ci to C6 alkyl radical, halogen, hydroxy, protected hydroxy, Cl to C7 alkoxy, trifluoromethyl, carboxy, protected carboxy, oxo, protected oxo, (monosubstituted) amino, protected (monosubstituted) amino (disubstituted) amino, phenyl, substituted phenyl, amino, or protected amino.

The term"heterocyclic ring"or"heterocyclic" denotes an optionally substituted five-membered or six- membered ring that has 1 to 4 heteroatoms, such as oxygen, sulfur and/or nitrogen and, in particular, nitrogen, either alone or in conjunction with sulfur or oxygen ring atoms. The five-membered or six-membered ring may be saturated, fully saturated or partially unsaturated, with a fully saturated ring being preferred.

An"amino-substituted heterocyclic ring"means any one of

the above-described heterocyclic rings is substituted with at least one amino group. Preferred heterocyclic rings include morpholino, piperidinyl, piperazinyl, tetrahydrofurano, pyrrolo, and tetrahydrothiophen-yl.

The term"substituted heterocycle"or "substituted heterocyclic ring"means the above-described heterocyclic ring is substituted with, for example, one or more, and preferably one or two, substituents which can be the same or different. The substituents can be halogen, hydroxy, protected hydroxy, cyano, nitro, C1 to <BR> <BR> <BR> C6 alkyl, Ci to C alkoxy, Cl to C substituted alkoxy, Ci<BR> <BR> <BR> <BR> <BR> to C acyl, Cl to C7 acyloxy, carboxy, protected carboxy, carboxymethyl, protected carboxymethyl, hydroxymethyl, protected hydroxymethyl, amino, protected amino, (monosubstituted) amino, protected (monosubstituted) amino, (disubstituted) amino carboxamide, protected carboxamide or trifluoromethyl groups.

The abbreviation"Ar"stands for an aryl group.

Aryl groups which can be used with present invention include phenyl, substituted phenyl, as defined above, heteroaryl, and substituted heteroaryl. The term "heteroaryl"means a heterocyclic aromatic derivative which is a five-membered or six-membered ring system having from 1 to 4 heteroatoms, such as oxygen, sulfur and/or nitrogen, in particular nitrogen, either alone or in conjunction with sulfur or oxygen ring atoms.

Examples of heteroaryls include pyridinyl, pyrimidinyl, and pyrazinyl, pyridazinyl, pyrrolo, furano, oxazolo, isoxazolo, thiazolo and the like.

The term"substituted heteroaryl"means the above-described heteroaryl is substituted with, for example, one or more, and preferably one or two,

substituents which are the same or different which substituents can be halogen, hydroxy, protected hydroxy, <BR> <BR> <BR> <BR> cyano, nitro, Ci to C6 alkyl, Ci to C7 alkoxy, C1 to C7<BR> <BR> <BR> <BR> <BR> <BR> acyl, Cl to C7 acyloxy, carboxy, protected carboxy, carboxymethyl, protected carboxymethyl, hydroxymethyl, protected hydroxymethyl, amino, protected amino, (monosubstituted) amino, protected (monosubstituted) amino, (disubstituted) amino carboxamide, protected carboxamide, N- (Cl to C6 alkyl) carboxamide, protected N- (Ci to C6 alkyl) carboxamide, N, N-di (C1 to C6 alkyl), trifluoromethyl, N-((C1 to C6 alkyl) sulfonyl) amino or N- (phenylsulfonyl) amino groups.

The term"C7 to C12 phenylalkyl"denotes a Cl to C6 alkyl group substituted at any position by a phenyl ring. Examples of such a group include benzyl, 2- phenylethyl, 3-phenyl (n-propyl), 4-phenylhexyl, 3- phenyl (n-amyl), 3-phenyl (sec-butyl) and the like.

Preferred C7 to C12 phenylalkyl groups are the benzyl and the phenylethyl groups.

The term"C7 to C12 substituted phenylalkyl" denotes a C7 to C12 phenylalkyl group substituted on the C, to C6 alkyl portion with one or more, and preferably one or two, groups chosen from halogen, hydroxy, protected hydroxy, oxo, protected oxo, amino, protected amino, monosubstituted) amino, protected (monosubstituted) amino, (disubstituted) amino, guanidino, heterocyclic ring, substituted heterocyclic ring, Ci to C7 alkoxy, Ci to C7 <BR> <BR> <BR> <BR> acyl, Ci to C7 acyloxy, nitro, carboxy, protected carboxy, carbamoyl, carboxamide, protected carboxamide, N- (Ci to C6 alkyl) carboxamide, protected N- (Ci to C6 alkyl) carboxamide, N, N- (Ci to C6 dialkyl) carboxamide, <BR> <BR> <BR> cyano, N- (C1 to C6 alkylsulfonyl) amino, thiol, C1 to C4<BR> <BR> <BR> <BR> <BR> <BR> alkylthio, C1 to C4 alkylsulfonyl groups ; and/or the

phenyl group may be substituted with one or more and, preferably, one or two substituents chosen from halogen, hydroxy, protected hydroxy, cyano, nitro, Ci to C6 alkyl, <BR> <BR> <BR> <BR> Ci to C7 alkoxy, C1to C7 acyl, C1 to C7 acyloxy, carboxy, protected carboxy, carboxymethyl, protected carboxymethyl, hydroxymethyl, protected hydroxymethyl, amino, protected amino, (monosubstituted) amino, protected (monosubstituted) amino, (disubstituted) amino, carboxamide, protected carboxamide, N- (Ci to C6 alkyl) carboxamide, protected N- (Cl to C6 alkyl) carboxamide, N, N-di (C1 to C6 alkyl) carboxamide, trifluoromethyl, N- ( (Ci to C6 alkyl) sulfonyl) amino, N- (phenylsulfonyl) amino or a phenyl group, substituted or unsubstituted, for a resulting biphenyl group. The substituted alkyl or phenyl groups may be substituted with one or more and, preferably, one or two substituents which can be the same or different.

Examples of the term"C7 to C12 substituted phenylalkyl"include groups such as 2-phenyl-1- chloroethyl, 2- (4-methoxyphenyl) ethyl, 4- (2,6-dihydroxy phenyl)-n-hexyl, 2- (5-cyano-3-methoxyphenyl)-n-pentyl, 3- (2,6-dimethylphenyl)-n-propyl, 4-chloro-3-aminobenzyl, 6- (4-methoxyphenyl)-3-carboxy (n-hexyl), 5- (4- aminomethylphenyl)-3- (aminomethyl)-n-pentyl, 5-phenyl-3- oxo-n-pent-1-yl and the like.

The term"substituted phenyl"specifies a phenyl group substituted with one or more, and preferably one or two, moieties chosen from the groups consisting of halogen, hydroxy, protected hydroxy, cyano, nitro, C1 to <BR> <BR> <BR> <BR> C6 alkyl, Ci to C7 alkoxy, C1to C7 acyl, C1 to C7 acyloxy, carboxy, protected carboxy, carboxymethyl, protected carboxymethyl, hydroxymethyl, protected hydroxymethyl, amino, protected amino, (monosubstituted) amino, protected

(monosubstituted) amino, (disubstituted) amino, carboxamide, protected carboxamide, N- (Ci to CE alkyl) carboxamide, protected N- (C1 to C6 alkyl) carboxamide, N, N-di (Cl to C6alkyl) carboxamide, trifluoromethyl, N-((C1 to C6 alkyl) sulfonyl) amino, N- (phenylsulfonyl) amino or phenyl, substituted or unsubstituted, such that, for example, a biphenyl results.

Examples of the term"substituted phenyl" include a mono-or di (halo) phenyl group such as 2,3 or 4-chlorophenyl, 2,6-dichlorophenyl, 2,5-dichlorophenyl, 3,4-dichlorophenyl, 2,3 or 4-bromophenyl, 3,4- dibromophenyl, 3-chloro-4-fluorophenyl, 2,3 or 4- fluorophenyl and the like; a mono or di (hydroxy) phenyl group such as 2,3 or 4-hydroxyphenyl, 2,4- dihydroxyphenyl, the protected-hydroxy derivatives thereof and the like ; a nitrophenyl group such as 2,3 or 4-nitrophenyl ; a cyanophenyl group, for example, 2,3 or 4-cyanophenyl ; a mono-or di (alkyl) phenyl group such as 2,3 or 4-methylphenyl, 2,4-dimethylphenyl, 2,3 or 4- (iso-propyl) phenyl, 2,3 or 4-ethylphenyl, 2,3 or 4- (n- propyl) phenyl and the like ; a mono or di (alkoxyl) phenyl group, for example, 2,6-dimethoxyphenyl, 2,3 or 4- methoxyphenyl, 2,3 or 4-ethoxyphenyl, 2,3 or 4- (isopropoxy) phenyl, 2,3 or 4- (t-butoxy) phenyl, 3-ethoxy- 4-methoxyphenyl and the like; 2,3 or 4- trifluoromethylphenyl ; a mono-or dicarboxyphenyl or (protected carboxy) phenyl group such as 2,3 or 4- carboxyphenyl or 2,4-di (protected carboxy) phenyl; a mono- or di (hydroxymethyl) phenyl or (protected hydroxymethyl) phenyl such as 2,3, or 4- (protected hydroxymethyl) phenyl or 3,4-di (hydroxymethyl) phenyl ; a mono-or di (aminomethyl) phenyl or (protected aminomethyl) phenyl such as 2,3 or 4- (aminomethyl) phenyl

or 2,4- (protected aminomethyl) phenyl ; or a mono-or di (N- (methylsulfonylamino)) phenyl such as 2,3 or 4- (N- (methylsulfonylamino)) phenyl. Also, the term "substituted phenyl"represents disubstituted phenyl groups wherein the substituents are different, for example, 3-methyl-4-hydroxyphenyl, 3-chloro-4- hydroxyphenyl, 2-methoxy-4-bromophenyl, 4-ethyl-2- hydroxyphenyl, 3-hydroxy-4-nitrophenyl, 2-hydroxy 4- chlorophenyl and the like.

The term"substituted aniline"specifies an aniline group substituted with one or more, and preferably one or two, moieties chosen from the groups consisting of halogen, hydroxy, protected hydroxy, cyano, <BR> <BR> <BR> <BR> <BR> nitro, C1 to C6 alkyl, Cl to C7 alkoxy, Cito Cy acyi, Ci to C7 acyloxy, carboxy, protected carboxy, carboxymethyl, protected carboxymethyl, hydroxymethyl, protected hydroxymethyl, amino, protected amino, (monosubstituted) amino, protected (monosubstituted) amino, (disubstituted) amino, carboxamide, protected carboxamide, N- (Cl to C6 alkyl) carboxamide, protected N- (Ci to C6 alkyl) carboxamide, N, N-di (Ci to C6 alkyl) carboxamide, trifluoromethyl, N-((C1 to C6 alkyl) sulfonyl) amino and N- (phenylsulfonyl) amino.

Examples of substituted anilines include, for example, 2-fluoroanilinyl, 3-fluoroanilinyl, 4- fluoroanilinyl, 2-chloroanilinyl, 3-chloroanilinyl, 4- chloroanilinyl, 2-bromoanilinyl, 3-bromoanilinyl, 4- bromoanilinyl, 2-methoxyanilinyl, 3-methoxyanilinyl, 4- methoxyanilinyl, 2-hydroxyanilinyl, 3-hydroxyanilinyl, 4- hydroxyanilinyl, 2-carboethoxyanilinyl, 3- carboethoxyanilinyl, 4-carboethoxyanilinyl, 2- trifluoromethylanilinyl, 3-trifluoromethylanilinyl, 4- trifluoromethylanilinyl, 2-dimethylaminoanilinyl, 3-

dimethylaminoanilinyl, 4-dimethylaminoanilinyl, 2- phenoxyanilinyl, 3-phenoxyanilinyl, 4-phenoxyanilinyl, 3,4-methylenedioxyanilinyl, 2,3-methylenedioxyanilinyl, 2,3-difluoroanilinyl, 2,3-dibromoanilinyl, 3,4- dibromoanilinyl, 2,3-dimethoxyanilinyl, 3,4- dimethoxyanilinyl, 1-amino-5,6,7,8-tetrahydronaphthyl, 2- hydroxy-3-amino-5,6,7,8-tetrahydronaphthyl, 2- aminonaphthyl, 1-amino-4-chloronaphthyl, 1-amino-4- bromonaphthyl, 5-amino-l-hydroxynaphthyl, 1-amino-2- hydroxynaphthyl, 5-aminoindanyl, 1-aminofluorenyl, 2- aminofluorenyl and N-methylanilinyl.

The term"substituted naphthyl"specifies a naphthyl group substituted with one or more, and preferably one or two, moieties either on the same ring or on different rings chosen from the groups consisting of halogen, hydroxy, protected hydroxy, cyano, nitro, Ci to C6 alkyl, C, to C alkoxy, C1 to C, acyl, Ci to C acyloxy, carboxy, protected carboxy, carboxymethyl, protected carboxymethyl, hydroxymethyl, protected hydroxymethyl, amino, protected amino, (monosubstituted) amino, protected (monosubstituted) amino, (disubstituted) amino, carboxamide, protected carboxamide, N- (Ci to C6 alkyl) carboxamide, protected N- (Ci to C6 alkyl) carboxamide, N, N-di (C1 to C6 alkyl) carboxamide, trifluoromethyl, N-((C1 to C6 alkyl) sulfonyl) amino or N- (phenylsulfonyl) amino.

Examples of the term"substituted naphthyl" include a mono or di (halo) naphthyl group such as 1,2,3, 7 or 8-chloronaphthyl, 2,6-dichloronaphthyl, 2, 5-dichloronaphthyl, 3,4-dichloronaphthyl, 1,2,3,4,5, 6,7 or 8-bromonaphthyl, 3,4-dibromonaphthyl, 3-chloro- 4-fluoronaphthyl, 1,2,3,4,5,6,7 or 8-fluoronaphthyl and the like ; a mono or di (hydroxy) naphthyl group such as

1,2,3,4,5,6,7 or 8-hydroxynaphthyl, 2,4- dihydroxynaphthyl, the protected-hydroxy derivatives thereof and the like; a nitronaphthyl group such as 3-or 4-nitronaphthyl; a cyanonaphthyl group, for example, 1, 2,3,4,5,6,7 or 8-cyanonaphthyl; a mono-or di (alkyl) naphthyl group such as 2,3,4,5,6,7 or 8- methylnaphthyl, 1,2,4-dimethylnaphthyl, 1,2,3,4,5, 6,7 or 8- (isopropyl) naphthyl, 1,2,3,4,5,6,7 or 8- ethylnaphthyl, 1,2,3,4,5,6,7 or 8- (n- propyl) naphthyl and the like; a mono or di (alkoxy) naphthyl group, for example, 2,6- dimethoxynaphthyl, 1,2,3,4,5,6,7 or 8- methoxynaphthyl, 1,2,3,4,5,6,7 or 8-ethoxynaphthyl, 1,2,3,4,5,6,7 or 8- (isopropoxy) naphthyl, 1,2,3, 4,5,6,7 or 8- (t-butoxy) naphthyl, 3-ethoxy-4- methoxynaphthyl and the like ; 1,2,3,4,5,6,7 or 8- trifluoromethylnaphthyl ; a mono-or dicarboxynaphthyl or (protected carboxy) naphthyl group such as 1,2,3,4,5, 6,7 or 8-carboxynaphthyl or 2,4-di (-protected carboxy) naphthyl; a mono-or di (hydroxymethyl) naphthyl or (protected hydroxymethyl) naphthyl such as 1,2,3,4,5, 6,7 or 8- (protected hydroxymethyl) naphthyl or 3,4- di (hydroxymethyl) naphthyl; a mono-or di (amino) naphthyl or (protected amino) naphthyl such as 1,2,3,4,5,6,7 or 8- (amino) naphthyl or 2,4- (protected amino)-naphthyl, a mono-or di (aminomethyl) naphthyl or (protected aminomethyl) naphthyl such as 2,3, or 4- (aminomethyl) naphthyl or 2,4- (protected aminomethyl)- naphthyl; or a mono-or di- (N-methylsulfonylamino) naphthyl such as 1,2,3,4,5,6,7 or 8- (N- methylsulfonylamino) naphthyl. Also, the term "substituted naphthyl"represents disubstituted naphthyl groups wherein the substituents are different, for example, 3-methyl-4-hydroxynaphth-1-yl, 3-chloro-4- hydroxynaphth-2-yl, 2-methoxy-4-bromonaphth-1-yl, 4-

ethyl-2-hydroxynaphth-1-yl, 3-hydroxy-4-nitronaphth-2-yl, 2-hydroxy-4-chloronaphth-1-yl, 2-methoxy-7-bromonaphth-1- yl, 4-ethyl-5-hydroxynaphth-2-yl, 3-hydroxy-8- nitronaphth-2-yl, 2-hydroxy-5-chloronaphth-1-yl and the like.

The terms"halo"and"halogen"refer to the fluoro, chloro, bromo or iodo groups. There can be one or more halogen, which are the same or different.

Preferred halogens are chloro and fluoro.

The term" (monosubstituted) amino" refers to an amino group with one substituent chosen from the group consisting of phenyl, substituted phenyl, Cl to C6 alkyl, <BR> <BR> <BR> <BR> Ci to C6 substituted alkyl, C1 to C7 acyl, C2 to C7 alkenyl, C2 to C7 substituted alkenyl, C2 to C, alkynyl, C2 to C7 substitued alkynyl, C7 to C12 phenylalkyl, C7 to CI-2 substituted phenylalkyl and heterocyclic ring. The (monosubstituted) amino can additionally have an amino- protecting group as encompassed by the term"protected (monosubstituted) amino." The term" (disubstituted) amino" refers to amino groups with two substituents chosen from phenyl, substituted phenyl, C1 to C6 alkyl, Ci to C6 substituted <BR> <BR> <BR> <BR> alkyl, C, to C7 acyl, C2 to C7 alkenyl, C2 to C7 alkynyl, C,<BR> <BR> <BR> <BR> <BR> <BR> to C12 phenylalkyl or C7 to C12 substituted phenylalkyl.

The two substituents can be the same or different.

The term"amino-protecting group"as used herein refers to substituents of the amino group commonly employed to block or protect the amino functionality while reacting other functional groups of the molecule.

The term"protected (monosubstituted) amino" means there is an amino-protecting group on the monosubstituted amino

nitrogen atom. In addition, the term"protected carboxamide"means there is an amino-protecting group on the carboxamide nitrogen.

Examples of such amino-protecting groups include the formyl ("For") group, the trityl group, the phthalimido group, the trichloroacetyl group, the chloroacetyl, bromoacetyl, and iodoacetyl groups, urethane-type blocking groups, such as t-butoxycarbonyl ("Boc"), 2- (4-biphenylyl) propyl-2-oxycarbonyl ("Bpoc"), 2-phenylpropyl-2-oxycarbonyl ("Poc"), 2- (4- xenyl) isopropoxycarbonyl, 1,1-diphenylethyl-l- oxycarbonyl, 1,1-diphenylpropyl-1-oxycarbonyl, 2- (3,5- dimethoxyphenyl) propyl-2-oxycarbonyl ("Ddz"), 2- (p- toluyl) propyl-2-oxycarbonyl, cyclopentanyloxycarbonyl, 1-methylcyclopentanyloxycarbonyl, cyclohexanyloxy- carbonyl, 1-methylcyclohexanyloxycarbonyl, 2-methylcyclohexanyloxycarbonyl, 2- (4- toluylsulfonyl) ethoxycarbonyl, 2- (methylsulfonyl) ethoxycarbonyl, 2- (triphenylphosphino)- ethoxycarbonyl, 9-fluorenylmethoxycarbonyl ("Fmoc"), 2- (trimethylsilyl) ethoxycarbonyl, allyloxycarbonyl, 1- (trimethylsilylmethyl) prop-1-enyloxycarbonyl, 5- benzisoxalylmethoxycarbonyl, 4-acetoxybenzyloxycarbonyl, 2,2,2-trichloroethoxycarbonyl, 2-ethynyl-2- propoxycarbonyl, cyclopropylmethoxycarbonyl, isobornyloxycarbonyl, 1-piperidyloxycarbonyl, benzyloxycarbonyl ("Cbz"), 4-phenylbenzyloxycarbonyl, 2- methylbenzyloxy-carbonyl, a-2,4,5,- tetramethylbenzyloxycarbonyl ("Tmz"), 4- methoxybenzyloxycarbonyl, 4-fluorobenzyloxycarbonyl, 4-chlorobenzyloxycarbonyl, 3-chlorobenzyloxycarbonyl, 2-chlorobenzyloxycarbonyl, 2,4-dichlorobenzyloxycarbonyl, 4-bromobenzyloxycarbonyl, 3-bromobenzyloxycarbonyl, 4-nitrobenzyloxycarbonyl, 4-cyanobenzyloxycarbonyl,

4- (decyloxy) benzyloxycarbonyl and the like ; the benzoylmethylsulfonyl group, dithiasuccinoyl ("Dts"), the 2- (nitro) phenylsulfenyl group ("Nps"), the diphenyl- phosphine oxide group and like amino-protecting groups.

The species of amino-protecting group employed is not critical so long as the derivatized amino group is stable to the conditions of the subsequent reaction (s) and can be removed at the appropriate point without disrupting the remainder of the compounds. Preferred amino- protecting groups are Boc, Cbz and Fmoc. Further examples of amino-protecting groups embraced by the above term are well known in organic synthesis and the peptide art and are described by, for example, T. W. Greene and P. G. M. Wuts,"Protective Groups in Organic Synthesis," 2nd ed., John Wiley and Sons, New York, NY, 1991, Chapter 7, M. Bodanzsky,"Principles of Peptide Synthesis,"1st and 2nd revised ed., Springer-Verlag, New York, NY, 1984 and 1993, and Stewart and Young,"Solid Phase Peptide Synthesis,"2nd ed., Pierce Chemical Co., Rockford, IL, 1984, each of which is incorporated herein by reference.

The related term"protected amino"defines an amino group substituted with an amino-protecting group discussed above.

The term"carboxy-protecting group"as used herein refers to one of the ester derivatives of the carboxylic acid group commonly employed to block or protect the carboxylic acid group while reactions are carried out on other functional groups on the compound.

Examples of such carboxylic acid protecting groups include t-butyl, 4-nitrobenzyl, 4-methoxybenzyl, 3,4- dimethoxybenzyl, 2,4-dimethoxybenzyl, 2,4,6- trimethoxybenzyl, 2,4,6-trimethylbenzyl, pentamethylbenzyl, 3,4-methylenedioxybenzyl, benzhydryl, 4,4'-dimethoxytrityl, 4,4', 4"-trimethoxytrityl, 2-

phenylpropyl, trimethylsilyl, t-butyldimethylsilyl, phenacyl, 2,2,2-trichloroethyl, P- (trimethylsilyl) ethyl, P- (di (n-butyl) methylsilyl) ethyl, p-toluenesulfonylethyl, 4-nitrobenzylsulfonylethyl, allyl, cinnamyl, 1- (trimethylsilylmethyl)-propenyl and like moieties. The species of carboxy-protecting group employed is not critical so long as the derivatized carboxylic acid is stable to the conditions of subsequent reaction (s) and can be removed at the appropriate point without disrupting the remainder of the molecule. Further examples of these groups are found in E. Haslam, "Protective Groups in Organic Chemistry,"J. G. W. McOmie, Ed., Plenum Press, New York, NY, 1973, Chapter 5, and T. W. Greene and P. G. M. Wuts,"Protective Groups in Organic Synthesis,"2nd ed., John Wiley and Sons, New York, NY, 1991, Chapter 5, each of which is incorporated herein by reference. A related term is"protected carboxy,"which refers to a carboxy group substituted with one of the above carboxy-protecting groups.

The term"protected hydroxy"denotes a hydroxy group bonded to a"hydroxy-protecting group."The term "hydroxy-protecting group"refers to a readily cleavable group bonded to a hydroxy group, such as the tetrahydropyranyl, 2-methoxypropyl, 1-ethoxyethyl, methoxymethyl, 2-methoxyethoxymethyl, methylthiomethyl, t-butyl, t-amyl, trityl, 4-methoxytrityl, 4,4'- dimethoxytrityl, 4,4', 4"-trimethoxytrityl, benzyl, allyl, trimethylsilyl, (t-butyl) dimethylsilyl, 2,2,2- trichloroethoxycarbonyl groups and the like. The term "protected hydroxymethyl"is similarly defined.

The species of hydroxy-protecting group is not critical so long as the derivatized hydroxyl group is stable to the conditions of subsequent reaction (s) and

can be removed at the appropriate point without disrupting the remainder of the molecule. Further examples of hydroxy-protecting groups are described by C. B. Reese and E. Haslam,"Protective Groups in Organic Chemistry,"J. G. W. McOmie, Ed., Plenum Press, New York, NY, 1973, Chapters 3 and 4, respectively, and T. W. Greene and P. G. M. Wuts,"Protective Groups in Organic Synthesis,"2nd ed., John Wiley and Sons, New York, NY, 1991, Chapters 2 and 3.

