This invention relates to p2 agonists of general formula : in which n and Q1 have the meanings indicated below, and to processes for the preparation of, intermediates used in the preparation of, compositions containing and the uses of, such derivatives.

Adrenoceptors are members of the large G-protein coupled receptor super-family. The adrenoceptor subfamily is itself divided into the a and ß subfamilies with the ß sub-family being composed of at least 3 receptor sub- types: ß1, (32 and 33. These receptors exhibit differential expression patterns in tissues of various systems and organs of mammals. (32 adrenergic ( (32) receptors are mainly expressed in smooth muscle cells (e. g. vascular, bronchial, uterine or intestinal smooth muscles), whereas ß3 adrenergic receptors are mainly expressed in fat tissues (therefore j33 agonists could potentially be useful in the treatment of obesity and diabetes) and pl adrenergic receptors are mainly expressed in cardiac tissues (therefore pi agonists are mainly used as cardiac stimulants).

The pathophysiology and treatments of airway diseases have been extensively reviewed in the literature (for reference see Barnes, P. J. Chest, 1997, 111 : 2, pp 17S-26S and Bryan, S. A. et al, Expert Opinion on investigational drugs, 2000,9 : 1, pp25-42) and therefore only a brief summary will be included here to provide some background information.

Glucocorticosteroids, anti-leukotrienes, theophylline, cromones, anti- cholinergics and ß2 agonists constitute drug classes that are currently used to treat allergic and non-allergic airways diseases such as asthma and chronic- obstructive airways disease (COPD). Treatment guidelines for these diseases include both short and long acting inhaled (32 agonists. Short acting, rapid onset (32 agonists are used for"rescue"bronchodilation, whereas, long-acting forms provide sustained relief and are used as maintenance therapy.

Bronchodilation is mediated via agonism of the (32 adrenoceptor expressed on airway smooth muscle cells, which results in relaxation and hence bronchodilation. Thus, as functional antagonists, (32 agonists can prevent and reverse the effects of all bronchoconstrictor substances, including leukotriene D4 (LTD4), acetylcholine, bradykinin, prostaglandins, histamine and endothelins. Because (32 receptors are so widely distributed in the airway, ß2 agonists may also affect other types of cells that play a role in asthma. For example, it has been reported that ß2 agonists may stabilize mast cells. The inhibition of the release of bronchoconstrictor substances may be how ß2 agonists block the bronchoconstriction induced by allergens, exercise and cold air. Furthermore, ß2 agonists inhibit cholinergic neurotransmission in the human airway, which can result in reduced cholinergic-reflex bronchoconstriction.

In addition to the airways, it has also been established that ß2 adrenoceptors are also expressed in other organs and tissues and thus ß2 agonists, such as those described in the present invention, may have application in the treatment of other diseases such as, but not limited to those of the nervous system, premature labor, congestive heart failure, depression, inflammatory and allergic skin diseases, psoriasis, proliferative skin diseases, glaucoma and in conditions where there is an advantage in lowering gastric acidity, particularly in gastric and peptic ulceration.

However, numerous ß2 agonists are limited in their use due to their low selectivity or adverse side-effects driven by high systemic exposure and mainly mediated through action at ß2 adrenoreceptors expressed outside the airways

(muscle tremor, tachycardia, palpitations, restlessness). Therefore there is a need for improved agents in this class.

Accordingly, there is still a need for novel ß2 agonists that would have an appropriate pharmacological profile, for example in terms of potency, selectivity, duration of action and/or pharmacodynamic properties. In this context, the present invention relates to novel ß2 agonists.

EP 0654534 B1 and EP0939134 B1 disclose a process for the preparation of compounds of formula (Xi) : These compounds are disclosed as anti-obesity and anti-diabetic agents having specific p3 activity.

US5,561, 142 discloses selective ß3 agonists of formula EP0236624 discloses compounds of formula

having anti-obesity and/or anti-hyperglycaemic activity coupled with good selectivity from cardiac side-effects.

The invention relates to compounds of general formula (1): wherein the (CH2) n-C(=O)Q1 group is in position meta or para, n is 1 or 2 and Q1 is a group selected from: and a group *-N (R8)-Q2-A, wherein Q2 is a single bond or a Ci-C4 alkylene, R8 is H or Ci-C4 alkyl, p is 1 or 2, and A is pyridyl, or a group of formula wherein R', R2, R3, R4 and R5 are the same or different and are selected from H, Ci-C4 alkyl, OR6, SR6, halo, CF3, OCF3, COOR6, S02NR6R', CONR6R7, NR6R7, NHCOR6, wherein at least 2 of R1 to R5 are equal to H;

wherein R6 and R7 are the same or different and are selected from H or Ci-C4 alkyl and the * represent the attachment point to the carbonyl group; or, if appropriate, their pharmaceutically acceptable salts and/or isomers, tautomers, solvates or isotopic variations thereof.

It has now been found that the compounds of formula (1) are agonists of the (32 receptors, that are particularly useful for the treatment of (32-mediated diseases and/or conditions, and show good potency, in particular when administered via the inhalation route.

In the present invention, the term"potent"means that the compounds of formula (1) show an agonist potency for the ß2 receptor, which is less than 10 nM as measured by the cell-based assay described herein.

Preferably, the compounds of the invention are selective agonists of the ß2 receptor receptors. Preferably, the compounds of the invention show an agonist potency for the ß2 receptor, which is at least about 1 00-fold higher as for the (33 receptor and at least about 500-fold higher as for the PI receptor.

In the here above general formula (1), Ci-C4 alkyl and Ci-C4 alkylen denote a straight-chain or branched group containing 1,2, 3 or 4 carbon atoms.

This also applies if they carry substituents or occur as substituents of other radicals, for example in 0- (Cl-C4) alkyl radicals, S- (CI-C4) alkyl radicals etc....

Examples of suitable (Ci-C4) alkyl radicals are methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl.... Examples of suitable 0- (Ci-C4) alkyl radicals are methoxy, ethoxy, n-propyloxy, iso-propyloxy, n-butyloxy, iso-butyloxy, sec-butyloxy and tert-butyloxy....

Finally, halo denotes a halogen atom selected from the group consisting of fluoro, chloro, bromo and iodo in particular fluoro or chloro.

In the following, the free bond on the phenyl group such as in the structure below, means that the phenyl can be substituted in the meta or para position.

The compounds of the formula (1)

can be prepared using conventional procedures such as by the following illustrative methods in which Q1, Q2, A and n are as previously defined for the compounds of the formula (1) unless otherwise stated.

The amide derivatives of the formula (1) may be prepared by coupling an acid of formula (2): with an amine of formula N (R8)-Q2-A (3),

wherein R8, Q2, A, p and R1 to R5 are as previously defined for compounds of formula (1) The coupling is generally carried out in an excess of said amine as an acid receptor, with a conventional coupling agent (e. g. 1- (3-dimethylaminopropyl)-3- ethylcarbodiimide hydrochloride or N, N'-dicyclohexylcarbodiimide), optionally in the presence of a catalyst (e. g. 1-hydroxybenzotriazole hydrate or 1-hydroxy-7- azabenzotriazole), and optionally in the presence of a tertiary amine base (e. g.

N-methylmorpholine, triethylamine or diisopropylethylamine). The reaction may be undertaken in a suitable solvent such as pyridine, dimethylformamide, tetrahydrofuran, dimethylsulfoxide, dichloromethane or ethyl acetate, and at temperature comprised between 10°C and 40°C (room temperature) for a period of 1-24 hours.

Said amine (3), (3') or (3") is either commercially available or may be prepared by conventional methods well known to the one skilled in the art (e. g. reduction, oxidation, alkylation, protection, deprotection etc...) from commercially available material.

The acid of formula (2) may be prepared from the corresponding ester of formula (4): wherein Ra is a suitable acid protecting group, preferably a (Ci-C4) alkyl group, which includes, but is not limited to, methyl and ethyl, according to any method

well-known to the one skilled in the art to prepare an acid from an ester, without modifying the rest of the molecule. For example, the ester may be hydrolyse by treatment with aqueous acid or base (e. g. hydrogen chloride, potassium hydroxide, sodium hydroxide or lithium hydroxide), optionally in the presence of a solvent or mixture of solvents (e. g. water, 1,4-dioxan, tetrahydrofuran/water), at a temperature comprised between 20°C and 100°C, for a period of 1 to 40 hours.

The ester of formula (4) may be prepared by reaction of an amine of formula (5): wherein Ra and n are as previously defined, with a bromide of formula (6): In a typical procedure, the amine of formula (5) is reacted with a bromide of formula (6) optionally in the presence of a solvent or mixture of solvents (e. g. dimethyl sulphoxide, toluene, N, N-dimethylformamide, acetonitrile), optionally in the presence of a suitable base (e. g. triethylamine, diisopropylethylamine, potassium carbonate) at a temperature comprised between 80°C and 120°C, for 12 to 48 hours.

The bromide of formula (6) may be prepared from the ester of formula (7):

according to any method well-known to the one skilled in the art to prepare an alcohol from an ester, without modifying the rest of the molecule.

In a typical procedure, the ester of formula (7) is reduced with borane dimethylsulfide complex in tetrahydrofuran at a reflux for a period of 2 hours.

The alcohol of formula (7) may be prepared as either the (R) or (S) enantiomer according to methods well described in the literature (Tetrahedron Letters 1994,35 (50), 9375).

The amine of formula (5) may be prepared as either the (R) or (S) enantiomer from the corresponding protected amine of formula (8) : wherein Ra and n are as previously defined and Rb and Rc represent any suitable substituents so that HNRbRc is a chiral amine (for example, Rb may be hydrogen and Rc may be a-methylbenzyl), provided that the bonds between N and Rb and N and Rc can be easily cleaved to give the free amine of formula (5) using standard methodology for cleaving nitrogen protecting groups, such as those found in the text book T. W. GREENE, Protective Groups in Organic Synthesis, A. Wiley-Interscience Publication, 1981.

The amine of formula (8) may be prepared as a single diastereomer by reaction of an amine of formula HNRbRc with a ketone of formula (9) :

wherein Ra, Rb, Re and n are as previously defined.

In a typical procedure, the reaction of the ketone of formula (9) with the amine of formula HNRbRc leads to a chiral intermediate which is in turn reduced by a suitable reducing agent (e. g. sodium cyanoborohydride of formula NaCNBH3 or sodium triacetoxyborohydride of formula Na (OAc) 3BH) optionally in the presence of a drying agent (e. g. molecular sieves, magnesium sulfate) and optionally in the presence of an acid catalyst (e. g. acetic acid) to give the amine of formula (8) as a mixture of diastereomers. The reaction is generally done in a solvent such as tetrahydrofuran or dichloromethane at a temperature comprised between 20°C and 80°C for 3 to 72 hours. The resulting product is then converted to the hydrochloride salt and selectively crystallised from a suitable solvent or mixture of solvents (e. g. isopropanol, ethanol, methanol, diisopropyl ether or diisopropyl ether/methanol) to give (8) as a single diastereomer.

The ketone of formula (9) where n=1 may be prepared by palladium mediated coupling of an aryl halide of formula (10): wherein Ra is as previously defined and Hal represents an halogen atom, which includes, but is not limited to bromo and iodo, with an enolate or enolate equivalent.

In a typical procedure, the aryl halide of formula (10) is reacted with a tin enolate generated in-situ by treatment of isoprenyl acetate with tri-n-butyltin methoxide of formula Bu3SnOMe in the presence of a suitable palladium

catalyst (palladium acetate/tri-ortho-tolylphosphine of formula Pd (OAc) 2/P (o- Tol) 3) in a non-polar solvent (e. g. toluene, benzene, hexane). Preferably, the reaction is carried out at a temperature comprised between 80°C and 110°C for 6 to 16 hours.

The aryl halide of formula (10) may be obtained by esterification of the corresponding acid of formula (11): wherein Hal is as previously defined, according to any method well-known to the one skilled in the art to prepare an ester from an acid, without modifying the rest of the molecule.

In a typical procedure, the acid of formula (11) is reacted with an alcoholic solvent of formula RaOH, wherein Ra is as previously defined, in the presence of an acid such as hydrogen chloride at a temperature between 10°C and 40°C (room temperature) for 8 to 16 hours.

The acid of formula (11) is a commercial product.

The ketone of formula (9) where n=2 may be prepared by reduction of an alkene of formula (12): In a typical procedure, a solution of the olefin of formula (12) in a suitable solvent (e. g. methanol, ethanol, ethyl acetate) is treated with a palladium catalyst (e. g. 10% palladium on charcoal) and stirred under an atmosphere of hydrogen, optionally at elevated pressure (e. g. 60 psi), at temperature between room temperature and 60°C for 8-24 hours.

The alkene of formula (12) may be prepared by a palladium mediated coupling of an activated olefin with an aryl halide of formula (13) :

In a typical procedure, the aryl halide (13) is coupled with a vinyl ester (e. g. methyl acrylate) in the presence of a suitable palladium catalyst (e. g. tetrakis (triphenylphosphine) palladium (0) of formula Pd (PPh3) 4, palladium acetate/tri-ortho-tolylphosphine of formula Pd (OAc) 2/P (o-tol) 3 or (diphenylphosphino) ferrocenyl palladium chloride of formula dppfPdCl2) in a sutiable solvent (e. g. acetonitrile, N, N-dimethylformamide, toluene), optionally in the presence of a base such as triethylamine at a temperature between 40°C and 110°C for 8 to 24 hours.

The ketone of formula (13) is a commercial product.

For some of the steps of the here above described process of preparation of the compounds of formula (1), it may be necessary to protect potential reactive functions that are not wished to react, and to cleave said protecting groups in consequence. In such a case, any compatible protecting radical can be used. In particular methods of protection and deprotection such as those described by T. W. GREENE (Protective Groups in Organic Synthesis, A. Wiley-Interscience Publication, 1981) or by P. J. Kocienski (Protecting groups, Georg Thieme Verlag, 1994), can be used.

All of the above reactions and the preparations of novel starting materials used in the preceding methods are conventional and appropriate reagents and reaction conditions for their performance or preparation as well as procedures for isolating the desired products will be well-known to those skilled in the art with reference to literature precedents and the examples and preparations hereto.

Also, the compounds of formula (1) as well as intermediate for the preparation thereof can be purified according to various well-known methods, such as for example crystallization or chromatography.

Compounds of formula (1) wherein n is 1 or 2, Q1 is a group *-NH-Q2-A, wherein Q2 is Ci-C4 alkylen and A is group of formula wherein R', R2, R3, R4 and R5 are as defined above, are particularly preferred.

Preferably n is 1.

Preferably, Q2 is selected from -CH2-, -(CH2)2-, -(CH2)3- and -CH(CH2)-.

More preferably, Q2 is-CH2-.

Preferably, R', R2, R3, R4 and R5 are the same or different and are selected from H, Ci-C4 alkyl, OR, Cl, F, CF3, OCF3, COUR', SO2NR6R7, provided at least 2 of R1 to R5 are equal to H, wherein R6 and R7 are the same or different and are selected from H or Ci-C4 alkyl.

Preferably, R', R2, R3, R4 and R5 are the same or different and are selected from H, CH3, OH, OCH3, OCH2CH3, Cl, F, CF3, OCF3, COOH, S02NH2, provided at least 2 of R1 to R5 are equal to H.

Preferably, R, R2, R3, R4 and R5 are the same or different and are selected from H, CH3, OH, OCH3, OCH2CH3, Cl, F, CF3, OCF3, COOH, S02NH2, provided at least 3 of R1 to R5 are equal to H.

Preferably, R, R2, R3, R4 and R5 are selected from Cl, provided at least 3 of R1 to R5 are equal to H.

Other preferred compounds are those wherein n is 1 or 2 and Q1 is

wherein p is 1 or 2, R1,, R2, R3 and R4 are the same or different and are selected from H, Ci-C4 alkyl, OR, SR6, halo, CF3, OCF3, COOR6, SO2NR6R7, CONR6R7, NR6R7, NHCOR6, provided at least 2 of R1 to R4 are equal to H; wherein R6 and R7 are the same or different and are selected from H or C1-C4 alkyl.

Preferably, R', R2, R3, and R4 are the same or different and are selected from H and OR6, provided at least 2 of R1 to R4 are equal to H.

Other preferred compounds are those wherein n is 1 or 2 and Q1 is Other preferred compounds are those wherein n is 1 or 2 and Q1 is a group *- NH-Q2-A, wherein Q2 is C1-C4 alkylene and A is pyridin-2-yl.

Other preferred compounds are those wherein n is 1 or 2 and Q1 is a group *- NH-Q2-A, wherein Q2 is C1-C4 alkylene and A is naphthyl.

Particularly preferred are the compounds of the formula (1) as described in the Examples section hereafter, i. e.: N- (2,6-Dimethoxybenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydr oxy-3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetamide ; N- (2-Ethoxybenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy-3 -hydroxymethyl- phenyl)-ethylamino]-propyl}-phenyl)-acetamide ;

N- (2-Hydroxybenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy- 3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetamide ; 2- (3-{(2R)-2-[(2R)-2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl-phen yl)- ethylamino]-propyl}-phenyl)-N-indan-2-yI-acetamide ; N-(3, 4-Dichlorobenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy- 3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetamide ; N- [4- (Aminosulfonyl) benzyl]-2- (3- { (2R)-2- [ (2R)-2-hydroxy-2- (4-hydroxy-3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetamide ; 2- (3-{(2R)-2-[(2R)-2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl-phen yl)- ethylamino]-propyl}-phenyl)-N-(pyridin-2-ylmethyl)-acetamide ; 4- {(2-(3-{(2R)-2-[(2R)-2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl- phenyl)- ethylamino]-propyl}-phenyl)-acetylamino)-methyl}-benzamide ; N- (3,4-Dimethoxybenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydr oxy-3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetamide ; 2- (3-{(2R)-2-[(2R)-2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl-phen yl)- ethylamino]-propyl}-phenyl)-N- (4-trifluoromethoxybenzyl)-acetamide ; <BR> <BR> N- (2-Chloro, 6-fluorobenzyl)-2- (3- { (2R)-2- [ (2R)-2-hydroxy-2- (4-hydroxy-3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetamide ; N- (3,4-Dimethylbenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydro xy-3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetamide ; N- [2-Fluoro-5-(trifluoromethyl)benzyl]-2-(3-{(2R)-2-[(2R)-2-hy droxy-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetamide ; N- (2, 6-Dichlorobenzyl)-2- (3- { (2R)-2- [ (2R)-2-hydroxy-2- (4-hydroxy-3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetamide ; 2- (3-{(2R)-2-[(2R)-2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl-phen yl)- ethylamino]-propyl}-phenyl)-N-(2-phenylethyl) acetamide; N-Benzyl-2- (3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy-3-hydroxymethyl-phen yl)- ethylamino]-propyl}-phenyl)-acetamide ; N- (3, 5-Dichlorobenzyl)-2- (3- { (2R)-2- [ (2R)-2-hydroxy-2- (4-hydroxy-3- hydroxymethyl-phenyl)-ethyWamino]-propyl}-phenyl)-acetamide ; N- (4-Chlorobenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy-3 -hydroxymethyl- phenyl)-ethylamino]-propyl}-phenyl)-acetamide ;

4- {([2-(3-{(2R)-2-[(2R)-2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl -phenyl)- ethylamino]-propyl}-phenyl)-acetyl]-amino)-methyl}-benzoic acid ; 2- [3-[(2R)-2-({(2R)-2-Hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl]ethyl}amino)propyl]phenyl}-N-[(1R)-1- phenylethyl] acetamide ; 4- {(1R)-2-[((1R)-2-{3-[2-(3,4-Dihydroisoquinolin-2(1H)-yl)-2-o xoethyl]phenyl}-1- methylethyl) amino]-1-hydroxyethyl}-2-(hydroxymethyl) phenol ; 4- {(1R)-2-[((1R)-2-{3-[2-(7-Ethoxy-6-methoxy-3,4-dihydroisoqui nolin-2(1H)-yl)-2- oxoethyl] phenyl}-1-methylethyl) amino]-1-hydroxyethyl}-2- (hydroxymethyl) phenol ; N- [2-(4-Chlorophenyl)ethyl]-2-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4 -hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} acetamide ; N- [2- (4-Ethylphenyl) ethyl]-2- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} acetamide; <BR> <BR> N- (1, 1-Dimethyl-2-phenylethyl)-2- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} acetamide; N- [2-(3,4-Dimethoxyphenyl)ethyl]-2-{3-[(2R)-2-({(2R)-2-hydroxy -2-{4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} acetamide; N- (3, 4-Difluorobenzyl)-2- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} acetamide; 4-{(1 R)-2-[((1 R)-2-{3-[2-(1, 3-Dihydro-2H-isoindol-2-yl)-2-oxoethyl] phenyl}-1- methylethyl) amino]-1-hydroxyethyl}-2-(hydroxymethyl)phenol ; 2- {3- ( (2R)-2- ( { (2R)-2-Hyd roxy-2- [4-hyd roxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-phenyiacetamide ; 2- {3- [ (2R)-2- ( { (2R)-2-Hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N- (1- naphthylmethyl) acetamide; N- (3,4-Dichlorobenzyl)-2-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4-hydr oxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-methylacetamide ; 2- {3- [ (2R)-2- ( { (2R)-2-Hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(2-pyridin-2- ylethyl) acetamide;

2- {3- [ (2R)-2- ( { (2R)-2-Hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-[(2R)-2- phenylpropyl] acetamide ; N-Benzyl-2- {3-[(2R)-2-({(2R)-2-hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-methylacetamide ; N- [3- (4-Fiuorophenyl) propyl]-2- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl)phenyl]ethyl} amino) propyl] phenyl} acetamide ; N-(2, 6-Dichlorobenzyl)-3-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy- 3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-propanamid e ; N- (2,6-Dimethoxybenzyl)-3-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4-hyd roxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide; N- (2-Ethxybenzyl)-3-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4-hydroxy-3 - (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide ; N- (3,4-Dimethylbenzyl)-3-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4-hydr oxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide; N- (2,3-Dihydro-1H-inden-2-yl)-3-{3-[(2R)-2-({(2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide; 4- {(1R)-2-[((1R)-2-{3-[3-(3,4-Dihydroisoquinolin-2(1H)-yl)-3-o xopropyl]phenyl}-1- methylethyl)amino]-1-hydroxyethyl}-2-(hydroxymethyl)phenol ; N- (2-Chloro-6-fluorobenzyl)-3- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide; N- (2-Chlorobenzyl)-3-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4-hydroxy- 3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide; 3- {3- [ (2R)-2- ( { (2R)-2-Hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(pyridin-2- ylmethyl) propanamide; N- (2-Chlorobenzyl)-3- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide; 3- {3- [ (2R)-2- ( { (2R)-2-Hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(pyridin-2- ylmethyl) propanamide;

M-Benzy)-3- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide ; 3- {3- [ (2R)-2- ( { (2R)-2-Hydroxy-2- [4-hydroxy-3- (hydroxymethyl), phenyl]ethyl}amino)propyl]phenyl}-N-(2- phenylethyl) propanamide; 3- {3-[(2R)-2-({(2R)-2-Hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(3- phenylpropyl) propanamide; <BR> <BR> 4- { (1 R)-2- [ ( (1 R)-2- {3- [3- (1, 3-Dihydro-2H-isoindol-2-yl)-3-oxopropyl] phenyl}-1- methylethyl)amino]-1-hydroxyethyl}-2-(hydroxymethyl)phenol ; N- [2-Fluoro-5- (trifluoromethyl) benzyl]-3- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4- hydroxy-3-(hydroxymethyl)phenyl]ethyl} amino) propyl] phenyl} propanamide; N- (2-Hydroxybenzyl)-3-{3-[(2R)-2-({(2R)2--hydroxy-2-[4-hydroxy -3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide; 3- {3- [ (2R)-2- ( { (2R)-2-Hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl]phenyl}-N-phenylpropanamide ; N-Benzyl-2-(4-{(2R)-2-[(2R)-2-hydroxy-2-(4-hyd roxy-3- hydroxymethylphenyl) ethyl-amino] propyl} phenyl) acetamide; 2- (4-{(2R)-2-[(2R)-2-Hydroxy-2-(4-hydroxy-3-hydroxymethylpheny l)ethyl- amino] propyl} phenyl)-N- (3-phenyl-propyl) acetamide; 2- (4- { (2R)-2- [ (2R)-2-Hydroxy-2- (4-hydroxy-3-hydroxymethylphenyl) ethyl- amino] propyl} phenyl)-N-indan-2-yl-acetamide ; <BR> <BR> 1- (3, 4-Dihydro-1 H-isoquinolin-2-yl)-2- (4- { (2R)-2- [ (2R)-2-hydroxy-2- (4-hydroxy-3- hydroxymethylphenyl)-ethylamino] propyl} phenyl) ethanone ; N- (2-Hydroxybenzyl)-2-(4-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy- 3- hydroxymethyl-phenyl)-ethylamino] propyl} phenyl)-acetamide ; N- (3-Chlorobenzyl)-2-(4-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy-3 -hydroxymethyl- phenyl)-ethylamino] propyl} phenyl)-acetamide ; <BR> <BR> N- (4-Ghlorobenzyl)-2- (4- { (2R)-2- [ (2R)-2-hydroxy-2- (4-hydroxy-3-hydroxymefihyl- phenyl)-ethylamino] propyl} phenyl)-acetamide ; <BR> <BR> 2-(4-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy-3-hydroxymethylphe nyl)-ethylamino]- propyl}phenyl)-N-(2-methoxybenzyl)-acetamide ;

2-(4-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy-3-hydroxymethylphe nyl)- ethylamino] propyl} phenyl)-N-(3-methoxybenzyl) acetamide; <BR> <BR> <BR> <BR> 2-(4-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy-3-hydroxymethylphe nyl)-ethylamino]- propyl}phenyl)-N-(4-methoxybenzyl)-acetamide ; <BR> <BR> <BR> <BR> N-(2, 6-Dimethoxybenzyl)-2-(4-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy -3-hydroxy- methylphenyl) -ethylamino]porpyl}phenyl)-acetamide, 2-(4-{(2R)-2-[(2R)-2-Hydroxy-2-(4-hydroxy-3-hydroxymethylphe nyl)-ethyl- amino] propyl} phenyl)-N- (pyridin-2-ylmethyl) acetamide, N- [2-Fluoro-5-(trifluoromethyl)benzyl]-2-{4-[(2R)-2-({(2R)-2-h ydroxy-2-[4- hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} acetamide, and, 2- {4- [ (2R)-2- ( { (2R)-2-Hydroxy-2- [4-hydroxy-3- (hydroxymethyi) phenyl] ethyll amino) propyl] phenyl}-N- (2-phenylethyl) acetamide.