The term"Ci to C4 alkylthio"refers to sulfide groups such as methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, t-butylthio and like groups.

The term"Cl to C4 alkylsulfoxide"indicates sulfoxide groups such as methylsulfoxide, ethylsulfoxide, n-propylsulfoxide, isopropylsulfoxide, n-butylsulfoxide, sec-butylsulfoxide and the like.

The term"Cl to C alkylsulfonyl"encompasses groups such as methylsulfonyl, ethylsulfonyl, n- propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, t- butylsulfonyl and the like.

By"substituted phenylthio,""substituted phenyl sulfoxide,"and"substituted phenylsulfonyl"is meant that the phenyl can be substituted as described above in relation to"substituted phenyl." <BR> <BR> <BR> <BR> <BR> <BR> <BR> <BR> The terms"cyclic C2 to C alkylene,"<BR> <BR> <BR> <BR> <BR> <BR> <BR> "substituted cyclic C2 to C7 alkylene,""cyclic C2 to C7 heteroalkylene,"and"substituted cyclic C2 to C7 heteroalkylene,"define such a cyclic group bonded to the phenyl radical resulting in a bicyclic ring system. The cyclic group may be saturated or contain one or two

double bonds. Furthermore, the cyclic group may have one or two methylene or methine groups replaced by one or two oxygen, nitrogen or sulfur atoms which are the the cyclic C2 to C-, heteroalkylene.

The cyclic alkylene or heteroalkylene group may be substituted once or twice by the same or different substituents selected from the group consisting of the following moieties: hydroxy, protected hydroxy, carboxy, protected carboxy, oxo, protected oxo, Ci to C4 acyloxy, <BR> <BR> <BR> <BR> formyl, C1 to C acyl, Ci to C6 alkyl, carbamoyl, C1 to C<BR> <BR> <BR> <BR> <BR> <BR> alkoxy, C, to C4 alkylthio, C, to C4 alkylsulfoxide, C, to<BR> <BR> <BR> <BR> <BR> <BR> <BR> C4 alkylsulfonyl, halo, amino, protected amino, (monosubstituted) amino, protected (monosubstituted) amino, (disubstituted) amino, hydroxymethyl or a protected hydroxymethyl.

The cyclic alkylene or heteroalkylene group fused onto the benzene radical preferably contains three to six members. Examples of such saturated cyclic groups are when the resultant bicyclic ring system is 2,3- dihydro-indanyl and a tetralin ring. When the cyclic groups are unsaturated, examples occur when the resultant bicyclic ring system is a naphthyl ring or indolyl.

Examples of fused cyclic groups which each contain one nitrogen atom and one or more double bond, preferably one or two double bonds, are when the phenyl is fused to a pyridino, pyrano, pyrrolo, pyridinyl, dihydropyrrolo, or dihydropyridinyl ring. Examples of fused cyclic groups which each contain one oxygen atom and one or two double bonds are when the phenyl ring is fused to a furo, pyrano, dihydrofurano, or dihydropyrano ring. Examples of fused cyclic groups which each have one sulfur atom and contain one or two double bonds are when the phenyl is fused to a thieno, thiopyrano, dihydrothieno or

dihydrothiopyrano ring. Examples of cyclic groups which contain two heteroatoms selected from sulfur and nitrogen and one or two double bonds are when the phenyl ring is fused to a thiazolo, isothiazolo, dihydrothiazolo or dihydroisothiazolo ring. Examples of cyclic groups which contain two heteroatoms selected from oxygen and nitrogen and one or two double bonds are when the benzene ring is fused to an oxazolo, isoxazolo, dihydrooxazolo or dihydroisoxazolo ring. Examples of cyclic groups which contain two nitrogen heteroatoms and one or two double bonds occur when the benzene ring is fused to a pyrazolo, imidazolo, dihydropyrazolo or dihydroimidazolo ring or pyrazinyl.

Unless otherwise defined herein, any substituent term ending in"ene"means that such substituent connects two separate additional groups. For example, the term"C3 to Cl cycloalkylene"means a cycloalkyl, as defined above, where the cycloalkyl radical connects two separate additional groups.

One or more of the isoquinoline derivatives, even within a given library, may be present as a salt.

The term"salt"encompasses those salts that form with the carboxylate anions and amine nitrogens and include salts formed with the organic and inorganic anions and cations discussed below. Furthermore, the term includes salts that form by standard acid-base reactions with basic groups (such as amino groups) and organic or inorganic acids. Such acids include hydrochloric, sulfuric, phosphoric, acetic, succinic, citric lactic, maleic, fumaric, palmitic, cholic, pamoic, mucic, D- glutamic, d-camphoric, glutaric, phthalic, tartaric, lauric, stearic, salicyclic, methanesulfonic,

benzenesulfonic, sorbic, picric, benzoic, cinnamic, and like acids.

The term"organic or inorganic cation"refers to counterions for the carboxylate anion of a carboxylate salt. The counter-ions are chosen from the alkali and alkaline earth metals, (such as lithium, sodium, potassium, barium, aluminum and calcium); ammonium and mono-, di-and tri-alkyl amines such as trimethylamine, cyclohexylamine ; and the organic cations, such as dibenzylammonium, benzylammonium, 2-hydroxyethylammonium, bis (2-hydroxyethyl) ammonium, phenylethylbenzylammonium, dibenzylethylenediammonium, and like cations. See, for <BR> <BR> <BR> <BR> example,"Pharmaceutical Salts,"Berge et al., J. Pharm. _ Sci., 66: 1-19 (1977), which is incorporated herein by reference. Other cations encompassed by the above term include the protonated form of procaine, quinine and N- methylglucosamine, and the protonated forms of basic amino acids such as glycine, ornithine, histidine, phenylglycine, lysine and arginine. Furthermore, any zwitterionic form of the instant compounds formed by a carboxylic acid and an amino group is referred to by this term. For example, a cation for a carboxylate anion will exist when R2 or R3 is substituted with a (quaternary ammonium) methyl group. A preferred cation for the carboxylate anion is the sodium cation.

The compounds of the above formula can also exist as solvates and hydrates. Thus, these compounds may crystallize with, for example, waters of hydration, or one, a number of, or any fraction thereof of molecules of the mother liquor solvent. The solvates and hydrates of such compounds are included within the scope of this invention.

One or more isoquinoline derivatives, even when in a combinatorial library, can be in the biologically active ester form, such as the non-toxic, metabolically- labile ester-form. Such ester forms induce increased blood levels and prolong the efficacy of the corresponding non-esterified forms of the compounds.

Ester groups which can be used include the lower alkoxymethyl groups, for example, methoxymethyl, ethoxymethyl, isopropoxymethyl and the like; the a- (C, to C,) alkoxyethyl groups, for example methoxyethyl, ethoxyethyl, propoxyethyl, isopropoxyethyl and the like; the 2-oxo-1,3-diooxlen-4-ylmethyl groups, such as 5- methyl-2-oxo-1,3-dioxolen-4-ylmethyl, 5-phenyl-2-oxo-1,3- dioxolen-4-ylmethyl and the like ; the C1 to C4 alkylthiomethyl groups, for example methylthiomethyl, ethylthiomethyl, iso-propylthiomethyl and the like ; the acyloxymethyl groups, for example pivaloyloxymethyl, pivaloyloxyethyl, a-acetoxymethyl and the like ; the ethoxycarbonyl-1-methyl group; the a-acetoxyethyl ; the 1- <BR> <BR> <BR> <BR> (C1 to C alkyloxycarbonyloxy) ethyl groups such as the 1-<BR> <BR> <BR> <BR> <BR> <BR> <BR> (ethoxycarbonyloxy) ethyl group ; and the l- (Ci to C, alkylaminocarbonyloxy) ethyl groups such as the 1- (methylaminocarbonyloxy) ethyl group.

The term"amino acid"includes any one of the twenty naturally-occurring amino acids or the D-form of any one of the naturally-occurring amino acids. In addition, the term"amino acid"also includes other non- naturally occurring amino acids besides the D-amino acids, which are functional equivalents of the naturally- occurring amino acids. Such non-naturally-occurring amino acids include, for example, norleucine ("Nle"), norvaline ("Nva"), (3-Alanine, L-or D-naphthalanine, ornithine ("Orn"), homoarginine (homoArg) and others well known in the peptide art, such as those described in M.

Bodanzsky,"Principles of Peptide Synthesis,"1st and 2nd revised ed., Springer-Verlag, New York, NY, 1984 and 1993, and Stewart and Young,"Solid Phase Peptide Synthesis,"2nd ed., Pierce Chemical Co., Rockford, IL, 1984, both of which are incorporated herein by reference.

Amino acids and amino acid analogs can be purchased commercially (Sigma Chemical Co.; Advanced Chemtech) or synthesized using methods known in the art.

The amino acids are indicated herein by either their full name or by the commonly known three letter code. Further, in the naming of amino acids,"D-" designates an amino acid having the"D"configuration, as opposed to the naturally occurring L-amino acids. Where no specific configuration is indicated, one skilled in the art would understand the amino acid to be an L-amino acid. The amino acids can, however, also be in racemic mixtures of the D-and L-configuration.

As used herein, the phrase"any one of the twenty naturally-occurring amino acids"means any one of the following: Ala, Arg, Asn, Asp, Cys, Gln, Glu, Gly, His, Ile, Leu, Lys, Met, Phe, Pro, Ser, Thr, Trp, Tyr, and Val. As used herein, the language"the D-form of a naturally-occurring amino acid"means the D-isomer of any one of these naturally-occurring amino acids, with the exception of Gly, which does not occur as D or L isomers.

The term"functionalized resin"means any resin, crosslinked or otherwise, where functional groups have been introduced into the resin, as is common in the art. Such resins include, for example, those functionalized with amino, alkylhalo, formyl or hydroxy groups. Such resins which can serve as solid supports are well known in the art and include, for example,

4-methylbenzhydrylamine-copoly (styrene-l% divinylbenzene) (MBHA), 4-hydroxymethylphenoxymethyl-copoly (styrene-1% divinylbenzene), 4-oxymethyl-phenyl-acetamido- copoly (stryene-l% divinylbenzene) (Wang), 4- (oxymethyl)- phenylacetamido methyl (Pam), and TentagelTM, from Rapp Polymere Gmbh, trialkoxy-diphenyl-methyl ester- copoly (styrene-l% divinylbenzene) (RINK) all of which are commercially available. Other functionalized resins are known in the art and can be use without departure from the scope of the current invention. Such resins may include those described in Jung, G., Combinatorial Peptide and Nonpeptide Libraties, A Handbook (VCH Verlag, 1996) or Bunin, B. A., The Combinatorial Index (Academic Press, 1998) and are incorporated herein by reference.

As used herein, a"combinatorial library"is an intentionally created collection of differing molecules which can be prepared by the means provided below or otherwise and screened for biological activity in a variety of formats (e. g., libraries of soluble molecules, libraries of compounds attached to resin beads, silica chips or other solid supports). A"combinatorial library,"as defined above, involves successive rounds of chemical syntheses based on a common starting structure.

The combinatorial libraries can be screened in any variety of assays, such as those detailed below as well as others useful for assessing their biological activity.

The combinatorial libraries will generally have at least one active compound and are generally prepared such that the compounds are in equimolar quantities.

Compounds disclosed in previous work that are not in an intentially created collection are not part of a"combinatorial library"of the invention. In addition, compounds that are in an unintentional or undesired

mixture are not part of a"combinatorial library"of the invention.

A combinatorial library of the invention can contain two or more of the above-described compounds.

The invention further provides a combinatorial library containing five or more of the above-described compounds.

In another embodiment of the invention, a combinatorial library can contain ten or more of the above-described compounds. In yet another embodiment of the invention, a combinatorial library can contain fifty or more of the above-described compounds. If desired, a combinatorial library of the invention can contain 100,000 or more, or even 1,000,000 or more, of the above-described compounds.

The compounds of the present formula and combinatorial libraries containing the same can be prepared as set forth below. It should be appreciated that the substituents discussed herein are merely exemplary and other groups can be used. For example, homophthalic anhydride, discussed below, wherein each of R3, R, R5, and R6 are a hydrogen atom, is only an exemplary anhydride, and that other anhydrides having the above-defined R3, R4, R5 and R6 substituents can alternatively be used.

In brief, the isoquinoline compounds of the present invention were prepared as follows. A solid support resin-bound amine was reacted with bromoacetic acid to produce resin bound-CH2NHC (O) CH2Br (i. e., -"Y"CH2Br). The Rl group, for example, R1l-NH2, was then coupled, displacing the bromine and thus yielding resin bound-CH2NHC (O) CH2NH-Rll. To this is coupled a protected amino acid (i. e., Boc-NH-CH2-R7-R8-R9-C (0) OH) which was then deprotected to form resin bound-CH2NHC (O) CH2NH-R---

C (o)-R9-R8-R7-CH2-NH2, which, for purposes of describing the remainder of the reaction scheme, is now referred to as"resin bound-Y-Rl-NH2." This resin bound amine is reacted with an aldehyde (2) and, thereby, converted to the corresponding imine (3). Addition of a cyclic anhydride, such as homophthalic anhydride (4), yields isoquinoline, as shown below in Reaction Scheme I. See also Figure 1.

REACTION SCHEME I

More specifically, preparation of the isoquinolines and libraries containing the same were prepared by the more detailed steps decribed in Example 52, below.

Exemplary aldehydes used in the above reaction scheme are 1,4-benzodioxan-6-carboxaldehyde, 1- methylindole-3-carboxaldehyde, 2,3-difluorobenzaldehyde, 2-bromobenzaldehyde, 2-chloro-5-nitrobenzaldehyde, 2- furaldehyde, 2-imidazolecarboxaldehyde, 2-naphthaldehyde,

2-pyridinecarboxaldehyde, 2-thiophenecarboxaldehyde, 3,4- dichlorobenzaldehyde, 3,5-bis (trifluoromethyl) benzaldehyde, 3,5-dihydroxybenzaldehyde, 3,5- dimethoxybenzaldehyde, 3,5,-dimethyl-4- hydroxybenzaldehyde, 3- (4-methoxyphenoxy) benzaldehyde, 3-furaldehyde, 3- hydroxybenzaldehyde, 3-methyl-4-methoxybenzaldehyde, 3- methylbenzaldehyde, 3-nitrobenzaldehyde, 3- pyridinecarboxaldehyde, 3-thiophenecarboxaldehyde, 4- (3- dimethylaminopropoxy) benzaldehyde, 4- (dimethylamino) benzaldehyde, 4- (methylthio) benzaldehyde, 4- (trifluoromethyl) benzaldehyde, 4-biphenylcarboxaldehyde, 4-bromo-2- thiophenecarboxaldehyde, 4-cyanobenzaldehyde, 4-methoxy- 1-naphthaldehyde, 4-nitrobenzaldehyde, 4-pyridinecarboxaldehyde, 5- (hydroxymethyl)-2- furaldehyde, 5-bromo-4-hydroxy-3-methoxybenzaldehyde, 5- nitro-2-furaldehyde, 6-methyl-2-pyridinecarboxaldehyde, and benzaldehyde.

Isoquinoline 4-carboxylic acids can be converted to alternatively substituted compounds having an amide or ester, or other functionality as defined by X, following Reaction Schemes III and IV. Briefly, as shown in Reaction Scheme III, condensation of the isoquinoline 4-carboxylic acid prepared by the above Reaction Schemes, is condensed with an amine or alcohol (4) in an aprotic solvent such as DMF to furnish the substituted isoquinoline (5).

REACTION SCHEME III

More specifically, as shown in Reaction Scheme IV, preparation of the library containing alternatively substituted isoquinolines other than 4-carboxylic acids involved the following steps described above but not performing the cleavage from the resin step once the carboxylic acid is formed. Instead the free carboxylic acid of the newly formed isoquinoline compounds is first treated with N- [(dimethylamino)-lH-1, 2,3-triazolo [4, 5-b] pyridin-1-ylmethylene]-N-methylmethanaminium hexafluorophosphate N-oxide (HATU, PerSeptive Biosystems, Farmingham, MA), and then different amines having varying R groups were added after dissolving in DMF, DMA, NMP, and the like. The reaction is allowed to proceed for 1 to 24 hrs at 20°C to 80°C, preferably at 25°C for 3 to 5 hrs to yield various carboxamide derivatives. Finally, the compounds were cleaved from the resin as described above and tested for biological activity.

REACTION SCHEME IV CONHR' CLEAVAGE C < N I R H, NOC o The present invention also provides libraries and individual compounds which are the corresponding 5 amines of the above-described isoquinoline amide derivatives. Once the isoquinoline amide derivatives are prepared by above the described methods, the mixture can be further chemically transformed to extend the range and chemical diversity of the compounds. Using the

"libraries from libraries"concept, as described in Ostresh et al., Proc. Natl. Acad. Sci., 91: 11138-11142 (1994), various libraries of isoquinoline derivatives can be prepared by chemically altering the isoquinoline library. Such libraries and compounds will have the following structure: The preparation of such amines are described in Examples 48 to 50 and 53.

The nonsupport-bound library mixtures were screened in solution in radio-receptor inhibition assays described in detail below. Deconvolution of highly active mixtures were carried out by iterative, and in one instance additionally, positional scanning methods.

These techniques, the iterative approach or the positional scanning approach, can be utilized for finding other active compounds within the libraries of the present invention using any one of the below-described assays or others well known in the art.

The iterative approach is well-known and is set forth in general in Houghten et al., Nature, 354,84-86 (1991); and Dooley et al., Science, 266,2019-2022

(1994); both of which are incorporated herein by reference. In the iterative approach, for example, sublibraries of a molecule having three variable groups are made wherein the first variable is defined. Each of the compounds with the defined variable group is reacted with all of the other possibilities at the other two variable groups. These sub-libraries are each tested to define the identity of the second variable in the sub- library having the highest activity in the screen of choice. A new sub-library with the first two variable positions defined is reacted again with all the other possibilities at the remaining undefined variable position. As before, the identity of the third variable position in the sub-library having the highest activity is determined. If more variables exist, this process is repeated for all variables, yielding the compound with each variable contributing to the highest desired activity in the screening process. Promising compounds from this process can then be synthesized on larger scale in traditional single-compound synthetic methods for further biological investigation.

The positional-scanning approach has been described for various organic libraries and for various peptide libraries (see, for example, R. Houghten et al.

PCT/US91/08694 and U. S. Patent 5,556,762, both of which are incorporated herein by reference). In the positional scanning approach sublibraries are made defining only one variable with each set of sublibraries-and all possible sublibraires with each single variable defined (and all other possibilities at all of the other variable positions) is made and tested. From the instant description one skilled in the art could synthesize libraries wherein 2 fixed positions are defined at a time. From the testing of each single-variable defined

library, the optimum substituent at that position is determined, pointing to the optimum or at least a series of compounds having a maximum of the desired biological activity. Thus, the number of sublibraries for compounds with a single position defined will be the number of different substituents desired at that position, and the number of all the compounds in each sublibrary will be the product of the number of substituents at each of the other variables.

Individual compounds and pharmaceutical compositions containing the new isoquinoline derivatives, as well as methods of using the same are included within the scope of the present invention. The new isoquinoline compounds of the present invention can be used for a variety of purposes and indications and as medicaments for any such purposes and indications. For example, isoquinolines are generally known to have antimicrobial activity. Thus the isoquinolines of the present invention can be used to treat infections. The ability of the compounds to inhibit bacterial growth can be determined by methods well known in the art. An exemplary in vitro antimicrobial activity assay is described in Bondelle and Houghten, Biochemistry 30: 4671-4678 (1991), which is incorporated herein by reference. In brief, Staphylococcus aureus ATCC 29213 (Rockville, MD) is grown overnight at 37°C in Mueller- Hinton broth, then re-inoculated and incubated at 37°C to reach the exponential phase of bacterial growth (i. e., a final bacterial suspension containing 105 to 5 x 105 colony-forming units/ml). The concentration n of cells is established by plating 100 ul of the culture solution using serial dilutions (e. g., 10-2,10-3 and 10-4) onto solid agar plates. In 96-well tissue culture plates isoquinolines, individual or in mixtures, are added to

the bacterial suspension at concentrations derived from serial two-fold dilutions ranging from 1500 to 2.9 ug/ml.

The plates are incubated overnight at 37°C and the growth determined at each concentration by OD62o nm. The IC, 50 (the concentration necessary to inhibit 50% of the growth of the bacteria) can then be calculated.

In addition, Compounds of the present invention were shown to have antimicrobial activity by the in vitro antimicrobial activity assay described in Example 54 below and, therefore, are useful as antimicrobial agents.

Isoquinolines are also known to be antiarrhythmic and cardioprotective agents as described, for example, in published European Patent Application 0 590 455 to Lal et al., which is incorporated herein by reference. Therein is also described assays for assessing the antiarrhythmic and cardioprotective properties of isoquinolines, such as the reperfusion induced arrhythmias assay in isolated rat heart.

Additional assays can be, and have been, used to test the biological activity of the instant isoquinolines. Such assays include a competitive enzyme- linked immunoabsorbent assay and, as described in Examples 44 and 47, radio-receptor assays. The latter test, the radio-receptor assay, can be selective for any <BR> <BR> <BR> <BR> one of the u, K, or 6 opiate receptors and is, therefore, an indication of isoquinolines'analgesic properties as described, for example, in Dooley et al., Proc. Natl.

Acad. Sci., 90: 10811-10815 (1993). Additionally, such compounds can, and have been as described in Example 47, <BR> <BR> <BR> <BR> tested in a o receptor assay. Ligands for the a receptor can be useful as antipsychotic agents, as described in

Abou-Gharbia et al., Annual Reports in Medicinal Chemistry, 28: 1-10 (1993).

Competitive Enzyme-Linked Immunosorbent Assay (ELISA): The competitive ELISA method which can be used here is a modification of the direct ELISA technique described previously in Appel et al., J. Immunol.

144: 976-983 (1990), which is incorporated herein by reference. It differs only in the MAb addition step.

Briefly, multi-well microplates are coated with the antigenic peptide (Ac-GASPYPNLSNQQT-NH2) at a concentration of 100 pmol/50 pi. After blocking, 25 pi of a 1.0 mg/ml solution of each isoquinoline mixture of a synthetic combinatorial library (or individual isoquinoline) is added, followed by MAb 125-lOF3 (Appel et al., supra) (25 pi per well). The MAb is added at a fixed dilution in which the isoquinoline in solution effectively competes for MAb binding with the antigenic peptide adsorbed to the plate. The remaining steps are the same as for direct ELISA. The concentration of isoquinoline necessary to inhibit 50% of the MAb binding to the control peptide on the plate (ICso) is determined by serial dilutions of the isoquinoline.

Radio-Receptor Assay: Particulate membranes can be prepared using a modification of the method described in Pasternak et al., Mol. Pharmacol. 11: 340-351 (1975), which is incorporated herein by reference. Rat brains frozen in liquid nitrogen can be obtained from Rockland (Gilbertsville, PA). The brains are thawed, the cerebella removed and the remaining tissue weighed. Each brain is individually homogenized in 40 ml Tris-HC1 buffer (50 mM, pH 7.4,4°C) and centrifuged (Sorvall RC5C SA-600: Du Pont, Wilmington, DE) (16,000 rpm) for 10 mins. The pellets are resuspended in fresh Tris-HCl

buffer and incubated at 37°C for 40 mins. Following incubation, the suspensions are centrifuged as before, the resulting pellets resuspended in 100 volumes of Tris buffer and the suspensions combined. Membrane suspensions are prepared and used in the same day.

Protein content of the crude homogenates generally range from 0.15-0.2 mg/ml as determined using the method described in M. M. Bradford, M. M., Anal. Biochem. 72: 248- 254 (1976), which is incorporated herein by reference.

Binding assays are carried out in polypropylene tubes, each tube containing 0.5 ml of membrane suspension. 8 nM of 3H- [D-Ala2, Me-Phe4, Gly-ol'] enkephalin (DAMGO) (specific activity = 36 Ci/mmol, 160,000 cpm per tube; which can be obtained from Multiple Peptide Systems, San Diego, CA, through NIDA drug distribution program 271-90-7302) and 80 ug/ml of isoquinoline, individual or as a mixture and Tris-HC1 buffer in a total volume of 0.65 ml. Assay tubes are incubated for 60 mins. at 25°C. The reaction is terminated by filtration through GF-B filters on a Tomtec harvester (Orange, CT).

The filters are subsequently washed with 6 ml of Tris-HC1 buffer, 4°C. Bound radioactivity is counted on a Pharmacia Biotech Betaplate Liquid Scintillation Counter (Piscataway, NJ) and expressed in cpm. To determine inter-and intra-assay variation, standard curves in which 3H-DAMGO is incubated in the presence of a range of concentrations of unlabeled DAMGO (0.13-3900 nM) are generally included in each plate of each assay (a 96-well format). Competitive inhibition assays are performed as above using serial dilutions of the isoquinolines, individually or in mixtures. ICso values (the concentration necessary to inhibit 50% of 3H-DAMGO <BR> <BR> <BR> binding) are then calculated. As opposed to this<BR> <BR> <BR> <BR> <BR> receptor selective assay, assays selective for K

receptors can be carried out using ['H]-U69,593 (3 nM, specific activity 62 Ci/mmol) as radioligand. Assays <BR> <BR> <BR> selective for 5 opiate receptors can be carried out using tritiated DSLET ([D-Ser2, D-Leu5]-threonine-enkephalin) as radioligand. Similarly, assays for the o receptor assay are the same as the p assay but use radiolabeled pentazocine as ligand.

As pharmaceutical compositions for treating infections, arrhythmia, pain, or other indications known to be treatable by isoquinolines, the isoquinoline compounds of the present invention are generally in a pharmaceutical composition so as to be administered to a subject at dosage levels of from 0.7 to 7000 mg per day, and preferably 1 to 500 mg per day, for a normal human adult of approximately 70 kg of body weight, this translates into a dosage of from 0.01 to 100 mg/kg of body weight per day. The specific dosages employed, however, can be varied depending upon the requirements of the patient, the severity of the condition being treated, and the activity of the compound being employed. The determination of optimum dosages for a particular situation is within the skill of the art.

For preparing pharmaceutical compositions containing compounds of the invention, inert, pharmaceutically acceptable carriers are used. The pharmaceutical carrier can be either solid or liquid.

Solid form preparations include, for example, powders, tablets, dispersible granules, capsules, cachets, and suppositories.

A solid carrier can be one or more substances which can also act as diluents, flavoring agents, solubilizers, lubricants, suspending agents, binders, or

tablet disintegrating agents; it can also be an encapsulating material.

In powders, the carrier is generally a finely divided solid which is in a mixture with the finely divided active component. In tablets, the active compound is mixed with the carrier having the necessary binding properties in suitable proportions and compacted in the shape and size desired.

For preparing pharmaceutical composition in the form of suppositories, a low-melting wax such as a mixture of fatty acid glycerides and cocoa butter is first melted and the active ingredient is dispersed therein by, for example, stirring. The molten homogeneous mixture is then poured into convenient-sized molds and allowed to cool and solidify.

Powders and tablets preferably contain between about 5% to about 70% by weight of the active ingredient.

Suitable carriers include, for example, magnesium carbonate, magnesium stearate, talc, lactose, sugar, pectin, dextrin, starch, tragacanth, methyl cellulose, sodium carboxymethyl cellulose, a low-melting wax, cocoa butter and the like.

The pharmaceutical compositions can include the formulation of the active compound with encapsulating material as a carrier providing a capsule in which the active component (with or without other carriers) is surrounded by a carrier, which is thus in association with it. In a similar manner, cachets are also included.

Tablets, powders, cachets, and capsules can be used as solid dosage forms suitable for oral administration.

Liquid pharmaceutical compositions include, for example, solutions suitable for oral or parenteral administration, or suspensions, and emulsions suitable for oral administration. Sterile water solutions of the active component or sterile solutions of the active component in solvents comprising water, ethanol, or propylene glycol are examples of liquid compositions suitable for parenteral administration.

Sterile solutions can be prepared by dissolving the active component in the desired solvent system, and then passing the resulting solution through a membrane filter to sterilize it or, alternatively, by dissolving the sterile compound in a previously sterilized solvent under sterile conditions.

Aqueous solutions for oral administration can be prepared by dissolving the active compound in water and adding suitable flavorants, coloring agents, stabilizers, and thickening agents as desired. Aqueous suspensions for oral use can be made by dispersing the finely divided active component in water together with a viscous material such as natural or synthetic gums, resins, methyl cellulose, sodium carboxymethyl cellulose, and other suspending agents known to the pharmaceutical formulation art.

Preferably, the pharmaceutical composition is in unit dosage form. In such form, the composition is divided into unit doses containing appropriate quantities of the active isoquinoline. The unit dosage form can be a

packaged preparation, the package containing discrete quantities of the preparation, for example, packeted tablets, capsules, and powders in vials or ampules. The unit dosage form can also be a capsule, cachet, or tablet itself, or it can be the appropriate number of any of these packaged forms.

The following Examples are intended to illustrate but not limit the present invention.

EXAMPLE 1 Combinatorial Library Of Dihydroisoquinoline Derivatives This Example provides a representative solid-phase combinatorial synthesis of a library which would contain approximately 525 derivatives of dihydroisoquinolines (DHQs).

Following the above Reaction Scheme II, preparation of a library containing the DHQs involves the following steps. Briefly, first, thirty five diverse amino carboxylic acid, varying at R1, and including various amino-protected amino acids, are coupled to MBHA resin employing the tea-bag method of Houghten, et. al, as described, for example in U. S. Patent No. 4,631,211 to Houghten and Houghten et al., Proc. Natl. Acad. Sci., 82: 5131-5135 (1985), both of which are incorporated herein by reference. After coupling and thorough washing the 35 tea-bags, each containing one resin-bound amino carboxylic acid, are opened and the resin beads combined and thoroughly mixed as a suspension in dichloromethane (DCM). The resins are isolated by filtration and dried under vacuum, then divided into 15 equal portions and resealed in 15 labeled tea-bags, each tea-bag now having

a mixture of the 35 amino carboxylic acids. This is followed by condensing 15 aldehydes, each differing by their R2 substituent, using triethylorthoformate as dehydrating agent with the tea-bag contained mixtures of resin-bound amino carboxylic acids. One tea-bag, each containing the 35 resin-bound carboxylic acids, is used for each aldehyde in a separate reaction. After washing with an anhydrous solvent the tea-bags are collectively reacted with homophthalic anhydride and triethylamine in anhydrous dimethylformamide (DMF) to arrive at a library of 525 derivatives of DHQ. Finally, the compounds are individually cleaved from the MBHA resin using a hydrogen fluoride (HF) procedure. The individual mixtures varying at RI and constant at R2, each a mixture containing 35 individual compounds can then be tested for biological activity using any one of a variety of screening assays, such as those described above or others well known in the art.

The individual amino carboxylic acids which can be used to prepare a library of 525 DHQs include the following: Ala, Arg, Asn, Asp, Cys, Gln, Glu, Gly, His, Ile, Leu, Lys, Met, Phe, Ser, Thr, Trp, Tyr, Val, D-Ala, D-Asp, D-Cys, D-Glu, D-Ile, D-Leu, D-Lys, D-Met, D-Phe, D-Ser, D-Thr, D-Tyr, and D-Val, ß-alanine, and 4-aminobutyric acid. All are amino-protected with Fmoc or Boc and carry appropriate side chain protecting group as required. Individual aldehydes which can be employed are as follows: benzaldehyde, 4-methoxybenzaldehyde, 4-nitrobenzaldehyde, 4-chlorobenzaldehyde, 2-methoxybenzaldehyde, 2-nitrobenzaldehyde, 2-chlorobenzaldehyde, 4-phenylbenzaldehyde, furfuraldehyde, 2-propionaldehyde, 2-methyl-2-buten-1-al, cyclohexane carboxaldehyde, butanal, cinnamaldehyde, acetaldehyde.

1. Coupling of Amino Carboxylic Acids to MBHA Resin Thirty five polypropylene mesh packets (T-bags,-2"square, 65u; McMaster Carr, Chicago, IL) of (0.6 g, 0.93 meq/g) MBHA resin are prepared, washed with DCM (2X,-5 ml each), neutralized with 5% diisopropylethylamine/dichloromethane (DIEA/DCM) (3X,-5 ml each), and washed with DCM (2X,-5 ~ 5 ml each). Each resin packet is individually coupled overnight (-16 hrs except for Gly, 1 hr) by adding 10X amino acid in DCM (0.2 M) or amino carboxylic acid in DMF followed by 10X diisopropylcarbodiimide/DCM (0.2 M) for a final reagent concentration of 0.1 M DMF (5%) used to solubilize the Arg and Ser derivatives. Hydroxybenzotriazole (HOBt) (10X) is added to the amino carboxylic acids couplings.

Following coupling completion, resin packets are washed with DCM (1X), isopropanol (IPA) (2X), and DCM (2X).

Each packet is then opened and the resin carefully washed into a common vessel using alternating DCM and methanol (MeOH) washes (final volume, ml). The resin is mixed using a magnetic stir bar for 2.5 hrs. Resin is then filtered, washed with MeOH, and dried under vacuum.

Based upon synthesis and cleavage of individual controls, reaction completion should be, and generally is, >95%.

2. Condensation of Benzaldehydes to the Mixture of Resin-Bound Amino Carboxylic Acids Each packet is next shaken twice in 20% (v/v) piperidine/DMF (30 ml, 5 min, then 15 min) then washed with DMF (3 x 30 ml) and DCM (3 x 30 ml). A solution of the respective aldehyde (0.203 ml, 2 mmoles) and anhydrous trimethylorthoformate (0.438 ml, 4 mmoles) is prepared in DMF (7.5 ml) ana added to the packet. After

shaking for 3 hrs the packet is washed with dry (<0.03% water) DMF (5 x 30 ml).

3. Condensation of Homophthalic Anhydride to Yield a Library of Dihydroisoquinolines A solution of homophthalic anhydride (324 mg, 2 mmoles) and triethylamine (0.021 ml, 0.15 mmoles) is prepared in DMF (5 ml) and added to each packet. After heating at 80°C for 16 hrs the packets are then washed with DMF (3 x 30 ml) and DCM (3 x 30 ml).

The isoquinolines are cleaved off of the resin by treatment with HF (liquid (1)) at-15°C for 2 hrs followed by warming to room temperature while removing HF (gaseous (g)) with a nitrogen stream.

EXAMPLE 2 trans-N- (2-acetamidoyl)-3-phenyl-4-carboxy-3,4-dihydro- 1 (2H)-isoquinolone This Example provides the solid-phase synthesis of trans-N- (2-acetamidoyl)-3-phenyl-4-carboxy-3,4 -dihydro-1 (2H)-isoquinolone by condensing, on a TentaGel resin, glycine, benzaldehyde and homophthalic anhydride.

The isoquinoline was cleaved from the resin by trifluoroacetic acid (TFA).

TentaGelTM S-NH2 resin (Rapp Polymere Gmbh, Federal Republic of Germany; 385 mg, 0.100 milliequivalents) was placed in a porous polypropylene packet. The packet was placed in a 60 ml bottle and washed with 5% (v/v) DIEA/DCM (3 x 30 ml) followed by DCM (5 x 30 ml). A solution of Rink linker (270 mg, 0.5 mmoles), HOBt (68 mg, 0.5 mmoles), and

diisopropylcarbodiimide (DIC, 0.094 ml, 0.6 mmoles) was prepared in DMF (5 ml) and added to the resin packet.

After shaking for 16 hrs the packet was washed with DMF (3 x 30 ml) and DCM (3 x 30 ml).

The packet was next shaken twice in 20% (v/v) piperidine/DMF (30 ml, 5 min, then 15 min), then washed with DMF (3 x 30 ml) and DCM (3 x 30 ml). A solution of N- (9-fluorenylmethoxycarbonyl) glycine (149 mg, 0.5 mmoles), HOBt (68 mg, 0.5 mmoles), and DIC (0.094 ml, 0.6 mmoles) was prepared in DMF (5 ml) and added to the resin packet. After shaking for 2 hrs the packet was washed with DMF (3 x 30 ml) and DCM (3 x 30 ml).

The packet was next shaken twice in 20% (v/v) piperidine/DMF (30 ml, 5 min, then 15 min) then washed with DMF (3 x 30 ml) and DCM (3 x 30 ml). A solution of benzaldehyde (0.203 ml, 2 mmoles) and anhydrous trimethylorthoformate (0.438 ml, 4 mmoles) was prepared in DMF (7.5 ml) and added to the packet. After shaking for 3 hrs the packet was washed with dry (<0.03% water) DMF (5 x 30 ml). A solution of homophthalic anhydride (324 mg, 2 mmoles) and triethylamine (0.021 ml, 0.15 mmoles) was prepared in DMF (5 ml) and added to the packet. After heating at 80°C for 16 hrs the packet was washed with DMF (3 x 30 ml) and DCM (3 x 30 ml).

The isoquinolone was cleaved off of the resin by addition of a solution of 75/20/5 (v/v/v) TFA/DCM/water (10 ml). After shaking for 135 min the acid solution was decanted into a round bottom flask.

The packet was then washed with TFA (1 x 10 ml) and this wash was also added to the round bottom flask. The solvent was removed under reduced pressure providing a clear oil.

The crude oil was dissolved in DCM (20 ml and extracted with 1 N hydrochloric acid (HC1; 1 x 10 ml).

The organic layer was next extracted with aqueous saturated sodium bicarbonate (NaHCO3) (2 x 10 ml). The NaHCO3 layers were combined and the pH of the solution was brought to 1-2 by addition of 2 N HC1, followed by extraction with DCM (2 x 10 ml). The final organic layers were combined and the solvent was removed under reduced pressure, providing a quantitative yield of a clear oil which crystallized overnight into a white solid. 1H NMR (DMSO-d6) d 7.98 (d, 1 H, J = 2.4 Hz), 7.46 (m, 3H), 7.25 (m, 5H), 7.11 (m, 2H), 5.41 (d, 1H, J = 1.7 Hz), 4.39 (d, 1H, J = 16.3 Hz), 4.14 (d, 1H, J = 1.7 Hz), 3.34 (d, 1H, J = 16.3 Hz). 13C NMR (DMSO-d6) d 172.98,169.77,163.41,138.86,133.46,132.34,129.25, 128.63,128.21,128.09,127.70,127.08,126.28,61.67, 50.41,49.89. Matrix Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry (MALDI-TOF MS; Kratos (division of Shimadzu Scientific), Columbia, MD): 364 (MW + 2 Na+), (347 (MW + Na+).

EXAMPLE 3 trans-N-(2-acetamidoyl)-3-phenyl-4-carboxy-3,(2-acetamidoyl) -3-phenyl-4-carboxy-3, 4-dihydro- 1 (2H)-isoquinolone This Example provides the solid-phase synthesis of trans-N- (2-acetamidoyl)-3-phenyl-4-carboxy-3,4 -dihydro-1 (2H)-isoquinolone by condensing, on a polystyrene benzhydrylamine resin, glycine, benzaldehyde and homophthalic anhydride. The final product was cleaved from the resin using an HF procedure.

Polystyrene benzhydrylamine (BHA) resin (189 mg, 0.100 milliequivalents) was placed in a porous polypropylene packet. The packet was placed in a 60 ml

bottle and washed with 5% (v/v) DIEA/DCM (3 x 30 ml) followed by DCM (5 x 30 ml). A solution of N- (9-fluorenylmethoxycarbonyl) glycine (149 mg, 0.5 mmoles), HOBt (68 mg, 0.5 mmoles), and DIC (0.094 ml, 0.6 mmoles) was prepared in DMF (5 ml) and added to the resin packet. After shaking for 2 hrs the packet was washed with DMF (3 x 30 ml) and DCM (3 x 30 ml).

The packet was next shaken twice in 20% (v/v) piperidine/DMF (30 ml, 5 min, then 15 min), then washed with DMF (3 x 30 ml) and DCM (3 x 30 ml). A solution of benzaldehyde (0.203 ml, 2 mmoles) and anhydrous trimethylorthoformate (0.438 ml, 4 mmoles) was prepared in DMF (7.5 ml) and added to the packet. After shaking for 3 hrs the packet was washed with dry (<0.03% water) DMF (5 x 30 ml). A solution of homophthalic anhydride (324 mg, 2 mmoles) and triethylamine (0.021 ml, 0.15 mmoles) was prepared in DMF (5 ml) and added to the packet. After heating at 80°C for 16 hrs the packet was washed with DMF (3 x 30 ml) and DCM (3 x 30 ml).

The isoquinoline was cleaved off of the resin by treatment with HF (1) at-15°C for 2 hrs followed by warming to room temperature while removing HF (g) with a nitrogen stream. The packet and HF tube were washed with TFA (2 x 8 ml) and the two washes were transferred to a round bottom flask and concentrated to a clear oil under reduced pressure.

The crude oil was dissolved in DCM (20 ml and extracted with 1 N HC1 (1 x 10 ml). The organic layer was next extracted with aqueous saturated NaHCO3 (2 x 10 ml). The NaHCO3 layers were combined and the pH of the solution was brought to 1-2 by addition of 2 N HC1, followed by extraction with DCM (2 x 10 ml). The final

organic layers were combined and the solvent was removed under reduced pressure, providing a quantitative yield of a clear oil which upon lyophilization provided a white crystalline solid. Spectral data was identical to the sample prepared in Example 2.

EXAMPLE 4 t. rans-N- (2- (s)-propionamidoyl)-3-phenyl-4-carboxy-3,4- dihydro-1 (2H)-isoquinolone Provided by this Example is the solid-phase synthesis of trans-N- (2- (s)-propionamidoyl)-3-phenyl -4-carboxy-3,4-dihydro-1 (2H)-isoquinolone prepared by condensing, on an MBHA resin, alanine, benzaldehyde and homophthalic anhydride. The final product was removed from the resin by HF cleavage.

N- (t-Butyloxycarbonyl)-L-alanine attached to MBHA resin (0.05 mmoles) was sealed in a polypropylene packet. The packet was shaken in 55% (v/v) TFA/DCM (30 ml, 30 min) then washed with DCM (1 x 30 ml), isopropyl alcohol (2 x 30 ml), 5% (v/v) DIEA/DCM (3 x 30 ml, 2 min each), DCM (2 x 30 ml), and anhydrous DMF (2 x 30 ml).

A solution of benzaldehyde (10 mmoles) and anhydrous trimethylorthoformate (20 mmoles) was prepared in DMF (20 ml) and added to the packet. After shaking for 3.75 hrs the packet was washed with dry (<0.03% water) DMF (5 x 30 ml). A solution of homophthalic anhydride (7.5 mmoles) and triethylamine (225 mmoles) was prepared in chloroform (15 ml) and added to the packet.

After shaking at room temperature for 17 hrs the packet was washed with DCM (3 x 30 ml), DMF (3 x 30 ml), shaken for 20 min in water (30 ml), washed with DMF (3 x 30 ml) and DCM (3 x 30 ml).

The isoquinolone was cleaved off of the resin using HF as in Example 3, but no aqueous extraction was performed. The residue was dissolved in deuterated DMSO to obtain NMR and mass spectral data after which the solvent was removed under reduced pressure providing a 1/1 mixture of the desired product and the amide arising from homophthalic acid and L-alaninamide as a clear oil.

(14 mg, 83%). MALDI-TOF MS: 338 (MW), 359 (MW + Na+).

EXAMPLE 5 trans-N- (3-propionamidoyl)-3-phenyl-4-carboxy-3,4- dihydro-1 (2H)-isoquinolone This Example provides the solid-phase synthesis of trans-N- (3-propionamidoyl)-3-phenyl-4-carboxy- 3,4-dihydro-1 (2H)-isoquinolone prepared by condensing, on a RINK linker derivatized TentaGel resin, aminopropionic acid, benzaldehyde and homophthalic anhydride. The final product was removed from the resin by TFA cleavage.

N- (9-Fluorenylmethoxycarbonyl)-3-aminopropionic acid was attached to RINK linker derivatized TentaGelTM resin as described in Example 2. The packet was next shaken twice in 20% (v/v) piperidine/DMF (30 ml, 5 min, then 15 min) then washed with DMF (3 x 30 ml) and DCM (3 x 30 ml).

A solution of benzaldehyde (0.203 ml, 2 mmoles) and anhydrous trimethylorthoformate (0.438 ml, 4 mmoles) was prepared in DMF (7.5 ml) and added to the packet.

After shaking for 3 hrs the packet was washed with dry (<0.03% water) DMF (5 x 30 ml) followed by chloroform (3 x 30 ml). A solution of homophthalic anhydride (324 mg, 2 mmoles) and triethylamine (0.021 ml, 0.15 mmoles) was prepared in chloroform (5 ml) and added to the packet.

After shaking at room temperature for 18 hrs the packet was washed with DCM (3 x 30 ml), DMF (3 x 30 ml) and water (1 x 30 ml). The packet was then shaken in water (30 ml) for 20 min followed by washing with DMF (3 x 30 ml) and DCM (3 x 30 ml).

The isoquinolone was cleaved off of the resin by addition of a solution of 75/20/5 (v/v/v) TFA/DCM/water (10 ml). After shaking for 135 min the acid solution was decanted into a round bottom flask.

The packet was then washed with TFA (1 x 10 ml) and this wash was also added to the round bottom flask. The solvent was removed under reduced pressure providing a clear oil.

The crude oil was dissolved in 1 ml methyl sulfoxide and half was stored at-20°C. The other half was mixed with 1 N NaOH (10 ml) and stirred at room temperature for 1 hr. Water (5 ml) was then added and the solution was extracted with DCM (1 x 10 ml). The pH of the aqueous layer was brought to 1-2 by addition of 2 N HC1, followed by extraction with DCM (2 x 10 ml). The final organic layers were combined and the solvent was removed under reduced pressure, providing a clear oil (15 mg, 89%). MALDI-TOF MS: 360 (MW + Na+).

EXAMPLE 6 TO EXAMPLE 28 Synthesis of Additional Substituted Isoquinolines With the exception of the amino carboxylic acid and aldehyde starting materials, Examples 6 to 28 were done using the procedures of Example 5. In place of the starting materials 3-aminopropionic acid and benzaldehyde of Example 5, Examples 6 to 28 provide all possible combinations of four different amino carboxylic acids and six unique benzaldehydes. The amino carboxylic acids and benzaldehydes used, along with the corresponding Example number is shown in TABLE I. As a reference, the compound prepared in Example 5 is shown in Table I at upper left.

TABLE I 3-Amino-4-Amino-6-Amino-Glycine propionic butyric hexanoic acid acid acid Benzaldehyde Example 5 Example 11 Example 17 Example 23 4-Methoxy-Example 6 Example 12 Example 18 Example 24 benzaldehyde 3,5-Dimethoxy- Example 7 Example 13 Example 19 Example 25 benzaldehyde 4-Cyano-Example 8 Example 14 Example 20 Example 26 benzaldehyde 2-Bromo-Example 9 Example 15 Example 21 Example 27 benzaldehyde 3-Hydroxy-Example 10 Example 16 Example 22 Example 28 benzaldehyde EXAMPLE 6 <BR> trans-N- (3-propionamidoyl)-3- (4-methoxyphenyl)-4-carboxy- 3,4-dihydro-1 (2H)-isoquinolone Yield: 16 mg, 87%. MALDI-TOF MS: 390 (MW + Na+), 406 (MW + K+).

EXAMPLE 7 trans-N- (3-propionamidoyl)-3- (3,5-dimethoxyphenyl)-4- carboxy-3,4-dihydro-1 (2H)-isoquinolone Yield: 15 mg, 75%. MALDI-TOF MS: 421 (MW + Na+).

EXAMPLE 8 <BR> <BR> <BR> <BR> trans-N- (3-propionamidoyl)-3- (4-cyanophenyl)-4-carboxy- 3,4-dihydro-1 (2H)-isoquinolone Yield: 9 mg, 50%. MALDI-TOF MS: 363 (MW), 385 (MW + Na+).

EXAMPLE 9 trans-N- (3-propionamidoyl)-3- (2-bromophenyl)-4-carboxy- 3,4-dihydro-1 (2H)-isoquinolone Yield: 17 mg, 82%. MALDI-TOF MS: 417 (MW), 439 (MW + Na+).

EXAMPLE 10 <BR> <BR> <BR> <BR> trans-N- (3-propionamidoyl)-3- (3-hydroxyphenyl)-4-carboxy- 3,4-dihydro-1 (2H)-isoquinolone Yield: 2 mg, 11%. MALDI-TOF MS: 354 (MW), 376 (MW + Na+).

EXAMPLE 11 <BR> <BR> <BR> <BR> trans-N- (4-butyramidoyl)-3- (phenyl)-4-carboxy-3,4-dihydro -1 (2H)-isoquinolone Yield: 17 mg, 97%. MALDI-TOF MS: 374 (MW + Na+).

EXAMPLE 12 <BR> trans-N- (4-butyramidoyl)-3- (4-methoxyphenyl)-4-carboxy-3, 4-dihydro-1 (2H)-isoquinolone Yield: 11 mg, 58%. MALDI-TOF MS: 382 (MW), 404 (MW + Na+).

EXAMPLE 13 trans-N- (4-butyramidoyl)-3- (3,5-dimethoxyphenyl)-4- carboxy-3,4-dihydro-1 (2H)-isoquinolone Yield: 17 mg, 83%. MALDI-TOF MS: 412 (MW), 434 (MW + Na+).

EXAMPLE 14 <BR> trans-N- (4-butyramidoyl)-3- (4-cyanophenyl)-4-carboxy-3,4- dihydro-1 (2H)-isoquinolone Yield: 13 mg, 69%. MALDI-TOF MS: 399 (MW + Na+).

EXAMPLE 15 <BR> trans-N- (4-butyramidoyl)-3- (2-bromophenyl)-4-carboxy-3,4- dihydro-1 (2H)-isoquinolone Yield: 18 mg, 84%. MALDI-TOF MS: 453 (MW + Na+).