According to one aspect of the present invention, the compounds of formula (1) wherein the (CH2) n-C (=O) Q1 group is in position meta are generally preferred.

The compounds of formula (1) may also be optionally transformed into pharmaceutical acceptable salts. In particular, these pharmaceutical acceptable salts of the compounds of the formula (1) include the acid addition and the base salts (including disalts) thereof.

Suitable acid addition salts are formed from acids which form non-toxic salts. Examples include the acetate, aspartate, benzoate, besylate, bicarbonate/carbonate, bisulphate/sulphate, borate, camsylate, citrate, edisylate, esylate, formate, fumarate, gluceptate, gluconate, glucuronate, hexafluorophosphate, hibenzate, hydrochloride/chloride, hydrobromide/bromide, hydroiodide/iodide, hydrogen phosphate, isethionate, D-and L-lactate, malate, maleat, malonate, mesylate, methylsulphate, 2- napsylate, nicotinate, nitrate, orotate, oxalate, palmitat, pamoate, phosphate/hydrogen, phosphate/phosphate dihydrogen"saccharate, stearate, succinate, D-and L-tartrate, 1-hydroxy-2-naphthoate and tosylat salts.

Suitable base salts are formed from bases which form non-toxic salts.

Examples include the aluminium, arginine, benzathine, calcium, choline, diethylamine, diolamine, glycine, lysine, magnesium, meglumine, olamine, potassium, sodium, tromethamine and zinc salts.

Hemisalts of acids and bases may also be formed, for example, hemisulphate and hemicalcium salts.

For a review on suitable salts, see Stahl and Wermuth, Handbook of Pharmaceutical Salts : Properties, Selection, and Use, Wiley-VCH, Weinheim, Germany (2002).

Pharmaceutical acceptable salts of compounds of formula (1) may be prepared by one or more of three methods: (i) by reacting the compound of formula (1) with the desired acid or base; (ii) by removing an acid-or base-labile protecting group from a suitable precursor of the compound of formula (1) or by ring-opening a suitable cyclic precursor, for example, a lactone or lactam, using the desired acid or base; or (iii) by converting one salt of the compound of formula (1) to another by reaction with an appropriate acid or base or by means of a suitable ion exchange column.

All three reactions are typically carried out in solution. The resulting salt may precipitate out and be collected by filtration or may be recovered by evaporation of the solvent. The degree of ionisation in the resulting salt may vary from completely ionised to almost non-ionised.

The compounds of the invention may exist in both unsolvated and solvate forms. The term'solvate'is used herein to describe a molecular complex comprising the compound of the invention and a stoichiometric amount of one or more pharmaceutically acceptable solvent molecules, for example, ethanol.

The term'hydrate'is employed when said solvent is water.

Included within the scope of the invention are complexes such as clathrates, drug-host inclusion complexes wherein, in contrast to the aforementioned solvates, the drug and host are present in stoichiometric or non-stoichiometric amounts. Also included are complexes of the drug containing two or more organic and/or inorganic components which may be in stoichiometric or non- stoichiometric amounts. The resulting complexes may be ionised, partially ionised, or non-ionised. For a review of such complexes, see J Pharm Sci, 64 (8), 1269-1288 by Haleblian (August 1975).

Hereinafter all references to compounds of formula (1) include references to salts, solvates and complexes thereof and to solvates and complexes of salts thereof.

The compounds of the invention include compounds of formula (1) as hereinbefore defined, including all polymorphs and crystal habits thereof, prodrugs and isomers thereof (including optical, geometric and tautomeric isomers) as hereinafter defined and isotopically-labeled compounds of formula (1).

As indicated, so-called'pro-drugs'of the compounds of formula (1) are also within the scope of the invention. Thus certain derivatives of compounds of formula (1) which may have little or no pharmacological activity themselves can, when administered into or onto the body, be converted into compounds of formula (1) having the desired activity, for example, by hydrolytic cleavage.

Such derivatives are referred to as'prodrugs'. Further information on the use of prodrugs may be found in'Pro-drugs as Novel Delivery Systems, Vol. 14, ACS Symposium Series (T. Higuchi and W. Stella) and'Bioreversible Carriers in Drug Design', Pergamon Press, 1987 (ed. E. B Roche, American Pharmaceutical Association).

Prodrugs in accordance with the invention can, for example, be produced by replacing appropriate functionalities present in the compounds of formula (1) with certain moities known to those skilled in the art as'pro-moieties'as described, for example, in"Design of Prodrugs"by H. Bundgaard (Elsevier, 1985).

Some examples of prodrugs in accordance with the invention include: (i) where the compound of formula (1) contains a carboxylic acid functionality (-COOH), an ester thereof, for example, a compound wherein the hydrogen of the carboxylic acid functionality of the compound of formula (1) is replaced by (Cl-C8) alkyl ; (ii) where the compound of formula (1) contains an alcohol functionality (- OH), an ether thereof, for example, a compound wherein the hydrogen of the alcohol functionality of the compound of formula (1) is replaced by (Ci-C6) alkanoyloxymethyl ; and (iii) where the compound of formula (1) contains a primary or secondary amino functionality (-NH2 or-NHR where R H), an amide thereof, for example, a compound wherein, as the case may be, one or both hydrogens of the amino functionality of the compound of formula (1) is/are replaced by (C1-C10) alkanol.

Further examples of replacement groups in accordance with the foregoing examples and examples of other prodrug types may be found in the aforementioned references.

Moreover, certain compounds of formula (1) may themselves act as prodrugs of other compounds of formula (1).

Also included within the scope of the invention are metabolites of compounds of formula (1), that is, compounds formed in vivo upon administration of the drug.

Some examples of metabolites in accordance with the invention include (i) where the compound of formula (1) contains a methyl group, an hydroxymethyl derivative thereof (-CH3->-CH2OH) : (ii) where the compound of formula (1) contains an alkoxy group, an hydroxy derivative thereof (-OR->-OH); (iii) where the compound of formula (1) contains a tertiary amino group, a secondary amino derivative thereof (-NR1R2->-NHR1 or-NHR2) ; (iv) where the compound of formula (1) contains a secondary amino group, a primary derivative thereof (-NHR1->-NH2) ; (v) where the compound of formula (1) contains a phenyl moiety, a phenol derivative thereof (-Ph->-PhOH); and (I). (vi) where the compound of formula (1) contains an amide group, a carboxylic acid derivative thereof (-CONH2-> COOH).

Compounds of formula (1) containing one or more asymmetric carbon atoms can exist as two or more stereoisomers. Where a compound of formula (1) contains an alkenyl or alkenylene group, geometric cisltrans (or Z/E) isomers are possible. Where the compound contains, for example, a keto orstructural isomers are interconvertible via a low oxime group or an aromatic moiety, energy barrier, tautomeric isomerism ('tautomerism') can occur. This can take the form of proton tautomerism in compounds of formula (1) containing, for example, an imino, keto, or oxime group, or so-called valence tautomerism in compounds which contain an aromatic moiety. It follows that a single compound may exhibit more than one type of isomerism.

Included within the scope of the present invention are all stereoisomers, geometric isomers and tautomeric forms of the compounds of formula (1), including compounds exhibiting more than one type of isomerism, and mixtures of one or more thereof. Also included are acid addition or base salts wherein the counterion is optically active, for example, d-lactate or l-lysine, or racemic, for example, dl-tartrate or d/-arginine..

Cisltrans isomers may be separated by conventional techniques well known to those skilled in the art, for example, chromatography and fractional crystal lisation.

Conventional techniques for the preparation/isolation of individual enantiomers include chiral synthesis from a suitable optically pure precursor or resolution of the racemate (or the racemate of a salt or derivative) using, for example, chiral high pressure liquid chromatography (HPLC).

Alternatively, the racemate (or a racemic precursor) may be reacted with a suitable optically active compound, for example, an alcohol, or, in the case where the compound of formula (1) contains an acidic or basic moiety, an acid or base such as tartaric acid or 1-phenylethylamine. The resulting diastereomeric mixture may be separated by chromatography and/or fractional crystallization and one or both of the diastereoisomers converted to the corresponding pure enantiomer (s) by means well known to a skilled person.

Chiral compounds of the invention (and chiral precursors thereof) may be obtained in enantiomerically-enriched form using chromatography, typically HPLC, on an asymmetric resin with a mobile phase consisting of a hydrocarbon, typically heptane or hexane, containing from 0 to 50% by volume of isopropanol, typically from 2% to 20%, and from 0 to 5% by volume of an alkylamine, typically 0. 1% diethylamine. Concentration of the eluate affords the enriched mixture.

Stereoisomeric conglomerates may be separated by conventional techniques known to those skilled in the art-see, for example,"Stereochemistry of Organic Compounds"by E. L. Eliel (Wiley, New York, 1994).

According to one aspect of the present invention, the (R, R)-stereoisomer of the formula below is generally preferred: wherein n and Q1 are as defined above for compounds of formula (1).

The present invention includes all pharmaceutically acceptable isotopically- labelled compounds of formula (1) wherein one or more atoms are replaced by atoms having the same atomic number, but an atomic mass or mass number different from the atomic mass or mass number which predominates in nature.

Examples of isotopes suitable for inclusion in the compounds of the invention include isotopes of hydrogen, such as H and 3H, carbon, such as 11C, 13C and 4C, chlorine, such as 36CI, fluorine, such as 13F, iodine, such as 123I and 125I, nitrogen, such as N and N, oxygen, such as 0, 17O and 18O, phosphorus, such as 32p, and sulphur, such as 35S.

Certain isotopically-labelled compounds of formula (1), for example, those incorporating a radioactive isotope, are useful in drug and/or substrate tissue distribution studies. The radioactive isotopes tritium, i. e. 3H, and carbon-14, i. e.

14C, are particularly useful for this purpose in view of their ease of incorporation and ready means of detection.

Substitution with heavier isotopes such as deuterium, i. e. 2H, may afford certain therapeutic advantages resulting from greater metabolic stability, for example, increased in vivo half-life or reduced dosage requirements, and hence may be preferred in some circumstances.

Substitution with positron emitting isotopes, such as 11C, 18F, 0 and 13N, can be useful in Positron Emission Topography (PET) studies for examining substrate receptor occupancy.

Isotopically-labeled compounds of formula (1) can generally be prepared by conventional techniques known to those skilled in the art or by processes analogous to those described in the accompanying Examples and Preparations using an appropriate isotopically-labeled reagents in place of the non-labeled reagent previously employed.

Pharmaceutical acceptable solvates in accordance with the invention include those wherein the solvent of crystallization may be isotopically substituted, e. g.

D2O, d6-acetone, d6-DMSO.

The compounds of formula (1), their pharmaceutical acceptable salts and/or derived forms, are valuable pharmaceutical active compounds, which are suitable for the therapy and prophylaxis of numerous disorders in which the ß2 receptor is involved or in which agonism of this receptor may induce benefit, in particular the allergic and non-allergic airways diseases but also in the treatment of other diseases such as, but not limited to those of the nervous system, premature labor, congestive heart failure, depression, inflammatory and allergic skin diseases, psoriasis, proliferative skin diseases, glaucoma and in conditions where there is an advantage in lowering gastric acidity, particularly in gastric and peptic ulceration.

The compounds of formula (1) and their pharmaceutically acceptable salts and derived forms as mentioned above can be administered according to the invention to animals, preferably to mammals, and in particular to humans,

as pharmaceuticals for therapy and/or prophylaxis. They can be administered per se, in mixtures with one another or in the form of pharmaceutical preparations which as active constituent contain an efficacious dose of at least one compounds of formula (1), its pharmaceutically acceptable salts and/or derived forms, in addition to customary pharmaceutically innocuous excipients and/or additives.

The compounds of formula (1), their pharmaceutical acceptable salts and/or derived forms may be freeze-dried, spray-dried, or evaporatively dried to provide a solid plug, powder, or film of crystalline or amorphous material.

Microwave or radio frequency drying may be used for this purpose.

The compounds of formula (1), their pharmaceutically acceptable salts and/or derived forms may be administered alone or in combination with other drugs and will generally be administered as a formulation in association with one or more pharmaceutically acceptable excipients. The term"excipient"is used herein to describe any ingredient other than the compound of the invention. The choice of excipient will to a large extent depend on the particular mode of administration.

ORAL ADMINISTRATION The compounds of the invention may be administered orally. Oral administration may involve swallowing, so that the compound enters the gastrointestinal tract, or buccal or sublingual administration may be employed by which the compound enters the blood stream directly from the mouth.

Formulations suitable for oral administration include solid formulations such as tablets, capsules containing particulates, liquids, or powders, lozenges (including liquid-filled), chews, multi-and nano-particulates, gels, solid solution, liposome, films, ovules, sprays and liquid formulations.

Liquid formulations include suspensions, solutions, syrups and elixirs. Such formulations may be employed as fillers in soft or hard capsules and typically comprise a carrier, for example, water, ethanol, polyethylene glycol, propylene glycol, methylcellulose, or a suitable oil, and one or more emulsifying agents and/or suspending agents. Liquid formulations may also be prepared by the reconstitution of a solid, for example, from a sachet.

The compounds of the invention may also be used in fast-dissolving, fast- disintegrating dosage forms such as those described in Expert Opinion in Therapeutic Patents, 11 (6), 981-986, by Liang and Chen (2001).

For tablet dosage forms, depending on dose, the drug may make up from 1 weight % to 80 weight % of the dosage form, more typically from 5 weight % to 60 weight % of the dosage form. In addition to the drug, tablets generally contain a disintegrant. Examples of disintegrants include sodium starch glycolat, sodium carboxymethyl cellulose, calcium carboxymethyl cellulose, croscarmellose sodium, crospovidone, polyvinylpyrrolidone, methyl cellulose, microcrystalline cellulose, lower alkyl-substituted hydroxypropyl cellulose, starch, pregelatinised starch and sodium alginate. Generally, the disintegrant will comprise from 1 weight % to 25 weight %, preferably from 5 weight % to 20 weight % of the dosage form.

Binders are generally used to impart cohesive qualities to a tablet formulation. Suitable binders include microcrystalline cellulose, gelatin, sugars, polyethylene glycol, natural and synthetic gums, polyvinylpyrrolidone, pregelatinised starch, hydroxypropyl cellulose and hydroxypropyl methylcellulose. Tablets may also contain diluents, such as lactose (monohydrate, spray-dried monohydrate, anhydrous and the like), mannitol, xylitol, dextrose, sucrose, sorbitol, microcrystalline cellulose, starch and dibasic calcium phosphate dihydrate.

Tablets may also optionally comprise surface active agents, such as sodium lauryl sulfate and polysorbate 80, and glidants such as silicon dioxide and talc.

When present, surface active agents may comprise from 0. 2 weight % to 5 weight % of the tablet, and glidants may comprise from 0. 2 weight % to 1 weight % of the tablet.

Tablets also generally contain lubricants such as magnesium stearate, calcium stearate, zinc stearate, sodium stearyl fumarate, and mixtures of magnesium stearate with sodium lauryl sulphate. Lubricants generally comprise from 0.25 weight % to 10 weight %, preferably from 0.5 weight % to 3 weight % of the tablet.

Other possible ingredients include anti-oxidants, colourants, flavouring agents, preservatives and taste-masking agents.

Exemplary tablets contain up to about 80% drug, from about 10 weight % to about 90 weight % binder, from about 0 weight % to about 85 weight % diluent, from about 2 weight % to about 10 weight % disintegrant, and from about 0.25 weight % to about 10 weight % lubricant.

Tablet blends may be compressed directly or by roller to form tablets. Tablet blends or portions of blends may alternatively be wet-, dry-, or melt-granulated, melt congealed, or extruded before tabletting. The final formulation may comprise one or more layers and may be coated or uncoated; it may even be encapsulated.

The formulation of tablets is discussed in Pharmaceutical Dosage Forms: Tablets, Vol. 1, by H. Lieberman and L. Lachman (Marcel Dekker, New York, 1980).

Consumable oral films for human or veterinary use are typically pliable water- soluble or water-swellable thin film dosage forms which may be rapidly

dissolving or mucoadhesive and typically comprise a compound of formula (1), a film-forming polymer, a binder, a solvent, a humectant, a plasticiser, a stabiliser or emulsifier, a viscosity-modifying agent and a solvent. Some components of the formulation may perform more than one function.

The compound of formula (1) may be water-soluble or insoluble. A water- soluble compound typically comprises from 1 weight % to 80 weight %, more typically from 20 weight % to 50 weight %, of the solutes. Less soluble compounds may comprise a greater proportion of the composition, typically up to 88 weight % of the solutes. Alternatively, the compound of formula (1) may be in the form of multiparticulate beads.

The film-forming polymer may be selected from natural polysaccharides, proteins, or synthetic hydrocolloids and is typically present in the range 0.01 to 99 weight %, more typically in the range 30 to 80 weight %.

Other possible ingredients include anti-oxidants, colorants, flavourings and flavour enhancers, preservatives, salivary stimulating agents, cooling agents, co-solvents (including oils), emollients, bulking agents, anti-foaming agents, surfactants and taste-masking agents.

Films in accordance with the invention are typically prepared by evaporative drying of thin aqueous films coated onto a pelable backing support or paper.

This may be done in a drying oven or tunnel, typically a combined coater dryer, or by freeze-drying or vacuuming.

Solid formulations for oral administration may be formulated to be immediate and/or modified release. Modified release formulations include delayed-, sustained-, pulsed-, controlled-, targeted and programmed release.

Suitable modified release formulations for the purposes of the invention are described in US Patent No. 6,106, 864. Details of other suitable release

technologies such as high energy dispersions and osmotic and coated particles are to be found in Pharmaceutical Technology On-line, 25 (2), 1-14, by Verma et al (2001). The use of chewing gum to achieve controlled release is described in WO 00/35298.

PARENTERAL ADMINISTRATION The compounds of the invention may also be administered directly into the blood stream, into muscle, or into an internal organ. Suitable means for parenteral administration include intravenous, intraarterial, intraperitoneal, intrathecal, intraventricular, intraurethral, intrasternal, intracranial, intramuscular and subcutaneous. Suitable devices for parenteral administration include needle (including microneedle) injectors, needle-free injectors and infusion techniques.

Parenteral formulations are typically aqueous solutions which may contain excipients such as salts, carbohydrates and buffering agents (preferably to a pH of from 3 to 9), but, for some applications, they may be more suitably formulated as a sterile non-aqueous solution or as a dried form to be used in conjunction with a suitable vehicle such as sterile, pyrogen-free water.

The preparation of parenteral formulations under sterile conditions, for example, by lyophilisation, may readily be accomplished using standard pharmaceutical techniques well known to those skilled in the art.

The solubility of compounds of formula (1) used in the preparation of parenteral solutions may be increased by the use of appropriate formulation techniques, such as the incorporation of solubility-enhancing agents.

Formulations for parenteral administration may be formulated to be immediate and/or modified release. Modified release formulations include delayed-, sustained-, pulsed-, controlled-, targeted and programmed release. Thus

compounds of the invention may be formulated as a solid, semi-solid, or thixotropic liquid for administration as an implanted depot providing modified release of the active compound. Examples of such formulations include drug- coated stents and PGLApoly (dl-lactic-coglycolic) acid (PGLA) microspheres.

TOPICAL ADMINISTRATION The compounds of the invention may also be administered topically to the skin or mucosa, that is, dermally or transdermally. Typical formulations for this purpose include gels, hydrogels, lotions, solutions, creams, ointments, dusting powders, dressings, foams, films, skin patches, wafers, implants, sponges, fibres, bandages and microemulsions. Liposomes may also be used. Typical carriers include alcohol ;-water, mineral oil, liquid petrolatum, white petrolatum, glycerin, polyethylene glycol and propylene glycol. Penetration enhancers may be incorporated-see, for example, J Pharm Sci, 88 (10), 955-958 by Finnin and Morgan (October 1999).

Other means of topical administration include delivery by electroporation, iontophoresis, phonophoresis, sonophoresis and microneedle or needle-free (e. g. Powderject, Bioject, etc.) injection.

Formulations for topical administration may be formulated to be immediate and/or modified release. Modified release formulations include delayed-, sustained-, pulsed-, controlled-, targeted and programmed release.

INHALED/INTRANASAL ADMINISTRATION The compounds of the invention can also be administered intranasally or by inhalation, typically in the form of a dry powder (either alone, as a mixture, for example, in a dry blend with lactose, or as a mixed component particle, for example, mixed with phospholipids, such as phosphatidylcholine) from a dry powder inhaler or as an aerosol spray from a pressurised container, pump,

spray, atomiser (preferably an atomiser using electrohydrodynamics to produce a fine mist), or nebuliser, with or without the use of a suitable propellant, such as 1,1, 1, 2-tetrafluoroethane or 1, 1, 1,2, 3,3, 3-heptafluoropropane. For intranasal use, the powder may comprise a bioadhesive agent, for example, chitosan or cyclodextrin.

The pressurised container, pump, spray, atomizer, or nebuliser contains a solution or suspension of the compound (s) of the invention comprising, for example, ethanol, aqueous ethanol, or a suitable alternative agent for dispersing, solubilising, or extending release of the active, a propellant (s) as solvent and an optional surfactant, such as sorbitan trioleate, oleic acid, or an oligolactic acid.

Prior to use in a dry powder or suspension formulation, the drug product is micronised to a size suitable for delivery by inhalation (typically less than 5 microns). This may be achieved by any appropriate comminuting method, such as spiral jet milling, fluid bed jet milling, supercritical fluid processing to form nanoparticles, high pressure homogenisation, or spray drying.

Capsules (made, for example, from gelatin or hydroxypropylmethylcellulose), blisters and cartridges for use in an inhaler or insufflator may be formulated to contain a powder mix of the compound of the invention, a suitable powder base such as lactose or starch and a performance modifier such as I-leucine, mannitol, or magnesium stearate. The lactose may be anhydrous or in the form of the monohydrate, preferably the latter. Other suitable excipients include dextran, glucose, maltose, sorbitol, xylitol, fructose, sucrose and trehalose.

A suitable solution formulation for use in an atomiser using electrohydrodynamics to produce a fine mist may contain from 1, ug to 20mg of the compound of the invention per actuation and the actuation volume may vary from 1//i to 100//L A typical formulation may comprise a compound of formula (1), propylene glycol, sterile water, ethanol and sodium chloride. Alternative

solvents which may be used instead of propylene glycol include glycerol and polyethylene glycol.

Suitable flavours, such as menthol and levomenthol, or sweeteners, such as saccharin or saccharin sodium, may be added to those formulations of the invention intended for inhaled/intranasal administration.

Formulations for inhaled/intranasal administration may be formulated to be immediate and/or modified release using, for example, PGLA. Modified release formulations include delayed-, sustained-, pulsed-, controlled-, targeted and programmed release.