EXAMPLE 16 trans-N- (4-butyramidoyl)-3- (3-hydroxyphenyl)-4-carboxy- 3,4-dihydro-1 (2H)-isoquinolone Yield: 2 mg, 11%. MALDI-TOF MS: 389 (MW + Na+).

EXAMPLE 17 trans-N-(6-hexanamidoyl)-3-(phenyl)-4-carboxy-3,(6-hexanamid oyl)-3-(phenyl)-4-carboxy-3, 4- dihydro-1 (2H)-isoquinolone Yield: quantitative. MALDI-TOF MS: 402 (MW + Na+).

EXAMPLE 18 <BR> <BR> <BR> <BR> trans-N- (6-hexanamidoyl)-3- (4-methoxyphenyl)-4-carboxy- 3,4-dihydro-1 (2H)-isoquinolone Yield: 16 mg, 78%. MALDI-TOF MS: 410 (MW), 432 (MW + Na+), 448 (MW + K+).

EXAMPLE 19 t. rans-N- (6-hexanamidoyl)-3- (3, 5-dimethoxyphenyl)-4- carboxy-3,4-dihydro-1 (2H)-isoquinolone Yield: 18 mg, 82%. MALDI-TOF MS: 440 (MW), 462 (MW + Na+), 478 (MW + K+).

EXAMPLE 20 <BR> <BR> <BR> <BR> trans-N- (6-hexanamidoyl)-3- (4-cyanophenyl)-4-carboxy-3,4- dihydro-1 (2H)-isoquinolone Yield: 15 mg, 74%. MALDI-TOF MS: 405 (MW), 427 (MW + Na+).

EXAMPLE 21 trans-N-(6-hexanamidoyl)-3-(2-bromophenyl)-4-carboxy-3,(6-he xanamidoyl)-3-(2-bromophenyl)-4-carboxy-3, 4- dihydro-1 (2H)-isoquinolone Yield: 19 mg, 83%. MALDI-TOF MS: 481 (MW + Na+).

EXAMPLE22 <BR> trans-N- (6-hexanamidoyl)-3- (3-hydroxyphenyl)-4-carboxy- 3,4-dihydro-1 (2H)-isoquinolone Yield: 3 mg, 15%. MALDI-TOF MS: 396 (MW), 418 (MW + Na+).

EXAMPLE 23 <BR> trans-N- (2-acetamidoyl)-3- (phenyl)-4-carboxy-3, 4-dihydro- 1 (2H)-isoquinolone Yield: 11 mg, 68%. MALDI-TOF MS: 324 (MW), 346 (MW + Na+).

EXAMPLE 24 trans-N- (2-acetamidoyl)-3- (4-methoxyphenyl)-4-carboxy- 3,4-dihydro-1 (2H)-isoquinolone Yield: 9 mg, 51%. MALDI-TOF MS: 376 (MW + Na+).

EXAMPLE 25 trans-N- (2-acetamidoyl)-3- (3,5-dimethoxyphenyl)-4- carboxy-3,4-dihydro-1 (2H)-isoquinolone Yield: 9 mg, 47%. MALDI-TOF MS: 406 (MW + Na+).

EXAMPLE 26 <BR> trans-N- (2-acetamidoyl)-3- (4-cyanophenyl)-4-carboxy-3,4- dihydro-1 (2H)-isoquinolone Yield: 9 mg, 52%. MALDI-TOF MS: 371 (MW + Na+).

EXAMPLE 27 <BR> <BR> <BR> <BR> trans-N- (2-acetamidoyl)-3- (2-bromophenyl)-4-carboxy-3,4- dihydro-1 (2H)-isoquinolone Yield: quantitative. MALDI-TOF MS: 425 (MW + Na+).

EXAMPLE 28 trans-N- (2-acetamidoyl)-3- (3-hydroxyphenyl)-4-carboxy- 3,4-dihydro-1 (2H)-isoquinolone Yield: 3 mg, 18%. MALDI-TOF MS: 362 (MW + Na+).

EXAMPLE 29 <BR> <BR> <BR> <BR> trans-N- (2-acetamidoyl)-3-methyl-4-carboxy-3,4-dihydro- 1 (2H)-isoquinolone This Example provides the solid-phase synthesis of trans-N- (2-acetamidoyl)-3-methyl-4-carboxy- 3,4-dihydro-1 (2H)-isoquinolone prepared by condensing, on an MBHA resin, glycine, acetaldehyde and homophthalic anhydride. The final product was removed from the resin by HF cleavage.

N- (t-Butyloxycarbonyl) glycine attached to MBHA resin (0.05 mmoles) was sealed in a polypropylene packet.

The packet was shaken in 55% (v/v) TFA/DCM (30 ml, 30 min) then washed with DCM (1 x 30 ml), isopropyl alcohol (2 x 30 ml), 5% (v/v) DIEA/DCM (3 x 30 ml, 2 min each), DCM (2 x 30 ml), and anhydrous DMF (2 x 30 ml).

A solution of acetaldehyde (5 mmoles) and anhydrous trimethylorthoformate (10 mmoles) was prepared in DMF (10 ml) and added to the packet. After shaking for 3.75 hrs the packet was washed with dry (<0.03%

water) DMF (5 x 30 ml). A solution of homophthalic anhydride (5 mmoles) and triethylamine (0.075 mmoles) was prepared in chloroform (10 ml) and added to the packet.

After shaking at room temperature for 17 hrs the packet was washed with DCM (3 x 30 ml), DMF (3 x 30 ml), shaken for 20 min in water (30 ml), washed with DMF (3 x 30 ml) and DCM (3 x 30 ml).

The isoquinolone was cleaved off of the resin using HF as in Example 3. The residue was dissolved in deuterated DMSO to obtain NMR and mass spectra after which the solvent was removed under reduced pressure providing a 2/1 mixture of the desired product and the amide of homophthalic acid and glycinamide as a clear oil (10 mg, 77%). MALDI-TOF MS: 283 (MW + Na+).

EXAMPLE 30 trans-N- (2-acetamidoyl)-3-cyclohexyl-4-carboxy-3,4- dihydro-1 (2H)-isoquinolone Synthesis was performed as in Example 29 with the exception of substituting cyclohexanecarboxaldehyde for acetaldehyde. Obtained after cleavage was a 2/1 mixture of the desired product and the amide of homophthalic acid and glycinamide as a clear oil (12 mg, 73%). MALDI-TOF MS: 329 (MW), 351 (MW + Na+).

EXAMPLE 31 trans-N-(2-acetamidoyl)-3-(E-2-but-2-enyl)-4-carboxy-3,(2-ac etamidoyl)-3-(E-2-but-2-enyl)-4-carboxy-3, 4- dihydro-1 (2H)-isoquinolone Synthesis was performed as in Example 29, excepting substitution of trans-2-methyl-2-butanal for acetaldehyde. Obtained after cleavage was a 2/1 mixture

of the desired product and the amide of homophthalic acid and glycinamide as a clear oil (15 mg, 100%). MALDI-TOF MS: 325 (MW + Na+).

EXAMPLE 32 <BR> <BR> <BR> <BR> trans-N- (2-acetamidoyl)-3-phenyl-4- (propylcarboxylate)- 3,4-dihydro-1 (2H)-isoquinolone Trans-N- (2-Acetamidoyl)-3- (3,5-dimethoxyphenyl) -4-carboxy-3,4-dihydro-1 (2H)-isoquinolone (0.05 mmoles) was prepared on MBHA polystyrene resin using the method described in Example 4 with the following changes: glycine was substituted for alanine, 3,5-dimethoxybenzaldehyde was substituted for benzaldehyde, and the product was further modified before cleavage off resin.

A solution of [0- (7-azabenzotriazol-1-yl)-1, 1, 3,3-tetramethyluronium hexafluorophosphate (HATU) in anhydrous DMF (0.93 mmoles, 3.1 ml, 300 mM solution) was added to the packet and shaken for 20 min. The HATU solution was decanted off of the tea-bag and anhydrous DMF (4.7 ml) and anhydrous 1-propanol (0.374 ml, 5 mmoles) were added. After shaking for 1 hr, the propanol solution was removed and the bag washed with anhydrous DMF (2 x 10 ml). The HATU treatment was repeated followed by decanting and addition of a second 1-propanol solution. This reaction was shaken at room temperature for 66 hrs. The bag was then washed with DMF (4 x 10 ml), DCM (3 x 10 ml), and allowed to dry.

Standard HF cleavage as in Example 4 provided a clear oil shown by NMR and mass spectra to contain a half

mixture of the desired ester and the free acid (18 mg, 85%) MALDI-TOF MS: 448 (MW + Na+).

EXAMPLE 33 trans-N- (2-acetamidoyl)-3-phenyl-4- (N- (isopropyl) carboxamido)-3,4-dihydro-1 (2H)-isoquinolone This product was prepared as in Example 32 but with the substitution ofisopropylamine for 1-propanol.

Yield: 20 mg, 94%. MALDI-TOF MS: 425 (MW), 447 (MW + Na+).

EXAMPLE 34 trans-N-(2-acetamidoyl)-3-phenyl-4-(N, N-(diethyl) carboxamido)-3,4-dihydro-1 (2H)-isoquinolone This product was prepared as in Example 32 but with the substitution of N, N-diethylamine for 1-propanol.

Yield: 21 mg, 96%. MALDI-TOF MS: 439 (MW), 461 (MW + Na+).

EXAMPLE 35 trans-N- (2-acetamidoyl)-3-phenyl-4- (N- (4-amino- morpholinyl) carboxamido)-3,4-dihydro-1 (2H)-isoquinolone This product was prepared as in Example 32 but with the substitution of 4-aminomorpholine for 1-propanol. Yield: 23 mg, 98%. MALDI-TOF MS: 468 (MW), 490 (MW + Na+).

EXAMPLE 36 trans-N- (2-acetamidoyl)-3-phenyl-4- (N- ( (+/-) 3-amino- quinuclidyl) carboxamido)-3,4-dihydro-1 (2H)-isoquinolone This product was prepared as in Example 32 but with the substitution of (+/-)-3-aminoquinuclidine, bis HC1 salt for 1-propanol; DIEA (200 mole % versus aminoquinuclidine) was also added to neutralize the HC1 salt. Yield: 23 mg, 98%. MALDI-TOF MS: 468 (MW), 490 (MW + Na+).

EXAMPLE 37 Solid-phase synthesis of a combinatorial library pool containing isoquinolines derived from five amino acids, benzaldehyde and homophthalic anhydride As described in Example 2, five porous polystyrene packets were prepared each containing TentaGelTM S-NH2 resin (385 mg, 0.100 milliequivalents) derivatized with the protected RINK linker. Following the procedure provided in Example 2, one bag each was then coupled with one each of five different amino acids, N- (9-fluorenylmethoxycarbonyl) -3-aminopropionic acid, N- (9-fluorenylmethoxycarbonyl) -4-aminobutyric acid, N- (9-fluorenylmethoxycarbonyl) -6-aminohexanoic acid, N- (9-fluorenylmethoxycarbonyl) -N-t-butoxycarbonyl- (s)-2,6-diaminohexanoic acid, and N- (9-fluorenylmethoxycarbonyl)-glycine.

The resin packets were dried at room temperature and cut open. The resin inside was pooled from all five bags and the resin was shaken in DCM (20 ml) for 75 min. The resin was filtered off and again dried before being divided into five equal portions and

resealed in porous polystyrene packets. One packet was then reacted with first benzaldehyde and then homophthalic anhydride as in Example 5. The resin was cleaved and worked up as in Example 5, providing a clear oil, 11 mg, 61% yield based on average molecular weight).

MALDI-TOF MS of the crude products after cleavage showed all five expected isoquinolines for each individual resin packet. Analysis of the final extract by proton NMR and MALDI-TOF MS indicated that only four isoquinolines were now present with the 2,6- (s)-diaminohexanoic acid based isoquinolone having been lost in the extraction procedure.

EXAMPLE 38 Solid-phase synthesis of a combinatorial library pool containing isoquinolines derived from five amino acids, 4-methoxybenzaldehyde and homophthalic anhydride This library pool was synthesized as in Example 37, with the exception of using 4-methoxybenzaldehyde instead of benzaldehyde. Cleavage from the resin was performed on all 100 mmoles of resin and yield and mass spectra were immediately obtained on the residue with no aqueous extraction being performed. Yield: 36 mg, 93%.

MALDI-TOF MS of the crude products after cleavage showed all five expected isoquinolines for each individual resin packet.

EXAMPLE 39 Solid-phase synthesis of a combinatorial library pool containing isoquinolines derived from five amino acids, 3,5-dimethoxybenzaldehyde and homophthalic anhydride This library pool was synthesized as in Example 37, with the exception of substituting 3,5-dimethoxybenzaldehyde for benzaldehyde used in Example 37. Cleavage from the resin was performed on all 100 umoles of resin and yield and mass spectra were immediately obtained on the residue with no aqueous extraction being performed. Yield: 35 mg, 84%.

MALDI-TOF MS of the crude products after cleavage showed all five expected isoquinolines for each individual resin packet.

EXAMPLE40 Solid-phase synthesis of a combinatorial library pool containing isoquinolines derived from five amino acids, 4-cyanobenzaldehyde and homophthalic anhydride This library pool was synthesized as in Example 37, with a substitution of 4-cyanobenzaldehyde for benzaldehyde used in Example 37. Cleavage from the resin was performed on all 100 umoles of resin and yield and mass spectra were immediately obtained on the residue with no aqueous extraction being performed. Yield: 34 mg, 89%. MALDI-TOF MS of the crude products after cleavage showed all five expected isoquinolines for each individual resin packet.

EXAMPLE 41 Solid-phase synthesis of a combinatorial library pool containing isoquinolines derived from five amino acids, 2-bromobenzaldehyde and homophthalic anhydride This library pool was synthesized as in Example 37, only instead of using benzaldehyde as in that Example, 2-bromobenzaldehyde was used. Cleavage from the resin was performed on all 100 umoles of resin and yield and mass spectra were immediately obtained on the residue with no aqueous extraction being performed.

Yield: 41 mg, 94%. MALDI-TOF MS of the crude products after cleavage showed all five expected isoquinolines for each individual resin packet.

EXAMPLE 42 Solid-phase synthesis of a combinatorial library pool containing isoquinolines derived from five amino acids, 3-hydroxybenzaldehyde and homophthalic anhydride This library pool was also synthesized following the procedures set forth in Example 37, with the exception of substituting 3-hydroxybenzaldehyde for the benzaldehyde. Cleavage from the resin was performed on all 100 umoles of resin and yield and mass spectra were immediately obtained on the residue with no aqueous extraction being performed. Yield: quantitative.

MALDI-TOF MS of the crude products after cleavage showed all five expected isoquinolines for each individual resin packet.

EXAMPLE43 Solid-phase synthesis of a library of 21,736 different isoquinoline amides and acids Eleven porous polypropylene tea-bags were prepared each containing polystyrene MBHA/resin (974 mg, 0.750 milliequivalents). One tea-bag was placed in a 60 ml bottle and washed with 5% (v/v) DIEA/DCM (3 x 30 ml) followed by DCM, 5 x 30 ml. A solution of N- (t-butyloxycarbonyl) glycine (657 mg, 3.75 mmoles), HOBt (507 mg, 3.75 mmoles), and DIC (0.705 ml, 4.5 mmoles) was prepared in DMF (37.5 ml) and added to the resin packet.

After shaking for 16 hrs the tea-bag was washed with DMF (3 x 30 ml) and DCM (3 x 30 ml). The same coupling procedure was performed on the remaining ten tea-bags, each being reacted with a separate amino acid from the list: N- (t-butyloxycarbonyl)-3-aminopropionic acid, N- (t-butyloxycarbonyl)-5-aminopentanoic acid, N- (t-butyloxycarbonyl)-7-aminoheptanoic acid, <BR> <BR> <BR> (s)-2-N- (t-butyloxycarbonyl)-3-N- (9-fluorenylmethoxycarbo nyl)-diaminopropionoic acid, (s)-2-N- (t-butyloxycarbonyl)-6-N- (9-fluorenylmethoxy carbonyl)-diaminohexanoic acid, (s)- (t-butyloxycarbonyl)-2-methyl-3-aminopropionic acid, (r)- (t-butyloxycarbonyl)-2-methyl-3-aminopropionic acid, N- (t-butyloxycarbonyl)-2- (2-aminoethoxyethoxy) acetic acid, N- (t-butyloxycarbonyl)-trans-4- (aminomethyl) cyclohexanecarboxylic acid, N- (t-butyloxycarbonyl)-4- (aminomethyl) benzoic acid. The tea-bags with attached (s)-2-N- (t-butyloxycarbonyl)- 3-N- (9-fluorenylmethoxycarbonyl)-diaminopropionic acid, and (s)-2-N- (t-butyloxycarbonyl)-6-N- (9-fluorenylmethoxy carbonyl)-diaminohexanoic acid were washed with DCM (2 x 50 ml), shaken twice in 20% (v/v) piperidine/DMF (30 ml, 5 min then 15 min), then washed with DMF (4 x 50 ml) and

DCM (4 x 50 ml). The remaining nine tea-bags were placed in one bottle and washed with DCM (150 ml, 15 min) and then treated with 55% (v/v) TFA/DCM (150 ml, 30 min). The bags were then washed with DCM (150 ml), isopropyl alcohol (2 x 150 ml), DCM (2 x 150 ml), 5% (v/v) DIEA/DCM (3 x 150 ml, 2 min each) and DCM (3 x 150 ml). After drying at room temperature the eleven tea-bags were cut open and the contents pooled in a bottle containing DCM (70 ml). The bottle was shaken for 90 min to thoroughly mix the resin. The DCM/resin slurry was then poured into a large (12 x 18 cm) tea-bag to separate the resin from the DCM and the resin was dried at 50°C. The resulting 11.042 g of resin (8.25 mmoles total of mixed amino acids) was divided into 39 tea-bags containing 38 x 0.241 g resin (each 180 micromoles total of mixed amino acids) and 1 x 1.204 g (900 micromoles total of mixed amino acids). Also prepared for use as a control were 38 additional tea-bags each containing 23 mg (18 micromoles) of glycine (containing a free amino group) attached to MBHA resin (coupled and deprotected as in Example 1, subheading 1, hereinafter referred to as the"glycine control tea-bags").

Placed in a 20 ml bottle were one of the small (0.241 g of mixed amino acid resin) tea-bags and one of the control (18 micromoles of glycine) tea-bags. The two tea-bags were treated with a solution of benzaldehyde (0.508 ml, 5 mmoles) and anhydrous trimethylorthoformate (1.094 ml, 10 mmoles) in anhydrous DMF (9 ml). After shaking for 3 hrs the packet was washed with anhydrous DMF (3 x 8 ml). A solution of homophthalic anhydride (801 mg, 5 mmoles) and triethylamine (0.044 ml, 0.3 mmoles) was prepared in chloroform (10 ml) and added to the tea-bag. After shaking at room temperature for 15.5 hrs the packet was washed with DMF (6 x 30 ml) and DCM (4

x 30 ml) and dried at room temperature. The remaining 37 tea-bags of mixed resin were each paired with one glycine control tea-bag and reacted as above in 37 separate reactions with the following aldehydes: 1,4-benzodioxan-6-carboxaldehyde, 1-methylindole-3-carboxaldehyde, 2,3-difluorobenzaldehyde, 2-bromobenzaldehyde, 2-chloro-5-nitrobenzaldehyde, 2-furaldehyde, 2-imidazolecarboxaldehyde, 2-naphthaldehyde, 2-pyridinecarboxaldehyde, 2-thiophenecarboxaldehyde, 3,4-dichlorobenzaldehyde, 3,5-bis (trifluoromethyl) benzaldehyde, 3,5-dihydroxybenzaldehyde, 3,5-dimethoxybenzaldehyde, 3,5-dimethyl-4-hydroxybenzaldehyde, 3- (4-methoxyphenoxy) benzaldehyde, 3-furaldehyde, 3-hydroxybenzaldehyde, 3-methyl-4-methoxybenzaldehyde, 3-methylbenzaldehyde, 3-nitrobenzaldehyde, 3-pyridinecarboxaldehyde, 3-thiophenecarboxaldehyde, 4- (3-dimethylaminopropoxy) benzaldehyde, 4- (dimethylamino) benzaldehyde, 4- (methylthio) benzaldehyde, 4- (trifluoromethyl) benzaldehyde, 4-biphenylcarboxaldehyde, 4-bromo-2-thiophenecarboxaldehyde, 4-cyanobenzaldehyde, 4-methoxy-l-naphthaldehyde, 4-nitrobenzaldehyde, 4-pyridinecarboxaldehyde, 5- (hydroxymethyl)-2-furaldehyde, 5-bromo-4-hydroxy-3-methoxybenzaldehyde, 5-nitro-2-furaldehyde and 6-methyl-2-pyridine- carboxaldehyde. The large tea-bag containing 1.204 g (900 micromoles total of mixed amino acids) of resin was reacted with 3,5-dimethoxybenzaldehyde in the same manner, but on a five times larger scale of all reagents and solvents and with no control tea-bag.

The 38 tea-bags containing mixed amino acid resin (now containing mixed isoquinolines after the anhydride condensation reaction) were cut open and the

contents pooled in a bottle containing DCM (70 ml). The bottle was shaken for 75 min to thoroughly mix the resin.

The DCM/resin slurry was then poured into a large (12 x 18 cm) tea-bag to separate the resin from the DCM and the resin was dried at room temperature. The resulting 10.144 g of resin (6.84 mmoles total of mixed isoquinolines) was divided into 52 tea-bags each containing 0.178 g resin (120 micromoles total of mixed isoquinolines). For use as a control the large tea-bag containing 900 micromoles total of mixed amino acid resin (now mixed isoquinolines) was cut open, weighed (1.331 g = 900 micromoles) and divided into 52 tea-bags each containing 22 mg (15 micromoles) of resin. Placed in a 20 ml bottle were one of the small (0.178 g of mixed isoquinoline resin) tea-bags and one of the second set of control (15 micromoles of mixed isoquinoline) tea-bags.

The two tea-bags were treated with a solution of HATU in anhydrous DMF (2.4 mmoles, 8 ml, 300 mM solution) and shaken for 20 min. The HATU solution was decanted off of the tea-bags and anhydrous DMF (6.9 ml) and cyclopropyl amine (0.52 ml, 7.5 mmoles) were added. After shaking for 1 hr the cyclopropyl amine solution was removed and the bags were washed with anhydrous DMF (2 x 8 ml). The HATU treatment was repeated followed by decanting and addition of a second cyclopropyl amine solution. This reaction was shaken at room temperature for 24 hrs. The bags were then washed with DMF (3 x 8 ml), water (8 ml, 60 min), DMF (3 x 8 ml), DCM (3 x 8 ml), and allowed to dry.

Fifty of the remaining tea-bags (each 0.178 g resin, 120 micromoles total of mixed isoquinolines) were each paired with one control tea-bag and reacted as above in 50 separate reactions with the following amines : isopropylamine, propylamine, ethanolamine,

(aminomethyl) cyclopropane, pyrrolidine, diethylamine, 2-methoxyethylamine, cyclopentylamine, piperidine, 3-pyrrolidinol, amylamine, N, N-dimethylethylenediamine, azetidine, furfurylamine, diallylamine, 2-aminothiazole, 1-aminopiperidine, 1-methylpiperazine, 4-aminomorpholine, diethanolamine, 2- (aminomethyl) pyridine, histamine, 1-(2-aminoethyl)(2-aminoethyl) pyrrolidine, 1-amino-4-methylpiperazine, tris (hydroxymethyl) aminomethane, 1-aminopyrrolidine, 1- (3-aminopropyl) imidazole, 1- (2-hydroxyethyl) piperazine, (s)-l-amino-2- (methoxymethyl) pyrrolidine, (+)-3-hydroxypiperidine, 1-amino-4- (2-hydroxyethyl) piperazine, trans-2-aminocyclohexanol, tryptamine, 1-adamantanemethylamine, (2-aminoethyl)-trimethylammonium chloride, (s)-O-t-butyl serine t-butyl ester, glycine benzyl ester, (s)-O-benzyl tyrosine benzyl ester, (s)- N'-carbobenzyloxy lysine benzyl ester, (s)-aspartic acid dibenzyl ester, (+)-3-amino-1,2-propanediol, (-)-3-amino-1,2-propanediol, (+)-tetrahydrofurfurylamine, (-)-tetrahydrofurfurylamine, (+)-exo-2-aminonorbornane, (-)-exo-2-aminonorbornane, cis-decahydroquinoline, trans-decahydroquinoline, (+)-3-aminoquinuclidine, (-)-3-aminoquinuclidine. The one remaining tea-bag was left as the free carboxylic acid. Also reacted with isopropyl amine in the same manner but on a 12.5 times larger scale were the 38 glycine control tea-bags.

The above procedures produced 52 tea-bags each containing a mixture of 418 isoquinoline amides or acids for a total library size of 21,736 compounds.

Also prepared as a control for the aldehyde reaction were 38 single compounds from the building blocks: glycine, one of 38 aldehydes and isopropyl amine. As described above, an additional control for the

amine reaction was performed resulting in 51 pools of 11 isoquinolines each prepared from the following building blocks: a mixture of the eleven amino acids, 3,5-dimethoxybenzaldehyde and, separately, each of the 51 amines. Each tea-bag prepared was cleaved separately via standard HF procedures with the addition of 0.2 ml anisole to each HF cleavage reaction as a scavenger and dissolved in an appropriate solvent and for testing in a variety of assays. The control tea-bags were cleaved in the same manner and characterized by NMR or mass spectra.

EXAMPLE44 Biological radioreceptor assay of 21,736 different isoquinoline amides and acids This example describes the identification of individual compounds contained within the synthetic combinatorial library of Example 43 which are selective inhibitors of the u and K-opioid ligands, [3H]-DAMGO and [3H]-U69,593, respectively and the o receptor ligand, radiolabeled pentazocine. Compounds were identified using the iterative approach and radioreceptor assays as described above.

Initially, libraries prepared according to Example 43, which are subsetted according to the X substituent, each subset having a unique X and every possible combination of R1 and R2, were screened in each of the u, K-opioid and a receptor assays. The subsets, identified by its pool number, and the chemical reagent used to provide the X variables are provided in Table II along with the results of the assays. Therefore, Table II identifies the relative importance of X's contribution to the activity.

TABLE II MU Kappa Sigma |Pool 1/% bound 1/% bound 1/% bound # 257 Cyclopropylamine 0. 01640 0. 01674 0.02 0.012540.014500.02073258Isopropylamine 0.011470.013650.02337259Propylamine 260 Ethanolamine 0. 01151 0. 01290 0.02270 261 (Aminomethyl) cyclo- 0. 01322 0. 01404 0.02606 propane 262 Pyrrolidine 0. 01172 0. 01539 0.01664 263 Diethylamine 0. 01124 0. 01419 0.01606 0.012230.014640.018992642-Methoxyethylamine 0.014160.038930.01841265Cyclopentylamine 266 Piperidine 0. 01250 0. 01772 0.01616 267 3-Pyrrolidinol 0. 01059 0. 01444 0.01716 268 Amylamine 0. 02391 0. 02101 0.02851 269 N, N-Dimethyl- 0. 02309 0. 01593 0.02870 ethylenediamine 270 Azetidine 0. 01179 0. 01481 0.02273 271 Furfurylamine 0. 02161 0. 01794 0.03440 272 Diallylamine 0. 01263 0. 01692 0.02539 273 2-Aminothiazole 0. 01645 0. 03261 0.01971 274 1-Aminopiperidine 0. 01031 0. 01577 0.01751 275 1-Methylpiperazine 0. 01000 0. 01652 0.01508 276 4-Aminomorpholine 0. 01000 0. 01188 0.02046 277 Diethanolamine 0. 02391 0. 01421 0.02500 278 2- (Aminomethyl)- 0. 02034 0. 01744 0.01680 pyridine 279 Histamine 0. 02381 0. 01591 0.02064 TABLE II

280 1- (2-aminoethyl)- 0.02606 0.01800 0.07710 pyrrolidine 281 1-Amino-4-0.01039 0.01497 0.01463 methylpiperazine 282 tris (Hydroxymethyl)-0.01193 0.01113 0.01808 aminomethane 283 1-Aminopyrrolidine 0.01080 0.01381 0.02244 284 1- (3-Aminopropyl)- 0.01429 0.01258 0.01484 imidazole 285 1- (2-Hydroxyethyl)- 0.01096 0.01382 0.01447 piperazine 286 (S)-1-Amino-2-0.01081 0.01185 0.01617 (methoxymethyl)- pyrrolidine 287 (+)-3-Hydroxy-0.01000 0.01222 0.02219 piperidine 288 1-Amino-4-(2-0.01153 0.01418 0.02048 hydroxyethyl)- piperazine 289 trans-2-0.01228 0.01515 0.02217 Aminocyclohexanol 290 Tryptamine 0.08613 0.02747 0.04335 291 1-Adamantanemethyl-0.01730 0.03842 1.13636 amine 292 (2-Aminoethyl)-0.01238 0.01511 0.02483 trimethylammonium 293 (L)-Serine 0.01115 0.01321 0.02116 294 Glycine 0.01113 0.01185 0.02100 295 (L)-Tyrosine 0.01129 0.01226 0.01500 296 (L)-Lysine 0.01078 0.01160 0.01611

TABLE IL 297 (L)-Aspartic Acid 0.01171 0.01245 0.01503 298 (+/-)-3-Amino-1,2- 0.01228 0.01372 0.02352 propanediol 299 (+/-)-3-Amino-1,2- 0.01237 0.02064 0.02179 propanediol 300 (+/-)-Tetrahydro-0.01383 0.02073 0.02443 furfurylamine 301 (+/-)-Tetrahydro-0.01394 0.02337 0.02210 furfurylamine 302 (+/-)-exo-2-0.01689 0.02270 0.03473 Aminonorbornane 303 (+/-)-exo-2-0.01566 0.02606 0.03446 Aminonorbornane 304 ci/trans-0.01327 0.01664 0.02764 Decahydroquinoline 305 ci/trans-0.01254 0.01606 0.02958 Decahydroquinoline 306 (+/-)-3-0.01608 0.01899 0.02530 Aminoquinuclidine 307 (+/-)-3-0.01640 0.01841 0.02342 Aminoquinuclidine

The results of the screen provide evidence that there is selectivity of certain compounds for one opioid receptor over another. More importantly, the assays identify certain classes of compounds which are particularly active. For instance, those compounds made from cyclopentylamine for X (pool # 265) are particularly good inhibitors of the [3H]-U69,593 ligand at the K-opioid receptor. Compounds made from 1-adamantanemethylamine at the X position (pool # 291) were identified as

significant inhibitors of pentazocine ligand at the o receptor.

From these results, additional subsets of compounds, keeping X constant as adamantanemethylamine and varying at R'and R, were prepared and screened in the a receptor assay to determine their relative contribution to the compounds'activity. As described below, an additional 418 compounds were prepared, subsetted by varying R2 substituents, and screened, followed by the synthesis of 11 compounds varying only at the R1 position to identify the lead compound.

Solid-phase synthesis of an iterative library of 418 different isoquinoline amides Thirty-eight tea-bags each containing a mixture of 11 amino acids on resin (7 mg, 5 micromoles) were prepared as in Example 43. Each tea-bag was reacted with a single aldehyde from the list: 1,4-benzodioxan-6-carboxaldehyde, 1-methylindole-3-carboxaldehyde, 2,3-difluorobenzaldehyde, 2-bromobenzaldehyde, 2-chloro-5-nitrobenzaldehyde, 2-furaldehyde, 2-imidazolecarboxaldehyde, 2-naphthaldehyde, 2-pyridinecarboxaldehyde, 2-thiophenecarboxaldehyde, 3,4-dichlorobenzaldehyde, 3,5-bis (trifluoromethyl) benzaldehyde, 3,5-dihydroxybenzaldehyde, 3,5-dimethoxybenzaldehyde, 3,5-dimethyl-4-hydroxybenzaldehyde, 3- (4-methoxyphenoxy) benzaldehyde, 3-furaldehyde, 3-hydroxybenzaldehyde, 3-methyl-4-methoxybenzaldehyde, 3-methylbenzaldehyde, 3-nitrobenzaldehyde, 3-pyridinecarboxaldehyde, 3-thiophenecarboxaldehyde, 4- (3-dimethylaminopropoxy)

benzaldehyde, 4- (dimethylamino) benzaldehyde, 4- (methylthio) benzaldehyde, 4- (trifluoromethyl) benzaldehyde, 4-biphenylcarboxaldehyde, 4-bromo-2-thiophenecarboxaldehyde, 4-cyanobenzaldehyde, 4-methoxy-l-naphthaldehyde, 4-nitrobenzaldehyde, 4-pyridinecarboxaldehyde, 5- (hydroxymethyl)-2-furaldehyde, 5-bromo-4-hydroxy-3-methoxybenzaldehyde, 5-nitro-2-furaldehyde, 6-methyl-2-pyridine- carboxaldehyde, and benzaldehyde as in Example 43, but scaled down to 80% as much aldehyde, TMOF, and solvent.

The dried tea-bags were all placed in a 60 ml bottle and washed with anhydrous DMF (2 x 30 ml).

Anhydrous DMF (30 ml) was then added to the tea-bags followed by HATU (3.5 g, 9.2 mmoles) and the tea-bags were shaken for 20 min. The HATU solution was next decanted and the tea-bags were washed with anhydrous DMF (1 x 20 ml). Anhydrous DMF (18.7 ml) was added to the tea-bags followed by 1-adamantanemethylamine (2.0 g, 12 mmoles). After shaking for 1 hour, the tea-bags were washed with anhydrous DMF (2 x 20 ml) and the HATU and 1- adamantanemethylamine treatments were repeated. After shaking for 16 hrs. the tea-bags were washed with DMF (4 x 20 ml), water (1 x 20 ml for 15 min., DMF (4 x 20 ml), and DCM (4 x 20 ml). After drying the tea-bags were cleaved as in Example 43, extracted into 1: 1 water/acetonitrile, examined by mass spectrometry, and <BR> <BR> <BR> <BR> <BR> tested in the o receptor assay as described above. Table III provides the results of that assay and evidences that pool # M367, derived from 5-hydroxymethylfuraldehyde, are the most active compounds. It was discovered in the course of identifying the individual compounds that the R2 group resulting from 5- (hyrdoxymethyl) furanaldehhyde, 5- (hydroxymethyl) furan-2-yl, reacted with the anisole scavenger during HF cleavage to yield the Freidel-Crafts alkylation product, 5- (4'-methoxybenzyl) furan-2-yl.

TABLE III Pool R2 1/IC50 IC50 (nM) C291 all mixed 0.00175 573 M250 3,5-Dimethoxybenzaldehyde 0.00065 1,534 M334 1,4-Benzodioxan-6-carboxaldehyde 0.00103 973 M335 1-Methylindole-3-carboxaldehyde 0.00104 963 M336 2,3-Difluorobenzaldehyde 0.00081 1,241 M337 2-Bromobenzaldehyde 0.00096 1,043 M338 2-Chloro-5-nitrobenzaldehyde 0.00065 1,527 M339 2-Furaldehyde 0.00147 682 M340 2-Imidazolecarboxaldehyde 0.00065 1,541 M341 2-Naphthaldehyde 0.00050 2,018 M342 2-Pyridinecarboxaldehyde 0.00063 1,579 M343 2-Thiophenecarboxaldehyde 0.00056 1,775 M344 3,4-Dichlorobenzaldehyde 0.00098 1,016 M345 3,5-Bis (trifluoromethyl) 0.00094 1,063 benzaldehyde M346 3,5-Dihydroxybenzaldehyde 0.00091 1,095 M347 5-Bromo-4-hydroxy-3-0.00109 921 methoxybenzaldehyde M348 1,415 hydroxybenzaldehyde M349 3- (4-Methoxyphenoxy) 0. 00102 977 benzaldehyde M350 3-Furaldehyde 0.00091 1.099 M351 3-Hydroxybenzaldehyde 0.00108 926

TABLE III M352 3-Methyl-4-methoxybenzaldehyde 0. 00078 1,286 0.000731,366M3533-Methylbenzaldehyde 0.000621,623M3543-Nitrobenzaldehyde 0.000631,575M3553-Pyridinecarboxaldehyde M356 3-Thiophenecarboxaldehyde 0. 00088 1,136 M357 4- (3-Dimethylaminopropoxy) 0.00075 1,325 benzaldehyde 0.00115869M3584-(Dimethylamino)benzaldehyde 0.00120834M3594-(Methylthio)benzaldehyde 0.00105950M3604-(Trifluoromethyl)benzaldehyde M361 4-Biphenylcarboxaldehyde 0. 00091 1,096 M362 4-Bromo-2-thiophene 0. 00093 1,071 carboxaldehyde M363 4-Cyanobenzaldehyde 0. 00067 1,490 M364 4-Methoxy-1-naphthaldehyde 0. 00084 1,187 0.000911,103M3654-Nitrobenzaldehyde M366 4-Pyridinecarboxaldehyde 0. 00101 995 M367 5- (Hydroxymethyl)-2-furaldehyde 0. 00234 428 M369 5-Nitro-2-furaldehyde 0. 00163 613 M370 6-Methyl-2-0. 00086 1,162 pyridinecarboxaldehyde M371 Benzaldehyde 0. 00103 969 Solid-phase synthesis of an iterative library of 11 different isoquinoline amides Ten tea-bags each containing one amino acid on resin (75 micromoles) were prepared as in Example 43. As identified in Example 43, one amino acid was in a racemic mixture, therefor accounting for 11 different compounds

in 10 bags. All of the tea-bags were placed in a 125 ml bottle and washed with anhydrous DMF (1 x 60 ml). Added to the tea-bags were anhydrous DMF (27 ml), 5- hydroxymethylfurfural (1.893 g, 15 mmoles), and anhydrous TMOF (3.282 ml, 30 mmoles). After shaking for 3.25 hr the tea-bags were washed with anhydrous DMF (3 x 50 ml) and anhydrous chloroform (1 x 50 ml). Next added to the tea-bags were anhydrous chloroform (30 ml), homophthalic anhydride (2.432 g, 15 mmoles), and triethylamine (0.133 ml, 1 mmole). After shaking for 15.5 hrs., the tea-bags were washed with DMF (5 x 50 ml) and DCM (4 x 50 ml).

The tea-bags were next washed with anhydrous DMF (2 x 50 ml). Added to the tea-bags were anhydrous DMF (48 ml) and HATU (5.47 g, 14.4 mmoles). After shaking for 20 min., the HATU solution was decanted and the tea-bags were washed with anhydrous DMF (1 x 50 ml). Anhydrous DMF (25 ml) was added to the tea-bags followed by 1- adamantanemethylamine (4.429 g, 25 mmoles). After shaking for 1 hr, the tea-bags were washed with anhydrous DMF (2 x 50 ml) and the HATU and 1-adamantanemethylamine treatments were repeated. After shaking for 18 hrs. the tea-bags were washed with DMF (4 x 50 ml), water (1 x 50 ml for 40 min., DMF (4 x 50 ml), and DCM (4 x 50 ml).

After drying the tea-bags were cleaved as in Example 43, extracted into 1: 1 water/acetonitrile, examined by mass spectrometry, and screened in the o receptor assay, the results of which are shown in Table IV.

TABLE IV Rl IC50 (nM) 1 7-Aminoheptanoic acid 56 2 trans-4- (Aminomethyl) 68 cyclohexanecarboxylic acid 1 3 (S)-2,4-Diaminopropionic acid 71

TABLE IV 4 (R/S)-3-Amino-2-86 methylpropionic acid 5 2- (2-Aminoethoxy (ethoxy)) 117 acetic acid 662-Aminoacetic acid 124 774-(Aminomethyl)benzoic acid 130 8 (S)-2,6-Diaminohexanoic acid 150 9 5-Aminopentanoic acid 231 10 3-Aminopropionic acid 355 From the results of the iterative approach and these screens as evidenced in Table IV, the most active compound from the library of Example 43 is one for which R1 is 1,6-hexyl, R2 is 5-(4'-methoxybenzyl)-furan-2-yl, R3 through R6 are, independently a hydrogen atom, X is 1- aminomethyladamantanyl, and Y is C (O) NH2.

EXAMPLE 45 Solid-phase synthesis of a library of 20,900 different isoquinoline amides and acids Eleven porous polypropylene tea-bags are prepared each containing polystyrene MBHA/resin (974 mg, 0.750 milliequivalents). One tea-bag is placed in a 60 ml bottle and washed with 5% (v/v) N, N,-diisopropylethylamine/dichloromethane (3 x 30 ml) followed by dichloromethane (DCM, 5 x 30 ml). A solution of N- (t-butyloxycarbonyl) glycine (657 mg, 3.75 mmoles), HOBt (507 mg, 3.75 mmoles), and DIC (0.705 ml, 4.5 mmoles) is prepared in DMF (37.5 ml) and added to the resin packet. After shaking for 16 hrs the tea-bag is washed with DMF (3 x 30 ml) and DCM (3 x 30 ml). The same coupling procedure is performed on the remaining ten

tea-bags, each being reacted with a separate amino acid from the list: N- (t-butyloxycarbonyl)-3-aminopropionic acid, N- (t-butyloxycarbonyl)-5-aminopentanoic acid, N- (t-butyloxycarbonyl)-7-aminoheptanoic acid, <BR> <BR> <BR> <BR> (s)-2-N- (t-butyloxycarbonyl)-3-N- (9-fluorenylmethoxycarbo nyl)-diaminopropionic acid, <BR> <BR> <BR> <BR> (s)-2-N- (t-butyloxycarbonyl)-6-N- (9-fluorenylmethoxycarbo nyl)-diaminohexanoic acid, (s)- (t-butyloxycarbonyl)-2-methyl-3-aminopropionic acid, (r)- (t-butyloxycarbonyl)-2-methyl-3-aminopropionic acid, N- (t-butyloxycarbonyl)-2- (2-aminoethoxyethoxy) acetic acid, N- (t-butyloxycarbonyl)-trans-4- (aminomethyl) cyclohexanecarboxylic acid, N- (t-butyloxycarbonyl)-4- (aminomethyl) benzoic acid. The tea-bags with attached <BR> <BR> <BR> <BR> (s)-2-N- (t-butyloxycarbonyl)-3-N- (9-fluorenylmethoxycarbo nyl)-diaminopropionic acid, and <BR> <BR> <BR> <BR> (s)-2-N- (t-butyloxycarbonyl)-6-N- (9-fluorenylmethoxycarbo nyl)-diaminohexanoic acid are washed with DCM (2 x 50 ml), shaken twice in 20% (v/v) piperidine/DMF (30 ml, 5 min then 15 min), then washed with DMF (4 x 50 ml) and DCM (4 x 50 ml). The remaining nine tea-bags are placed in one bottle and washed with DCM (150 ml, 15 min) and then treated with 55% (v/v) TFA/DCM (150 ml, 30 min).

The bags are then washed with DCM (150 ml), isopropyl alcohol (2 x 150 ml), DCM (2 x 150 ml), 5% (v/v) DIEA/DCM (3 x 150 ml, 2 min each) and DCM (3 x 150 ml). After drying at room temperature the eleven tea-bags are cut open and the contents pooled in a bottle containing DCM (70 ml). The bottle is shaken for 90 min to thoroughly mix the resin. The DCM/resin slurry is then poured into a large (12 x 18 cm) tea-bag to separate the resin from the DCM and the resin is dried at 50°C. The resulting 11.042 g of resin (8.25 mmoles total of mixed amino acids) is divided into 39 tea-bags containing 38 x 0.241

g resin (each 180 micromoles total of mixed amino acids) and 1 x 1.204 g (900 micromoles total of mixed amino acids). Also prepared for use as a control are 38 additional tea-bags each containing 23 mg (18 micromoles) of glycine (containing a free amino group) attached to MBHA resin (coupled and deprotected as in Example 43).

Placed in a 20 ml bottle are one of the small (0.241 g of mixed amino acid resin) tea-bags and one of the control (18 micromoles of glycine) tea-bags. The two tea-bags are treated with a solution of benzaldehyde (0.508 ml, 5 mmoles) and anhydrous trimethylorthoformate (1.094 ml, 10 mmoles) in anhydrous DMF (9 ml). After shaking for 3 hrs the packet is washed with anhydrous DMF (3 x 8 ml). A solution of homophthalic anhydride (801 mg, 5 mmoles) and triethylamine (0.044 ml, 0.3 mmoles) is prepared in chloroform (10 ml) and added to the tea-bag.

After shaking at room temperature for 15.5 hrs the packet is washed with DMF (6 x 30 ml) and DCM (4 x 30 ml) and dried at room temperature. The remaining 37 tea-bags of mixed resin are each paired with one glycine control tea- bag and reacted as in Example 43 in 37 separate reactions with the following aldehydes: 1,4-benzodioxan-6-carboxaldehyde, 1-methylindole-3-carboxaldehyde, 2,3-difluorobenzaldehyde, 2-bromobenzaldehyde, 2-chloro-5-nitrobenzaldehyde, 2-furaldehyde, 2-imidazolecarboxaldehyde, 2-naphthaldehyde, 2-pyridinecarboxaldehyde, 2-thiophenecarboxaldehyde, 3,4-dichlorobenzaldehyde, 3,5-bis (trifluoromethyl) benzaldehyde, 3,5-dihydroxybenzaldehyde, 3,5-dimethoxybenzaldehyde, 3,5-dimethyl-4-hydroxybenzaldehyde, 3- (4-methoxyphenoxy) benzaldehyde, 3-furaldehyde, 3-hydroxybenzaldehyde, 3-methyl-4-methoxybenzaldehyde, 3-methylbenzaldehyde,

3-nitrobenzaldehyde, 3-pyridinecarboxaldehyde, 3-thiophenecarboxaldehyde, 4- (3-dimethylaminopropoxy) benzaldehyde, 4- (dimethylamino) benzaldehyde, 4- (methylthio) benzaldehyde, 4- (trifluoromethyl) benzaldehyde, 4-biphenylcarboxaldehyde, 4-bromo-2-thiophenecarboxaldehyde, 4-cyanobenzaldehyde, 4-methoxy-l-naphthaldehyde, 4-nitrobenzaldehyde, 4-pyridinecarboxaldehyde, 5- (hydroxymethyl)-2-furaldehyde, 5-bromo-4-hydroxy-3-methoxybenzaldehyde, 5-nitro-2-furaldehyde and 6-methyl-2-pyridinecarboxaldehyde. The large tea-bag containing 1.204 g (900 micromoles total of mixed amino acids) of resin is reacted with 3,5-dimethoxybenzaldehyde in the same manner, but on a five times larger scale of all reagents and solvents and with no control tea-bag.

The 38 tea-bags containing mixed amino acid resin (now containing mixed isoquinolines after the above reaction) are cut open and the contents pooled in a bottle containing DCM (70 ml). The bottle is shaken for 75 min to thoroughly mix the resin. The DCM/resin slurry is then poured into a large (12 x 18 cm) tea-bag to separate the resin from the DCM and the resin is dried at room temperature. The resulting 10.144 g of resin (6.84 mmoles total of mixed isoquinolines) is divided into 49 tea-bags each containing 0.178 g resin (120 micromoles total of mixed isoquinolines). For use as a control the large tea-bag containing 900 micromoles total of mixed amino acid resin (now mixed isoquinolines) is cut open, weighed (1.331 g = 900 micromoles) and divided into 50 tea-bags each containing 22 mg (15 micromoles) of resin.

Placed in a 20 ml bottle are one of the small (0.178 g of mixed isoquinoline resin) tea-bags and one of the second set of control (15 micromoles of mixed isoquinoline) tea-

bags. The two tea-bags are treated with a solution of HATU in anhydrous DMF (2.4 mmoles, 8 ml, 300 mM solution) and shaken for 20 min. The HATU solution is decanted off of the tea-bags and anhydrous DMF (6.9 ml) and aniline (0.683 ml, 7.5 mmoles) are added. After shaking for 1 hr the aniline solution is removed and the bags are washed with anhydrous DMF (2 x 8 ml). The HATU treatment is repeated followed by decanting and addition of a second aniline solution. This reaction is shaken at room temperature for 24 hrs. The bags are then washed with DMF (3 x 8 ml), water (8 ml, 60 min), DMF (3 x 8 ml), DCM (3 x 8 ml), and allowed to dry. Forty eight of the remaining tea-bags (each 0.178 g resin, 120 micromoles total of mixed isoquinolines) are each paired with one control tea-bag and reacted as in Example 43 in 48 separate reactions with the following amines : 2-fluoroaniline, 3-fluoroaniline, 4-fluoroaniline, 2-chloroaniline, 3-chloroaniline, 4-chloroaniline, 2-bromoaniline, 3-bromoaniline, 4-bromoaniline, 2-methoxyaniline, 3-methoxyaniline, 4-methoxyaniline, 2-hydroxyaniline, 3-hydroxyaniline, 4-hydroxyaniline, 2-carboethoxyaniline, 3-carboethoxyaniline, 4-carboethoxyaniline, 2-trifluoromethylaniline, 3-trifluoromethylaniline, 4-trifluoromethylaniline, 2-dimethylaminoaniline, 3-dimethylaminoaniline, 4-dimethylaminoaniline, 2-phenoxyaniline, 3-phenoxyaniline, 4-phenoxyaniline, 3,4-methylenedioxyaniline, 2,3-methylenedioxyaniline, 2,3-difluoroaniline, 3,4-difluoroaniline, 2,3-dichloroaniline, 3,4-dichloroaniline, 2,3-dibromoaniline, 3,4-dibromoaniline, 2,3-dimethoxyaniline, 3,4-dimethoxyaniline, 1-amino-5,6,7,8-tetrahydronaphthalelene, 2-hydroxy-3-amino-5,6,7,8-tetrahydronaphthalelene, 2-aminonaphthalene, 1-amino-4-chloronaphthalene,

1-amino-4-bromonaphthalene, 5-amino-1-hydroxynaphthalene, 1-amino-2-hydroxynaphthalene, 5-aminoindane, 1-aminofluorene, 2-aminofluorine, N-methylaniline. The remaining tea-bag is left as the free carboxylic acid.