In the case of dry powder inhalers and aerosols, the dosage unit is determined by means of a valve which delivers a metered amount. Units in accordance with the invention are typically arranged to administer a metered dose or"puff' containing from 0. 001mg to 10mg of the compound of formula (1). The overall daily dose will typically be in the range 0. 001 mg to 40mg which may be administered in a single dose or, more usually, as divided doses throughout the day.

The compounds of formula (1) are particularly suitable for an administration by inhalation RECTAL/INTRAVAGINAL ADMINISTRATION The compounds of the invention may be administered rectally or vaginally, for example, in the form of a suppository, pessary, or enema. Cocoa butter is a traditional suppository base, but various alternatives may be used as appropriate.

Formulations for rectal/vaginal administration may be formulated to be immediate and/or modified release. Modified release formulations include delayed-, sustained-, pulsed-, controlled-, targeted and programmed release.

OCULAR/AURAL ADMINISTRATION The compounds of the invention may also be administered directly to the eye or ear, typically in the form of drops of a micronised suspension or solution in isotonic, pH-adjusted, sterile saline. Other formulations suitable for ocular and aural administration include ointments, biodegradable (e. g. absorbable gel sponges, collagen) and non-biodegradable (e. g. silicone) implants, wafers, lenses and particulate or vesicular systems, such as niosomes or liposomes. A polymer such as crossed-linked polyacrylic acid, polyvinylalcohol, hyaluronic acid, a cellulosic polymer, for example, hydroxypropylmethylcellulose, hydroxyethylcellulose, or methyl cellulose, or a heteropolysaccharide polymer, for example, gelan gum, may be incorporated together with a preservative, such as benzalkonium chloride. Such formulations may also be delivered by iontophoresis.

Formulations for ocular/aural administration may be formulated to be immediate and/or modified release. Modified release formulations include delayed-, sustained-, pulsed-, controlled-, targeted, or programmed release.

OTHER TECHNOLOGIES The compounds of the invention may be combined with soluble macromolecular entities, such as cyclodextrin and suitable derivatives thereof or polyethylene glycol-containing polymers, in order to improve their solubility, dissolution rate, taste-masking, bioavailability and/or stability for use in any of the aforementioned modes of administration.

Drug-cyclodextrin complexes, for example, are found to be generally useful for most dosage forms and administration routes. Both inclusion and non-inclusion complexes may be used. As an alternative to direct complexation with the drug, the cyclodextrin may be used as an auxiliary additive, iee. as a carrier, diluent, or solubiliser. Most commonly used for these purposes are alpha-, beta-and gamma-cyclodextrins, examples of which may be found in International Patent Applications Nos. WO 91/11172, WO 94/02518 and WO 98/55148.

KIT-OF-PARTS Inasmuch as it may desirable to administer a combination of active compounds, for example, for the purpose of treating a particular disease or condition, it is within the scope of the present invention that two or more pharmaceutical compositions, at least one of which contains a compound in accordance with the invention, may conveniently be combined in the form of a kit suitable for coadministration of the compositions.

Thus the kit of the invention comprises two or more separate pharmaceutical compositions, at least one of which contains a compound of formula (1) in accordance with the invention, and means for separately retaining said compositions, such as a container, divided bottle, or divided foil packet. An example of such a kit is the familiar blister pack used for the packaging of tablets, capsules and the like.

The kit of the invention is particularly suitable for administering different dosage forms, for example parenteral, for administering the separate compositions at different dosage intervals, or for titrating the separate compositions against one another. To assist compliance, the kit typically comprises directions for administration and may be provided with a so-called memory aid.

DOSAGE

For administration to human patients, the total daily dose of the compounds of the invention is typically in the range 0. 001 mg to 5000mg depending, of course, on the mode of administration. For example, an intravenous daily dose may only require from 0. 001 mg to 40mg. The total daily dose may be administered in single or divided doses and may, at the physician's discretion, fall outside of the typical range given herein.

These dosages are based on an average human subject having a weight of about 65kg to 70kg. The physician will readily be able to determine doses for subjects whose weight falls outside this range, such as infants and the elderly.

For the avoidance of doubt, references herein to"treatment"include references to curative, palliative and prophylactic treatment.

According to another embodiment of the present invention, the compounds of the formula (1), or pharmaceutically acceptable salts, derived forms or compositions thereof, can also be used as a combination with one or more additional therapeutic agents to be co-administered to a patient to obtain some particularly desired therapeutic end result such as the treatment of pathophysiologically-relevant disease processes including, but not limited to (i) bronchoconstriction, (ii) inflammation, (iii) allergy, (iv) tissue destruction, (v) signs and symptoms such as breathlessness, cough. The second and more additional therapeutic agents may also be a compound of formula (1), or a pharmaceutical acceptable salt, derived forms or compositions thereof, or one or more j32 agonists known in the art. More typically, the second and more therapeutic agents will be selected from a different class of therapeutic agents.

As used herein, the terms"co-administration","co-administered"and"in combination with", referring to the compounds of formula (1) and one or more other therapeutic agents, is intended to mean, and does refer to and include the following :

simultaneous administration of such combination of compound (s) of formula (1) and therapeutic agent (s) to a patient in need of treatment, when such components are formulated together into a single dosage form which releases said components at substantially the same time to said patient, substantially simultaneous administration of such combination of compound (s) of formula (1) and therapeutic agent (s) to a patient in need of treatment, when such components are formulated apart from each other into separate dosage forms which are taken at substantially the same time by said patient, whereupon said components are released at substantially the same time to said patient, sequential administration of such combination compound (s) of formula (1) and therapeutic agent (s) to a patient in need of treatment, when such components are formulated apart from each other into separate dosage forms which are taken at consecutive times by said patient with a significant time interval between each administration, whereupon said components are released at substantially different times to said patient; and sequential administration of such combination of compound (s) of formula (1) and therapeutic agent (s) to a patient in need of treatment, when such components are formulated together into a single dosage form which releases said components in a controlled manner whereupon they are concurrently, consecutively, and/or overlapingly administered at the same and/or different times by said patient, where each part may be administered by either the same or different route.

Suitable examples of other therapeutic agents which may be used in combination with the compound (s) of formula (1), or pharmaceutical acceptable salts, derived forms or compositions thereof, include, but are by no means limited to:

(a) 5-Lipoxygenase (5-LO) inhibitors or 5-lipoxygenase activating protein (FLAP) antagonists, (b) Leukotriene antagonists (LTRAs) including antagonists of LTB4, LTC4, LTD4, and LTE4, (c) Histamine receptor antagonists including H1 and H3 antagonists, (d) ai-and as-adrenoceptor agonist vasoconstrictor sympathomimetic agents for decongestant use, (e) muscarinic M3 receptor antagonists or anticholinergic agents, (f) PDE inhibitors, e. g. PDE3, PDE4 and PDE5 inhibitors, (g) Theophylline, (h) Sodium cromoglycate, (i) COX inhibitors both non-selective and selective COX-1 or COX-2 inhibitors (NSAIDs), Oral and inhaled glucocorticosteroids, (k) Monoclonal antibodies active against endogenous inflammatory entities, (I) Anti-tumor necrosis factor (anti-TNF-o) agents, (m) Adhesion molecule inhibitors including VLA-4 antagonists, (n) Kinin-B1-and B2-receptor antagonists, (o) Immunosuppressive agents, (p) Inhibitors of matrix metalloproteases (MMPs), (q) Tachykinin NK1, NK2 and NK3 receptor antagonists, (r) Elastase inhibitors, (s) Adenosine A2a receptor agonists, (t) Inhibitors of urokinase, (u) Compounds that act on dopamine receptors, e. g. D2 agonists, (v) Modulators of the NFKß pathway, e. g. IKK inhibitors, (w) modulators of cytokine signaling pathyways such as p38 MAP kinase or syk kinase, (x) Agents that can be classed as mucolytics or anti-tussive, and (y) Antibiotics.

According to the present invention, combination of the compounds of formula (1) with: -glucocorticosteroids, in particular inhaled glucocorticosteroids with reduced systemic side effects, including prednisone, prednisolone, flunisolide, triamcinolone acetonide, beclomethasone dipropionate, budesonide, fluticasone propionate, ciclesonide, and mometasone furoate, or - muscarinic M3 receptor antagonists or anticholinergic agents including in particular ipratropium salts, namely bromide, tiotropium salts, namely bromide, oxitropium salts, namely bromide, perenzepine, and telenzepine, are preferred.

It is to be appreciated that all references herein to treatment include curative, palliative and prophylactic treatment. The description, which follows, concerns the therapeutic applications to which the compounds of formula (1) may be put.

The compounds of formula (1) have the ability to interact with the (32 receptor and thereby have a wide range of therapeutic applications, as described further below, because of the essential role which the ß2 receptor plays in the physiology of all mammals.

Therefore, a further aspect of the present invention relates to the compounds of formula (1), or pharmaceutical acceptable salts, derived forms or compositions thereof, for use in the treatment of diseases, disorders, and conditions in which the (32 receptor is involved. More specifically, the present invention also concerns the compounds of formula (1), or pharmaceutically acceptable salts, derived forms or compositions thereof, for use in the treatment of diseases, disorders, and conditions selected from the group consisting of:

asthma of whatever type, etiology, or pathogenesis, in particular asthma that is a member selected from the group consisting of atopic asthma, non-topic asthma, allergic asthma, atopic bronchial IgE-mediated asthma, bronchial asthma, essential asthma, true asthma, intrinsic asthma caused by pathophysiologic disturbances, extrinsic asthma caused by environmental factors, essential asthma of unknown or inapparent cause, non-atopic asthma, bronchitic asthma, emphysematous asthma, exercise-induced asthma, allergen induced asthma, cold air induced asthma, occupational asthma, infective asthma caused by bacterial, fungal, protozoal, or viral infection, non-allergic asthma, incipient asthma, wheezy infant syndrome and bronchiolytis, chronic or acute bronchoconstriction, chronic bronchitis, small airways obstruction, and emphysema, obstructive or inflammatory airways diseases of whatever type, etiology, or pathogenesis, in particular an obstructive or inflammatory airways disease that is a member selected from the group consisting of chronic eosinophilic pneumonia, chronic obstructive pulmonary disease (COPD), COPD that includes chronic bronchitis, pulmonary emphysema or dyspnea associated or not associated with COPD, COPD that is characterized by irreversible, progressive airways obstruction, adult respiratory distress syndrome (ARDS), exacerbation of airways hyper- reactivity consequent to other drug therapy and airways disease that is associated with pulmonary hypertension, bronchitis of whatever type, etiology, or pathogenesis, in particular bronchitis that is a member selected from the group consisting of acute bronchitis, acute laryngotracheal bronchitis, arachidic bronchitis, catarrhal bronchitis, croupus bronchitis, dry bronchitis, infectious asthmatic bronchitis, productive bronchitis, staphylococcus or streptococcal bronchitis and vesicular bronchitis, acute lung injury,

bronchiectasis of whatever type, etiology, or pathogenesis, in particular bronchiectasis that is a member selected from the group consisting of cylindric bronchiectasis, sacculated bronchiectasis, fusiform bronchiectasis, capillary bronchiectasis, cystic bronchiectasis, dry bronchiectasis and follicular bronchiectasis.

A still further aspect of the present invention also relates to the use of the compounds of formula (1), or pharmaceutical acceptable salts, derived forms or compositions thereof, for the manufacture of a drug having a ß2 agonist activity. In particular, the present inventions concerns the use of the compounds of formula (1), or pharmaceutically acceptable salts, derived forms or compositions thereof, for the manufacture of a drug for the treatment of P2- mediated diseases and/or conditions, in particular the diseases and/or conditions listed above.

As a consequence, the present invention provides a particularly interesting method of treatment of a mammal, including a human being, including treating said mammal with an effective amount of a compound of formula (1), or a pharmaceutical acceptable salt, derived form or composition thereof. More precisely, the present invention provides a particularly interesting method of treatment of a mammal, including a human being, to treat a ß2- mediated diseases and/or conditions, in particular the diseases and/or conditions listed above, including treating said mammal with an effective amount of a compound of formula (1), its pharmaceutical acceptable salts and/or derived forms.

The following examples illustrate the preparation of the compounds of the formula (1): Example 1: N-(2, 6-Dimethoxybenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetamide

A solution of 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-h ydroxy-3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N- (2, 6-dimethoxybenzyl)- acetamide (Preparation 1) (125mg, 0. 20mmol) in methanol (6ml) was treated with acetic acid (6ml) and ammonium fluoride (74mg, 2. Ommol) and the reaction heated to 40°C for 16 hours. The solvent was removed in vacuo and the residue purified by flash column chromatography on silica gel eluting with dichloromethane : methanol : 880 ammonia (95: 5: 0.5 changing to 93: 7: 0.7, by volume) to give the title compound as a white solid after trituration with diethyl ether (59mg).

1H NMR (400MHz, CD30D) : 8 = 7.24-7. 15 (3H, m), 7.09-7. 07 (1H, m), 7.02- 6.97 (3H, m), 6.70-6. 68 (1H, d), 6.61-6. 59 (2H, d), 4.61 (2H, s), 4.61-4. 58 (1H, m), 4.41 (2H, s), 3.75 (6H, s), 3.43 (2H, s), 2.92-2. 84 (2H, m), 2.71-2. 67 (2H, m), 2.57-2. 52 (1 H, dd), 1.05-1. 03 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 509, [M-H]-507.

CHN analysis: found C 67.00%, H 7. 48%, N 5. 11% ; C29H36N206+0. 2Et20+ 0. 6H20 requires C 67.00%, H 7.40%, N 5.24%.

Example 2 : N-(2-Ethoxybenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy -3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetamide

Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl)dimethyl)silyl]oxy}-2-(4-h ydroxy- 3-hydroxymethyl-pehnyl)-ethylamino]-propyl}-phenyl)-N- (2-ethoxy benzyl)- acetamide (Preparation 2) according to the method for example 1 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 6 = 7.22-7. 18 (3H, m), 7.13-7. 11 (2H, d), 7.07 (1H, s), 7.03-7. 01 (2H, d), 6.90-6. 88 (1H, d), 6.85-6. 81 (1H, t), 6.71-6. 69 (1H, d), 4.65-4. 59 (1H, m), 4.62 (2H, s), 4.35 (2H, s), 4.03-3. 98 (2H, q), 3.50 (2H, s), 2.99-2. 85 (2H, m), 2.77-2. 70 (2H, m), 2.59-2. 54 (1H, dd), 1.34-1. 31 (3H, t), 1.07-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 493, [M-H]-491.

CHN analysis : found C 69.25%, H 7.59%, N 5. 31% ; C29H36N2O5+0.15Et2O+ 0. 55H20 requires C 69.22%, H 7. 57%, N 5.45%.

Example 3: N-(2-Hydroxybenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydrox y- 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetamid e Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl)dimethyl)silyl]oxy}-2-(4-h ydroxy- <BR> <BR> 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N-(2-hyd roxy benzyl)- acetamide (Preparation 3) according to the method for example 1, using water

instead of acetic acid as the co-solvent, to give the title compound as a white foam.

H NMR (400MHz, CD3OD) : 8 = 7. 23 (1H, s), 7. 19-7. 17 (1H, d), 7. 12-7. 00 (6H, m), 6.77-6. 73 (2H, t), 6.71-6. 69 (1H, d), 4. 65-4.60 (1H, m), 4. 62 (2H, s), 4.32 (2H, s), 3.50 (2H, s), 3.00-2. 86 (2H, m), 2. 75-2. 70 (2H, m), 2. 60-2. 55 (1H, m), 1.07-1. 06 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 465, [M+Na] + 487, [M-H]-463.

CHN analysis : found C 67. 46%, H 7.03%, N 5.66% ; C27H32N205+0. 9H20 requires C 67.45%, H 7.09%, N 5. 83%.

Example 4: 2-(3-{(2R)-2-[(2R)-2-Hydroxy-4-(4-hydroxy-3-hydroxymethyl- phenyl)-ethylamino]-propyl}-phenyl)-N-indan-2-yl-acetamide Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl)dimethyl)silyl]oxy}-2-(4-h ydroxy- <BR> <BR> <BR> 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N-indan- 2-yl-acetamide (Preparation 4) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8= 7.22-7. 16 (4H, m), 7.14-7. 09 (3H, m), 7.05 (1H, s), 7.03-6. 99 (2H, t), 6.70-6. 68 (1 H, d), 4.63-4. 60 (1 H, t), 4.61 (2H, s), 4.57-4. 53 (1 H, m), 3.43 (2H, s), 3.25-3. 20 (2H, dd), 2.98-2. 93 (1 H, q), 2.90-2. 85 (1 H, dd), 2.84-2. 79 (2H, dd), 2.74-2. 69 (2H, m), 2.60-2. 55 (1H, dd), 1.08-1. 07 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 475, [M-H]-473.

CHN analysis : found C 72.29%, H 7. 28%, N 5.79% ; C29H34N204+0. 4H20 requires C 72.29%, H 7. 28%, N 5. 81 %. Example 5: N-(3,4-Dichlorobenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetamide

Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-h ydroxy- <BR> <BR> <BR> 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N- (3, 4-dichloro benzyl)- acetamide (Preparation 5) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 6 = 7.41-7. 38 (1H, d), 7.33 (1H, d), 7.21-7. 17 (2H, m), 7.13-7. 11 (2H, d), 7.06 (1H, s), 7.01-6. 99 (2H, m), 6.69-6. 67 (1H, d), 4.60 (2H, s), 4.60-4. 57 (1H, m), 4.30 (2H, s), 3.50 (2H, s), 2.96-2. 91 (1H, m), 2.88- 2.83 (1 H, dd), 2.73-2. 68 (2H, m), 2.60-2. 57 (1 H, dd), 1.06-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 517/519, [M-H]-515/517.

CHN analysis : found C 61.95%, H 5.93%, N 5.37% ; C27H30Cl2N2O4+0.35H2O requires C 61.92%, H 5. 91 %, N 5.35%.

Example 6: N- [4- (Aminosulfonyl) benzyl]-2- (3- ( (2R)-2- [ (2R)-2-hydroxy-2- (4- <BR> <BR> <BR> hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetamide Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-h ydroxy- 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N- [4- (aminosulfonyl)

benzyl]-acetamide (Preparation 6) according to the method for example 3 to give the title compound as a white foam.

H NMR (400MHz, CD3OD) : 8 = 7. 82-7. 79 (2H, d), 7. 38-7. 36 (2H, d), 7. 25-7. 13 (3H, m), 7. 09 (1H, s), 7. 05-7. 03 (2H, d), 6. 72-6. 70 (1H, d), 4.65-4.62 (1H, m), 4.62 (2H, s), 4. 42 (2H, s), 3.53 (2H, s), 3.04-2. 98 (1H, m), 2.93-2. 86 (1H, m), 2. 80-2. 75 (2H, m), 2. 63-2. 57 (1 H, m), 1. 09-1. 08 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 528, [M+Na] + 550, [M-H]-526.

CHN analysis : found C 59. 44%, H 6.44%, N 7.65% ; C27H33N306S+1. OHzO requires C 59.43%, H 6.47%, N 7.70%.

Example 7: 2-(3-{(2R)-2-[(2R)-2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl- phenyl)-ethylamino]-propyl}-phenyl)-N-(pyridin-2-ylmethyl)-a cetamide Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-h ydroxy- 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N- (pyridin-2-ylmethyl)- acetamide (Preparation 7) according to the method for example 3 to give the title compound as a white foam.

H NMR (400MHz, CD30D) : 5 = 8. 44-8. 42 (1H, d), 7.75-7. 71 (1H, t), 7.28-7. 14 (5H, m), 7.11 (1H, s), 7.04-7. 01 (2H, t), 6.70-6. 68 (1H, d), 4.63-4. 60 (1H, m), 4.62 (2H, s), 4.47 (2H, s), 3.57 (2H, s), 3.03-2. 95 (1H, m), 2.91-2. 86 (1H, dd), 2.77-2. 72 (2H, m), 2.64-2. 59 (1 H, dd), 1.11-1. 09 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 450, [M+Na] + 472, [M-H]-448.

CHN analysis : found C 67. 06%, H 6.94%, N 8. 96%; C26H31N3O4+0. 9H2O requires C 67.05%, H 7.10%, N 9.02%. Example 8: 4-{(2-(3-{(2R)-2-l (2R)-2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl- phenyl)-ethylamino]-propyl}-phenyl)-acetylamino)-methyl}-ben zamide

Prepared from 4-{(2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2- (4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetylamino)- methyl}-benzamide (Preparation 8) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.80-7. 78 (2H, d), 7.31-7. 29 (2H, d), 7.21-7. 12 (3H, m), 7.09 (1H, s), 7.03-7. 01 (2H, d), 6.70-6. 68 (1H, d), 4.61-4. 59 (1H, m), 4.61 (2H, s), 4.40 (2H, s), 3.52 (2H, s), 2.98-2. 94 (1H, m), 2.90-2. 85 (1H, m), 2.74-2. 70 (2H, m), 2.61-2. 56 (1 H, dd), 1.08-1. 06 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 492, [M+Na] + 514, [M-H]-490.

CHN analysis: found C 65.27%, H 6.73%, N 8.20% ; C28H33N3O5+1.3H2O requires C 65.30%, H 6.97%, N 8.16%.

Example 9: N-(3, 4-Dimethoxybenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4- <BR> <BR> <BR> hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetamide Prepared from 2-(3-{(2R)-2-[(2R)-2-{[teff-butyl (dimethyl) silyl] oxy}-2-(4-hydroxy- 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N- (3,4-dimethoxy benzyl)-

acetamide (Preparation 9) according to the method for example 3 to give the title compound as a white foam. aH NMR (400MHz, CD3OD) : s = 7.21-7. 13 (3H, m), 7. 08 (1H, s), 7. 02-7.00 (2H, d), 6. 86-6. 77 (3H, m), 6. 70-6. 68 (1H, d), 4. 65-4.59 (1H, m), 4. 61 (2H, s), 4. 28 (2H, s), 3. 78 (3H, s), 3.71 (3H, s), 3.49 (2H, s), 2.96-2. 84 (2H, m), 2.73-2. 66 (2H, m), 2.59-2. 54 (1 H, dd), 1. 07-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 509, [M+Na] + 531, [M-H]'507.

CHN analysis : found C 66.69%, H 7. 44%, N 5.14% ; C29H36N206+0. 2Et2O+0.75H2O requires C 66.66%, H 7. 41%, N 5.22%.

Example 10: 2-(3-{(2R)-2-[(2R)-2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl- <BR> <BR> <BR> phenyl)-ethylamino]-propyl}-phenyl)-N- (4-trifluoromethoxybenzyl)- acetamide Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl)dimethyl)silyl]oxy}-2-(4-h ydroxy- 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N- (4- trifluoromethoxybenzyl)-acetamide (Preparation 10) using the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.32-7. 30 (2H, d), 7.22-7. 12 (5H, m), 7.08 (1H, s), 7.03-7. 01 (2H, d), 6.70-6. 68 (1H, d), 4.62-4. 59 (1H, m), 4.61 (2H, s), 4.36 (2H, s), 3.51 (2H, s), 3.00-2. 93 (1H, m), 2.90-2. 85 (1H, dd), 2.73-2. 69 (2H, m), 2.61-2. 56 (1 H, dd), 1. 08-1. 06 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 533, [M-H]-531.

CHN analysis : found C 62.12%, H 5.98%, N 5.15% ; C28H31F3N2O5+0.5H2O requires C 62.10%, H 5.96%, N 5.17%. Example 11: N-(2-Chloro, 6-fluorobenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetamide

Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-h ydroxy- 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N-(2-chl oro, 6- fluorobenzyl)-acetamide (Preparation 11) using the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.33-7. 28 (1H, m), 7.25-7. 22 (2H, m), 7.18- 7.15 (1H, t), 7.09-6. 97 (5H, m), 6.70-6. 68 (1H, d), 4.63-4. 60 (1H, m), 4.61 (2H, s), 4.53 (2H, s), 3.45 (2H, s), 2.97-2. 91 (1H, m), 2.90-2. 85 (1H, dd), 2. 74-2. 69 (2H, m), 2.57-2. 52 (1 H, dd), 1.06-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 501/503, [M-H]-499/501.

CHN analysis : found C 62.90%, H 6.06%, N 5.34% ; C27H30CIF N204+0. 8H2O requires C 62.92%, H 6.18%, N 5.44%.

Example 12: N-(3,4-Dimethylbenzyl)-2-(3-{(2R)-2-[(2R)-2-hydrxy-2-(4- <BR> <BR> hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetamide Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-h ydroxy- <BR> <BR> 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N-(3, 4-dimethylbenzyl)-

acetamide (Preparation 12) using the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz. CD3OD): # = 7. 21-7. 12 (3H, m), 7. 07 (1H, s), 7. 05-7. 00 (3H, m), 6.95-6. 91 (2H, m), 6. 70-6. 68 (1H, d), 4.62-4. 59 (1H, m), 4. 61 (2H, s), 4.26 (2H, s), 3.49 (2H, s), 2. 98-2. 90 (1H, m), 2. 90-2. 85 (1H, dd), 2.74-2. 69 (2H, m), 2.60-2. 55 (1 H, dd), 2.20 (3H, s), 2.19 (3H, s), 1. 07-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 477, [M-H]- 475.