Also reacted with aniline in the same manner but on a 12.5 times larger scale are the 38 glycine control tea- bags as in Example 43. The above procedures produced 50 tea-bags each containing a mixture of 418 isoquinoline amides or acids for a total library size of 20900 compounds.

Also prepared as a control for the aldehyde reaction are 38 single compounds from the building blocks: glycine, one of 38 aldehydes and aniline. An additional control for the amine reaction is performed resulting in 49 pools of 11 isoquinolines each prepared from the following building blocks: a mixture of the eleven amino acids, 3,5-dimethoxybenzaldehyde and, separately, each of the 49 amines. Each tea-bag prepared is cleaved separately via standard HF procedures (Example 3), dissolved in an appropriate solvent and tested in a variety of assays. The control tea-bags are cleaved in the same manner and characterized by NMR or mass spectra.

EXAMPLE 46 Solid-phase synthesis of a library of 459,000 different isoquinoline amides and acids This example describes an expanded library compared to that provided in Example 43, having even more possibilities at R1, R2 and X positions.

Seventy-two porous polypropylene tea-bags were prepared each containing polystyrene MBHA/resin (1.111 g,

1.0 milliequivalents). Six tea-bags were placed in a 500 ml bottle. A solution of N- (t-butyloxycarbonyl)-3- aminopropionic acid (beta alanine) (6.237 g, 33 mmoles), HOBt (4.458 g, 33 mmoles), and DIC (6.2 ml, 39.6 mmoles) was prepared in DMF (275 ml) and added to the resin packet. After shaking for 22 hrs N, N- dimethylaminopyridine (164 mg, 1.3 mmoles) was added and the solution shaken for an additional 18 hrs. The tea- bags were then washed with DMF (3 x 300 ml) and DCM (3 x 300 ml). The same coupling procedure was performed on the remaining 66 tea-bags in groups of six at a time, each six being reacted with a separate amino acid from the list: N- (t-butyloxycarbonyl) glycine, N- (t-butyloxycarbonyl)-5-aminopentanoic acid, N- (t-butyloxycarbonyl)-7-aminoheptanoic acid, <BR> <BR> <BR> <BR> (s)-2-N- (t-butyloxycarbonyl)-3-N- (9-fluorenylmethoxycarbo nyl)-diaminopropionic acid, <BR> <BR> <BR> <BR> (s)-2-N- (t-butyloxycarbonyl)-6-N- (9-fluorenylmethoxycarbo nyl)-diaminohexanoic acid, (s)- (t-butyloxycarbonyl)-2-methyl-3-aminopropionic acid, (r)- (t-butyloxycarbonyl)-2-methyl-3-aminopropionic acid, N- (t-butyloxycarbonyl)-trans-4- (aminomethyl) cyclohexanecarboxylic acid, N- (t-butyloxycarbonyl)-4- (aminomethyl) benzoic acid, (t-butyloxycarbonyl)-6-aminohexanoic acid, and (t-butyloxycarbonyl)-4-aminobutyric acid.

An additional 36 tea-bags, each containing 1.111 g of MBHA resin (1.0 mmole) were also prepared.

Eighteen of these bags were added to a preformed solution of 4- (bromomethyl) phenylacetic acid (20.61 g, 90 mmoles) and DIC (4.29 ml, 108 mmoles) in DMF (200 ml) and shaken at room temperature for 16 hrs. Eighteen additional bags were coupled identically, but to bromoacetic acid. After 16 hrs the two sets of tea-bags were each washed with DMF

(3 x 300 ml) and DCM (3 x 300 ml) and allowed to dry at room temperature. Six bags of bromoacetic acid on resin were paired with six bags of 4- (bromomethyl) phenylacetic acid on resin and added to a preformed solution of the HC1 salt of 2-aminoethanethiol (19.88 g, 175 mmoles) in DMF (200 ml). After shaking 116 hrs DIEA (33.53 ml, 193 mmoles) was added and the bags shaken an additional 126 hrs. Identical conditions were used for the attachment of two other nucleophiles (1-amino-2-methyl-2- propanethiol and delta-Boc-ornithine methyl ester) to the bromoalkyl derivatized resins. Cleavage of a small aliquot of each and characterization by NMR and mass spectroscopy showed that the expected amino-derivatized resin had formed in 5 of the 6 examples. The reaction between bromoacetic-derivatized resin and the Boc- ornithine nucleophile provided only low yields of product; these tea-bags were therefore discarded. The 30 tea-bags resulting from the five successful reactions were used for further synthesis as described below.

The tea-bags with attached <BR> <BR> <BR> <BR> (s)-2-N- (t-butyloxycarbonyl)-3-N- (9-fluorenylmethoxycarbo nyl)-diaminopropionic acid, and <BR> <BR> <BR> <BR> (s)-2-N- (t-butyloxycarbonyl)-6-N- (9-fluorenylmethoxycarbo nyl)-diaminohexanoic acid were washed with DCM (2 x 300 ml), shaken twice in 20% (v/v) piperidine/DMF (300 ml, 5 min then 15 min), then washed with DMF (4 x 300 ml) and DCM (4 x 300 ml).

The 24 tea-bags containing amino-derivatized resin prepared from the two thiol nucleophiles required no deprotection. All of the remaining 66 tea-bags carried Boc-protected derivatives on resin and were therefore deprotected. These tea-bags were placed in two bottles, each of which was treated identically as

follows. Each set of bags were first washed with DCM (900 ml, 15 min) and then treated with 55% (v/v) TFA/DCM (900 ml, 30 min). The bags were then washed with DCM (900 ml for each set), isopropyl alcohol (2 x 900 ml for each set), DCM (2 x 900 ml for each set), 5% (v/v) DIEA/DCM (3 x 900 ml, 2 min each set) and DCM (3 x 900 ml for each set).

After drying at room temperature all 102 of the tea-bags were cut open and 5.85 mmoles of each acid attached to resin was pooled in a bottle containing DCM (600 ml). The bottle was shaken for 180 min to thoroughly mix the resin. The DCM/resin slurry was then poured into two large (12 x 18 cm) tea-bag to separate the resin from the DCM and the resin was dried at room temperature. The resulting 121.6 g of resin (99.45 mmoles of mixed amino acids) was divided into 90 tea-bags each containing 0.673 g resin (each 550 micromoles total of mixed amino acids). An additional identical 90 bags were prepared for use in later iterational deconvolution.

Also prepared for use as a control were 90 additional tea-bags each containing 49 mg (45 micromoles) of glycine (containing a free amino group) attached to MBHA resin (coupled and deprotected as described previously in this example).

Placed in a 60 ml bottle were one of the library (0.673 g, 550 umoles of mixed amino acid resin) tea-bags and one of the control (45 micromoles of glycine) tea-bags. The two tea-bags were treated with a solution of benzaldehyde (2.135 ml, 21 mmoles) and anhydrous trimethylorthoformate (4.6 ml, 42 mmoles) in anhydrous DMF (38 ml). After shaking for 4 hrs the packets were washed with anhydrous DMF (3 x 20 ml) and anhydrous chloroform (1 x 20 ml). A solution of

homophthalic anhydride (2.4 g, 15 mmoles) and triethylamine (0.132 ml, 0.9 mmoles) was prepared in chloroform (30 ml) and added to the tea-bag. After shaking at room temperature for 16 hrs the packets were washed with DMF (4 x 30 ml) followed by DCM (3 x 30 ml) and dried at room temperature. The remaining 89 tea-bags of mixed resin were each paired with one glycine control tea-bag and reacted as described for benzaldehyde in 89 separate reactions with the following aldehydes: 2- bromobenzaldehyde, 2-cyanobenzaldehyde, 2- fluorobenzaldehyde, 2-hydroxybenzaldehyde (salicylaldehyde), 2-methoxybenzaldehyde (o- anisaldehyde), 3-bromobenzaldehyde, 3- carboxybenzaldehyde, 3-cyanobenzaldehyde, 3- fluorobenzaldehyde, 3-hydroxybenzaldehyde, 3- methoxybenzaldehyde (m-anisaldehyde), 3- methylbenzaldehyde (m-tolualdehyde), 3-nitrobenzaldehyde, 3- (trifluoromethyl) benzaldehyde, 4-acetamidobenzaldehyde, 4-bromobenzaldehyde, 4-carboxybenzaldehyde, 4- cyanobenzaldehyde, 4- (3- dimethylaminopropoxy) benzaldehyde, 4-fluorobenzaldehyde, 4- (dimethylamino) benzaldehyde, 4-hydroxybenzaldehyde, 4- isopropylbenzaldehyde, 4-methoxybenzaldehyde (p- anisaldehyde), 4-methylbenzaldehyde (p-tolualdehyde), 4- (methylcarboxylate) benzaldehyde, 4- methylsulphonylbenzaldehyde, 4- (methylthio) benzaldehyde, 4-nitrobenzaldehyde, 4-propoxybenzaldehyde, 4- (trifluoromethyl) benzaldehyde, 3,5- bis (trifluoromethyl) benzaldehyde, 3,5- dimethoxybenzaldehyde, 3,5-dibenzyloxybenzaldehyde, 3,5- dichlorobenzaldehyde, 2,3-difluorobenzaldehyde, 2,4- dichlorobenzaldehyde, 2-chloro-5-nitrobenzaldehyde, 2- chloro-6-fluorobenzaldehyde, 2,6-difluorobenzaldehyde, 3- bromo-4-fluorobenzaldehyde, 3,4-dibenzyloxybenzaldehyde, 3,4-dichlorobenzaldehyde, 3,4-difluorobenzaldehyde, 3-

fluoro-4-methoxybenzaldehyde, 3-nitro-4- chlorobenzaldehyde, 3-hydroxy-4-methoxybenzaldehyde, 3- hydroxy-4-nitrobenzaldehyde, 4-methoxy-3- (sulfonic acid sodium salt) benzaldehyde, 3-methyl-4-methoxybenzaldehyde, 2,3,4-trifluorobenzaldehyde, 2,3,5-trichlorobenzaldehyde, 3,5-dimethyl-4-hydroxybenzaldehyde, 3-methoxy-4-hydroxy- 5-bromobenzaldehyde, 3-methoxy-4-hydroxy-5- nitrobenzaldehyde, 1,4-benzodioxan-6-carboxaldehyde, 2,3- (methylenedioxy) benzaldehyde, 3,4- (methylenedioxy) benzaldehyde, 3,4- (methylenedioxy)-6- nitrobenzaldehyde, 9-formyl-8-hydroxyjulolidine, 3- (3,4- dichlorophenoxy) benzaldehyde, 3- (4- methoxyphenoxy) benzaldehyde, 3-phenoxybenzaldehyde, 4- phenoxybenzaldehyde, 4-biphenylcarboxaldehyde, 1- napthaldehyde, 2-naphthaldehyde, 4-methoxy-1- naphthaldehyde, 2-quinolinecarboxaldehyde, 3- quinolinecarboxaldehyde, 4-quinolinecarboxaldehyde, 8- hydroxyquinoline-2-carboxaldehyde, 9-ethyl-3- carbazolecarboxaldehyde, 2-thiophenecarboxaldehyde, 3- thiophenecarboxaldehyde, 5-methyl-2- thiophenecarboxaldehyde, 2-furaldehyde, 3-furaldehyde, 5- methyl-2-furaldehyde, 2-pyridinecarboxaldehyde, 3- pyridinecarboxaldehyde, 4-pyridinecarboxaldehyde, 6- methyl-2-pyridinecarboxaldehyde, pyrrole-2- carboxaldehyde, 1-methyl-2-pyrrolecarboxaldehyde, 2- imidazolecarboxaldehyde, 2-thiazolecarboxaldehyde, 5- (hydroxymethyl)-2-furaldehyde, and 5-nitro-2-furaldehyde.

Twelve additional tea-bags each containing 1 mmole of glycine on MBHA resin (prepared as described previously in this example) was reacted with benzaldehyde in the same manner, but on a ten times larger scale of all reagents and solvents and with no control tea-bag.

The 90 tea-bags containing mixed amino acid resin (now containing mixed isoquinolines after the above reaction) were cut open and the contents pooled in a bottle containing DCM (400 ml). The bottle was shaken for 70 min to thoroughly mix the resin. The DCM/resin slurry was then poured into a large (45 x 23 cm) tea-bag to separate the resin from the DCM and the resin was dried at room temperature. The resulting 76.58 g of resin (49.5 mmoles total of mixed isoquinolines) was divided into 160 tea-bags each containing 0.154 g resin (100 micromoles each of mixed isoquinolines) and 160 tea- bags each containing 0.309 g resin (200 micromoles each of mixed isoquinolines) for use in preparation of a reduced library (Example 50).

For use as controls the twelve tea-bags containing a total of 12 mmoles of the isoquinoline prepared from glycine, homophthalic anhydride and benzaldehyde were cut open, weighed (total 17.17 g = 12 mmoles) and divided into 160 tea-bags each containing 72 mg (50 micromoles) of resin (35 tea-bags each containing 144 mg (100 micromoles) of resin were also prepared for use as controls in the reduced library synthesis (Example 50).

Placed in a 20 ml bottle were one of the library (154 mg, 100 umoles of mixed isoquinoline resin) tea-bags and one of the second set of control tea-bags containing 72 mg of the isoquinoline prepared from glycine, homophthalic anhydride and benzaldehyde. The two tea-bags were treated with a solution of HATU in anhydrous DMF (6 mmoles, 20 ml, 300 mM solution) and shaken for 20 min. The HATU solution was decanted off of the tea-bags and anhydrous DMF (20 ml) and aniline (1.823 ml, 20 mmoles) were added. After shaking for 1 hr the

aniline solution was removed and the bags were washed with anhydrous DMF (2 x 20 ml). The HATU treatment was repeated followed by decanting and addition of a second aniline solution as before. This reaction was shaken at room temperature for 14 hrs. The bags were then washed with DMF (4 x 20 ml), water (20 ml, 2 x 20 min), DMF (4 x 20 ml), DCM (4 x 20 ml), and allowed to dry at room temperature. One hundred forty-two of the remaining tea- bags (each 154 mg resin, 100 micromoles total of mixed isoquinolines) were each paired with one control tea-bag and reacted as described above for aniline in 148 separate reactions with the following amines : 2- fluoroaniline, 2-methoxyaniline (o-anisidine), 2- (methylmercapto) aniline, benzylamine, 2- methylbenzylamine, 2-chlorobenzylamine, 2- methoxybenzylamine, 2-trifluoromethylbenzylamine, 3- fluoroaniline, 3-trifluoromethylaniline (3- aminobenzotrifluoride), 3-methoxyaniline (m-anisidine), 3- (methylmercapto) aniline, 3-trifluoromethylbenzylamine, 3-methylbenzylamine, 3-fluorobenzylamine, 4- fluoroaniline, 4-methylaniline (p-toluidine), 4- propylaniline, 4-pentylaniline, 4- (methylmercapto) aniline, 4-fluorobenzylamine, 4- chlorobenzylamine, 4-methoxybenzylamine, 4- methylbenzylamine, 3- (1-hydroxyethyl) aniline, 4- bromoaniline, 4-chloroaniline, 2,3-dimethylaniline, 4- methoxyaniline (p-anisidine), 4-carboxamidoaniline (4- aminobenzamide), 2,4-difluoroaniline, 4-bromo-2- methylaniline, 2,5-dimethoxyaniline, 2-methoxy-5- methylaniline, 2-methoxy-5-nitroaniline, 3,4,5- trimethoxyaniline, 3-chloro-4-fluoroaniline, 3-bromo-4- methylaniline, 4-bromo-3-methylaniline, 3,4- dimethoxyaniline (4-aminoveratrole), 3,4-dimethylaniline, 3,5-dimethoxyaniline, 2-methylaniline (o-toluidine), 3- ethoxyaniline (m-phenetidine), 3,4-difluorobenzylamine,

3,4-dimethoxybenzylamine (veratrylamine), 3,4- dichlorobenzylamine, 3,4,5-trimethoxybenzylamine, phenethylamine, 2- (2-chlorophenyl) ethylamine, 2- (3- chlorophenyl) ethylamine, 2- (4-chlorophenyl) ethylamine, 4- methoxyphenethylamine, 3,4-dimethoxyphenethylamine, N- benzylmethylamine, N-benzylethanolamine, aminodiphenylmethane, 1,2,3,4-tetrahydroisoquinoline, 1- phenylpiperazine, 1-(a-trifluoro-m-tolyl) piperazine, 1,4-benzodioxan-6-amine, 4- (aminomethyl) pyridine, 3- (aminomethyl) pyridine, 1- (2-pyridyl) piperazine, cycloheptylamine, cyclohexylamine, 2-bromo-4- methylaniline, 5-fluoro-2-methylaniline, 3- carboxamidoaniline (3-aminobenzamide), 1-methyl-3- phenylpropylamine, 1-adamantanemethylamine, 1,3,3- trimethyl-6-azabicyclo [3.2.1] octane, 2-ethoxyaniline (o- phenetidine), 4-isopropylaniline, 3-phenyl-1-propylamine, trans-2-phenylcyclopropylamine, 3-nitrobenzylamine, 4- bromobenzylamine, 2-bromobenzylamine, 3-bromobenzylamine, 4-ethoxyaniline (p-phenetidine), 2-aminoindan, 3-amino- 2,6-dimethoxypyridine, 4-nitrobenzylamine, 4- benzyloxyaniline, 5-bromo-2-fluorobenzylamine, 6,7- dimethoxy-1,2,3,4-tetrahydroisoquinoline, 2,4- dimethoxybenzylamine, 3-methylsulphonylaniline, 4- (dimethylamino) benzylamine, 4- (dimethylamino) aniline (N, N-dimethyl-1,4-phenylenediamine), pyridoxamine, 2- fluorophenethylamine, 3-fluorophenethylamine, 4- fluorophenethylamine, 2,4-dichlorophenethylamine, 3- iodoaniline, 3-chloro-2-methylaniline, 5-chloro-2- methoxyaniline (5-chloro-o-anisidine), 2-chloro-4- fluoroaniline, 4-methoxy-2-methylaniline, 2,4- dimethoxyaniline, 2,5-dimethylaniline, 2-fluoro-5- methylaniline, 3,5-dimethylaniline, 2,3- dimethoxybenzylamine, 2,4-difluorobenzylamine, 2,5- difluorobenzylamine, 2,6-difluorobenzylamine, 5-chloro-2- methylaniline, 2,4-dimethylaniline, 2-fluoro-4-

methylaniline, 4- (diethylamino) aniline (N, N-diethyl-1,4- phenylenediamine), cytosine, 2-aminobenzothiazole, 2- amino-6-fluorobenzothiazole, 2-amino-6- methoxybenzothiazole, 2- (4-aminophenyl)-6- methylbenzothiazole, 3-phenoxyaniline, 4-phenoxyaniline, 1-amino-4-bromonaphthalene, 2-aminofluorene, 1- naphthalenemethylamine, 3-benzyloxyaniline, 4- aminopyridine, 2-amino-4-picoline, 5-aminoindan, 1-amino- 5,6,7,8-tetrahydronaphthalene, tyramine, 2-amino-1- phenylethanol, 1-adamantanamine, tryptamine, 2- aminothiazole, 2-iodoaniline, 4-iodoaniline, 2-chloro-5- methylaniline, 4-hydroxy-4-phenylpiperidine, 4-chloro-2- methoxy-5-methylaniline, 4-morpholinoaniline, 3-chloro-4- methoxyaniline (3-chloro-p-anisidine). Four additional library tea-bags were each paired with a control tea-bag and each coupled as above, but to a racemic mixture of two amines from the following list: (+/-)-alpha- methylbenzylamine, (+/-)-exo-2-aminonorbornane, (+/-)- alpha- (methylaminomethyl) benzyl alcohol and (+/-)-endo-2- aminonorbornane. One additional library tea-bag was left as the free carboxylic acid.

Reacted with p-toluidine in the same manner but on a 40.5 times larger scale were the 90 glycine control tea-bags (45 micromoles each of the isoquinoline formed from glycine and, separately, each of the 90 aldehydes used for imine formation). The above procedures produced 142 tea-bags each containing a mixture of 3060 isoquinoline amides or acids plus 4 tea-bags each containing a mixture of 6120 isoquinoline amides for a total library size of 459,000 compounds.

Each tea-bag prepared was cleaved separately via standard HF procedures (Example 3 with the modification of an addition of 0.2 ml anisole to each HF

cleavage reaction as a scavenger), extracted into 45: 45: 10 water/acetonitrile/acetic acid, examined by HPLC coupled with mass spectrometry, and tested in a variety of assays. The control tea-bags were cleaved in the same manner and characterized by NMR or HPLC and mass spectra.

EXAMPLE 47 Biological radioreceptor assay of 459,000 different isoquinoline amides and acids This example describes an initial screen of libraries prepared according to Example 46 in the 5- opioid receptor assay and the a receptor assay described above. The results of those screens are provided in ensuing Tables V and VI.

TABLE V Pool # Percent Bound 0.495Pyridoxamine 2934-(Dimethylamino)benzylamine 41032-Chloro-4-fluoroaniline 65 3- (Aminomethyl) pyridine 5 94 4- (Dimethylamino) aniline 5 (N, N-dimethyl-1,4-phenylenediamine) 73 1-Adamantanemethylamine 5 76 4-Isopropylaniline 5 49 3, 4-Dichlorobenzylamine 5 58 N-Benzylethanolamine 5 62 1-(-Trifluro-m-tolyl) piperazine 6 87 4-Nitrobenzylamine 6

TABLE V Pool PercentX Bound 61325-Aminoindan 668Cyclohexylamine 6661-(2-Pyridyl)piperazine 6554-Methoxyphenethylamine 71271-Naphthalenemethylamine 7912,4-Dimethoxybenzylamine 116 7 ethylamine7522-(2-Chlorophenyl) 71352-Amino-1-phenylethanol 7631,4-Benzodioxan-6-amine 7895-Bromo-2-fluorobenzylamine 7644-(Aminomethyl)pyridine 7611-Phenylpiperazine 81262-Aminofluorene 8483,4-Dimethoxybenzylamine (veratrylamine) 8542-(4-Chlorophenyl)ethylamine 859Aminodiphenylmethane 851Phenethylamine 857N-Benzylmethylamine 81404-Iodoaniline 8793-Nitrobenzylamine 81 8 ethylamine8532-(3-Chlorophenyl) 8773-Phenyl-1-propylamine 91083,5-Dimethylaniline 9601,2,3,4-Tetrahydroisoquinoline

TABLE V Pool PercentX Bound 9741,3,3-Trimethyl-6- azabicyclo[3.2.1] octane 91412-Chloro-5-methylaniline 91453-Chloro-4-methoxyaniline 145 3-Chloro-4-methoxyaniline 9 (3-chloro-p-anisidine) 101424-Hydroxy-4-Phenylpiperidine 10705-Fluoro-2-methylaniline 101244-Phenoxyaniline 10137Tryptamine 1067Cycloheptylamine 101102,4-Difluorobenzylamine 101072-Fluoro-5-methylaniline 10473,4-Difluorobenzylamine 10721-Methyl-3-phenylpropylamine 10992,4-Dichlorophenethylamine 10852-Aminoindan 10503,4,5-Trimethoxybenzylamine 11822-Bromobenzylamine 11692-Bromo-4-methylaniline 1178trans-2-Phenylcyclopropylamine 11863-Amino-2,6-dimethoxypyridine 121025-Chloro-2-methoxyaniline (5-chloro-o-anisidine) 121392-Iodoaniline 121092,3-Dimethoxybenzylamine 121122,6-Difluorobenzylamine 121052,4-Dimethoxyaniline

TABLE V Pool PercentX Bound 121434-Chloro-2-methoxy-5-methylaniline 121251-Amino-4-bromonaphthalene 13143-Trifluoromethylbenzylamine 131013-Chloro-2-methylaniline 13713-Carboxamidoaniline (3-aminobenzamide) 13962-Fluorophenethylamine 14833-Bromobenzylamine 151003-Iodoaniline 151233-Phenoxyaniline 15563,4-Dimethoxyphenethylamine 161444-Morpholinoaniline 75752-Ethoxyaniline (o-phenetidine) 16 16134Tyramine 1692-Trifluoromethylbenzylamine 16804-Bromobenzylamine 17204-Pentylaniline 906,7-Dimethoxy-1,2,3,4- 17 Tetrahydroisoquinoline aniline18263-(1-Hydroxyethyl) 181361-Adamantanamine 181382-Aminothiazole 191293-Benzyloxyaniline 191222-(4-Aminophenyl)-6- methylbenzothiazole 19923-Methylsulphonylaniline 19194-Propylaniline