CHN analysis : found C 71. 69, H 7. 70, N 5. 72 ; C29H36N2O4+0.5H2O requires C 71.73%, H 7.68%, N 5. 77%.

Example 13: N-[2-Fluoro-5-(trifluoromethyl)benzyl]-2-(3-{(2R)-2-[(2R)-2- hydroxy-2- (4-hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}- phenyl)-acetamide Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-h ydroxy- 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N- [2-fluroo-5- (trifluoromethyl) benzyl]-acetamide (Preparation 13) using the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 5 = 7.61-7. 57 (1H, m), 7.55-7. 52 (1H, m), 7.28- 7.18 (3H, m), 7.14-7. 12 (1H, m), 7.07 (1H, s), 7.03-7. 01 (2H, d), 6.70-6. 68 (1H, d), 4.63-4. 60 (1 H, m), 4.61 (2H, s), 4.44 (2H, s), 3.52 (2H, s), 3.00-2. 93 (1 H, m), 2.91-2. 86 (1H, dd), 2.76-2. 70 (2H, m), 2.60-2. 55 (1H, dd), 1.07-1. 06 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H]+ 535, [M-H]-533.

CHN analysis : found C 62.26%, H 5. 81%, N 5. 09%; C28H30F4N204+0. 30H2O requires C 62.28%, H 5. 71%, N 5.19%.

Example 14: N- (2,6-Dichlorobenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetamide Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-h ydroxy- 3-hydroxymethyl-phenyl)-ethylamino]-propyi}-phenyl)-N-(2, 6-dichlorobenzyl)- acetamide (Preparation 14) using the method for example 3 to give the title compound as a white foam.

'H NMR (400MHz, CD30D) : 6 = 7.38-7. 36 (2H, d), 7.27-6. 97 (7H, m), 6.70-6. 68 (1H, d), 4.69-4. 55 (5H, m), 3.46 (2H, s), 3.00-2. 83 (2H, m), 2.79-2. 68 (2H, m), 2.61-2. 50 (1 H, m), 1.07-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 517/519, [M+Na] 539/541, [M-H]-515/ 517.

CHN analysis: found C 61.40%, H 6.13%, N 5.15% ; C27H30Cl2N2O4+0. 6H20 requires C 61. 39%, H 5.95%, N 5.30%.

Example 15: 2-(3-{(2R-2-[(2R)-2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl- phenyl)-ethylamino]-propyl}-phenyl)-N- (2-phenylethyl) acetamide

Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-h ydroxy- 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N-(2- phenylethyl) acetamide (Preparation 15) using the method for example 3 to give the title compound as a white solid.

'H NMR (400MHz, CD3OD) : 8 = 7.49-7. 30 (8H, m), 7. 26-7. 22 (3H, m), 6.90- 6. 88 (1H, d), 4.81-4. 78 (3H, m), 3.60-3. 54 (4H, m), 3.16-3. 00 (2H, m), 2.96-2. 87 (4H, m), 2. 80-2. 75 (1 H, dd), 1. 28-1. 26 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 463, [M+Na] + 485, [M-H]-461.

CHN analysis: found C 69.89%, H 7.63%, N 5.98% ; C28H34N204+1. 30H20 requires C 69.20%, H 7. 59%, N 5.76%.

Example 16: N-Benzyl-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy-3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetamide Prepared from N-Benzyl-2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]ox y}-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetamide (Preparation 16) using the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.29-7. 18 (7H, m), 7.14-7. 12 (1H, m), 7.08 (1H, s), 7.05-6. 99 (2H, m), 6.71-6. 69 (1H, d), 4.64-4. 62 (1H, m), 4.61 (2H, s), 4.34 (2H, s), 3.51 (2H, s), 3.02-2. 93 (1 H, m), 2.91-2. 86 (1 H, m), 2.76-2. 72 (2H, dd), 2.61-2. 56 (1 H, dd), 1.08-1. 07 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 449, [M+Na] +471, [M-H]-447.

CHN analysis: found C 69. 02%, H 7.24%, N 5.95% ; C27H32N204+1. 15H20 requires C 69. 11%, H 7.37%, N 5.97%. Example 17: N-(3,5-Dichlorobenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4- <BR> <BR> hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetamide

Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-h ydroxy- 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N-(3, 5-dichlorobenzyl)- acetamide (Preparation 17) using the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 6 = 7. 28-7. 13 (6H, m), 7.08 (1H, s), 7.04-7. 01 (2H, m), 6. 71-6.69 (1 H, d), 4.62 (2H, s), 4.62-4. 59 (1 H, m), 4.31 (2H, s), 3.52 (2H, s), 3.02-2. 92 (1H, m), 2.90-2. 85 (1H, m), 2.77-2. 69 (2H, m), 2.62-2. 57 (1H, dd), 1.08-1. 06 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 517/519, [M+Na] + 539 / 541, [M-H]- 515 / 517.

CHN analysis : found C 60. 61%, H 5.86%, N 5. 14% ; C27H30Cl2N2O4+0.95H2O requires C 60.67%, H 6. 01 %, N 5.24%.

Example 18: N-(4-Chlorobenzyl)-2-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4-hydroxy - 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetamid e

Prepared from 2-(3-{(2R)-2-[(2R)-2-[[tert-butyl(dimethyl)silyl]oxy}-2-(4-h ydroxy- 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N- (4-chlorobenzyl)- acetamide (Preparation 18) using the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD3OD) : 6 = 7. 28-7. 18 (6H, m), 7.13-7. 11 (1 H, m), 7. 06 (1 H, s), 7.02-7. 00 (2H, d), 6.70-6. 68 (1H, d), 4.61 (2H, s), 4.61-4. 58 (1H, m), 4.32 (2H, s), 3.50 (2H, s), 2. 95-2. 90 (1H, m), 2. 89-2. 84 (1H, dd), 2. 72-2. 67 (2H, m), 2.60-2. 55 (1 H, dd), 1. 07-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 483/485, [M+Na] + 505 / 507, [M-H]-481 / 483.

CHN analysis : found C 64.92%, H 6.46%, N 5. 61% ; C27H31ClN2O4+0.9H2O requires C 64.96%, H 6.62%, N 5. 61 %.

Example 19: 4-{([2-{(2R)-2-[(2R)-2-Hydroxy-2-(4-hydroxy-3- hydroxymethyl-phenyl)-ethylami no]-propyl}-phenyl)-acetyl]-amino)- methyl}-benzoic acid Prepared from 4-{([2-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4 - <BR> <BR> hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetyl]-amino)- methyl}-benzoic acid (Preparation 19) using the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 6 = 7. 86-7. 84 (2H, d), 7.33 (1H, s), 7.28-7. 09 (7H, m), 6. 78-6. 76 (1 H, d), 4.80 (1 H, m, partially obscured by solvent), 4. 65 (2H, s), 4.38 (2H, s), 3.54 (2H, s), 3.43-3. 36 (1H, m), 3.13-3. 05 (3H, m), 2.71-2. 65 (1H, m), 1.16-1. 14 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 493, [M+Na] +515, [M-H]- 491.

Example 20 : 2-{3-[(2R)-2-({(2R)-2-Hydroxy-2-[4-hydroxy-3- (hydroxymethyl)phenyl]ethyl}amino)propyl]phenyl}-N-[(1R)-1- phenylethyl] acetamide Prepared from 2-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy- 3- (hydroxymethyl)phenyl]ethyl}amino)propyl]phenyl}-N-[(1R)-1- phenylethyl] acetamide (Preparation 21) according to the method for example 3 using dichloromethane : methanol : 880 ammonia (90: 10: 1 by volume) as the column eluent to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.27-7. 01 (11H, m), 6.73-6. 71 (1H, d), 5.01- 4.94 (1H, m), 4.69-4. 63 (1H, m), 4.63 (2H, s), 3.49 (2H, s), 3.09-3. 01 (1H, m), 2.98-2. 89 (1H, m), 2.85-2. 76 (2H, m), 2.64-2. 56 (1H, m), 1.44-1. 42 (3H, d) 1.09-1. 08 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 463, [M+Na] + 485, [M-H]-461.

CHN analysis : found C 69.24%, H 7.35%, N 5.73% ; C28H34N204+1. 30H20 requires C 69.20%, H 7.59%, N 5.76%.

Example 21: 4- (1R)-2- [ ( (1R)-2- {3- [2- (3, 4-Dihydroisoquinolin-2 (1lH)-yl)-2- oxoethyl] phenyl}-1-methylethyl) amino]-1-hydroxyethyl}-2- (hydroxymethyl) phenol

Prepared from 4-{(1 R)-1-{[fert-butyl (dimethyl) silyl] oxy}-2-[((1 R)-2-{3-[2-(3, 4- dihydroisoquinolin-2 (1 H)-yl)-2-oxoethyl] phenyl}-1-methylethyl) amino] ethyl}-2- (hydroxymethyl) phenol (Preparation 22) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7. 24-6. 94 (10H, m), 6.70-6. 68 (1H, d), 4.69- 4. 67 (2H, m), 4. 61 (2H, s), 4.61-4. 58 (1 H, m), 3. 83-3. 82 (2H, m), 3. 81-3. 70 (2H, m), 2.95-2. 80 (3H, m), 2.74-2. 62 (3H, m), 2.60-2. 46 (1H, m), 1.05-0. 97 (3H, m) ppm.

LRMS (electrospray) : m/z [M+H] + 475, [M+Na] + 497, [M-H]-473.

CHN analysis: found C 71. 47%, H 7.29%, N 5. 71% ; C29H34N204+0. 70H2O requires C 71.49%, H 7.32%, N 5.75%.

Example 22 : 4-{(1R)-2-[((1R)-2-{3-[2-(7-Ethoxy-6-methoxy-3, 4- dihydroisoquinolin-2 (1 H)-yl)-2-oxoethyl] phenyl}-1-methylethyl) amino]-1- hydroxyethyl}-2- (hydroxymethyl)phenol Prepared from 4-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[((1R)-2-{3-[2- (7- ethoxy-6-methoxy-3, 4-dihydroisoquinolin-2(1H)-yl)-2-oxoethyl]phenyl}-1- methylethyl) amino] ethyl}-2- (hydroxymethyl) phenol (Preparation 23) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.23-6. 93 (6H, m), 6.70 (1 H, s), 6.70-6. 68 (1 H, d), 6.65-6. 56 (1H, m), 4.61-4. 57 (5H, m), 4.02-3. 92 (2H, m), 3.82 (2H, s), 3.76 (3H, s), 3.82-3. 67 (2H, m), 2.98-2. 44 (7H, m), 1.38-1. 33 (3H, m), 1.06-0. 96 (3H, m) ppm.

LRMS (electrospray) : m/z [M+H] + 549, [M+Na] + 571, [M-H]-547.

CHN analysis : found C 68.60%, H 7. 47%, N 4.96% ; C32H40N2O6+0.70H2O requires C 68.48%, H 7.43%, N 4.99%. Example 23: N- [2-(4-Chlorophenyl)ethyl]-2-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4 - hydroxy-3- (hydroxymethyl)phenyl]ethyl}amino)propyl]phenyl}acetamide

Prepared from 2-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy- 3-(hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-[2-(4- chlorophenyl) ethyl] acetamide (Preparation 24) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.22-7. 16 (4H, m), 7.09-7. 01 (6H, m), 6.70- 6.68 (1H, d), 4.62-4. 59 (1H, m), 4.61 (2H, s), 3.39 (2H, s), 3.39-3. 35 (2H, t), 3.00-2. 92 (1H, m), 2.90-2. 85 (1H, dd), 2.75-2. 68 (4H, m), 2.61-2. 56 (1H, dd), 1.09-1. 07 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 497, [M+Na] + 519, [M-H]-495.

CHN analysis : found C 66.68%, H 6.77%, N 5.66% ; C28H33ClN2O4+0.40H2O requires C 66.70%, H 6.76%, N 5.56%.

Example 24: N-[2-(4-Ethylphenyl)ethyl]-2-{3-[(2R)-2-({(2R)-2-hydroxy-2-[ 4- hydroxy-3- (hydroxymethyl) phenyl] ethyl) amino) propyl] phenyl) acetamide Prepared from 2-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy- 3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N- [2- (4- ethylphenyl) ethyl] acetamide (Preparation 25) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.22-7. 16 (2H, m), 7.07-7. 01 (8H, m), 6.70- 6. 68 (1H, d), 4.64-4. 60 (1H, m), 4.61 (2H, s), 3.41 (2H, s), 3.37-3. 34 (2H, t), 3.02-2. 95 (1H, m), 2.91-2. 86 (1H, dd), 2.75-2. 68 (4H, m), 2. 62-2. 55 (3H, m), 1. 20-1. 16 (3H, t), 1. 09-1. 08 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 491, [M+Na]+ 513, [M-H]- 489.

CHN analysis : found C 71. 77%, H 7. 84%, N 5. 58% ; C3oH38N204+0. 60H20 requires C 71. 86%, H 7. 88%, N 5.59%.

Example 25: N-(1,1-Dimethyl-2-phenylethyl)-2-{3-[(2R)-2-({(2R)-2-hydroxy -2- [4-hydroxy-3-(hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} acetamide Prepared from 2-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy- 3-(hydroxymethyl)phenyl]ethyl} amino) propyl]phenyl}-N-(1,1-dimethyl-2- phenylethyl) acetamide (Preparation 26) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 5 = 7.24-7. 20 (2H, m), 7.14-7. 11 (4H, m), 7.07- 7.02 (3H, m), 6.97-6. 95 (2H, m), 6.71-6. 69 (1 H, d), 4. 65-4. 61 (1 H, m), 4.61 (2H, s), 3.38 (2H, s), 3.01-2. 95 (1H, m), 2.99 (2H, s), 2.92-2. 87 (1H, dd), 2.79-2. 73 (2H, m), 2.62-2. 57 (1 H, dd), 1.27 (3H, s), 1.26 (3H, s), 1.08-1. 07 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 491, [M+Na] + 513, [M-H]-489.

CHN analysis : found C 71.96%, H 7. 81%, N 5. 51% ; C3oH38N204+0. 60H20 requires C 71.86%, H 7. 88%, N 5.59%.

Example 26: N-[2-(3,4-Dimethoxyphenyl)ethyl]-2-{3-[(2R)-2-({(2R)-2- hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyllacetamide

Prepared from 2- {3- [ (2R)-2- ( { (2R)-2- { [tert-butyl (dimethyl) silyl] oxy)-2- [4-hydroxy- 3- (hydroxymethyl)phenyl]ethyl}amino)propyl]phenyl}-N-[2-(3,4- dimethoxyphenyl) ethyl] acetamide (Preparation 27) according to the method for example 3 to give the title compound as a white foam after trituration with ether.

1H NMR (400MHz, CD30D) : 8 = 7.21-7. 15 (2H, m), 7.06-7. 00 (4H, m), 6. 82- 6.77 (2H, m), 6.70-6. 65 (2H, m), 4.64-4. 59 (1H, m), 4.61 (2H, s), 3.78 (3H, s), 3.75 (3H, s), 3.41 (2H, s), 3.40-3. 37 (2H, t), 2.98-2. 91 (1H, m), 2.90-2. 85 (1 H, dd), 2.74-2. 67 (4H, m), 2.60-2. 55 (1 H, dd), 1.08-1. 07 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 523, [M+Na] + 545, [M-H]-521.

CHN analysis : found C 67.27%, H 7.73%, N 4.96% ; C3oH38N206+0. 70H2O+0. 20Et20 requires C 67.25%, H 7.59%, N 5.09%.

Example 27: N- (3, 4-Difluorobenzyl)-2- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4- hydroxy-3-(hydroxymethyl) phenyl] ethyl} amino) propyl]phenyl}acetamide Prepared from 2-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy- 3-(hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(3, 4- difluorobenzyl) acetamide (Preparation 28) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 5 = 7.21-7. 15 (3H, m), 7. 13-7. 08 (3H, m), 7.06- 7.00 (3H, m), 6.70-6. 68 (1H, d), 4.61-4. 57 (3H, m), 4.30 (2H, s), 3.50 (2H, s),

2.94-2. 83 (2H, m), 2.71-2. 66 (2H, m), 2.59-2. 54 (1H, dd), 1.06-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 485, [M+Na] + 507, [M-H]- 483.

CHN analysis : found C 65.60%, H 6. 32%, N 5. 76% ; C27H3oF2N204+0. 50H20 requires C 65. 71%, H 6.33%, N 5. 68%.

Example 28 : 4- ((1R)-2- [ (1R)-2- 3- [2- (1, 3-Dihydro-2H-isoindol-2-yl)-2- oxoethyl] phenyl}-1-methylethyl) amino]-1-hydroxyethyl}-2- (hydroxymethyl) phenol Prepared from 4-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[((1R)-2-{3-[2- (1, 3- dihydro-2H-isoindol-2-yl)-2-oxoethyl] phenyl}-1-methylethyl) amino] ethyl}-2- (hydroxymethyl) phenol (Preparation 29) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.29-7. 27 (4H, m), 7.23-7. 19 (2H, m), 7.15- 7.13 (1H, d), 7.09 (1H, s), 7.02-6. 96 (2H, m), 6.68-6. 66 (1H, d), 4.74 (2H, s), 4.61-4. 58 (3H, m), 3.77 (2H, s), 3.29 (2H, s), 2.96-2. 83 (2H, m), 2.71-2. 65 (2H, m), 2.62-2. 57 (1 H, dd), 1.07-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H]+ 461, [M-H]- 459.

Example 29: 2-{3-[(2R)-2-({(2R)-2-Hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-phenylacetamide

Prepared from 2-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy- 3-(hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-phenylacetamide (Preparation 30) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.53-7. 51 (2H, d), 7.29-7. 10 (6H, m), 7.08-6. 99 (3H, m), 6.70-6. 68 (1 H, d), 4.66-4. 58 (3H, m), 3.62 (2H, s), 3.01-2. 85 (2H, m), 2.74-2. 68 (2H, m), 2.62-2. 57 (1 H, dd), 1.08-1. 06 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 435, [M+Na] + 457, [M-H]-433.

Example 30: 2- {3-[(2R)-2-({(2R)-2-Hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(1- naphthylmethyl) acetamide Prepared from 2-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy- 3-(hydroxymethyl)phenyl]ethyl} amino) propyl] phenyl}-N- (l- naphthylmethyl) acetamide (Preparation 31) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.96-7. 94 (1 H, d), 7.86-7. 83 ( (1 H, d), 7.79-7. 76 (1H, dd), 7. 48-7. 42 (2H, m), 7.40-7. 36 (2H, m), 7.20-7. 09 (3H, m), 7.00-6. 96 (3H, m), 6.70-6. 68 (2H, d), 4. 80 (2H, s), 4.61-4. 55 (3H, m), 3.49 (2H, s), 2. 83- 2.78 (2H, m), 2.66-2. 60 (2H, m), 2.50-2. 45 (1 H, dd), 1.00-0. 99 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 499, [M+Na] + 521, [M-H]-497. Example 31: N- (3, 4-Dichlorobenzyl)-2- (3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4- hydroxy-3- (hydroxymethyl)phenyl]ethyl}amino)propyl]phenyl}-N- methylacetamide

Prepared from (3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hyd roxy-3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine, using the amide coupling procedure of preparation 5 and the deprotection procedure of example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : s = 7.44-7. 36 (2H, m), 7.23-7. 13 (2H, m), 7.10- 7.04 (2H, m), 7.02-6. 93 (3H, m), 6.70-6. 67 (1 H, d), 4.69-4. 61 (5H, m), 3. 78-3.76 (2H, d), 2.96 (2H, s), 2.93-2. 83 (3H, m), 2.69-2. 63 (2H, m), 2.60-2. 49 (1H, m), 1.07-1. 00 (3H, m) ppm.

LRMS (electrospray) : m/z [M+H] + 531, [M+Na] + 553, [M-H]-529.

Example 32: 2-{3-[(2R)-2-({(2R)-2-Hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(2-pyridin-2- ylethyl) acetamide Prepared from 2-(3-{(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy- 3-(hydroxymethyl)phenyl]ethyl} amino) propyl] phenyl}-N- (2-pyridin-2-

ytethyt) acetamide (Preparation 32) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : s = 8. 40-8.39 (1H, d), 7. 69-7. 65 (1H, m), 7. 24-7. 16 (4H, m), 7. 06-7. 00 (4H, m), 6. 70-6. 68 (1 H, d), 4. 61-4. 59 (3H, m), 3. 53-3. 50 (2H, t), 3.40 (2H, s), 2. 96-2. 84 (4H, m), 2. 72-2. 66 (2H, m), 2. 60-2.55 (1H, m), 1. 08- 1. 06 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 464, [M+Na] + 486, [M-H]-462.

CHN analysis : found C 67. 36%, H 7. 21%, N 8. 95%; C27H33N3O4+1. OOH20 requires C 67.34%, H 7.33%, N 8.73%.

Example 33: 2-{3-[(2R)-2-({(2R)-2-Hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-[(2R)-2- phenylpropyl] acetamide Prepared from 2-(3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy- 3-(hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-[(2R)-2- phenylpropyl] acetamide (Preparation 33) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.31-7. 21 (4H, m), 7. 18-7. 12 (3H, m), 7.03- 6.97 (4H, m), 6.70-6. 68 (1 H, d), 4.61-4. 57 ( (3H, m), 3.37 (2H, s), 2.93-2. 79 (4H, m), 2.71-2. 64 (2H, m), 2.57-2. 52 (1H, m), 1.26-1. 24 (1H, m), 1. 20-1.18 (3H, d), 1.07-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 477, [M+Na]+ 499, [M-H]- 475.

CHN analysis: found C 71.73%, H 7.75%, N 6.12% ; C29H36N204+0. 50H20 requires C 71.73%, H 7. 68%, N 5.77%. Example 34 : N-Benzyl-2-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-methylacetamide

Prepared from N-benzyl-2-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]o xy}-2-[4- hydroxy-3-(hydroxymethyl)phenyl]ethyl} amino) propyl] phenylen methylacetamide (Preparation 34) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.33-7. 17 (6H, m), 7.11-7. 06 (2H, m), 7.03- 7.00 (3H, m), 6.71-6. 69 (1H, d), 4.62-4. 53 (5H, m), 3. 78-3. 76 (2H, m), 2.96-2. 84 (5H, m), 2.75-2. 67 (2H, m), 2.60-2. 52 (1 H, m), 1.03 (3H, m) ppm.

LRMS (electrospray) : m/z [M+H] + 463 ; [M+Na] + 485, [M-H]-461.

CHN analysis: found C 70.58%, H 7. 38%, N 5. 78% ; C28H34N204+0. 75H2O requires C 70.64%, H 7.52%, N 5. 88%.

Example 35 : N- [3- (4-Fluorophenyl) propyl]-2- {3- [ (2R)-2- ( ( (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} acetamide Prepared from 2-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy- 3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-[3-(4- fluorophenyl) propyl] acetamide (Preparation 35) according to the method for example 3 to give the title compound as a white foam.

HNMR (400MHz, CD30D) 8 : 7.25-7. 22 (2H, m), 7. 17-7. 12 (4H, m), 7.06-6. 96 (4H, m), 6.74 (1H, d), 4.67-4. 62 (m, 3H), 3.49 (2H, s), 3.22-3. 19 (2H, s), 2. 99-

2.87 (2H, m), 2.75-2. 70 (2H, m), 2.63-2. 57 (3H, m), 1.81-1. 76 (2H, m), 1.09 (3H, s) ppm.

MS (electrospray) : 495 [M+H] +, 517 [M+Na] +, 493 [M-H]- Example 36: N-(2,6-Dichlorobenzyl)-3-(3-{(2R)-2-[(2R)-2-hydroxy-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- propanamide Prepared from 2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-h ydroxy - 3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-N- (2,6-dichlorobenzyl)- propanamide (Preparation 45) using the method for example 3 to give the title compounds as a white foam.

1H NMR (400MHz, CD30D) : 6 = 7.39-7. 37 (2H, d), 7.28-7. 22 (2H, m), 7. 15-7. 11 (1H, t), 7.03-7. 01 (2H, d), 6.98 (1H, s), 6.95-6. 93 (1H, d), 6.71-6. 69 (1H, d), 4.66-4. 58 (5H, m), 3.05-2. 09 (1H, m), 2.94-2. 84 (3H, m), 2.79-2. 71 (2H, m), 2.60-2. 54 (1 H, dd), 2.48-2. 41 (2H, t), 1.09-1. 08 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 531/533, [M+Na] + 553/555, [M-H]-529/ 531.