TABLE V Pool PercentX Bound 221152-Fluoro-4-methylaniline 22234-Chlorobenzylamine 22163-Fluorobenzylamine 22404-Bromo-3-methylaniline 128 22a-(Methylaminomethyl)benzyl alcohol 1331-Amino-5,6,7,8-tetrahydronapthalene 23 24153-Methylbenzylamine 24214-(Methylmercapto)aniline 251135-Chloro-2-methylaniline (Diethylamino)aniline251174- (N,N-diethyl-1,4-phenylenediamine) 44 26 2672-Chlorobenzylamine 27224-Fluorobenzylamine 2782-Methoxybenzylamine 2762-Methylbenzylamine 27393-Bromo-4-methylaniline 28984-Fluorophenethylamine 84844-Ethoxyaniline (p-phenetidine) 29 291112,5-Difluorobenzylamine 29292,3-Dimethylaniline 295Benzylamine 301304-Aminopyridine 30284-Chloroaniline 30973-Fluorophenethylamine 30274-Bromoaniline

TABLE V Pool PercentX Bound 30884-Benzyloxyaniline 30334-Bromo-2-methylaniline 311192-Aminobenzothiazole 321212-Amino-6-methoxybenzothiazole 32254-Methylbenzylamine 321142,4-Dimethylaniline 321202-Amino-6-fluorobenzothiazole 33133-(Methylmercapto)aniline 45452-Methylaniline (o-toluidine) 34 341312-Amino-4-picoline 36383-Chloro-4-fluoroaniline 37174-Fluoroaniline 38244-Methoxybenzylamine (m-phenetidine)463-Ethoxyaniline 38 381044-Methoxy-2-methylaniline 18184-Methylaniline (p-toluidine) 39 391062,5-dimethylaniline 332-Methyoxyaniline (o-anisidine) 40 4222-Fluoroaniline 43433,5-Dimethoxyaniline 43352-Methoxy-5-methylaniline 43362-Methoxy-5-nitroaniline 4342-(Methylmercapto)aniline 43118Cytosine 43113-Trifluoromethylaniline (3-aminobenzotrifluoride) 441Aniline

TABLE V Pool # Percent Bound 42 3,4-Dimethylaniline 46 37 3,4,5-Trimethoxyaniline 48 34 2,5-Dimethoxyaniline 52 10 3-Fluoroaniline 56 41 3,4-Dimethoxyaniline 56 (4-aminoveratrole) 31 4-Carboxamidoaniline 61 (4-aminobenzamide) 32 2,4-Difluoroaniline 63 12 3-Methoxyaniline (m-anisidine) 64 30 4-Methoxyaniline (p-anisidine) 66 TABLE VI Pool # R3 Percent Bound 27 4-Bromoaniline 6 137 Tryptamine 7 140 4-Iodoaniline 7 49 3, 4-Dichlorobenzylamine 8 142 4-Hydroxy-4-phenylpiperidine 8 97 3-Fluorophenethylamine 8 51 Phenethylamine 10 98 4-Fluorophenethylamine 11 96 2-Fluorophenethylamine 11 99 2, 4-Dichlorophenethylamine 12 129 3-Benzyloxyaniline 12 43 3, 5-Dimethoxyaniline 12

TABLE VI Pool R3 Percent 12532-(3-Chlorophenyl)ethylamine 121304-Aminopyridine 135 2-Amino-l-phenylethanol 13 21 4- (Methylmercapto) aniline 14 76 4-Isopropylaniline 14 41 3, 4-Dimethoxyaniline 15 (4-aminoveratrole) 73 1-Adamantanemethylamine 15 89 5-Bromo-2-fluorobenzylamine 15 15522-(2-Chlorophenyl)ethylamine 16661-(2-Pyridyl)piperazine 40 4-Bromo-3-methylaniline 16 18184-Methylaniline (p-toluidine) 16 171392-Iodoaniline 17284-Chloroaniline 17423,4-Dimethylaniline 171325-Aminoindan 17944-(Dimethylamino)aniline (N,N-dimethyl-1,4-phenylenediamine) 123 3-Phenoxyaniline 17 37 3,4,5-Trimethoxyaniline 18 128 ()-a- (Methylaminomethyl) benzyl 18 alcohol 100 3-Iodoaniline 19 127 1-Naphthalenemethylamine 19 138 2-Aminothiazole 19 191312-Amino-4-picoline 119 2-Aminobenzothiazole 20

TABLE VI Pool R3 Percent Bound 107 2-Fluoro-5-methylaniline 20 54 2-(4-Chlorophenyl)ethylamine 20 13 3-(Methylmercapto)aniline 20 17 4-Fluoroaniline 20 93 4-(Dimethylamino)benzylamine 20 134 Tyramine 20 145 3-Chloro-4-methoxyaniline 20 (3-chloro-p-anisidine) 108 3,5-Dimethylaniline 20 10 3-Fluoroaniline 21 19 4-Propylaniline 21 12 3-Methoxyaniline (m-anisidine) 21 58 N-Benzylethanolamine 21 111 2,5-Difluorobenzylamine 21 143 4-Chloro-2-methoxy-5-methylaniline 21 78 trans-2-Phenylcyclopropylamine 21 117 4-(Diethylamino)aniline 22 (N,N-diethyl-1,4-phenylenediamine) 102 5-Chloro-2-methoxyaniline 22 (5-chloro-o-anisidine) 141 2-Chloro-5-methylaniline 22 90 22 Tetrahydroisoquinoline 114 2,4-Dimethylaniline 22 8 2-Methoxybenzylamine 22 11 3-Trifluoromethylaniline 23 (3-aminobenzotrifluoride) 20 4-Pentylaniline 23

TABLE VI Pool PercentR3 Bound 231062,5-Dimethylaniline 23554-Methoxyphenethylamine 23263-(1-Hydroxyethyl)aniline 23254-Methylbenzylamine 231102,4-Difluorobenzylamine 231013-Chloro-2-methylaniline 1331-Amino-5,6,7,8-tetrahydronapthalene 23 24473,4-Difluorobenzylamine 241092,3-Dimethoxybenzylamine 241122,6-Difluorobenzylamine 30304-Methoxyaniline (p-anisidine) 24 24692-Bromo-4-methylaniline 25234-Chlorobenzylamine 25923-Methylsulphonylaniline 251032-Chloro-4-fluoroaniline 2592-Trifluoromethylbenzylamine 25334-Bromo-2-methylaniline 25721-Methyl-3-phenylpropylamine 25912,4-Dimethoxybenzylamine 25773-Phenyl-1-propylamine 26713-Carboxamidoaniline (3-aminobenzamide) 261052,4-Dimethoxyaniline 26822-Bromobenzylamine 26833-Bromobenzylamine 26644-(Aminomethyl)pyridine 261444-Morpholinoaniline

TABLE VI Pool # R3 Percent Bound 74 1,3,3-Trimethyl-6-26 azabicyclo [3.2.1] octane 120 2-Amino-6-fluorobenzothiazole 26 15 3-Methylbenzylamine 50 3,4,5-Trimethoxybenzylamine 27 24 4-Methoxybenzylamine 27 3 2-Methoxyaniline (o-anisidine) 27 39 3-Bromo-4-methylaniline 27 pyridine28653-(Aminomethyl) 2872-Chlorobenzylamine 281152-Fluoro-4-methylaniline 44 28-a-Methylbenzylamine 2857N-Benzylmethylamine 28631,4-Benzodioxan-6-amine 28383-Chloro-4-fluoroaniline 281212-Amino-6-methoxybenzothiazole 46 3-Ethoxyaniline (m-phenetidine) 28 124 4-Phenoxyaniline 28 22 4-Fluorobenzylamine 29 60 1,2,3,4-Tetrahydroisoquinoline 29 86 3-Amino-2, 6-dimethoxypyridine 29 29 2, 3-Dimethylaniline 29 68 Cyclohexylamine 29 80 4-Bromobenzylamine 29 30342,5-Dimethoxyaniline 30852-Aminoindan 305Benzylamine 16 3-Fluorobenzylamine 30

TABLE VI Pool # R3 Percent Bound 62 1-(a-Trifluro-m-tolyl)(a-Trifluro-m-tolyl) piperazine 30 122 2- (4-Aminophenyl)-6- 30 methylbenzothiazole 126 2-Aminofluorene 30 311251-Amino-4-bromonaphthalene aniline3242-(Methylmercapto) 45 2-Methylaniline (o-toluidine) 32 1 Aniline 32 14 3-Trifluoromethylbenzylamine 32 32793-Nitrobenzylamine 116 33 3367Cycloheptylamine 33352-Methoxy-5-methylaniline 33563,4-Dimethoxyphenethylamine 33483,4-Dimethoxybenzylamine (Veratrylamine) 87 4-Nitrobenzylamine 33 113 5-Chloro-2-methylaniline 33 6 2-Methylbenzylamine 34 136 1-Adamantanamine 34 59 Aminodiphenylmethane 34 95 Pyridoxamine 35 75 2-Ethoxyaniline (o-phenetidine) 35 88 4-Benzyloxyaniline 35 104 4-Methoxy-2-methylaniline 35 70 5-Fluoro-2-methylaniline 37 81 (+/-)-endo-2-Aminonorbornane 38 84 4-Ethoxyaniline (p-phenetidine) 38

TABLE VI Pool # R3 Percent Bound 32 2,4-Difluoroaniline 39 2 2-Fluoroaniline 39 61 1-Phenylpiperazine 39 31 4-Carboxamidoaniline 45 (4-Aminobenzamide) 36 2-Methoxy-5-nitroaniline 52 118 Cytosine 54 EXAMPLE 48 Solid-phase synthesis of a library of 21,318 different isoquinoline amines Fifty one tea-bags are prepared as in Example 43 with each containing a mixture of 418 isoquinoline amides. While still attached to the resin the isoquinoline amides are reduced to the isoquinoline amines via the procedure of Cuervo et al., Peptides 1994, Proceedings of the 23rd European Peptide Symposium, H. L. S. Maia, Editor, Escom Publishers, Leiden, pp 465-466 (1995), which is incorporated herein by reference, modified for solid-phase use as described in published WO 94/26775, which is incorporated herein by reference. One tea-bag (0.178 g resin, 120 micromoles total of mixed isoquinolines) is placed in a 50 ml KIMAX glass tube and treated under nitrogen gas with a solution of: 1 M BH3 in anhydrous tetrahydrofuran (15 ml), boric acid (315 mg) and trimethyl borate (0.5 ml). After the solution is bubbling slows to a slight fizz the tube is capped tightly and heated at 65°C for 96 hrs. After cooling the borane solution is decanted and the bag washed with methanol (lx 25 ml), tetrahydrofuran (1 x 25 ml), and

again with methanol (4 x 25 ml). After drying the bag is returned to a 50 ml KIMAX glass tube, submerged completely in piperidine, sealed and heated at 65°C for 16 hrs. After cooling the piperidine is decanted off of the tea-bag and the bag is washed with DMF (2 x 25 ml), DCM (2 x 25 ml), methanol (1 x 25 ml), DMF (2 x 25 ml), DCM (2 x 25 ml), and again with methanol (1 x 25 ml).

After drying the tea-bag is cleaved via the HF protocols described in Example 43, but for 9 hrs instead of 2 hrs.

The remaining 50 tea-bags are treated in the same manner resulting in 51 pools of 418 isoquinoline amines, for a total library size of 21,318.

EXAMPLE 49 Solid-phase synthesis of a library of 20,482 different isoquinoline aromatic amines Forty nine tea-bags are prepared as in Example 45 with each containing a mixture of 418 isoquinoline amides. While still attached to the resin the isoquinoline amides are reduced to the isoquinoline amines and cleaved off the resin as in Example 48, resulting in 49 pools of 418 isoquinoline amines for a total library size of 20,482.

EXAMPLE 50 Solid-phase synthesis of a library of 332,860 different isoquinoline amines One-hundred seven tea-bags were prepared as in Example 46 but on two-fold larger scale (each bag containing 200 micromoles of resin) with each containing a mixture of isoquinoline amides or acids. A subset of the amines used in Example 44 were used consisting of

aniline, 2-fluoroaniline, 2-methoxyaniline, 2- chlorobenzylamine, 2-methoxybenzylamine, 2- trifluoromethylbenzylamine, 3-fluoroaniline, 3- methylaniline, 3-trifluoromethylaniline, 3- (methylmercapto) aniline, 3-trifluoromethylbenzylamine, 3- methylbenzylamine, 4-propylaniline, 4-pentylaniline, 4- (methylmercapto) aniline, 4-fluorobenzylamine, 4- methoxybenzylamine, 4-methylbenzylamine, 3- (1- hydroxyethyl) aniline, 4-chloroaniline, 2,3- dimethylaniline, 4-methoxyaniline, 2,5-dimethoxyaniline, 3-chloro-4-fluoroaniline, 3-bromo-4-methylaniline, 3,4- dimethoxyaniline, 3,4-dimethylaniline, 3,5- dimethoxyaniline, 2-methylaniline, 3,4- dimethoxybenzylamine, 3,4-dichlorobenzylamine, 2- (3- chlorophenyl) ethylamine, 4-methoxyphenethylamine, N- benzylethanolamine, aminodiphenylmethane, 1- phenylpiperazine, 1-(a-trifluoro-m-tolyl) piperazine, 1,4-benzodioxan-6-amine, 4- (aminomethyl) pyridine, 3- (aminomethyl) pyridine, 1- (2-pyridyl) piperazine, cycloheptylamine, cyclohexylamine, 5-fluoro-2- methylaniline, 3-carboxamidoaniline, 1-methyl-3- phenylpropylamine, 1-adamantanemethylamine, 1,3,3- trimethyl-6-azabicyclo [3.2.1] octane, 2-ethoxyaniline, 4- isopropylaniline, 3-phenyl-1-propylamine, trans-2- phenylcyclopropylamine, 3-nitrobenzylamine, 4- bromobenzylamine, 2-bromobenzylamine, 3-bromobenzylamine, 4-ethoxyaniline, 2-aminoindan, 3-amino-2,6- dimethoxypyridine, 4-nitrobenzylamine, 4- benzyloxyaniline, 5-bromo-2-fluorobenzylamine, 6,7- dimethoxy-1,2,3,4-tetrahydroisoquinoline, 2- adamantanamine, 2,4-dimethoxybenzylamine, 3- methylsulphonylaniline, 3- (dimethylamino) aniline, 4- (dimethylamino) aniline, pyridoxamine, 2- fluorophenethylamine, 3-fluorophenethylamine, 4- fluorophenethylamine, 2,4-dichlorophenethylamine, 3-

iodoaniline, 3-chloro-2-methylaniline, 5-chloro-2- methoxyaniline (5-chloro-o-anisidine), 4-methoxy-2- methylaniline, 2,4-dimethoxyaniline, 2,5-dimethylaniline, 2-fluoro-5-methylaniline, 2,3-dimethoxybenzylamine, 2,4- difluorobenzylamine, 2,5-difluorobenzylamine, 2,6- difluorobenzylamine, 5-chloro-2-methylaniline, 2,4- dimethylaniline, 2-fluoro-4-methylaniline, 3- phenoxyaniline, 4-phenoxyaniline, 2-aminofluorene, 1- naphthalenemethylamine, 3-benzyloxyaniline, 4- aminopyridine, 2-amino-4-picoline, 5-aminoindan, 1-amino- 5,6,7,8-tetrahydronaphthalene, tyramine, 2-amino-1- phenylethanol, 1-adamantanamine, 4-hydroxy-4- phenylpiperidine, 4-chloro-2-methoxy-5-methylaniline, 4- morpholinoaniline, 3-chloro-4-methoxyaniline (3-chloro-p- anisidine), carboxyl group, (+/-)-exo-2-aminonorbornane, (+/-)-endo-2-aminonorbornane, and (+/-)-a- methylbenzylamine. One bag was left as the carboxylic acid.

While still attached to the resin, the isoquinoline amides and acids were reduced to the isoquinoline amines and alcohols via the procedure of Cuervo et al., supra, modified for solid-phase use. One- half of the library tea-bags and one-half of the control tea-bags were placed in a 5 L glass reactor vessel under nitrogen gas containing boric acid (66.1 g, 1.07 moles) and anhydrous trimethyl borate (107 mL, 0.955 moles). A 1M solution of borane-tetrahydrofuran complex in tetrahydrofuran (3.2 L) was added slowly to the reaction.

After sealing the reaction vessel was heated at 65°C for 96 hrs. After cooling the borane solution was decanted and the bag washed with methanol (lx 25 ml), tetrahydrofuran (1 x 25 ml), and again with methanol (4 x 25 ml). After drying the bags were returned to the reaction vessel, submerged completely in piperidine,

sealed and heated at 65°C for 16 hrs. After cooling the piperidine was decanted off of the tea-bags and the bags were washed with DMF (2 x 25 ml), DCM (2 x 25 ml), methanol (1 x 25 ml), DMF (2 x 25 ml), and DCM (3 x 25 ml).

After drying the tea-bags were cleaved as in Example 48, extracted into 45: 45: 10 water/acetonitrile/acetic acid and examined by HPLC coupled with mass spectrometry. The control tea-bags were cleaved in the same manner and characterized by NMR or HPLC and mass spectra.

EXAMPLE 51 Isoquinoline Library Positional Scan Format In this example the positional scan format, as described above, is used to identify additional compounds which are significant inhibitors of the o receptor ligand, pentazocine. Subsets of compounds were prepared <BR> <BR> <BR> <BR> as described below and screened in the o receptor assay.

The experimental procedure was as follows. Two 0.30 umol bags each of either FMOC or BOC protected aminoacids were prepared using MBHA resin (0.90 umol/g) as previously described (DIC, HOBt, DMF/DCM). The amino acids used were: N- (t-butyloxycarbonyl) glycine, N- (t-butyloxycarbonyl)-3-aminopropionic acid, N- (t-butyloxycarbonyl)-5-aminopentanoic acid, N- (t-butyloxycarbonyl)-7-aminoheptanoic acid, (s)-2-N- (t-butyloxycarbonyl)-3-N- (9-fluorenylmethoxy- carbonyl)-diaminopropionoic acid, (s)-2-N- (t-butyloxycarbonyl)-6-N- (9-fluorenylmethoxy carbonyl)-diaminohexanoic acid, (s)- (t-butyloxycarbonyl)-2-methyl-3-aminopropionic acid,

(r)- (t-butyloxycarbonyl)-2-methyl-3-aminopropionic acid, N- (t-butyloxycarbonyl)-2- (2-aminoethoxyethoxy) acetic acid, N- (t-butyloxycarbonyl)-trans-4- (aminomethyl) cyclohexanecarboxylic acid, N- (t-butyloxycarbonyl)-4- (aminomethyl) benzoic acid. After standard deprotection procedures (BOC: lx 15 min DCM, lx 30 min 55% TFA/DCM, lx 5 min DCM, 2x 5 min IPA, 2x 5 min DCM, 3x 2 min 5% DIEA/DCM, 3x 5 min DCM ; FMOC: lx 15 min DCM, lx 5 min 20% piperidine/DMF, lx 15 min 20% piperidine/DMF, 4x 5 min DMF, 4x 5 min DCM) and drying under vacuum the resin- bound-aminoacids were selectively portioned into three subsets in order to prepare the library in the desired postional scan format. Control bags for library analysis were prepared using Resin-Glycine.

Subset 1 consisted of 11 bags containing 55 umol of a mixture of all 11 the resin-aminoacids. Subset 2 contained 11 bags of 240 umol of the 11 resin- aminoacids mixture. Subset 3 had each individual resin- aminoacid subdivided into 11x11 22 umol bags for a total of 121 bags.

For reaction with each of the benzaldehydes and homophatlic anhydride, the bags from Subset 1,2 and 3 were divided into 11 groups. The aldehydes used were benzaldehyde, 5-nitro-2-furaldehyde, 4- nitrobenzaldehyde, 5- (hydroxymethyl)-2-furaldehyde, 4- (dimethylamino)-benzaldehyde, 3-methylbenzaldehyde, 3,5- dimethoxybenzaldehyde, 2-pyridinecarboxaldehyde, 2- naphthaldehyde, 2-furaldehyde, and 2-bromobenzaldehyde.

Each group was composed of one bag each from Subset 1 and 2 and 11 bags of each individual resin-aminoacid from Subset 3 and at least one sibling bag (total 14 bags, 520 umol). The formation of the imine intermediate was performed by placing a series of bags in 75 ml of a 0.5 M

solution (37.5 mmol) of the benzaldehyde. The solution contained 8.2 ml (75 mmol) of trimethylorthoformate as a dehydrating agent. The resin bags were shaken in the reaction solution for 3 to 3 1/2 hrs at room temperature then the solution decanted and bags quickly washed lx with 30 ml anhydrous DMF and lx 30 ml anhydrous CHCl3.

Seventy-five ml of a stock solution of 0.5 M homophatlic anhydride in CHC13 (66.88 g in 825 ml plus 2.6 ml triethylamine catalyst) was added to each of the reaction vessels which were shaken at room temperature for 18 hrs.

The reaction solution was decanted and the resin-bags washed 3x 30 ml DMF, 3x 30 ml DCM, lx 30 ml MeOH and the bags dried 3-4 hrs under vacuum.

The Subsets now contained the intermediate tetrahydroisoquinoline acids with a single benzaldehyde derived fragment in combination with either a mixture of all the 11 aminoacid derived fragment (Subset 1 and 2) or a single aminoacid derived fragment (Subset 3). The Subsets where reapportioned according to the following scheme. Subset 1: all the resin-bound intermediates from original Subset 1, mixed into a single portion by combining the dry solids into a large (5cm x 5cm) resin bag and mixing for 30 min in DCM. After a MeOH wash and vacuum drying the mixed resin was divided into 12 equal portions to provide 50 umol scale bags. Subset 1 now represented mixtures from both the aminoacid and benzaldehyde building blocks. Subset 2: each of the 240 mol bags from original Subset 2 was divided into 12 equal portions of 20 umol to create bags which were mixed aminoacid fragments but contained sets of individual benzaldehyde fragments. Subset 3: for every individual resin-aminoacid set from original Subset 3 all the different benzaldehyde derived fragments were pooled into separate bags, mixed by treatment with DCM, then MeOH and

dried under vacuum. These 11 new mixtures were subdivided into 12 equal portions to generate 20 umol bags that contained a single aminoacid fragment and a mixture of the 11 benzaldehyde fragments.

The bags were once again separated into 11 groups which contained 1 bag from Subset 1,11 bags from Subset 2, and 11 bags from Subset 3, and a sibling bag prepared from resin-glycine-3,5-dimethoxybenzaldehyde.

The groups of bags were treated with 30 ml of a 0.3 M DMF stock solution of (0- (7-azabenzotriazol-1-yl)-1, 1,3,3- tetramethyluronium hexafluorophosphate (HATU: 79.84 g in 700 ml anhydrous DMF) by shaking for 30 min. The HATU solution was decanted and the bags shaken for 2 hrs in 40 ml of a 1 M DMF solution of an amine (75 mmol in 75 ml).

The amines used were 1- (2-aminoethyl) pyrrolidine, 1- adamantanemethylamine, 1- (2-hydroxyethyl) piperazine, piperidine, (aminomethyl) cyclohexane, 4-aminomorpholine, amylamine, aniline, cyclopentylamine, ethanolamine, and tryptamine. The amine solution was decanted and the bags washed 2x 30 ml DMF. The HATU treatments was repeated with an additional 30 ml of a 0.3 M DMF stock solution and 1 hr on the shaker then pouring off the solutions.

Thirty-five ml of 1 M amine/DMFsolution was added and the reactions allowed to shake for 24 hrs. The solutions were decanted and the bags washed with 3x 30 ml DMF, 3x 30 ml DCM and 1 x 30 ml MeOH. After drying under vacuum the resin was distributed according to the following scheme. Subset 1: The bags from Subset 1 contained mixtures from both the aminoacid and benzaldehyde building blocks but had a single amine fragment. These 50 umol bags were used directly in the HF cleavage step.

Subset 2: The 11 amine bags of the same resin- benzaldehyde-mixed amino acid fragments were combined into a bag in order to create a mixture of all the

amines. After shaking for 30 min in DCM, then 30 min in MeOH, the resin was dried 3-4 hrs under vacuum. A 50 umol sample bag was prepared from each of the fixed benzaldehyde mixtures for HF cleavage. Subset 3: The 11 amine bags containing the same resin-aminoacid-mixed benzaldehyde were mixed with the DCM/MeOH/vacuum drying procedure. Fifty umol sample bags were created from each of the mixtures with the fixed amino acid position.

Standard liquid HF/anisole MBHA-resin cleavage was carried out on the 33 bags and the product mixtures extracted 3x 5 ml of 50% acetonitrile/water. The solvent was removed by lypholization (2x) to yield 12 to 26 mg of solids. Each sample represented a 50 umol mixture of 242 compounds with one of the variable building blocks (aminoacid, benzaldehyde, amine) as a defined compentent of the library thus producing the postional scan format.