CHN analysis: found C 60.34%, H 6.00%, N 4.89% ; C28H32Cl2N2O4+1. 45 H20 requires C 60. 31%, H 6. 31%, N 5.02%.

Example 37: N- (2, 6-Dimethoxybenzyl)-3- 3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4- hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide

Prepared from 3-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(2, 6- dimethoxybenzyl) propanamide (Preparation 46) according to the method for example 1 using methanol : water (2.4 : 1 v/v) instead of acetic acid as solvent and using dichloromethane : methanol : 880 ammonia (97.5 : 2.5 : 0.25 by volume) as the column eluent to give the title compound as a white solid after trituration with diethyl ether.

1H NMR (400MHz, CD30D) : 6 = 7.24-7. 19 (2H, m), 7.13-7. 09 (1H, t), 7.01-6. 99 (2H, d), 6.95-6. 90 (2H, m), 6.70-6. 68 (1H, d), 6.61-6. 59 (2H, d), 4.65-4. 60 (1H, m), 4.60 (2H, s), 4.38 (2H, s), 3.78 (6H, s), 2.97-2. 81 (4H, m), 2.73-2. 64 (2H, m), 2.57-2. 52 (1 H, dd), 2.43-2. 39 (2H, t), 1. 07-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 523, [M+Na] + 545, [M-H]-521.

Example 38 : N-(2-Ethoxybenzyl)-3-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4-hydrox y- 3-(hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide Prepared from 3-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy- 3-(hydroxymethyl)phenyl]ethyl} amino) propyl] phenyl}-N- (2- ethoxybenzyl) propanamide (Preparation 47) according to the method for example 1 using methanol : water (2.4 : 1 v/v) instead of acetic acid as solvent

and using dichloromethane : methanol : 880 ammonia (94: 6: 0.6 by volume) as the column eluent to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 6 = 7.24 (1H, s), 7.19-7. 15 (2H, t), 7. 07-6. 98 (4H, m), 6. 93-6. 87 (2H, dd), 6. 81-6. 77 (1H, t), 6. 72-6. 70 (1H, d), 4. 70-4.64 (1H, m), 4.62 (2H, s), 4.31 (2H, s), 4. 05-4. 00 (2H, q), 3.10-3. 04 (1H, m), 2.97-2. 88 (3H, m), 2. 83-2. 74 (2H, m), 2. 62-2. 50 (3H, m), 1. 39-1. 36 (3H, t), 1. 09-1.08 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] 507, [M+Na] + 529, [M-H]-505.

CHN analysis: found C 69. 31%, H 7. 53%, N 5.20% ; C3oH38N205+0. 75H20 requires C 69.27%, H 7.65%, N 5.39 %.

Example 39: N-(3,4-Dimethylbenzyl)-3-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4- hydroxy-3- (hydroxymethyl) phenyl] ethyllamino) propyl] phenyllpropanamide Prepared from 3-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy-3- (hydroxymethyl) phenyl] ethyl}amino)propyl]phenyl}-N-(3, 4- dimethylbenzyl) propanamide (Preparation 48) according to the method for example 1 using methanol : water (2.4 : 1 v/v) instead of acetic acid as solvent and using dichloromethane : methanol : 880 ammonia (94: 6: 0.6 by volume) as the column eluent to give the title compound as a white solid.

H NMR (400MHz, CD3OD) : 6 = 7.21 (1H, s), 7.16-7. 12 (1H, t), 7.04-6. 92 (6H, m), 6.82-6. 81 (1H, d), 6.70-6. 68 (1H, d), 4.65-4. 61 (1H, m), 4.61 (2H, s), 4.22 (2H, s), 2.97-2. 85 (4H, m), 2.72-2. 64 (2H, m), 2.57-2. 52 (1H, dd), 2.51-2. 47 (2H, t), 2.20 (6H, s), 1.06-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H]+ 491, [M+Na]+ 513, [M-H]- 489.

CHN analysis : found C 71.55%, H 7. 71 %, N 5.59% ; C3oH38N204+0. 70H20 requires C 71.60%, H 7. 89%, N 5.57 %.

Example 40: N- (2,3-Dihydro-1H-inden-2-yl)-3-{3-[(2R)-2-({(2R)-2-hydroxy-2- [4- hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide Prepared from 3-{3-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(2, 3-dihydro-1 H-inden-2- yl) propanamide (Preparation 49) according to the method for example 1 using methanol : water (2.4 : 1 v/v) instead of acetic acid as solvent and using dichloromethane : methanol : 880 ammonia (94: 6: 0.6 by volume) as the column eluent to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 8 = 7. 21-7.09 (6H, m), 7.02-6. 92 (4H, m), 6.69- 6.67 (1H, d), 4.65-4. 56 (1H, m), 4.60 (2H, s), 4.53-4. 50 (1H, t), 3.20-3. 14 (2H, dd), 2.94-2. 81 (4H, m), 2.76-2. 64 (4H, m), 2.57-2. 52 (1 H, dd), 2.43-2. 40 (2H, t), 1.06-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 489, [M+Na] + 511, [M-H]-487.

CHN analysis : found C 71.08%, H 7.35%, N 5. 58% ; C3oH36N204+1. 05H20 requires C 71.00%, H 7.57%, N 5.52 %.

Example 41: 4-{(1R)-2-[((1R)-2-{3-[3-(3,4-Dihydroisoquinolin-2(1H)-yl)-3 - oxopropyl] phenyl}-1-methylethyl) amino]-1-hydroxyethyl}-2- (hydroxymethyl) phenol

Prepared from 4- {(1R)-1-{[tert-butyl(dimethyl)siyl]oxy}-2-[((1R)-2-{3-[3-(3, 4- dihydroisoquinolin-2 (1 H)-yl)-3-oXopropyl] phenyl}-1-methylethyl) amino] ethyl}-2- (hydroxymethyl) phenol (Preparation 50) according to the method for example 1 using methanol : water (2.4 : 1 v/v) instead of acetic acid as solvent and using dichloromethane : methanol : 880 ammonia (95: 5: 0.5 by volume) as the column eluent to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 5 = 7.22 (1H, s), 7.16-6. 93 (8H, m), 6.87-6. 85 (1H, bd), 6.71-6. 68 (1 H, m), 4.65-4. 55 (2H, m), 4.63-4. 60 (1H, m), 4.61 (2H, s), 3.75- 3.60 (2H, m), 2.95-2. 85 (4H, m), 2.80-2. 60 (6H, m), 2.53-2. 47 (1H, dd), 1.05- 1.02 (3H, m) ppm.

LRMS (electrospray) : m/z [M+H] + 489, [M+Na] + 511, [M-H]-487.

CHN analysis: found C 71. 06%, H 7. 27%, N 5.46% ; C30H36N2O4+1.05H2O requires C 71.00%, H 7. 57%, N 5.52 %.

Example 42: N- (2-Chloro-6-fluorobenzyl)-3- 3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4- hydroxy-3-(hydroxymethyl)phenyl]ethyl} amino) propyt] phenyl} propanamide A solution of 3- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanoic acid (Preparation 60) (150mg, 0. 29mol), O-(1H-benzotrizol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate (133mg, 0. 35mmol), 2-fluoro-6-chlorobenzylamine (56mg, 0. 35mmol) and triethylamine (0. 12ml, 0. 88mmol) were stirred at room

temperature for 16 hours in N, N-dimethylformamide (3ml). The solvent was removed in vacuo and the resulting brown oil was purified by flash column chromatography on silica gel eluting with dichloromethane : methanol : 880 ammonia (98 : 2 : 0. 2 followed by 94 : 6 : 0. 6 by volume) to give the title compound as a white foam (30mg).

1H NMR (400MHz, CD3OD) : 6 = 7. 32-7. 20 (3H, m), 7. 12-6. 98 (4H, m), 6.95 (1H, s), 6.92-6. 90 (1H, d), 6.70-6. 68 (1H, d), 4. 64-4.60 (3H, m), 4.49 (2H, s), 2. 98- 2.83 (4H, m), 2.75-2. 66 (2H, m), 2. 58-2. 53 (1 H, dd), 2. 47-2. 43 (2H, t), 1.08-1. 07 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 517, [M+Na] + 537, [M-H]-513.

CHN analysis : found C 62.04%, H 6. 11%, N 5.15% ; C28H32N204CIF+0. 05H20+0. 40CH2CI2 requires C 62.03%, H 6.03%, N 5.09%.

Example 43: N- (2-Chlorobenzyl)-3- 3- [ (2R)-2- ( (2R)-2-hydroxy-2- [4-hydroxy- 3-(hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide Prepared according to the procedure used for example 42 using 3- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanoic acid (Preparation 60) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 5 = 7.35-7. 01 (10H, m), 6.76-6. 74 (1H, d), 4.77- 4.74 (1H, dd), 4.64 (2H, s), 4.39 (2H, s), 3.07-2. 90 (6H, m), 2.67-2. 55 (3H, m), 1.14-1. 13 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 497, [M+Na] + 519, [M-H]-495. Example 44 : 3- {3- [ (2R)-2- ( ( (2R)-2-Hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl]ethyl}amino)propyl]phenyl}-N-(pyridin-2- ytmethyt) propanam ! de

Prepared according to the procedure used for example 42 using 3- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanoic acid (Preparation 60) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 8.42-8. 41 (1H, d), 7.71-7. 67 (1H, m), 7.27-7. 14 (3H, m), 7.06-6. 96 (5H, m), 6.71-6. 68 (1H, d), 4.63-4. 59 (3H, m), 4.42 (2H, s), 2.96-2. 85 (4H, m), 2.72-2. 65 (2H, m), 2.59-2. 53 (3H, m), 1.06-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 464, [M+Na] + 486, [M-H]-462.

CHN analysis : found C 66. 60%, H 6.97%, N 8. 54%; C27H33N304+0. 05H20+0. 35CH2CI2 requires C 66.47%, H 6.89%, N 8.50%.

Example 45: N-Benzyl-3-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide Prepared according to the procedure used for example 42 using 3- {3- [ (2R)-2- ( { (2R)-2-hyd roxy-2- [4-hyd roxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl]phenyl} propanoic acid (Preparation 60) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.26-6. 90 (11H, m), 6.70-6. 68 (1H, d), 4.61- 4.58 (3H, m), 4.30 (2H, s), 2.94-2. 83 (4H, m), 2.70-2. 63 (2H, m), 2.57-2. 49 (3H, m), 1.06-1. 04 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H]+ 463, [M+Na]+ 485, [M-H]- 461.

CHN analysis : found C 68. 16%, H 7.16%, N 5. 66% ; C28H34N204+0. 05H20+0. 25CH2C) 2 requires C 68. 11%, H 7. 03%, N 5. 58%.

Example 46 : 3- (3- [ (2R)-2- ( ( (2R)-2-Hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(2- phenylethyl) propanamide Prepared according to the procedure used for example 42 using 3- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanoic acid (Preparation 60) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.26-7. 22 (3H, m), 7. 18-7. 12 (4H, m), 7.03- 7.01 (2H, d), 6.97-6. 94 (2H, d), 6.71-6. 69 (1 H, d), 4. 64-4. 58 (3H, m), 3. 36-3. 30 (2H, m), 3.00-2. 81 (4H, m), 2.75-2. 68 (4H, m), 2.59-2. 54 (1H, dd), 2. 42-2. 39 (2H, t), 1.08-1. 06 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 477, [M+Na] + 499, [M-H]-475.

Example 47: 3-{3-[(2R)-2-({(2R)-2-Hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(3- phenylpropyl) propanamide

Prepared according to the procedure used for example 42 using 3- {3- [ (2R)-2- ({(2R)-2-hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl amino) propyl] phenyl} propanoic acid (Preparation 60) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD3OD) : 8 = 7.25-7. 21 (3H, m), 7.15-7. 11 (4H, m), 7.04- 7.00 (2H, m), 6.97 (1H, s), 6.92-6. 91 (1H, d), 6.71-6. 69 (1H, d), 4.62-4. 58 (3H, m), 3.14-3. 11 (2H, t), 2. 93-2.83 (4H, m), 2. 70-2.62 (2H, m), 2.54-2. 49 (3H, m), 2.45-2. 42 (2H, t), 1.73-1. 66 (2H, m), 1.04-1. 03 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 491, [M+Nal+ 513, [M-H]-489.

Example 48: 4- { (1R)-2- [ ( (1R)-2- {3- [3- (1, 3-Dihydro-2H-isoindo)-2-y !)-3- oxopropyl] phenyl}-1-methylethyl) amino]-1-hydroxyethyl}-2- (hydroxymethyl) phenol Prepared according to the procedure used for example 42 using 3- {3- [ (2R)-2- ({(2R)-2-hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanoic acid (Preparation 60) and the appropriate amine to give the title compound as a pale grey foam.

1H NMR (400MHz, CD30D) : 8 = 7.30-7. 21 (5H, m), 7.17-7. 13 (1H, t), 7.10-7. 08 (1H, d), 7.03-6. 99 (2H, m), 6.93-6. 92 (1H, d), 6.70-6. 68 (1H, d), 4.71-4. 69 (4H, d), 4.65-4. 58 (3H, m), 2.97-2. 84 (4H, m), 2.74-2. 65 (4H, m), 2.56-2. 51 (1H, dd), 1.02-1. 01 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 475, [M+Na] + 497, [M-H]-473.

CHN analysis : found C 70.10%, H 7. 03%, N 5.66% ; C29H34N204+1. 20H20 requires C 70. 19%, H 7.39%, N 5.65%.

Example 49: N- [2-Fluoro-5- (trifluoromethyl) benzyl]-3- {3- [ (2R)-2- ( ( (2R)-2- hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide Prepared according to the procedure used for example 42 using 3- {3- [ (2R)-2- ( { (2R)-2-hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanoic acid (Preparation 60) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.63-7. 59 (2H, m), 7.28-7. 21 (2H, m), 7.12- 7.08 (1 H, m), 7.02-6. 91 (4H, m), 6.70-6. 68 (1 H, d), 4.63-4. 58 (3H, m), 4.40 (2H, s), 2.96-2. 84 (4H, m), 2.72-2. 64 (2H, m), 2.57-2. 48 (3H, m), 1.06-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 549, [M+Na] + 571, [M-H]-547.

CHN analysis: found C 60.76%, H 5. 79%, N 4.87% ; C29H32N204F4+1. 35H20 requires C 60.80%, H 6. 11%, N 4. 89%.

Example 50 : N-(2-Hydroxybenzyl)-3-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4-hydro xy- 3-(hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanamide

Prepared according to the procedure used for example 42 using 3- {3- [ (2R)-2- ({(2R)-2-hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl) amino) propyl] phenylopropanoic acid (Preparation 60) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 6 = 7.21 (1H, m), 7. 12-6.99 (4H, m), 6.95-6. 91 (3H, m), 6. 77-6. 68 (3H, m), 4. 65-4. 59 (3H, m), 4. 27 (2H, s), 2.94-2. 84 (4H, m), 2. 70- 2.61 (2H, m), 2.55-2. 47 (3H, m), 1.05-1. 04 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 479, [M+Na] + 501, [M-H]-477.

CHN analysis: found C 66. 61%, H 6. 91%, N 5.57% ; C28H34N205+0. 40 CH2CI2 requires C 66.55%, H 6.84%, N 5.47%.

Example 51: 3-{3-[(2R)-2-({(2R)-2-Hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-phenylpropanamide Prepared according to the procedure used for preparation 1 using 3-{3-[(2R)-2- ({(2R)-2-hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanoic acid (Preparation 60) and the appropriate amine, substituting dichloromethane instead of ethyl acetate as the extraction solvent to give the title compound as a white foam.

H NMR (400MHz, CD30D) : 8 =7.49-7. 47 (2H, d), 7.28-7. 21 (3H, m), 7.17-7. 13 (1H, t), 7.08-7. 00 (4H, m), 6.94-6. 92 (1H, d), 6.71-6. 69 (1 H, d), 4.63-4. 58 (3H, m), 2.97-2. 84 (4H, m), 2.71-2. 52 (5H, m), 1.04-1. 02 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 449, [M+Na] + 471, [M-H]-447.

Examples 52-63 Examples 52 to 63 are of formula:

A solution of (4- {2- [2- (tert-butyldimethylsilanyloxy)-2- (4-hydroxy-3- hydroxymethyl-phenyl) ethylamino] propyl} phenyl) acetic acid (Preparation 61) (150mg, 0. 32mol), 1- (3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (67mg, 0. 34mmol), 1-hydroxybenzotriazole monohydrate (54mg, 0. 34mol) and diisopropylethylamine (82mg, 0. 63mmol) were stirred in N, N- dimethylformamide (3ml) with the appropriate amine (0. 34mmol) at room temperature for 18 hours. The solvent was removed in vacuo and the crude material taken up in a mixture of dichloromethane (5ml) and saturated potassium carbonate (3moi) and passed through a phase separating column.

The organic layer was concentrated in vacuo and the material taken up in methanol (1ml) and treated with ammonium fluoride (117mg, 3. 20mmol) in water (0. 5ml) and the resulting mixture heated to 40°C for 20 hours The solvent was removed in vacuo and dimethylsulfoxide (2ml) added and the mixture filtered before being purified by reverse phase chromatography (A- acetonitrile, B-H2O buffered with 0. 1% diethylamine : 0-1.90min 5% B, 1.90- 2. 00min 5-10% B, 2.00-10. 50min 10-95% B, 10.50-13. 80min 95% B) using a 150 x 21.2mm C8 (2) column (0-3. 00min 10-95% B). Amine used HRMS HRMS Exemple Retention Name (intermediate [M+H] + [M+H] number minutes (3), (3') or (3")) calculated found N-Benzyl-2-(4-{(2R)-2-[(2R)-2- hydroxy-2- 52 449. 2442 449. 2471 1. 64 hydroxymethylphenyl) ethyl- amino] propyl} phenyl) acetamide 2- hydroxy-3- 53 hydroxymethylphenyl) 477. 2755 477. 2730 1. 86 amino] propyl} propyl) acetamide 2- hydroxy-3- 54 hydroxymethylphenyl) 475. 2574 1. 81 amino] propyl acetamide 1- 55-2-(4-{(2R)-2-[(2R)-2-hydroxy-2-(4-HN93 hydroxy-3-hydroxymethylphenyl)- ethylamino] propyl} phenyl) ethanone N [ 56 hydroxymethyl-phenyl)-483. 2052 483. 2029 1. 79 ethylamino] acetamide N- [(2R)-2-hydroxy-2-(4-hydroxy-3-q 57 hydroxymethyl-phenyl)-HN 483. 2052 483. 2028 1. 83 ethylamino] acetamide N- [ 58 hydroxymethyl-phenyl)-H2N93scl 2052 483. 2028 1. 83 ethylamino] acetamide 2- hydroxy-3-hydroxymethylphenyl)- 59 H2NX 479. 2547 479. 2522 1. 74 ethylamino]-propyl} methoxybenzyl)-acetamide 2- 60 hydroxy-3-hydroxymethylphenyl)-HN--Cro-479. ethylamino] methoxybenzyl) acetamide 2-(4-{(2R)-2-[(2R)-2-hydroxy-2-(4- hydroxy-3-hydroxymethylphenyi)-H2NX 61 ethylamino]-propyl} methoxybenzyl)-acetamide N- {(2R)-2-[(2R)-2-hydroxy-2-(4-o' 62 hydrpw-3-hydroxy-methylphenyl)-H2N 509. 2653 509. 2627 1. 79 o ethylamino] propyl} acetamide 2- hydroxy-3-hydroxymethylphenyl)- 63 2 N 450. 2394 450. 2375 1. 38 ethyl-amino] (pyridin-2-ylmethyl) acetamide + RetentionExample 64: N- [2-Fluoro-5- (trifluoromethyl) benzyl]-2- (4- [ (2R)-2- ( ( (2R)-2- hydroxy-2- [4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} acetamide

Prepared from 2-{4-[(2R)-2-({(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-[4- hydroxy- 3-(hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N- [2-fluoro-5- (trifluoromethyl) benzyl] acetamide (Preparation 67) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.61-7. 53 (2H, m), 7.35-6. 98 (7H, m), 6.65 (1 H, d), 4.60 (3H, m), 4.46 (2H, s), 3.55 (2H, s), 3.00-2. 90 (2H, m), 2.75 (2H, m), 2.60 (1 H, m), 1.05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 535, [M+Na] + 557, [M-H]-533. Example 65: 2- {4-[(2R)-2-({(2R)-2-Hydroxy-2-[4-hydroxy-3- (hydroxymethyl)phenyl]ethyl}amino)propyl]phenyl}-N-(2- phenylethyl) acetamide

Prepared from 2- {4- [ (2R)-2- ( { (2R)-2- { [tert-butyl (dimethyl) silyl] oxy}-2- [4-hydroxy- 3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(2- phenylethyl) acetamide (Preparation 68) according to the method for example 3 to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.26-7. 00 (11 H, m), 6.69 (1 H, d), 4.60 (3H, m), 3.40 (4H, m), 2. 98 (2H, m), 2.70 (4H, m), 2. 58 (1H, m), 1.07 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 463, [M+Na] + 485, [M-H]-461. Preparation 1: 2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N-(2, 6- dimethoxybenzyl)-acetamide A solution of (3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hyd roxy-3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-acetic acid (Preparatiori 36)

(150mg, 0. 32mol), 1- (3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (67mg, 0. 35mmol), hydroxybenzotriazole monohydrate (47mg, 0. 35mmol) in N, N-dimethylformamide (3ml) was treated with triethylamine (0. 09moi, 0. 63mmol) and 2, 6-dimethoxybenzylamine (58mg, 0. 35 mmol) and the resulting suspension left to stir at room temperature under a nitrogen atmosphere for 18 hours. The solvent was removed in vacuo and the residue partitioned between ethyl acetate (10moi) and saturated aqueous sodium bicarbonate (10ml). The organic phase was separated, and the aqueous phase extracted with further ethyl acetate (2x10ml). The combined organic extracts were washed with water (5ml), brine (5ml), dried (sodium sulphate) and the solvent removed in vacuo. The residue was purified by fiash column chromatography on silica gel eluting with dichloromethane : methanol : 880 ammonia (95: 5: 0.5 by volume) to give the title compound as a pale yellow oil (128mg).

1H NMR (400MHz, CD30D) : 8 = 7.23-7. 14 (3H, m), 7.09-7. 07 (1H, d), 6.99-6. 93 (3H, m), 6.69-6. 67 (1H, d), 6.59-6. 61 (2H, d), 4. 70-4. 67 (1H, m), 4.61 (2H, d), 4.41 (2H, s), 3.75 (6H, s), 3.42 (2H, s), 2. 89-2. 81 (2H, m), 2.67-2. 60 (2H, m), 2.53-2. 48 (1H, dd), 1.02-1. 01 (3H, d), 0.84 (9H, s), 0.00 (3H, s), -0. 19 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 623, [M+Na] + 645, [M-H]-621.

Preparation 2: 2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N-(2- ethoxybenzyl)-acetamide

Prepared according to the procedure used for preparation 1 using (3- { (2R)-2- [(2R)-2-{[teff-butyl (dimethyl) silyi] oxy}-2-(4-hydroxy-3-hydroxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 6 = 7.21-7. 17 (3H, m), 7.14-7. 12 (2H, d), 7.04 (1H, s), 7. 00-6. 98 (2H, d), 6.91-6. 89 (1h, d), 6. 85-6. 81 (1H, t), 6. 70-6. 68 (1h, d), 4. 72-4. 68 (1H, t), 4.62-4. 61 (2H, d), 4.35 (2H, s), 4. 04-3. 98 (2H, q), 3.50 (2H, s), 2.94-2. 84 (2H, m), 2.72-2. 62 (2H, m), 2.56-2. 51 (1h, dd), 1.34-1. 30 (3H, t), 1.04-1. 02 (3H, d), 0. 84 (9H, s), 0.00 (3H, s), -0. 19 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 607, [M+Na] + 629, [M-H]-605.

Preparation 3: 2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- <BR> <BR> <BR> hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N-(2-<BR> <BR> <BR> <BR> <BR> hydroxybenzyl)-acetamide Prepared according to the procedure used for preparation 1 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine, substituting dichloromethane as the reaction solvent to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 5 = 7.19-7. 02 (6H, m), 6.99-6. 95 (2H, m), 6.75- 6.70 (2H, m), 6. 68-6. 66 (1H, d), 4.71-4. 67 (1H, t), 4.61 (2H, d), 4.32 (2H, s), 3.49 (2H, s), 2.91-2. 84 (2H, m), 2.70-2. 61 (2H, m), 2.55-2. 50 (1H, dd), 1.04- 1.03 (3H, d), 0. 84 (9H, s), 0.01 (3H, s), -0. 18 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 579, [M+Na] + 601, [M-H]-577. Preparation 4: 2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl[oxy}-2-(4- <BR> <BR> hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N-indan-2-<BR> <BR> yl-acetamide

Prepared according to the procedure used for preparation 3 using (3-{(2R)-2- [ (2R)-2- { [tert-butyl (dimethyl) silyl] oxy}-2- (4-hydroxy-3-hydroxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 5 = 7.20-7. 09 (7H, m), 7.02 (1 H, s), 6.99-6. 96 (2H, t), 6.69-6. 67 (1H, d), 4.71-4. 68 (1H, m), 4.61-4. 60 (2H, d), 4.56-4. 52 (1H, t) 3.42 (2H, s), 3.26-3. 20 (2H, dd), 2.92-2. 79 (4H, m), 2.69-2. 62 (2H, m), 2.56- 2.51 (1 H, m), 1.05-1. 03 (3H, d), 0. 83 (9H, s), 0.00 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 589, [M+Na] + 611, [M-H]'587.

Preparation 5: 2-(3-{[(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N- (3, 4- dichlorobenzyl)-acetamide Prepared according to the procedure used for preparation 1 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)-

ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine substituting dichloromethane instead of ethyl acetate as the extraction solvent to give the title compound as a white solid. iH NMR (400MHz, CD3OD) : 6 = 7. 41-7. 39 (1H, d), 7. 34 (1H, s), 7. 20-7. 16 (2H, m), 7. 14-7. 10 (2H, t), 7.03 (1H, s), 7.00-6. 96 (2H, d), 6.68-6. 66 (1H, d), 4.70- 4. 67 (1H, t), 4. 61-4. 60 (2H, d), 4.30 (2H, s), 3.49 (2H, s), 2. 92-2. 84 (2H, m), 2.70-2. 60 (2H, m), 2.56-2. 51 (1H, dd), 1.03-1. 01 (3H, d), 0. 82 (9H, s), -0. 01 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 631 / 633, [M+Na]+ 653 / 655, [M-H]- 629 / 631.

Preparation 6: 2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N- [4- (aminosulfonyl) benzyl]-acetamide Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

H NMR (400MHz, CD30D) : 8 = 7.82-7. 79 (2H, d), 7.38-7. 36 (2H, d), 7.22-7. 13 (3H, m), 7.05 (1H, s), 7.01-6. 99 (2H, d), 6.70-6. 67 (1H, d), 4.72-4. 69 (1H, t), 4.62-4. 61 (2H, d), 4.42 (2H, s), 3.51 (2H, s), 2.95-2. 84 (2H, m), 2.71-2. 63 (2H, m), 2.57-2. 52 (1H, dd), 1.05-1. 03 (3H, d), 0.83 (9H, s), 0.00 (3H, s), -0. 19 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 642, [M+Na] + 664, [M-H]-640.

Preparation 7: 2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- <BR> hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N- (pyridin- 2-ylmethyl)-acetamide

Prepared according to the procedure used for preparation 5 using (3-{(2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 8 = 8.44-8. 42 (1H, d), 7.74-7. 70 (1H, t), 7.27-7. 23 (2H, m), 7.20-7. 13 (3H, m), 7.06 (1H, s), 6.99-6. 97 (2H, m), 6.68-6. 66 (1H, d), 4.71-4. 67 (1H, t), 4.61 (2H, d), 4.46 (2H, s), 3.55 (2H, s), 2.93-2. 85 (2H, m), 2.71-2. 63 (2H, m), 2. 58-2. 53 (1 H, dd), 1.06-1. 04 (3H, d), 0.84 (9H, s), 0. 01 (3H, s), -0. 18 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 564, [M+Na] + 586, [M-H]-562.

Preparation 8: 4-{[(2-(3-{[(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}- 2-(4- <BR> <BR> hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- <BR> <BR> <BR> <BR> <BR> acetylamino)-methyl}-benzamide Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [ (2R)-2- { [tert-butyl (dimethyl) silyl] oxy}-2- (4-hydroxy-3-hydroxymethyl-phenyl)-

ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white solid.

1H NMR (400MHz, CD3OD) : 8 = 7. 79-7. 77 (2H, d), 7.31-7. 28 (2H, d), 7. 20-7. 11 (3H, m), 7. 04 (1H, s), 6. 99-6. 97 (2H, m), 6. 68-6. 66 (1H, d), 4. 71-4. 69 (1H, t), 4.61-4. 60 (2H, d), 4. 40 (2H, s), 3.51 (2H, s), 2.92-2. 83 (2H, m), 2.70-2. 61 (2H, m), 2. 58-2. 53 (1H, m), 1. 06-1. 04 (3H, d), 0. 83 (9H, s), 0.00 (3H, s),-0. 18 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 606, [M+Na] + 628, [M-H]-604.

Preparation 9: 2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N- (3, 4- dimethoxybenzyl)-acetamide Prepared according to the procedure used for preparation 1 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 8 = 7.20-7. 13 (3H, m), 7.05 (1H, s), 7.00-6. 98 (2H, d), 6.86-6. 84 (1H, d), 6.79-6. 77 (2H, m), 6.70-6. 68 (1H, d), 4.72-4. 68 (1H, m), 4.62-4. 61 (2H, d), 4.29 (2H, s), 3.78 (3H, s), 3.71 (3H, s), 3. 48 (2H, s), 2.94- 2.83 (2H, m), 2.70-2. 60 (2H, m), 2.57-2. 51 (1 H, m), 1.04-1. 03 (3H, d), 0. 83 (9H, s), 0.00 (3H, s), -0. 19 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 623, [M+Na] + 645, (M-H]-621. Preparation 10: 2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- <BR> hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N- (4- <BR> <BR> trifluoromethoxybenzyl)-acetamide

Prepared according to the procedure used for preparation 5 using (3-{(2R)-2- [ (2R)-2- { [tert-butyl (dimethyl) silyl] oxy}-2- (4-hydroxy-3-hydroxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 8 = 7.32-7. 30 (2H, d), 7.21-7. 12 (5H, m), 7.05 (1H, s), 7.00-6. 97 (2H, m), 6.69-6. 67 (1H, d), 4.71-4. 68 (1H, t), 4.60 (2H, d), 4.36 (2H, s), 3.49 (2H, s), 2.93-2. 85 (2H, m), 2.70-2. 60 (2H, m), 2.57-2. 52 (1H, dd), 1.04-1. 03 (3H, d), 0.83 (9H, s), 0.00 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 647, [M-H]-645.

Preparation 11 : 2-(3-{[2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N-(2- chloro, 6-fluorobenzyl)-acetamide Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 8 = 7.33-7. 14 (4H, m), 7.10-7. 06 (2H, m), 7.02- 6.95 (3H, m), 6.69-6. 67 (1H, d), 4.72-4. 68 (1H, t), 4.61-4. 60 (2H, s), 4.52 (2H, s), 3.44 (2H, s), 2.93-2. 85 (2H, m), 2.71-2. 61 (2H, m), 2.54-2. 49 (1H, dd), 1. 04- 1. 02 (3H, d), 0. 83 (9H, s), 0.00 (3H, s),-0. 19 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] 615/617, [M+Na] + 637/639, [M-H]-613/ 615.

Preparation 12: 2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N- (3, 4- dimethylbenzyl)-acetamide Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [ (2R)-2- { [tert-butyl (dimethyl) silyl] oxy}-2- (4-hydroxy-3-hydroxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 8 = 7.19-7. 11 (3H, m), 7.04-6. 90 (6H, m), 6.68- 6.66 (1H, d), 4.70-4. 67 (1H, t), 4.61-4. 60 (2H, d), 4.26 (2H, s), 3.47 (2H, s), 2.91-2. 84 (2H, m), 2.69-2. 60 (2H, m), 2.55-2. 50 (1H, dd), 2.20 (3H, s), 2.18 (3H, s), 1.03-1. 02 (3H, d), 0.82 (9H, s), -0. 01 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 591, [M-H]-589. Preparation 13: 2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- <BR> <BR> hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N-[2-fluoro-<BR> <BR> 5-(trifluoromethyl) benzyl]-aciamide

Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white solid.

H NMR (400MHz, CD30D) : 8 = 7.61-7. 58 (1H, m), 7.55-7. 53 (1H, d), 7. 28-7. 12 (4H, m), 7.05 (1H, s), 7.02-6. 97 (2H, m), 6.69-6. 67 (1H, d), 4.72-4. 69 (1H, t), 4.61 (2H, d), 4.45 (2H, s), 3.51 (2H, s), 2.93-2. 84 (2H, m), 2.74-2. 60 (2H, m), 2.57-2. 51 (1H, dd), 1.04-1. 03 (3H, d), 0.83 (9H, s), 0.00 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 649, [M-H]-647.

Preparation 14: 2- (3- { (2R)-2- [ (2R)-2- { [tert-Butyl (dimethyl) silyl] oxy}-2- (4- hydroxy-3-hydroxymethyl_phenyl)-ethylamino]-propyl}-phenyl)- N-(2, 6- dichlorobenzyl)-acetamide

Prepared according to the procedure used for preparation 5 using (3-{(2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 8 = 7.35-7. 33 (2H, m), 7.25-7. 21 (1H, m), 7.17 (1H, s), 7. 14-7. 10 (1H, m), 7. 07-7. 05 (1H, m), 7. 00 (1H, s), 6.97-6. 91 (2H, m), 6.66- 6.64 (1H, d), 4. 68-4. 65 (1H, t), 4.61 (2H, s), 4. 58-4. 57 (2H, d), 3.42 (2H, s), 2. 89-2. 82 (2H, m), 2. 67-2.60 (2H, m), 2.51-2. 47 (1H, dd), 1.00-0. 99 (3H, d), 0. 80 (9H, s), -0. 04 (3H, s), -0. 23 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 631/633, [M+Na] + 653/655, [M-H]-629/ 631.

Preparation 15: 2- {3- { (2R)-2- [ (2R)-2- { [tert-Butyl (dimethyl) silyl] oxy)-2- (4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N-(2- phenylethyl) acetamide Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-[{tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a brown oil. rH NMR (400MHz, CD30D) : 8 = 7.31-7. 11 (7H, m), 7.07-7. 05 (1 H, d), 6.99-6. 97 (3H, m), 6. 68-6. 66 (1H, d), 4.70-4. 67 (1H, t), 4.61-4. 60 (2H, d), 3.41-3. 37 (2H, m), 3.34 (2H, s), 2.95-2. 84 (2H, m), 2.81-2. 73 (2H, m), 2.68-2. 61 (2H, m), 2.56- 2.51 (1 H, dd), 1.05-1. 03 (3H, d), 0. 82 (9H, s), -0. 01 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 577, [M+Na] + 599, [M-H]-575.

Preparation 16: N-Benzyl-2-(3-{(2R)-2-[(2R)-2-{lferf-Butyl (dimethyl) silyl <BR> oxy}-2- (4-hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-pheny l)- acetamide

Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a colourless oil.

1H NMR (400MHz, CD30D) : ô = 7.35-7. 12 (8H, m), 7.04 (1H, s), 6.99-6. 97 (2H, d), 6.69-6. 67 (1H, d), 4.70-4. 67 (1H, t), 4.61-4. 60 (2H, d), 4.35 (2H, s), 3.49 (2H, s), 2.90-2. 83 (2H, m), 2.69-2. 61 (2H, m), 2.55-2. 50 (1H, dd), 1.04-1. 02 (3H, d), 0.83 (9H, s), 0.00 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+Na] + 585, [M-H]-561.

Preparation 17: 2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N- (3, 5- dichlorobenzyl)-acetamide Prepared according to the procedure used for preparation 5 using (3- {(2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)-

ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a colourless oil.

1H NMR (400MHz, CD3OD) : 5 = 7.33-7. 28 (2H, m), 7. 22-7. 12 (4H, m), 7. 05 (1H, s), 7. 01-6. 98 (2H, m), 6. 69-6. 67 (1H, d), 4. 71-4. 68 (1H, t), 4. 62-4.. 61 (2H, d), 4.32 (2H, s), 3.51 (2H, s), 2.91-2. 84 (2H, m), 2.71-2. 61 (2H, m), 2.57-2. 52 (1H, dd), 1. 04-1. 03 (3H, d), 0. 83 (9H, s), 0.00 (3H, s),-0. 19 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] 631/633, [M+Na] + 653/655, [M-H]-629/ 631.

Preparation 18: 2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- N- (4- chlorobenzyl)-acetamide Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl)dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a colourless oil.

1H NMR (400MHz, CD30D) : 5 = 7.31 (1H, s), 7.28-7. 25 (1H, d), 7.21-7. 16 (4H, m), 7.13-7. 11 (1H, m), 7.03 (1H, s), 6.99-6. 97 (2H, d), 6.69-6. 67 (1H, d), 4.70- 4.67 (1H, t), 4.62-4. 62 (2H, d), 4.32 (2H, s), 3. 48 (2H, s), 2. 88-2. 83 (2H, m), 2.68-2. 60 (2H, m), 2.55-2. 50 (1H, dd), 1.03-1. 02 (2H, d), 0.83 (9H, s), -0. 01 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 597/599, [M+Na] 619/621, [M-H]-595/ 597. Preparation 19: 4-{[[2-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2 -(4- <BR> <BR> hydroxy-3-hydroxymethyl-phenyl)-athylamino]-propyl)-phenyl)- acetyl]-<BR> <BR> amino)-methyl-benzoic acid

Prepared according to the procedure used for preparation 36, using methyl 4- {[[2-(3-{[2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-( 4-hydroxy-3- hydroxymethyl-phenyl) -ethylamino]-propyl}-phenyl)-acdtyl]-amino)-methyl}- benzoate (Preparation 20), to give the title compound as a white solid which was used without further purification.

1H NMR (400MHz, CD30D) : 5 = 7.89-7. 87 (2H, d), 7.34-7. 20 (5H, m), 7.15-7. 09 (3H, m), 6.80-6. 78 (1H, d), 5.00-4. 97 (1H, m), 4.67-4. 66 (2H, d), 4.40 (2H, s), 3.55 (2H, s), 3.45-3. 38 (1H, m), 3. 28-3. 23 (1H, dd), 3.15-3. 11 (1H, dd), 3.03- 2.98 (1H, dd), 2.72-2. 66 (1H, dd), 1.17-1. 16 (3H, d), 0.86 (9H, s), 0.07 (3H, s),- 0.12 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 607, [M+Na] + 629, [M-H]-605.

CHN analysis: found C 62.04%, H 7.50% N 3.79% ; C34H46N206Si+0. 5MeOH+2. 6H20 requires C 61.97%, H 7.87%, N 4.19%.

Preparation 20: Methyl-4-{[2-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl) silyl] oxy}-2- (4-hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}- <BR> phenyl)-acetyl]-amino)-methyl}-benzoate

Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as an orange oil.

1H NMR (400MHz, CD30D) : 6 = 7.93-7. 91 (2H, d), 7.33-7. 31 (2H, d), 7.21-7. 13 (3H, m), 7.05 (1H, s), 7.00-6. 97 (2H, m), 6.69-6. 67 (1H, d), 4.70-4. 67 (1H, m), 4.62-4. 61 (2H, d), 4.42 (2H, s), 3.87 (3H, s), 3.52 (2H, s), 2.91-2. 84 (2H, m), 2.69-2. 60 (2H, m), 2.56-2. 51 (1 H, dd), 1.04-1. 02 (3H, d), 0.84 (9H, s), 0.01 (3H, s), -0. 19 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 621.

Preparation 21: 2- (2R)-2-({(2R)-2-{ltert-Butyl (dimethyl) silylloxy}-2-l4- hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N- [ (1 R)-1- phenylethyl] acetamide Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [ (2R)-2- { [terf-butyl (dimethyl) silyl] oxy}-2- (4-hydroxy-3-hydroxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white solid.

1H NMR (400MHz, CD30D) : 8 = 7.27-7. 26 (4H, d), 7.21-7. 09 (4H, m), 7.01-6. 95 (3H, m), 6.69-6. 67 (1 H, d), 5.00-4. 95 (1 H, q), 4. 70-4. 67 (1 H, dd), 4.62-4. 61 (2H,

d), 3.46 (2H, s), 2.88-2. 83 (2H, m), 2.69-2. 61 (2H, m), 2.53-2. 48 (1 H, dd), 1.44- 1.42 (3H, d), 1.02-1. 01 (3H, d), 0.83 (9H, s), 0.00 (3H, s), -0. 19 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 577, [M+Na] + 599, [M-H]-575.

Preparation 22: 4-{(1R)-1-{[tert-Butyl (dimethyl) silyl] oxy}-2-[((1R)-2-C3-[2- (3, 4-dihydroisoquinolin-2(1H)-yl)-2-oxoethyl]phenyl}-1- methylethyl) amino] ethyl}-2- (hydroxymethyl) phenol Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.23-7. 07 (7H, m), 7.03-6. 92 (3H, m), 6.68- 6.66 (1H, d), 4.70-4. 66 (3H, m), 4.61 (2H, s), 3.82 (2H, s), 3.81-3. 70 (2H, m), 2.90-2. 81 (3H, m), 2.71-2. 43 (4H, m), 1.02-0. 94 (3H, m), 0.82 (9H, s), -0. 01 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 589, [M+Na] + 611, [M-H]-587.

Preparation 23: 4- {(1R)-1-{[tert-Butyl(dimethyl)silyl]oxy}-2-[((1R)-2-{3-[2-(7 - ethoxy-6-methoxy-3, 4-dihydroisoquinolin-2(1H)-yl)-2-oxoethyl]phenyl}-1- methylethyl) amino] ethyl}-2- (hydroxymethyl) phenol

Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [ (2R)-2- { [fert-butyl (dimethyl) silyl] oxy}-2- (4-hydroxy-3-hydroxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.23-6. 91 (6H, m), 6.71-6. 55 (3H, m), 4.69- 4. 64 (1H, m), 4. 61 (2H, s), 4. 61-4. 56 (2H, m), 4. 03-3.93 (2H, m), 3. 81 (2H, s), 3.76 (3H, s), 3. 79-3. 66 (2H, m), 2.90-2. 40 (7H, m), 1. 38-1. 33 (3H, m), 1.02- 0.94 (3H, m), 0. 82 (9H, s), -0. 01 (3H, s), -0. 21 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 663, [M-H]-661.

Preparation 24: 2-{3-[(2R)-2-{[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-[4- hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N- [2- (4- <BR> chlorophenyl) ethyl] acetamide Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.21-7. 15 (4H, m), 7.09-7. 03 (3H, m), 7.00- 6.97 (3H, m), 6.69-6. 66 (1H, d), 4.71-4. 68 (1H, t), 4.60 (2H, d), 3. 38 (2H, s), 3.40-3. 36 (2H, t), 2.93-2. 85 (2H, m), 2.75-2. 72 (2H, t), 2.69-2. 62 (2H, m), 2.57- 2.52 (1 H, dd), 1.06-1. 04 (3H, d), 0.82 (9H, s), -0. 01 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 611, [M-H]-609.

Preparation 25: 2-{3-[(2R)-2-({(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-[4- hydroxy-3- (hydroxymethyl)phenyl]ethyl}amino)propyl}phenyl}-N-[2-(4- ethylphenyl) ethyl] acetamide

Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl)dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.18 (1H, s), 7.16-7. 14 (1H, d), 7. 06-6. 95 (8H, m), 6.67-6. 65 (1H, d), 4.69-4. 66 (1H, t), 4.60-4. 59 (2H, d), 3.39 (2H, s), 3.37- 3.34 (2H, t), 2.92-2. 84 (2H, m), 2.72-2. 68 (2H, t), 2.66-2. 51 (5H, m), 1.19-1. 16 (3H, t), 1.05-1. 03 (3H, d), 0.81 (9H, s), -0. 02 (3H, s), -0. 21 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 605, [M-H]-603.

Preparation 26: 2-{3-[(2R)-2-({(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-[4- hydroxy-3- (hydroxymethyl)phenyl]ethyl}amino)propyl]phenyl}-N-(1,1- dimethyl-2-phenylethyl) acetamide Prepared according to the procedure used for preparation 5 using (3-{(2R)-2- [ (2R)-2- {[tert-butyl (dimethyl) silyl] oxy}-2- (4-hydroxy-3-hydroxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.22-7. 18 (2H, m), 7.14-7. 11 (4H, m), 7.03- 6.95 (5H, m), 6.69-6. 67 (1H, d), 4.71-4. 68 (1H, q), 4.61 (2H, d), 3.37 (2H, s), 2.99 (2H, s), 2.92-2. 84 (2H, m), 2.72-2. 62 (2H, m), 2.57-2. 52 (1H, dd), 1.26 (6H, s), 1.04-1. 03 (3H, d), 0.83 (9H, s), 0.00 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 605, [M-H]-603.

Preparation 27 : 2-{3-[(2R)-2-({(2R)-2-{[tert-Bubyl(dimethyl)silyl]oxy}-2-[4- hydroxy-3- (hydroxymethyl)phenyl[ethyl}amino)propyl]phenyl}-N-[2-(3,4- dimethoxyphenyl) ethyl] acetamide Prepared according to the procedure used for preparation 1 using (3- { (2R)-2- [ (2R)-2- { [tert-butyl (dimethyl) silyl] oxy}-2- (4-hydroxy-3-hydroxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

H NMR (400MHz, CD30D) : 8 = 7.19-7. 14 (2H, m), 7.05-7. 04 (1H, d), 7.01-6. 98 (3H, m), 6.82-6. 77 (2H, m), 6.69-6. 66 (2H, m), 4.71-4. 69 (1H, m), 4. 62-4. 61 (2H, d), 3.78 (3H, s), 3.76 (3H, s), 3.41 (2H, s), 3.41-3. 37 (2H, t), 2.95-2. 86 (2H, m), 2.73-2. 69 (2H, t), 2.67-2. 62 (2H, m), 2.57-2. 52 (1 H, dd), 1.06-1. 04 (3H, d), 0. 83 (9H, s), 0.00 (3H, s), -0. 19 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 637, [M-H]- 635.

Preparation 28 : 2-{3-[(2R)-2-({(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-[4- hydroxy-3-(hydroxymethyl)phenyl]ethyl} amino) propyl] phenyll-N- (3, 4- difluorobenzyl) acetamide Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)-

ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

1H NMR (40OMHz, CD30D) : 6 = 7. 20-7. 07 (5H, m), 7.04-6. 97 (4H, m), 6.97- 6. 69 (1H, d), 4. 70-4. 67 (1 H, dd), 4. 62-4. 61 (2H, d), 4. 31 (2H, s), 3. 49 (2H, s), 2.90-2. 83 (2H, m), 2.69-2. 60 (2H, m), 2.55-2. 50 (1 H, m), 1.03-1. 02 (3H, d), 0. 83 (9H, s),-0. 01 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 599, [M-H]-597.

Preparation 29: 4-{(1R)-1-{[tert-Butyl(dimethyl)silyl]oxy}-2-[((1R)-2-{3-[2- (1, 3-dihydro-2H-isoindol-2-yl)-2-oxoethyl] phenyl}-1- methylethyl) amino] ethyl}-2- (hydroxymethyl) phenol Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a yellow oil.

1H NMR (400MHz, CD30D) : 6 = 7.26-7. 13 (7H, m), 7.07 (1H, s), 6.99-6. 97 (1H, d), 6.94-6. 91 (1H, dd), 6.66-6. 64 (1H, d), 4.74 (2H, s), 4.67-4. 64 (1H, t), 4.61 (2H, d), 3.76 (2H, s), 3.34 (2H, s), 2.93-2. 82 (2H, m), 2.67-2. 55 (3H, m), 1.06- 1.04 (3H, d), 0.80 (9H, s), -0. 03 (3H, s), -0. 21 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 575, [M+Na] + 597, [M-H]- 573.

Preparation 30: 2- {3-[(2R)-2-({(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-[4- hydroxy-3- (hydroxymethyl) phenyl] ethyl amino) propyl] phenyl}-N- <BR> phenylacetamide

Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy]-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 5 = 7.53-7. 51 (2H, d), 7.28-7. 24 (2H, m), 7.18 (3H, s), 7.11-7. 03 (2H, m), 6. 98-6. 94 (1H, m), 6.68-6. 66 (1H, d), 4.69-4. 66 (1H, m), 4.62-4. 61 (2H, d), 3.62 (2H, s), 2.94-2. 85 (2H, m), 2.70-2. 55 (3H, m), 1.07-1. 05 (3H, d), 0.81 (9H, s), -0. 02 (3H, s), -0. 21 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H]+ 549, [M+Na] + 571, [M-H]-547.