The results of the positional scan approach and <BR> <BR> <BR> <BR> the o receptor screen evidenced the most active compound similar to that in Example 44, wherein Ru ils 1,6-hexyl, R2 is 5- (4'-methoxybenzyl)-furan-2-yl, R3 through R6 is, independently, a hydrogen atom, Y is C (O) NH2, and the one distinction being at the X position, (aminomethyl) cyclohexyl in place of 1- aminomethyladamantanyl. The compound having (aminomethyl) cyclohexyl at the X position was seen to have virtually equal activity.

Example 52 Solid phase synthesis of a combinatorial library of isoquinoline derivatives of the structure

1. Bromoacetic Acid Coupling: MBHA resin containing T-bags (1.2g x 1.15 mmol/g per bag) were placed into Nalgene bottles (60 bags per 2L bottle) and washed with DMF 1X (-500mL, 20 min), washed with 50% piperidine/DMF 1X (700 mL for 2L bottle, 20 min), washed with DMF 4X, washed with 0.3M HoBt/DMF 1X (700 mL) and finally washed with DMF 4X containing 1% bromophenol blue in the last wash (2 mL per 2L bottle).

A bromoacetic acid/DMFsolution (104gm, 750mmol) was prepared and to this was added DIC (140mL, 750mmol) into the bromoacetic acid solution, stirred for about 30 seconds, then poured into the 2L bottle containing the T-bags immediately. The reaction was shaken at r. t. for 1 h (2 h max).

2. R1 (e. g., R11-Amine) Coupling: The T-bags from the reaction above were washed with DMF 3X (500mL), with DMSO 2X (500mL). The appropriate number of R11-amine/DMSO solutions (0.5mol of

amine, 440mL) were prepared and placed in 1L Nalgene bottles with the appropriate T-bags (30 bags per 1 L bottle). The reactions were shaken overnight.

3. Amino Acid Coupling: The T-bags from the reaction above were washed with DMSO 1X (500mL), and with DMF 5X (500mL) containing 1% bromophenol blue in the last wash (0.5mL mL per 2L bottle).

The amino acid/DMF solution was prepared as follows: a 0.3M HOBt/860mL DMF solution and in this was dissolved the amino acid (0.259mol), to this was added DMAP (3.2gm) and then was added DIC (40.5mL) right before use. The T-bags were placed into 2L Nalgene bottles (60 bags per bottle), then the amino acid solution prepared as above was added. The reactions were shaken overnight.

The T-bags were washed with DMF (4X 500mL), with DCM (4X, 500mL) and air dried in fume hood overnight.

4. Boc-Deprotection: The appropriate T-bags were placed into 2L Nalgene bottles (50 bags per 2L bottle) and washed with DCM 1X, 1000mL, 20 min), then washed with 55% TFA/DCM for 1 h (960mL, add slowly). The TFA solution was poured off and the T-bags washed with DCM (2X, 1000mL), with 5% DIEA/DCM (2X, 1000mL), with DCM (1X, 1000mL), with DMF (2X, 1000mL), with 50% piperidine/DMF 1X (700 mL, 10 min) and, finally, with DMF (5X, 1000mL).

5. R2-Aldehyde Reaction: For the appropriate T-bags, an 0.8M aldehyde/DMF solution was prepared in 1L bottles containing 0.225mol of aldehyde. A 1.6M TMOF trimethyl ortho formate

solution in DMF was prepared. To the 1L bottle of aldehyde solution and T-bags (25 bags per 1L bottle) was added the TMOF solution (292mL). The reactions were shaken 3-3.5h.

6. Homophthalic anhydride Reaction: At the end of the reaction above, the T-bags were washed with 0.2M TMOF/DMF 2X (500 mL per 1L bottle each time). A homophthalic anhydride/DMF solutions in 2L bottles was prepared containing 864mL DMF and 56gm of anhydride and to this was added DIEA (4.5mL), then added in T-bags immediately (60 bags per2L bottle). The reactions were shaken overnight.

The T-bags were washed with DMF (5X, 500mL), and with methyl t-butyl ether 4X, 500mL). The T-bags were air dried bags overnight.

7. X-amine Coupling: The resin from each T-bag was placed into each well of a 96-well microtiter plate (-20 mg per well).

All wells were washed with DMF (2X, l. OmL). The following solutions were prepared and added to the appropriate wells. 0.3 mL of a solution of HATU/DMF was added to each well as was 0.175mL of DIEA and the plates shaken for 20 min.. The required 48 different X-amine solutions were prepared at 0.2M in DMF. The X-amine solution (0.3mL) was added to each appropriate well. The microtiter plates were capped and shaken at rt overnight.

The resin in each well was washed with DMF (2X, l. OmL per well). This procedure was repeated to affect a double coupling of the amine to the resin bound carboxylic acid.

The wells on all plates were washed with DMF (10X, l. OmL), with 50% methyl t-butyl ether/DCM (3X,

l. OmL), and with MeOH (3X, l. OmL). The plates were air-dried in a fume hood for three days.

8. Gaseous HF Cleavage: The plates in batches of-15 were treated by passing N2 through chamber for 30 min, then passing HF gas for 15 min. The chamber was isolated under HF for 1.5 h, then the HF was removed by passing N2 through the chamber overnight. The plates were removed and the residual HF removed under vacuum in desiccator overnight.

9. AcOH Extraction: To extract the cleaved compound from the spent resin, 0.1 mL of AcOH was added into each well and shaken for 20 min. Extraction of each well was accomplished with 4x0.3 mL of AcOH per well to yield the final compound in acetic acid solution. The acetic acid was removed by lyophilization.

Based on the above, isoquinoline derivative compounds and combinaotrial libraries of the subject invention were made where Z is =0, R3 to R6 are each hydrogen, R'and R9 are each absent, Y is C (O) NH2, and R1, R2, R3 and X are as follows (with"r3"corresponding to X and"rl"generally corresponding to R1l of the subject invention): r2 building block name 1-naphthaldehyde 2-chloro-5-nitrobenzaldehyde 2-chloro-6-fluorobenzaldehyde 2-cyanobenzaldehyde 2-imidazolecarboxaldehyde 2-naphthaldehyde r2 radical name 1-naphthyl 2-chloro-5-nitrophenyl 2-chloro-6-fluorophenyl 2-cyanophenyl 2-imidazolyl 2-naphthyl

2-pyridinecarboxaldehyde 2-quinolinecarboxaldehyde 3,4,5-trimethoxybenzaldehyde 3,4- (methylenedioxy) benz aldehyde 3,5-bis (trifluoromethyl) benz aldehyde 3-methylbenzaldehyde 3-nitrobenzaldehyde 3-phenoxybenzaldehyde 4- (3-dimethylaminopropoxy) benzaldehyde 4- (methylthio) benzaldehyde 4- (trifluoromethyl) benz-aldehyde 4-biphenylcarboxaldehyde <BR> <BR> <BR> <BR> 4-bromobenzaldehyde<BR> <BR> <BR> <BR> <BR> <BR> <BR> 4-dimethylaminobenzaldehyde 4-ethylbenzaldehyde 4-hydroxybenzaldehyde 4-propoxybenzaldehyde 5-nitrovanillin 6-methyl-2-pyridinecarboxaldehyde benzaldehyde o-anisaldehyde p-tolualdehyde 2-pyridinyl 2-quinolinyl 3,4,5-trimethoxyphenyl 3,4- (methylenedioxy) phenyl 3,5-bis (trifluoromethyl) phenyl 3-methylphenyl 3-nitrophenyl 3-phenoxyphenyl 4- (3-dimethylaminopropoxy) phenyl 4- (methylthio) phenyl 4- (trifluoromethyl) phenyl 4-biphenylyl 4-bromophenyl 4-dimethylaminophenyl 4-ethylphenyl 4-hydroxyphenyl 4-propoxyphenyl 5-nitrovanillin 6-methyl-2-pyridinyl phenyl 2-methoxyphenyl 4-methylphenyl r3 building blocks names <BR> <BR> <BR> (r)- (-)-1-cyclohexylethylamine 1,2,3,4-tetrahydroisoquinoline 1- (2-aminoethyl) pyrrolidine 1- (2-furoyl) piperazine <BR> <BR> <BR> 1- (3-aminopropyl)-2-pipecoline 1- (3-aminopropyl) imidazole 1-benzylpiperazine 1-bis (4-fluorophenyl) methyl piperazine 1-methylpiperazine 2-amino-5-diethylaminopentane 2-chlorobenzylamine 2-methoxyethylamine 3,3'-dipicolylamine 3- (aminomethyl) pyridine 3-butoxypropylamine r3 radical names <BR> <BR> <BR> (r)- (-)-1-cyclohexylethylamino 1,2,3,4-tetrahydroisoquinolyl 2- (n-pyrrolidyl)-ethylamino 4- (2-furoyl) piperazyl 3- (2-pipecolyl) propylamino 3- (n-imidazoyl) propylamino 4-benzylpiperazyl 4-bis (4-fluorophenyl) methyl piperazyl 4-methylpiperazyl 5-diethylamino-2-pentylamino 2-chlorobenzylamino 2-methoxyethylamino 3,3'-dipicolylamino (3-pyridyl) methylamino 3-butoxypropylamino

3-dimethylaminopropylamine 3-ethoxypropylamine 3-methylbenzylamine 4- (1-pyrrolidinyl) piperidine 4- (aminomethyl) pyridine 4- (ethylaminomethyl) pyridine 4- (trifluoromethyl) benzylamine 4-amino-2,2,6,6-tetramethyl piperidine 4-bromopiperidine hydrobromide 4-tert-butylcyclohexylamine allylamine benzylamine beta-alanine ethyl ester hydrochloride cyclohexylamine dodecylamine ethyl-1-piperazinecarboxylate ethyl-3-aminobutyrate isoamylamine isonipecotamide 1-leucine methyl ester hydrochloride methyl isobutylamine morpholine n, n, n', n'-tetraethyldiethylene triamine n, n, n'-triethylethylenediamine n, n-diethyl-n'-methylethylene diamine n, n-dimethylethylenediamine n- (2-aminoethyl)-n-ethyl-m- toluidine n- (3-aminopropyl) morpholine neopentylamine pyrrolidine tetrahydrofurfurylamine thiomorpholine rl building block names 1- (2-aminoethyl) piperidine 1- (3-aminopropyl) imidazole 3-dimethylaminopropylamino 3-ethoxypropylamino 3-methylbenzylamino 4- (1-pyrrolidinyl) piperidyl 4- (aminomethyl) pyridyl n-ethyl- (4-pyridyl) methylamino 4- (trifluoromethyl) benzylamino 4-amino-2,2,6,6-tetramethyl piperidine 4-bromopiperidinyl 4-tert-butylcyclohexylamino allylamino benzylamino 2-carboethoxy-1-ethylamino cyclohexylamino dodecylamino 4-carboethoxypiperazinyl 3-amino-ethylbutyrate isoamylamino 4-carboxamidopiperidinyl 1-leucine methyl ester hydrochloride methyl isobutylamino morpholinyl n, n, n', n'-tetraethyldiethylene triamino n, n, n'-triethylethylenediamino n, n-diethyl-n'-methylethylene diamino n, n-dimethylethylenediamino <BR> <BR> <BR> <BR> 2- (n-ethyl-n- (2-methylphenyl) ethylamino 3- (n-morpholinyl) propylamino neopentylamino pyrrolidinyl tetrahydrofurfurylamino thiomorpholyl rl radical names (2-piperidinyl) ethyl 3- (imidazoyl) propyl

2,3-dimethoxybenzylamine 2,3-dimethoxyphenylmethyl 2,4-dichlorophenethylamine 2,4-dichlorophenethyl 2-(2-aminoethyl) pyridine 2-(2-pyridinyl)(2-aminoethyl) pyridine 2-(2-pyridinyl) ethyl 2- (4-methoxyphenyl) ethylamine 2- (4-methoxyphenyl) ethyl (1-ethyl-2-pyrrolidinyl)methyl2-(aminomethyl)-1-ethyl-pyrrol idine 2-thiophene methylamine 2-thiophenyl methyl 3- (aminomethyl) pyridine (3-pyridinyl) methyl 3- (trifluoromethyl) benzylamine 3- (trifluoromethyl) phenylmethyl 3-ethoxypropylamine 3-ethoxypropyl 3-methoxybenzylamine 3-methoxyphenylmethyl 4- (2-aminoethyl) morpholine 2- (4-morpholinyl) ethyl acethydrazide n-acetylamino allylamine allyl benzylamine phenylmethyl cyclopropylamine cyclopropyl methyl hydrazinocarboxylate carbomethyoxyamino n, n-di-n-butylethylenediamine 2- (n, n-di-n-butylamino) ethyl n, n-dimethylethylenediamine 2-(n, n-dimethylamino) ethyl piperazine piperazine propylamine propyl tyramine tyramine 2-methoxyethylamine 2-methoxyethyl 4-chlorobenzylamine 4-chlorophenylmethyl n, n-diethyl-1,3-propanediamine 3- (n, n-diethylamino) propyl r8 building blocks names beta alanine 4-aminomethylcyclohexane carboxylic acid 4-aminomethyl benzoic acid r8 radical names 1,2-ethylenyl 1,4-cyclohexylenyl 1,4-phenylenyl

EXAMPLE 53 Solid-phase synthesis of a combinatorial library of isoquinoline amines Tea-bags are prepared as in Example 52 with each containing a mixture of isoquinoline amides. While still attached to the resin the isoquinoline amides are reduced to the isoquinoline amines and cleaved off the resin as described in Example 48, resulting in a mixture of isoquinoline amines.

Example 54 Anti-microbial Screen Streptococcus pyogenes (ATCC&num 97-03 14289) were grown in Todd Hewitt Broth (THB) (Difco Laboratories #0492-17-6) overnight until they reached an optical density of (OD = 0.636@ 570 nm) by reading 0.1 ml in a 96 well microtiter plate in a Molecular Devices Thermomax. This preparation was kept frozen as stocks in 30% v/v glycerol in 1.5 ml aliquots at-70°C until use.

Prior to experiments 1.5 ml aliquots were thawed and diluted into 50 ml THB. 200 ul of this dilution was added to 92 wells of microtiter plate. To three wells THB (200 ul) was added to serve as a blank and a sterility control. Test compounds in DMSO and appropriate concentrations of DMSO were added to Growth/Solvent Controls at 0 time. Plates were read at 0 time at 570 nm in the Molecular Devices plate reader to obtain compounds correction factors for insoluble or colored compounds.

Plates were read again at 4 hrs.

Percent inhibition was calculated with the following formulae: Color correct = (O. D. 0 hr-Blank 0 hr)- (Solvent Control Ohr-Blank 0 hr) % Inhibition = 100-O. D. test compound 4 hr-Blank 4 hr-color correct O. D. growth/solvent control 4 hr-Blank 4 hr Percent inhibition for compounds of the subject invention are listed in the table below. It should be noted that, in the table below,"rl"is the building block that corresponds with R1 of the subject formula; "r2"is the building block that corresponds with R2 of the subject formula; and"r3"is the building block that corresponds with X of the subject formula. % LIDrary Compoun Inhibttlon t1 strvcture S MN 0 HC, Nlcp, two 0 2520 1 9 N, N-DIMETHYLETHYLENEDIAMINE 3, 4-(METHYLENEDIOXY) BENZALDEHYDE 1-(2-AMINOEtHYL) PYRROLIDINE ° ° cC H, benz 0 Ha Jo 4-TERT-NN'Nh5 2520 2 94 N, N-DIMETHYLETHYLENEDIAMINE 3, 4- (METHYLENEDIOXY) BENZALDEHYDE BUTYLCYCLOHEXYLAMINE ° ° cr 6 SN CC CR h1N 0 N- (2-AMINOETHYLYN-ETHYL-M- 2520 7216 N, N-DI-N-BUTYLETHYLENEDIAMINE 3, 4- (METHYLENEDIOXY) BENZALDEHYDE TOLUIDINE ° 0 rc \ o . eM RC ro o"MCrS N 2520 722 St N, N-DI-N-BLZYLETHYLENEDIAMINE 3, 6 (METHYLENEDIOXY) BENZALDEHYDE 3-BUTOXYPROPYLAMINE o' ON O F2C*N-CH, Br 0 NN N 2520 1521 35 N, N-DIMETHYLETHYLENEDIAMINE 4-BROMOBENZALDEHYDE PYRROLIDINE ° 0 H,CH, L HN 0 HC C MJ4NHZ ber 0 2520 1522 102 N, N-DIMETHYLETHYLENEDIAMINE 4-BROMOBENZALDEHYDE ISOAMYLAMINE 0 0 wo Cn, 1-(3-AMINOPROPYL2- H 0 2520 2325 38 PIPERAZINE 4-BROMOBENZALDEHYDE PIPECOLINE ° ° E YOE PIPECOIINE o 0 c F"0 I FN O/vC O 2iAMINOMETHYL>1-ETHYL-1-(3-AMINOPROPYL>2-o-ta 2520 2341 104 PYRROLIDINE 3-NITROBENZALDEHYDE PIPECOLINE o' o ew, , N'CH, roi0 'c I N- (2-AMINOETHYL)-N-ETHYL-M- 2520 3137 B6 BENZYLAMINE 4-DIMETHYLAMINOBENZALDEHYDE TOLUIDINE ° 0 rc 1 o 1 o c O N N H C I 2520 3138 19 BENZYLAMINE 4-DIMETHYLAMINOBENZALDEHYDE 3-BUTOXYPROPYLAMINE o 0 fun 0 c% 0 0 4- (3- 0 0 4-(3-X, cCDIMETHYLAMINOPROPOXY) BENZALDEHY 2520 3954 89 N, N-DI-N-BUTYLETHYLENEDIAMINE DE ISOAMYLAMINE 0 N 0 N f1. 4- (3- o °\CH. DIMETHYLAMINOPROPOXY) BENZALDEHY N' 2520 3956 86 N, N-DI-N-BUTYLETHYLENEDIAMINE DE 1-BENZYLPIPERAZINE OtOwCA YCC 0 FC.. Ch YCH, ANA 2520 4745 99 N, N-DIMETHYLETHYLENEDIAMINE 3-PHENOXYBENZALDEHYDE ETHYL-3-AMINOBUTYRATE 0 0 HN o FÆ N-CHN a N II 2520 4746 100 N, N-DIMETHYLETHYLENEDIAMINE 3-PHENOXYBENZALDEHYDE ALLYLAMINE ° ° CH, I con F I F OSC. O ONi O 3. 5- N- (2-AMINOETHYL)-N-ETHYL-M- F N" 2520 5545 86 METHYL HYDRAZtNOCARBOXYLATE BIS (TRIFLUOROMETHYL) BENZALDEHYDE TOLUIDINE F O O P% C F I F o He. O F N'-"Y 2520 5518 43 METHYL HYDRAZINOCARBOXYLATE BIS (TRIFLUOROMETHYL) BENZALDEHYDE 3-BUTOXYPROPYLAMINE ? 4 Y PN CH, O 2- (AMINOMETHYLl-ETHYL- 2520 6332 98 PYRROLIDINE 4-BIPHENYLCARBOXALDEHYDE 1-BENZYLPIPERAZINE ° 0 rc, 4 Y PN CH, O 2-(AMINOMETHYLk1-ETHYL-XNH, 2S20 6333 78 PYRROLIDINE 4-BIPHENYLCARBOXALDEHYDE l-METHYLPIPERAZINE ° ° CX, CH, "\ t4 0 0 zon 2- (AMINOMETHYLl-ETHYL. 1- (3-AMINOPROrTL)-Z- N 2520 7t25 100 PYRROLIDINE M'4 ZON OxOwCA 0,, Cbz Ch N O 2- (AMINOMETHYLy-1-ETHYL i N BETA-ALANINE ETHYL EStER 2520 7126 26 PYRROLIDINE 4-DIMETHYLAMINOBENZALDEHYDE HYDROCHLORIDE 0 0 SNCH, hN O NCF so 2-(AMINOMETHYL>1-ETHYL-N-(2-AMINOETHYL)-N-ETHYL-M-<8NH , 2520 7921 100 ) rr PYRROLIDINE 4- (METHYLTHIO) BENZALDEHYDE TOLUIDINE ° ° ? % C 0 o rriCR rr 2- (AMINOMEThiYL1-ETFiYL. 2520 7922 87 PYRROLIDINE 4- (METHYLTHIO) BENZALDEHYDE 3-BUTOXYPROPYLAMINE ° o N tBr 0 OH i w w I N.. O _ o o N 0 0 O SOCcHHa CH ; -cl, cl % Library Compoun tnhibXton r1 r2 r3 structure 0NH N I i N 0 N, N- 0 0 DIMETHYLETHYLENED 2530 1 44 IAMINE BENZALDEHYDE IDINE IDINE N N 0 H N N0 09 H2N<N>ON,N-3. ° % DIMETHYLETHYLENED 2530 2 51 IAMINE BENZALDEHYDE INE HC CH 0 NH FN 0) YN O0 1- (2- N AMINOETHYL) PIPERIDI AMINOETHYL)PYRROL tX,) 2530 tSS 20 NE BENZALDEHYDE IDOINE fi 0NH w Y v HL'N) fN ON 0 FN N0 0 N AMINOETHYL) PIPERIDI (AMINOMETHYL) PYRID 2530 866 11 NE BENZALDEHYDE INE N ? CH, 0NON CH, N 0 0 SMETHYL-2-1-(2-O 4 PYRIDINECARBOXALDAMINOETHYL) PYRROL 2530 1537 4 PROPYLAMINE EHYDE D ! NE' N 0 NHN I i H, N zozo HN II 0 6-METHYL-2-3° 0 PYRIDINECARBOXALD(AMINOMETHYL) PYRID 2530 1538 15 PROPYLAMINE EHYDE p N i 0 N i N 0 Ns 0 4- (2- 4. CL J AMINOETHYL) MORPH BIPHENYLCARBOXALD 2530 2501 109 OLINE EHYDE 1-BENZYLPIPERAZINE -CH, H, C N N eN CH2 I l 0 FUNCH, 0 4- (2- 4-N, N, N', N- N AMINOETHYL) MORPH BIPHENYLCARBOXALD tETRAETHYLOtETHYL 25302517 61 OLINE EHYDE ENETRIAMINE HLC Nt CHL c NWH c w w i i N 0 N) f CH20 9 gwN O4-2-AMINO-5,, o 2-(AMINOMETHYL)-1-HYDROXYBENZALDEH DIETHYLAMINOPENTA r 2530 3185 4 ETHYL-PYRROLIDINE YDE NE NH2 CH, 3Cl 0 Mi 0 N I i N 0 CON N YNO 4-4 TERT-0 2- (AMINOMETHYL)-t-HYDROXYBENZALDEH BUTYLCYCLOHEXYLA 2530 3186 101 ETHYL-PYRROLIDINE YDE MINE 'N ? CF 0 NH I i N O N HL N) ( N O FN N 0 2-4-N, N- METHOXYETHYLAMIN ETHYLBENZALDEHYD DIMETHYLETHYLENED E E IAMINE CH,CH2 0 N N 0t 2-4-N,N-DIETHYL-N'- METHOXYETHYLAMIN ETHYLBENZALDEHYD METHYLETHYLENEDIA o'CH, 2530 4164 9 E E MINE l H2 0 nu 0 NH O-NH N 0 NnN No 4TERT- AMINOPROPYL) IMIDAZ BUTYLCYCLOHEXYLA 2530 4818 61 OLE BENZALDEHYDE MINE 3NNIO 0 N i N 0 NEZ N 0 1-(3- 4- (1-Y° AMINOPROPYL) IMIDAZ PYRROLIDINYL) PIPERI NH, 2530 4819 20 OLE BENZALDEHYDE DINE XCY, 0 N S i N 0t FN 0 cl 2,4- 4- DICHLOROPHENETHY(METHYLTHIO) BENZAL 4-BROMOPIPERIDINE 2530 4401 45 LAMINE DEHYDE HYDROBROMIDE 'N 20 ÇH2 o rrr, s N I i N 0 N 0 0 ci 2. 4- 4-N, N. w I DICHLOROPHENETHY (METHYLTHIO) BENZAL DIPAETHYLETHYLENED 2530 4402 96 LAMINE DEHYDE IAMINE r, o 0N 0 N 0 'N--.-N 0 4-0l HYDROXYBENZALDEH Coi 2530 6447 8 ALLYLAMINE YDE MORPHOLINE CH2 0OH i N N H2NtNO 4-0 HYDROXYBENZALDEH C CH1 2530 6448 53 ALLYLAMINE YDE DODECYLAMINE 43 Br i N 0 H2NtN0 0 cl 2,4- 4- DICHLOROPHENETHY BROMOBENZALDEHY 2530 6805 LAMINE DE CI / Po '0 0 rr" 0 NH Br WN) 0 ? HN \ I Han nez c 1 , cl M 3. DICHLOROPHENETHYBROMOBENZALDEHY BUTOXYPROPYLAMIN 2530 6806 LAMINE DE E ci

Although the invention has been described with reference to the examples provided above, it should be understood that various modifications can be made by those skilled in the art without departing from the invention. Accordingly, the invention is set out in the following claims.