Preparation 31: 2- {3- [ (2R)-2- ( ( (2R)-2- { [tert-Butyl (dimethyl) silyl] oxy)-2- [4- hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N- (1- naphthylmethyl) acetamide Prepared according to the procedure used for preparation 5 using (3-{(2R)-2- [ (2R)-2- { [tert-butyl (dimethyi) silyl] oxy}-2- (4-hydroxy-3-hydroxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

H NMR (400MHz, CDsOD) : 8 = 7.96-7. 94 (1 H, d), 7.85-7. 82 (1 H, d), 7.78-7. 75 (1H, d), 7.55-7. 35 (4H, m), 7.19-7. 09 (3H, m), 6. 98-6. 93 (3H, m), 6.70-6. 68 (1H, d), 4.79 (2H, s), 4.68-4. 58 (3H, m), 3.47 (2H, s), 2. 82-2. 72 (2H, m), 2.60-2. 54

(2H, m), 2.45-2. 40 (1H, m), 0.96-0. 95 (3H, d), 0.83 (9H, s), -0. 01 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 613, [M+Na] + 635, [M-H]-611.

Preparation 32: 2- (3- [ (2R)-2- ( { (2R)-2- { [tert-Butyl (dimethyl) silyl] oxy)-2- [4- hydroxy-3- (hydroxymeethyl)phenyl]ethyl]amino)propyl]phenyl}-N-(2- pyridin-2-ylethyl) acetamide Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 8.41-8. 39 (1H, d), 7.68-7. 64 (1H, m), 7. 23-7. 14 (4H, m), 7.06-7. 04 (1H, d), 6. 98-6. 96 (3H, d), 6.69-6. 67 (1 H, d), 3.53-3. 50 (1H, t), 3.39 (2H, s), 2.94-2. 84 (4H, m), 2.67-2. 61 (2H, m), 2.55-2. 50 (1H, m), 1.04- 1.03 (3H, d), 0.82 (9H, s), -0. 01 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 578, [M+Na] + 600, [M-H]-576.

Preparation 33: 2- {3- [ (2R)-2- ( { (2R)-2- ( [tert-Butyl (dimethyl) silyl] oxy)-2- [4- hydroxy-3-(hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-[(2R)-2- phenylpropyl] acetamide

Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : â = 7.24-7. 11 (7H, m), 7.00-6. 94 (4H, m), 6.68- 6.66 (1 H, d), 4. 69-4.66 (1 H, m), 4. 61-4. 60 (2H, d), 3. 31-3. 28 (3H, m), 2.93-2. 83 (3H, m), 2.78 (1H, s), 2.66-2. 60 (2H, m), 2. 53-2. 48 (1H, m), 1.19-1. 17 (3H, d), 1.03-1. 01 (3H, d), 0. 82 (9H, s), -0. 02 (3H, s), -0. 21 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 591, [M+Na]+ 613, [M-H]-589.

Preparation 34: N-Benzyl-2-{3-[(2R)-2-({(2R)-2-{[tert- butyl (dimethyl) silyl] oxy}-2-14-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-methylacetamide Prepared according to the procedure used for preparation 5 using (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a colourless oil.

1H NMR (400MHz, CD30D) : 8 = 7.52-7. 36 (6H, m), 7.30-7. 25 (2H, m), 7.19- 7.16 (3H, m), 6.89-6. 87 (1 H, d), 4.90-4. 87 (1 H, m), 4.83-4. 73 (4H, m), 3.97-3. 95 (2H, d), 3.11-3. 03 (5H, m), 2.88-2. 79 (2H, m), 2.75-2. 70 (1 H, m), 1.23-1. 20 (3H, m), 0.79 (9H, s), -0. 05 (3H, s), -0. 23 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 577, [M+Na] + 599, [M-HJ-575.

Preparation 35: 2- {3- [ (2R)-2- ( { (2R)-2- { [tert-Butyl (dimethyl) silyl] oxy)-2- [4- hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-[3-(4- fluorophenyl) propyl] acetamide

Prepared according to the procedure used for preparation 5 using (3-{(2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-acetic acid (Preparation 36) and the appropriate amine to give the title compound as a white foam.

1HNMR (400MHz, CD30D) 8 : 7.22-6. 92 (10H, m), 6.69 (1 H, d), 4.71-4. 66 (1 H, m), 4.62 (2H, s), 3.44 (2H, s), 3.20-3. 16 (2H, m), 2.94-2. 52 (7H), m), 1.80-1. 73 (2H, m), 1.03 (3H, d), 0.83 (9H, s), 0.00 (3H, s), -0. 19 (3H, s) ppm.

LRMS (electrospray) : 609 [M+H] +, 631 [M+Na] + Preparation 36: (3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetic acid A solution of methyl (3-{(2R)-2-[(2R)-2-{[teff-butyl (dimethyl) silyl] oxy}-2-(4- hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- acetate (Preparation 37) (7.04g, 14. 4mmol) in tetrahydrofuran (40ml) was treated with lithium hydroxide (28. 9m1 of a 1 M aqueous solution, 28. 9mmol) and the reaction left to stir at room temperature for 16 hours. Hydrochloric acid (28. 9mi of a 1M aqueous solution, 28. 9mmol) was added and then the tetrahydrofuran was removed in vacuo. The remaining aqueous layer was decanted and the residue washed with further water (10mut). The residue was redisolved in

methanol (30ml) and the solvent removed in vacuo to give the title compound as a colorless foam (5.95g) which was used without further purification.

1H NMR (400MHz, CD30D) : 8 = 7. 32 (1H, s), 7. 25-7. 18 (2H, m), 7. 13 (1H, s), 7. 12-7. 10 (1H, d), 7. 02-7. 01 (1H, d), 6. 79-6. 77 (1H, d), 4. 98-4. 95 (1H, m), 4. 65- 4. 64 (2H, d), 3. 48 (2H, s), 3. 48-3. 43 (1H, m), 3. 28-3. 23 (1H, dd), 3.13-3. 09 (1H, dd), 2. 98-2. 93 (1 H, dd), 2. 77-2. 72 (1 H, dd), 1. 23-1. 21 (3H, d), 0. 86 (9H, s), 0.06 (3H, s), -0. 13 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 474, [M+Na]+ 496, [M-H]- 472.

CHN analysis: found C 64. 15%, H 8.25%, N 2. 84% ; C26H39NO5Si+0.7H2O requires C 64.22%, H 8. 37%, N 2. 88%.

Preparation 37: Methyl-(3-{[(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}- 2- (4-hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-pheny l)-acetate A suspension of methyl (3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4- [benzyloxy]-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phen yl)-acetate (Preparation 38) (5.27g, 9. 12mmol) and 10% palladium on carbon (1. 00g) in ethanol (50moi) was stirred under an atmosphere of hydrogen (60psi) at room temperature for 16 hours. The catalyst was filtered off through arbocel and the filtrate concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with dichloromethane : methanol : 880 ammonia (96: 4: 0.4 changing to 95: 5: 0.5, by volume) to give the title compound as a pale yellow oil (1.99g) which was used without further purification.

1H NMR (400MHz, CD30D) : 8 = 7.21-7. 17 (2H, m), 7. 11-7.09 (1H, d), 7.03-6. 98 (3H, m), 6.69-6. 67 (1H, d), 4.71-4. 68 (1H, t), 4.62-4. 61 (2H, d), 3.67 (3H, s), 3. 59 (2H, s), 2.96-2. 86 (2H, m), 2.69-2. 55 (3H, m), 1.07-1. 05 (3H, d), 0. 82 (9H, s), -0. 01 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H]+ 488, [M+Na]+ 510 [M-H]- 486 Preparation 38: Methyl- (3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2- (4- [benzyloxy]-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phen yl)- acetate A solution of [2-(benzyloxy)-5-((1R)-2-bromo-1-{[tert-butyl(dimethyl) silyl] oxy} ethyl) phenyl] methanol (Preparation 39) (12.5g, 27. 7mmol) and the amine from preparation 27 (11.5g, 55. 4mmol) in dichloromethane (130mol) was heated to 90°C, allowing the dichloromethane to evaporate. The resulting melt was left at 90°C for a further 16 hours. The reaction mixture was cooled to room temperature and purified by flash column chromatography on silica gel eluting with dichloromethane : methanol : 880 ammonia (98: 2: 0.2 changing to 97: 3: 0.3, by volume) to give the title compound (12. 1g) as a colourless oil.

1H NMR (400MHz, CD30D) : s = 7.47-7. 45 (2H, m), 7.39-7. 29 (4H, m), 7.19- 7.15 (1H, t), 7.13-7. 07 (2H, m), 7.03 (1H, s), 7.01-6. 99 (1H, d), 6.93-6. 91 (1H, d), 5.12 (2H, s), 4.76-4. 73 (1H, t), 4.67-4. 66 (2H, d), 3.66 (3H, s), 3.58 (2H, s), 2.95-2. 80 (2H, m), 2.68-2. 55 (3H, m), 1.06-1. 05 (3H, d), 0.83 (9H, s), 0.00 (3H, s), -0. 19 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 578, [M+Na] + 600.

Preparation 39: [2-(Benzyloxy)-5-((1R)-2-bromo-1-{[tert-butyl(dimethyl) silyl] oxy} ethyl) phenyl] methanol

Borane dimethylsulfide complex (42. 4ml of 10M solution in tetrahydrofuran, 424mol) was added dropwise to a solution methyl-2-(benzyloxy)-5-((1R)-2- bromo-1-f [tert-butyl (dimethyl) silyl] oxylethyl) benzoate (Preparation 40) (91. 0g, 189mmol) in tetrahydrofuran (1600ml). The resulting mixture was then heated to reflux for 2 hours and then cooled to 0°C before quenching with methanol (270ml). The mixture was left to stir at room temperature for 16 hours and then the solvent removed in vacuo. The residue was partitioned between dichloromethane (500ml) and water (500ml). The aqueous phase was separated and extracted with dichloromethane (500ml) and the combined organic extracts washed with brine (500ml), dried (magnesium sulfate) and the solvent removed in vacuo. The residue was purified by flash column chromatography on silica gel eluting with cyclohexane : ethyl acetate (100: 0 changing to 80 : 20, by volume) to give the title compound (68. 7g) as a colourless oil.

1H NMR (400MHz, CDCI3) : 8 = 7.42-7. 36 (5H, m), 7.29-7. 25 (3H, m), 6.94 (1H, d), 5.12 (2H, s), 4.84-4. 81 (1H, m), 4.74 (2H, s), 3.48-3. 40 (2H, m), 0.90 (9H, s), 0.11 (3H, s), -0. 07 (3H, s) ppm.

LRMS (electrospray) : m/z [M+Na] + 473/475.

Preparation 40: Methyl-2-(benzyloxy)-5-((1R)-2-bromo-1-{[tert-butyl (dimethyl) silyl] oxy} ethyl) benzoate

A solution of methyl 2- (benzyloxy)-5- [ (11R)-2-bromo-1-hydroxyethyl] benzoate (71. Og, 195mmol), imidazole (18. 5g, 272mol), Sff-butyldimethylsilyl chloride (32.2g, 214mmol) and 4-(N, N-dimethylamino) pyridine (440mg, 3. 60mmol) in N, N-dimethylformamide (270ml) was left to stir at room temperature under a nitrogen atmosphere for a period of 24 hours. The solvent was removed in vacuo and the residue partitioned between ethyl acetate (500mi) and water (500ml). The organic phase was separated and washed with 2N aqueous hydrochloric acid (2#500ml), saturated aqueous sodium bicarbonate (2x500m1), brine (500mut), dried (magnesium sulfate) and the solvent removed in vacuo to give the title compound as a colourless oil (91. 0g).

1H NMR (400MHz, CDCl3) : 5 = 7.81 (1H, bs), 7.51-7. 30 (6H, m), 7.01 (1H, d), 5.19 (2H, s), 4.85-4. 82 (1H, m), 3.91 (3H, s), 3.48-3. 39 (2H, m), 0.90 (9H, s), 0.11 (3H, s), -0. 08 (3H, s) ppm.

LRMS (electrospray) : m/z [M+Na] + 501/503.

Preparation 41: Methyl-{3-[(2R)-2-aminopropyl] phenyl} acetate A solution of methyl-[3-((2R)-2-{[(1R)-1-phenyl-ethyl]-amino}-propyl)-phen yl}- acetate hydrochloride (Preparation 42) (7.69g, 22. 0mmol) and ammonium formate (6.94g, 110mmol) was heated to 75°C in the presence of 20% palladium hydroxide-on-charcoal (Pd (OH) 2/C, 2. 00g). After 90 minutes the reaction mixture was cooled to room temperature, filtered through arbocel and the filtrate concentrated in vacuo. The residue was partitioned between

dichloromethane (100ml) and 880 ammonia (100moi) and the organic phase separated. The aqueous phase was extracted dichloromethane (100ml) and the combined organic extracts dried (magnesium sulfate) and reduced in vacuo to give the title compound as a colourless oil (4. 78g).

1H NMR (400MHz, CD30D) : 6 = 7.27-7. 23 (1H, t), 7.13-7. 09 (3H, m), 3.67 (3H, s), 3.63 (2H, s), 3. 12-3. 05 (1H, m), 2. 67-2. 57 (2H, m), 1. 06 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 208, [M+Na] + 230.

Preparation 42: Methyl--[3-((1R)-2-{[(1R)-1-phenyl-ethyl]-amino}-propyl)- phenyl]-acetate hydrochloride A solution of methyl- [3- (2-oxopropyl) phenyl] acetate (Preparation 43) (8.50g, 41. 2mmol), (R)-a-methyl benzylamine (4. 8ml, 37. 2mmol), sodium triacetoxyborohydride (11.6g, 56. Ommol) and acetic acid (2. 2moi, 38. Ommol) in dichloromethane (400ml) was stirred at room temperature for 48 hours. The reaction mixture was quenched by addition of saturated aqueous sodium bicarbonate (200ml) and allowed to stir until effervescence ceased. The organic phase was separated and the aqueous phase extracted with dichloromethane (100ml). The combined organic extracts were dried (magnesium sulfate) and reduced in vacuo. Purification by flash column chromatography eluting with dichloromethane : methanol : 880 ammonia (99: 1: 0.1 to 95: 5: 0.5 by volume) gave a 4: 1 mixture of diastereomers (R, R major) as a pale yellow oil (8. 71 g).

Treatment with hydrogen chloride (40moi of a 1 M solution in methanol, 40. Ommol) followed by three successive crystallisations (diisopropylether/methanol) gave the title compound as a white crystalline solid (5. 68g).

1H NMR (400MHz, CD3OD) : 8 = 7.52-7. 48 (5H, m), 7. 28-7. 25 (1H, m), 7.18- 7.16 (1H, m), 7.02-6. 99 (2H, m), 4.59 (1H, q), 3.62 (2H, s), 3. 30 (3H, s), . 3.30-

3.25 (1H, m), 3.26-3. 15 (1H, m), 2. 66-2. 60 (1H, m), 1.68 (3H, d), 1.18, (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 312, [M+Naf 334.

Preparation 43: Methyl- [3- (2-oxopropyl) phenyl] acetate

Tributyltin methoxide (28. 3 ml, 98. 0mmo !), methyt- (3-bromopheny !) acetate (Preparation 44) (15. 0g, 65. Ommol), isopropenyl acetate (10. 8moi, 98. 0mmol), palladium (ll) acetate (750mg, 3. 30mmol) and tri-ortho-tolylphosphine (2. 00g, 6. 5mmol) were stirred together in toluene (75ml) at 100°C under nitrogen for 5 hours. After cooling the reaction was diluted with ethyl acetate (150ml) and 4M aqueous potassium fluoride solution (90m1) and stirred for 15 minutes. The mixture was filtered through arbocel and the organic phase separated and reduced in vacuo. The residue was purified by flash column chromatography silica gel eluting with a solvent gradient of diethyl ether : pentane (0: 100 to 25: 75, by volume) changing to dichloromethane to give the title compound as a pale yellow oil (12. 6g).

1H NMR (400MHz, CDCl3) : 8 = 7.30 (1H, t), 7.19 (1H, d), 7.13-7. 10 (2H, m), 3.69 (5H, s), 3.61 (2H, s), 2.15 (3H, s) ppm.

LRMS (electrospray) : m/z [M+NH4] + 224, [M+Na] + 229.

Preparation 44: Methyl- (3-bromophenyl) acetate

Acetyl chloride (0. 70ml, 9. 30mmol) was slowly added to a solution of (3-bromo- phenyl)-acetic acid (20. 0g, 93mmol) in methanol (500ml) at 0°C under nitrogen and the reaction was allowed to warm gradually to room temperature over a period of 5 hours. The solvent was removed in vacuo and the residual oil was

dissolved in dichloromethane, dried (sodium sulfate) and concentrated in vacuo to give the title compound as a colourless oil (20. 6g).

1H NMR (400MHz, CDCI3) : s = 7. 37-7.45 (2H, m), 7. 24-7. 17 (2H, m), 3.70 (3H, s), 3. 59 (2H, s) ppm.

LRMS (electrospray) : m/z [M+Na] + 253.

Preparation 45: 3-{3-[(2R)-2-({(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-[4- hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N- (2, 6- dichlorobenzyl) propanamide Prepared using the method for preparation 5 using 3-(3-{(2R)-2-[(2R)-2-{[tert- butyl (dimethyl) silyl] oxy}-2- (4-hydroxy-3-hydroxymethyl-phenyl)-ethylamino]- propyl}-phenyl)-propanoic acid (Preparation 51) and the appropriate amine to give the title compound as a white solid.

H NMR (400MHz, CD30D) : 8 = 7.39-7. 37 (2H, d), 7.28-7. 24 (1H, m), 7.20-7. 19 (1H, d), 7. 14-7. 10 (1H, t), 7.03-6. 97 (2H, m), 6.94-6. 90 (2H, m), 6.69-6. 67 (1H, d), 4.73-4. 69 (1H, t), 4.64-4. 56 (4H, m), 2.95-2. 84 (4H, m), 2.69-2. 63 (2H, m), 2.56-2. 50 (1H, m), 2.48-2. 44 (2H, t), 1.06-1. 04 (3H, d), 0. 82 (9H, s), -0. 01 (3H, s), -0. 19 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 645/647, [M+Na] + 667/669, [M-H]-643/ 645.

Preparation 46: 3- {3- [ (2R)-2- ( { (2R)-2- ( [tert-Butyl (dimethyl) silyl] oxyl-2- [4- hydroxy-3-(hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(2, 6- dimethoxybenzyl) propanamide

Prepared according to the procedure used for preparation 1 using 3- (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-propanoic acid (Preparation 51) and the appropriate amine, substituting dichloromethane instead of ethyl acetate as the extraction solvent to give the title compound as a yellow foam.

1H NMR (400MHz, CD30D) : 5 = 7.20-7. 15 (2H, m), 7.09-7. 06 (1H, t), 6.98-6. 93 (2H, m), 6.89-6. 86 (2H, m), 6.66-6. 64 (1 H, d), 6.57-6. 55 (2H, d), 4.70-4. 67 (1 H, t), 4.57-4. 56 (2H, d), 4.34 (2H, s), 3.74 (6H, s), 2.94-2. 86 (2H, m), 2. 81-2. 77 (2H, t), 2.67-2. 59 (2H, m), 2.52-2. 46 (1 H, dd), 2.39-2. 35 (2H, t), 1.02-1. 00 (3H, d), 0.78 (9H, s), -0. 04 (3H, s), -0. 23 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 637, [M+Na] + 659, [M-H]-635.

Preparation 47: 3- {3- [ (2R)-2- ( (2R)-2- { [tert-Butyl (dimethyl) silyl] oxy}-2- [4- hydroxy-3-(hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N-(2- ethoxybenzyl) propanamide Prepared according to the procedure used for preparation 1 using 3- (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-propanoic acid (Preparation 51) and the appropriate amine, substituting dichloromethane instead of ethyl acetate as the

extraction solvent, and dichloromethane : methanol : 880 ammonia (98: 2: 0.2 by volume) instead of (95: 5: 0.5 by volume) as column eluent to give the title compound as a colourless oil.

'H NMR (400MHz, CDsOD) : s = 7. 17-7. 07 (3H, m), 7. 00-6. 98 (1H, d), 6.94-6. 88 (4H, m), 6. 84-6. 82 (1H, d), 6.76-6. 72 (1H, t), 6.64-6. 62 (1H, d), 4. 67-4. 64 (1H, t), 4. 57-4.56 (2H, d), 4. 28 (2H, s), 4. 01-3. 96 (2H, q), 2. 90-2. 82 (4H, m), 2. 63- 2.57 (2H, m), 2.51-2. 45 (3H, m), 1.37-1. 33 (3H, t), 1.01-0. 99 (3H, d), 0.79 (9H, s), -0. 04 (3H, s), -0. 23 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 621, [M-H]-620.

Preparation 48: 3- {3- [ (2R)-2- ( ( (2R)-2- { [tert-Butyl (dimethyl) silyl] oxy)-2- [4- hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N- (3, 4- dimethylbenzyl) propanamide Prepared according to the procedure used for preparation 1 using 3- (3- { (2R)-2- [(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydr oxymethyl-phenyl)- ethylamino]-propyl}-phenyl)-propanoic acid (Preparation 51) and the appropriate amine, substituting dichloromethane instead of ethyl acetate as the extraction solvent, and dichloromethane : methanol : 880 ammonia (98 : 2: 0.2 by volume) instead of (95: 5: 0.5 by volume) as column eluent to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 6 = 7.19-7. 18 (1H, d), 7.15-7. 11 (1H, t), 7.04-6. 92 (6H, m), 6.84-6. 82 (1H, d), 6.68-6. 66 (1H, d), 4.70-4. 67 (1H, t), 4.61-4. 60 (2H, d), 4.23 (2H, s), 2.90-2. 84 (4H, m), 2.64-2. 59 (2H, m), 2.53-2. 46 (3H, m), 2.20 (6H, s), 1.03-1. 02 (3H, d), 0.82 (9H, s), -0. 01 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 605, [M+Na] + 627, [M-H]-603.

Preparation 49: 3- {3-[(2R)-2-({(2R)-2-{[tert-Butyl(dimethyl)silyl]oxyl}-2-[4- hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N- (2, 3- dihydro-1 H-inden-2-yl) propanamide

Prepared according to the procedure used for preparation 1 3- (3- { (2R)-2- [ (2R)- 2- {[tert-butyl(dimethyl)silyl]oxy}-2-(4-hydroxy-3-hydroxymethy l-phenyl)- ethylamino]-propyl}-phenyl)-propanoic acid (Preparation 51) and the appropriate amine, substituting dichloromethane instead of ethyl acetate as the extraction, and dichloromethane : methanol : 880 ammonia (97: 3: 0.3 by volume) instead of (95: 5: 0.5 by volume) as column eluent to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.19-7. 09 (6H, m), 7. 02-6. 90 (4H, m), 6. 68- 6.66 (1H, d), 4.70-4. 67 (1H, dd), 4.60 (2H, s), 4.56-4. 49 (1H, m), 3.21-3. 15 (2H, dd), 2.91-2. 81 (4H, m), 2.73-2. 68 (2H, dd), 2.65-2. 60 (2H, dd), 2.54-2. 49 (1H, dd), 2.43-2. 40 (2H, t), 1.04-1. 02 (3H, d), 0.82 (9H, s), -0. 01 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 603, [M+Na] + 625, [M-H]-601.

Preparation 50: 4- ((1R)-1- { [fert-Butyl (dimethyl) silyl] oxy}-2- [ ( (1R)-2- {3- [3- (3, 4- dihydroisoquinolin-2 (1l)-yl)-3-oxopropyl] phenyl}-1- methylethyl)amino]ethyl}-2- (hydroxymethyl)phenol

Prepared according to the procedure used for preparation 1 using 3- (3- { (2R)-2- <BR> <BR> <BR> [(2R)-2-{[teff-butyl (dimethyl) silyl] oxy}-2-(4-hYdroxy-3-hydroxymethyl-phenyl)- <BR> <BR> <BR> <BR> <BR> ethylamino]-propyl}-phenyl)-propanoic acid (Preparation 51) and the- appropriate amine, substituting dichloromethane instead of ethyl acetate as the extraction solvent, and dichloromethane : methanol : 880 ammonia (96: 4: 0.4 by volume) instead of (95: 5: 0.5 by volume) as column eluent to give the title compound as a white foam.

1H NMR (4001XAHz, CD30D) : s = 7.19 (1H, s), 7.16-7. 01 (5H, m), 6.99-6. 90 (3H, m), 6.84-6. 82 (1 H, d), 6.70-6. 67 (1 H, m), 4.71-4. 68 (1 H, dd), 4.65+4. 54 (2H, m), 4.62-4. 60 (2H, m), 3.76-3. 60 (2H, m), 2.93-2. 85 (4H, m), 2.80-2. 69 (4H, m), 2.66-2. 53 (2H, m), 2.50-2. 45 (1H, dd), 1.03-1. 00 (3H, m), 0.82 (9H, s),-0. 01 (3H, s), -0. 19 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] +603,[M+Na]+ 625, [M-H]- 601.

Preparation 51: 3-(3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4- <BR> <BR> <BR> hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)- propanoic acid Prepared according to the procedure used for preparation 36, using methyl-3- (3-{(2R)-2-[(2R)-2-{[tert-butyl(bimethyl)silyl]oxy}-2-(4-hyd roxy-3-hydroxymethyl- phenyl)-ethylamino]-propyl}-phenyl)-propanoate (Preparation 52) to give the title compound as a brown solid.

1H NMR (400MHz, CD30D) : 8 = 7.27 (1H, s), 7.19-7. 14 (1H, t), 7.09-7. 02 (3H, m), 6.95-6. 93 (1H, d), 6.75-6. 73 (1H, d), 4.92-4. 90 (1H, m), 4.61-4. 60 (2H, d), 3.37-3. 32 (1H, m), 3.20-3. 15 (1H, m), 3.04-3. 00 (1H, dd), 2.91-2. 83 (3H, m), 2.68-2. 62 (1H, m), 2.45-2. 40 (2H, t), 1.15-1. 14 (3H, d), 0.81 (9H, s), -0. 01 (3H, s), -0. 18 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 488, [M+Na] + 510, [M-H]-486.

Preparation 52: Methyl-3-(3-{(2R)-2-[(2R)-2-{[tert-butyl(dimethyl)silyl] oxyl}- 2- (4-hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-propyl}-pheny l) propanoate Prepared according to the procedure used for preparation 37, using methyl-3- (3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4-[be nzyloxy]-3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-propanoate (Preparation 53) to give the title compound as a brown oil.

1H NMR (400MHz, CD30D) : 8 = 7. 08-7. 15 (2H, m), 6.99-6. 88 (4H, m), 6.65- 6.62 (1H, d), 4.67-4. 64 (1H, m), 4. 58-4. 57 (2H, d), 3.59 (3H, s), 2.90-2. 80 (4H, m), 2.61-2. 49 (5H, m), 1.01-1. 00 (3H, d), 0.78 (9H, s), -0. 06 (3H, s), -0. 24 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 502, [M+Na] + 524, [M-H]-500.

Preparation 53: Methyl-3- (3- { (2R)-2- [ (2R)-2- { [tert-Butyl (dimethyl) silyll oxy)- 2-(4-lbenzyloxyl-3-hydroxymethyl-phenyl)-ethylamino]-propyl} -phenyl)- propanoate Prepared according to the procedure used for preparation 38 using methyl-3- [(2R)-2-aminopropyl) phenyl] propanoate (Preparation 54) and [2- (benzyloxy)-5-

((1R)-2-bromo-1-{[tert-butyl(bimethyl)silyl] oxy} ethyl) phenyl] methanol (Preparation 39) to give the title compound as a brown oil.

1H NMR (400MHz, CD30D) : 8 = 7. 43-7.24 (6H, m), 7.11-7. 04 (2H, m), 6.69- 6. 95 (1 H, d), 6. 91-6. 86 (3H, m), 5. 07 (2H, s), 4. 71-4. 66 (1 H, m), 4. 63-4. 62 (2H, d), 3. 58 (3H, s), 2. 89-2. 79 (4H, m), 2. 63-2.47 (5H, m), 1.02-1. 00 (3H, d), 0. 78 (9H, s), -0. 05 (3H, s),-0. 23 (3H, s) ppm.

LRMS (electrospray) : m/z [M+HI+ 592, [M+Na] + 614.

Preparation 54: Methyl-3-[(2R)-2-aminopropyl) phenyl] propanoate Prepared according to the procedure used for preparation 41, using methyl- [3- ((2R)-2-{[(1R)-1-phenyl-ethyl]-amino}-propyl)-phenyl]-propan oate hydrochloride (Preparation 55) to give the title compound as a brown oil.

1H NMR (400MHz, CD30D) : 6 = 7. 21-7.17 (1H, t), 7.03-7. 01 (3H, m), 3.61 (3H, s), 3.11-3. 03 (1H, m), 2.91-2. 87 (2H, t), 2.64-2. 54 (4H, m), 1.07-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 222.

Preparation 55: Methyl-[3-((2R)-2-{[(1R)-1-phenyl-ethyl]amino}-propyl)- phenyl]-propanoate hydrochloride Prepared according to the procedure used for preparation 52, using methyl-3- [3- (2-oxopropyl) phenyl] propanoate (Preparation 56) to give the title compound as a white crystalline solid.

H NMR (400MHz, CD30D) : 5 = 7.54-7.47 (5H, m), 7.23-7. 19 (1H, t), 7.12-7. 10 (1H, d), 6.92-6. 91 (2H, d), 4.64-4. 59 (1H, q), 3.61 (3H, s), 3.34-3. 29 (1H, m), 3.20-3. 12 1 H, m), 2. 89-2. 85 (2H, t), 2. 62-2. 56 (3H, m), 1. 71-1. 69 (3H, d), 1. 18- 1. 16 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 326.

Preparation 56: Methyl-3-[3-(2-oxopropyl)phenyl]propanoate

Prepared according to the procedure used for preparation 37 using methyl (2E)- 3- [3- (2-oxopropyl) phenyl] acrylate (Preparation 57) to give the title compound as an orange oil.

1H NMR (400MHz, CD30D) : 8 = 7.27-7. 23 (1H, q), 7.11-7. 09 (1H, d), 7.05-7. 04 (2H, d), 3.66 (5H, s), 2.96-2. 92 (2H, t), 2.64-2. 60 (2H, t), 2.14 (3H, s) ppm.

LRMS (electrospray) : m/z [M+Na] + 243, [M-H]-219.

Preparation 57: Methyl (2E)-3- [3- (2-oxopropyl) phenyl] acrylate

A solution of 3-bromophenylacetone (50. 0g, 235mmol), methyl acrylate (40.4g, 469mol), palladium (ll) acetate (7 9g, 35. 2mmol), tri-ortho-tolylphosphine (21.4g, 70. 4mmol) and triethylamine (82ml) in acetonitrile (900moi) was heated at reflux under a nitrogen atmosphere for a period of 16 hours. The reaction mixture was cooled to room temperature and the solvent removed in vacuo.

Purification by flash column chromatography eluting with pentane : ethyl acetate (90: 10 changing to 70: 30 by volume) gave the title compound as an orange oil (54.3g).

rH NMR (400MHz, CD30D) : 8 = 7.66-7. 62 (1 H, d), 7.41-7. 39 (1 H, d), 7.34-7. 31 (2H, t), 7.20-7.18 (1H, d), 6.43-6.39 (1H, d), 3.77 (3H, s), 3.70 (2H, s), 2.15 (3H, s) ppm.

LRMS (electrospray) : m/z [M+Na]+ 241, [M-H]- 217.

Preparation 58 : Methyl-3- {3- [ (2R)-2- ( ( (2R)-2- [4- (benzyloxy)-3- (hydroxymethyl) phenyll-2-hydroxyethyl} amino) propyl]phenyl}propanoate Ammonium fluoride (2. 80g, 75. 5mmol) was added in one portion to a solution of methyl-3- (3-{(2R)-2-[(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-(4-[be nzyloxy]-3- hydroxymethyl-phenyl)-ethylamino]-propyl}-phenyl)-propanoate (Preparation 53) (4.47g, 7. 55mmol) in water (20ml) and methanol (30ml) at room temperature. The reaction was heated at 40°C for 18 hours and then allowed to cool to room temperature. The methanol was removed in vacuo and the resulting aqueous extracted with dichloromethane (3x75ml), the combined organics were washed with water (25ml), dried (sodium sulfate) and the solvent removed in vacuo to yield an orange foam. This was purified by flash column chromatography on silica gel eluting with dichloromethane : methanol : 880 ammonia (95: 5: 0.5 by volume) to give the title compound as a yellow oil (3.21 g).

1H NMR (400MHz, CD30D) : 6 = 7.46-7. 44 (2H, d), 7.38-7. 28 (4H, m), 7.15-7. 11 (2H, m), 7.00-6. 90 (4H, m), 5.12 (s, 2H), 4.67-4. 63 (3H, m), 3.62 (3H, s), 2.96- 2. 84 (4H, m), 2.74-2. 66 (2H, m), 2.61-2. 55 (3H, m), 1.09-1. 07 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 478, [M+Na] + 500.

Preparation 59: Methyl3-{3-[(2R)-2-({(2R)-2-hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ehyl}amino)propyl]phenyl}propanoate

Prepared according to the procedure used for preparation 37 using methyl-3- {3- [(2R)-2-({(2R)-2-[4-(benzyloxy)-3-(hydroxymethyl)phenyl]-2- hydroxyethyl}amino)propyl]phenyl}propanoate (Preparation 58), substituting dichloromethane : methanol : 880 ammonia (95: 5: 0.5 changing to 90: 10: 1 by volume) as column eluent to give the title compound as a colourless oil.

1H NMR (400MHz, CD30D) : 6 = 7.21 (1H, m), 7.16-7. 13 (1H, t), 7.02-7. 00 (2H, m), 6.97-6. 93 (2H, m), 6.70-6. 68 (1 H, d), 3.63-3. 60 (3H, m), 3.34 (3H, s), 2.95- 2.84 (4H, m), 2.72-2. 65 (2H, m), 2.61-2. 53 (3H, m), 1.07-1. 05 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 388, [M+Na] + 410, [M-H]- 386.

Preparation 60: 3-{3-[(2R)-2-({(2R)-2-Hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl} propanoic acid Prepared according to the procedure used for preparation 36 using methyl-3- {3- [(2R)-2-({(2R)-2-hydroxy-2-[4-hydroxy-3- (hydroxymethyl) phenyl] ethyl}amino)propyl]phenyl} propanoate to give the title compound as a white foam.

1H NMR (400MHz, CD30D) : 8 = 7.17-7. 13 (3H, m), 7.35-7. 33 (1H, m), 7.24- 7.20 (1H, m), 7.07-7. 03 (2H, d), 6.79-6. 77 (1H, d), 4.87 (1H, s), 4.65 (2H, s), 3.52-3. 47 (1H, m), 3.16-3. 06 (3H, m), 2.91-2. 87 (2H, t), 2.77-2. 71 (1H, m), 2. 48-2. 44 (2H, t), 1.23-1. 21 (3H, d) ppm.

LRMS (electrospray) : m/z [M+H] + 374, [M-H]-372. Preparation 61: (4-{2-[2-(tert-Butyldimethylsilanyloxy)-2-(4-hydroxy- 3hydroxymethyl-phenyl) ethylamino] propylphenyl) acetic acid

Prepared according to the procedure used for preparation 36, using methyl- (4- {2 (2R)-[(2R)-2-(tert-butyldimethylsilanyloxy)-2-(4-hydroxy-3- hydroxymethylphenyl) ethylamino] propyl} phenyl) acetate (Preparation 62) to give the title compound as a brown solid.

1H NMR (400 MHz, CD30D) : 8 7.15 (2H, d), 6.92 (2H, m), 7.00 (1H, d), 6.83 (1 H, m), 6.64 (2H, bd), 4.67 (1H, s), 4.60 (2H, m), 3.43 (2H, m), 2.71-2. 92 (3H, m), 2.55 (2H, m), 1.04 (3H, m), 0.83 (9H, s), 0.00 (3H, s), -0. 18 (3H, s).

LRMS (electrospray) : m/z [M-H] + 472.

Preparation 62: Methyl- (4-{2(2R)-[(2R)-2-(tert-butyldimethylsilanyloxy)-2- (4-hydroxy-3-hydroxymethylphenyl) ethylamino] propyl} phenyl) acetate Prepared according to the procedure used for preparation 37, using methyl-(4- {(2R)-2-[(2R)-2-(4-benzyloxy-3-hydroxymethyl-phenyl)-2-(tert - butyldimethylsilanyloxy) ethylamino] propyl} phenyl) acetate (Preparation 63) to give the title compound as a yellow coloured foam.

1H NMR (400 MHz, CDCI3) : # 7. 14 (2H, d), 7.04 (1H, d), 7.02 (1H, d), 7. 00 (1H, d), 6.90 (1H, d), 6. 70 (1H, d), 4.76 (1H, s), 4.73 (2H, s), 3.71 (3H, s), 3.59 (2H,

s), 2.92 (2H, m), 2.73 (1H, m), 2.66 (2H, m), 1.12 (3H, m), 0.81 (9H, s), -0. 02 (3H, s), -0. 19 (3H, s).

LRMS (electrospray) : m/z [M+H] + 488, [M+Na] + 510.

Preparation 63: Methyl-(4-{(2R)-2-[(2R)-2-(4-benzyloxy-3-hydroxymethyl- phenyl)-2- (tert-butyldimethylilanyloxy)ethylamino]propyl}phenyl)acetat e

Methyl- {4- [ (2R)-2-amino-propyl] phenyl} acetate (Preparation 64) (7. 00g, 33. 8mmol), [2-(benzyloxy)-5-((1R)-2-bromo-1-{[tert- butyl (dimethyl) silyl] oxy} ethyl) phenyl] methanol (Preparation 39) (15. 2g, 33. 8mmol) and diisopropylethylamine (4.36 g, 33. 8mmol) were heated in diemthylsulfoxide (50ml) at 90 °C under nitrogen for 16 hours. The mixture was cooled and diluted with ethyl acetate (250moi) and basified with 1 M aqueous sodium hydroxide. The aqueous was extracted with ethyl acetate (250 mi) and the combined organics washed with brine (3x200 ml) and dried (magnesium sulfate). The crude material was purified by chromatography (90: 10 dichloromethane : methanol) to furnish an orange coloured oil (9.86g).

1H NMR (400 MHz, CDCl3) : 8 7.32-7. 43 (5H, m), 7.13 (1H, d), 7.17 (1H, m), 7.15 (2H, d), 7.07 (2H, d), 6.88 (1H, d), 5.10 (2H, s), 4.73 (1H, m), 4.70 (2H, d), 3.67 (3H, s), 3.57 (2H, s), 2. 68-2. 91 (4H, m), 2.48 (1H, m), 2.37 (1H, m), 1.01 (3H, d), 0.84 (9H, s), 0.00 (3H, s), -0. 18 (3H, s).

LRMS (electrospray) : m/z [M+H] + 578, [M+Na] + 600.

Preparation 64: Methyl-{4-[(2R)-2-amino-propyl]phenyl} acetate

Prepared according to the procedure used for preparation 41, using methyl-(4- {(2R)-2-[(1R)-1-phenylethylamino]propyl}phenyl) acetate hydrochloride (Preparation 65) to give the title compound as white crystals.

1H NMR (4û0 MHz, CDCl3) : 8 7. 22 (2H, d), 7. 17 (2H, d), 3. 69 (3H, s), 3. 60 (2H, s), 3.35 (1 H, m), 2.79 (1 H, m), 1. 24 (3H, d).

LRMS (electrospray) : m/z [M+H] + 208, [M+Na]+ 230.

Preparation 65 : Methyl-(4-{(2R)-2-[(1R)-1- phenylethylamino] propyl} phenyl) acetate hydrochloride Prepared according to the procedure used for preparation 42, using methyl- [4- (2-oxo-propyl) phenyl] acetate (Preparation 66) to give the title compound as white crystals.

1H NMR (400 MHz, CD30D) : 8 7.53 (5H, m), 7.21 (2H, d), 7.06 (2H, d), 4.61 (1H, q), 3.66 (3H, s), 3.62 (2H, s), 3.30 (2H, m), 3.18 (1H, m), 2.63 (1H, dd), 1.70 (3H, d), 1. 18 (3H, d).

LRMS (electrospray) : m/z [M+H] 312, [M+Na] + 334.

Preparation 66: Methyl- [4- (2-oxo-propyl) phenyl] acetate Prepared according to the procedure used for preparation 43, using methyl-4- bromophenylacetate to give the title compound as a clear oil.

LRMS (electrospray) : m/z [M+Na] + 229, [M-H]-205. Preparation 67: 2-{4-[(2R)-2-({(2R)-2-{[tert-Butyl(dimethyl)siyl]oxy}-2-[4- <BR> <BR> hydroxy-3- (hydroxymethyl) phenyl] ethyl} amino) propyl] phenyl}-N- [2-fluoro- 5- (trifluoromethyl) benzyl] acetamide

Prepared according to the procedure used for preparation 3 using (4- {2- [2- (tert- butyldimethylsilanyloxy)-2- (4-hydroxy-3hydroxymethyl- phenyl) ethylamino] propyl} phenyl) acetic acid (Preparation 61) and the appropriate amine to give the title compound as a white foam.

H NMR (400MHz, CD30D) : 8 = 7.55 (2H, m), 7.31-6. 82 (7H, m), 6.62 (1H, d), 6.05 (1 H, m), 4.75 (2H, s), 4.61 (2H, t), 4.55 (2H, d), 3.68 (2H, s), 2.95 (1 H, m), 2.83 (1 H, m), 2.56 (3H, m), 1.05 (3H, d), 0.90 (9H, s), 0.00 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 649.

Preparation 68: 2- (4-[(2R)-2-({(2R)-2-{[tert-Butyl(dimethyl)silyl]oxy}-2-[4- hydroxy-3- (hydroxymethyl) phenyl] ethyl amino) propyl] phenyl}-N- (2- phenylethyl) acetamide

Prepared according to the procedure used for preparation 3 using (4- {2- [2- (tert butyidimethylsilanyloxy)-2- (4-hydroxy-3hydroxymethyl- phenyl) ethylaminolpropyl} phenyl) acetic acid (Preparation 61) and the appropriate amine to give the title compound as a white foam.

1H NMR (400MHz, CD3OD) : 8 = 7.31-6. 85 (11H, m), 6.62 (1 H, d), 5.63 (1H, m), 4. 75 (2H, s), 4.66 (1 Hs, t), 3.55 (2H, m), 3. 48 (2H, s), 2. 88 (7H, m), 1.05 (3H, d), 0.90 (9H, s), 0.00 (3H, s), -0. 20 (3H, s) ppm.

LRMS (electrospray) : m/z [M+H] + 577, [M+Na] + 599, [M-H]-575.

Abbreviations TBDMS = tert-butyl (dimethyl) silyl In vitro activity of the compounds of formula (1) The ability of the compounds of the formula (1) to act as potent p2 agonists therefore mediating smooth muscle relaxation may be determined by the measure of the effect of beta-2 adrenergic receptor stimulation on electrical field stimulated-contraction of guinea pig trachea strips.

Guinea-pig trachea Male, Dunkin-Hartley guinea pigs (475-525g) are killed by CO2 asphyxiation and exsanguination from the femoral artery and the trachea is isolated. Four preparations are obtained from each animal, starting the dissection immediately below the larynx and taking 2.5 cm length of trachea. The piece of trachea is opened by cutting the cartilage opposite the trachealis muscle, then transverse sections, 3-4 cartilage rings wide, are cut. The resulting strip preparations are suspended in 5 ml organ baths using cotton threads tied through the upper and lower cartilage bands. The strips are equilibrated, un-tensioned, for 20 minutes in a modified Krebs Ringer buffer (Sigma K0507) containing 3 pM Indomethacin (Sigma 17378), 10 µM Guanethidine (Sigma G8520) and 10 jn. M Atenotoi (Sigma A7655), heated at 37°C and gassed with 95% O2/5% CO2, before applying an initial tension of 1 g. The preparations are allowed to equilibrate for a further 30-

45 minutes, during which time they are re-tensioned (to 1 g) twice at 15-minute intervals. Changes in tension are recorded and monitored via standard isometric transducers coupled to a data-collection system (custom-designed at Pfizer). Following the tensioning equilibration, the tissues are subjected to electrical field stimulation (EFS) using the following parameters: 10 s trains every 2 minutes, 0. 1 ms pulse width, 10 Hz and just-maximal voltage (25 Volts) continuously throughout the length of the experiment. EFS of post-ganglionic cholinergic nerves in the trachea results in monophasic contractions of the smooth muscle and twitch height is recorded. The organ baths are constantly perfused with the above-described Krebs Ringer buffer by means of a peristaltic pump system (pump flow rate 7.5 ml/minute) throughout the experiment, with the exception of when a beta-2 agonist according to the present invention is aided, the pump is then stopped for the time of the cumulative dosing to the bath and started again after maximal response is reached for the wash-out period.

Experimental protocol for assessment of potency and efficacy Following equilibration to EFS, the peristaltic pump is stopped and the preparations'primed'with a single dose of 300 nM isoprenaline (Sigma 15627) to establish a maximal response in terms of inhibition of the contractile EFS response. The isoprenaline is then washed out over a period of 40 minutes.

Following the priming and wash-out recovery, a standard curve to isoprenaline is carried out on all tissues (Isoprenaline Curve 1) by means of cumulative, bolus addition to the bath using half log increments in concentration. The concentration range used is 1e9 to 1e/3e-6 M. At the end of the isoprenaline curve the preparations are washed again for 40 minutes before commencing a second curve, either to isoprenaline (as internal control) or a beta-2 agonist according to the present invention. Beta-2 agonist responses are expressed as percentage inhibition of the EFS response. Data for beta-2 agonist are normalised by expressing inhibition as a percentage of the maximal inhibition induced by isoprenaline in Curve 1. The EC50 value for beta-2 agonist according to the present invention refers to the concentration of compound required to produce half maximal effect. Data for beta-2 agonists according to

the present invention are then expressed as relative potency to isoprenaline defined by the ratio (EC50 beta-2 agonist)/(EC50 Isoprenaline).

Confirmation of beta-2 mediated functional activity Beta-2 agonist activity of test compounds is confirmed using the protocol above, however, prior to constructing the curve to beta-2 agonist according to the present invention, the preparations are pre-incubated (for a minimum of 45 minutes) with 300 nM ICI 118551 (a selective (32 antagonist) which results in the case of a beta-2 mediated effect in a rightward-shift of the test compound dose response curve.

It has thus been found that the compounds of formula (1) according to the present invention that have been tested show a relative potency to Isoprenaline which is comprised between 0.002 and 2.0.

According to another alternative, the agonist potency for the ß2 receptor of the compounds of the formula (1) may also be determined by the measure of the concentration of compound according to the present invention required to produce half maximal effect (ECso) for the 32 receptor.

Compound Preparation 10 mM/100% DMSO (dimethylsulfoxide) stock of compound is diluted to required top dose in 4 % DMSO. This top dose is used to construct a 10-point semi-log dilution curve, all in 4 % DMSO. Isoprenaline (Sigma, I-5627) was used as a standard in every experiment and for control wells on each plate.

Data was expressed as % Isoprenaline response.

Cell Culture CHO (Chinese Hamster Ovary) cells recombinantly expressing the human p2 adrenergic receptor (from Kobilka et al., PNAS 84: 46-50, 1987 and Bouvier et al., Mol Pharmacol 33: 133-139 1988 CHOhß2) were grown in Dulbeccos MEM/ NUT MIX F12 (Gibco, 21331-020) supplemented with 10 % foetal bovine serum (Sigma, F4135, Lot 90K8404 Exp 09/04), 2 mM glutamin (Sigma, G7513),

500 ug/ml geneticin (Sigma, G7034) and 10 ug/ml puromycin (Sigma, P8833).

Cells were seeded to give about 90 % confluency for testing.

Assay Method 25 µl / well each dose of compound was transferred into a cAMP-FlashplateX (NEN, SMP004B), with 1% DMSO as basal controls and 100 nM Isoprenaline as max controls. This was diluted 1: 2 by the addition of 25 µl / well PBS. Cells were trypsinised (0.25% Sigma, T4049), washed with PBS (Gibco, 14040-174) and resuspended in stimulation buffer (NEN, SMP004B) to give 1#106 cells / ml CHOhB2. Compounds were incubated with 50 ui/well cells for 1 hour. Cells were then lysed by the addition of 100 uI/well detection buffer (NEN, SMP004B) containing 0. 18 EuCi/ml 1251-cAMP (NEN, NEX-130) and plates were incubated at room temperature for a further 2 hours. The amount of 125I-cAMP bound to the Flashplate was quantified using a Topcount NXT (Packard), normal counting efficiency for 1 minute. Dose-response data was expressed as % Isoprenaline activity and fitted using a four parameter sigmoid fit.

It has thus been found that the compounds of formula (1) according to the present invention that are illustrated in examples 1 to 65 above show a j32 cAMP EC50 between 0.006 nM and 0.467 nM.

The results below illustrate the activity of the compounds of formula (1): Example Number Cell based cAMP 32 activity (nM 1 0. 017 3 0. 007 4 0. 012 5 0. 024 6 0. 007 7 0 028 8 0. 010 10 0. 114 12 0. 009 13 0. 013 15 0. 056