wherein A is an unsubstituted or substituted cyclic group ; and R is hydrogen or tower alkyl ; and pharmaceutically acceptable acid addition salts thereof.

Especially preferred compounds are those, wherein the cyclic group A is

R1-R4 are independently from each other hydrogen, halogen, CF3, CHF2, C (CH3) F2, C3-C6-cycloalkyl, lower alkoxy, lower alkyl, OCFs or phenyl; R5-R'° are independently from each other hydrogen, halogen, lower alkyl, lower alkoxy or CHF2 ; R11-R16 are independently from each other hydrogen, halogen, lower alkoxy or lower alkyl ; R is hydrogen or CHF2 ; R18-R20 are independently from each other hydrogen, lower alkyl or lower alkoxy.

The following types of compounds are encompassed by the present formula I :

The substituents are described above.

Preferred are compounds of formulas IAl, IA2, IA3, IA4, IA5, IA6, IA7, IA8, IA9, IA10 and IA11.

The compounds of formula I and their salts are distinguished by valuable therapeutic properties. Compounds of the present invention are NMDA (N-methyl-D- aspartate)-receptor subtype selective blockers, which have a key function in modulating

neuronal activity and plasticity which makes them key players in mediating processes underlying development of CNS as well as learning and memory formation.

Under pathological conditions of acute and chronic forms of neurodegeneration overactivation of NMDA receptors is a key event for triggering neuronal cell death.

NMDA receptors are composed of members from two subunit families, namely NR-1 (8 different splice variants) and NR-2 (A to D) originating from different genes. Members from the two subunit families show a distinct distribution in different brain areas.

Heteromeric combinations of NR-1 members with different NR-2 subunits result in NMDA receptors displaying different pharmaceutical properties. Possible therapeutic indications for NMDA NR-2B receptor subtype specific blockers include acute forms of neurodegeneration caused, e. g., by stroke and brain trauma, and chronic forms of neurodegeneration such as Alzheimer's disease, Parkinson's disease, Huntington's disease, ALS (amyotrophic lateral sclerosis) and neurodegeneration associated with bacterial or viral infections, and, in addition, depression and chronic and acute pain.

Furthermore, EP 1254661 describes a method for preventing dyskinesias with selective NMDA antagonists and WO 02H5352 discloses the usefulness of NMDA modulators for the treatment of addictive illnesses, such as smoking cessation.

Most important indications are Parkinson's disease, (neuropatic) pain and stroke.

Objects of the invention are the compounds of formula IA or IB and pharmaceutically acceptable acid addition salts thereof, the preparation of the compounds of formula IA or IB and salts thereof, medicaments containing a compound of formula IA or IB or a pharmaceutically acceptable acid addition salt thereof, the manufacture of such medicaments and the use of the compounds of formula IA or IB and their pharmaceutically acceptable salts in the control or prevention of illnesses, especially of illnesses and disorders of the kind referred to earlier, and, respectively, for the manufacture of corresponding medicaments.

The following definitions of the general terms used in the present description apply irrespective of whether the terms in question appear alone or in combination.

As used herein, the term"lower alkvl"denotes a straight-or branched-chain alkyl group containing from 1 to 7 carbon atoms, for example, methyl, ethyl, propyl, isopropyl, butyl and the like. Preferred tower alkyl groups contain from 1 to 4 carbon atoms.

The term"halogen"denotes chlorine, iodine, fluorine and bromine.

The term"lower alkoxy"denotes a group wherein the alkyl residue is as defined above and the alkyl group is connected via an oxygen atom.

The term"cycloalkyl"denotes a carbon ring with 3 to 6 carbon atoms, preferred is cyclopropyl.

The term"pharmaceutically acceptable acid addition salts"embraces salts with inorganic and organic acids, such as hydrochloric acid, nitric acid, sulfuric acid, phosphoric acid, citric acid, formic acid, fumaric acid, maleic acid, acetic acid, succinic acid, tartaric acid, methane-sulfonic acid, p-toluenesulfonic acid and the like.

Preferred compounds of the present invention are those, wherein A is the group a).

Specific preferred compounds, which fall under this group are the followings : 5- (3-chloro-4-fluoro-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine, 3- (2-methyl-imidazol-1-yl-methyl)-5- (3-trifluoromethyl-phenyl) -pyridazine, 5- (3-difluoromethyl-4-fluoro-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine, 5- [3- (I, l-difluoro-ethyl)-phenyl]-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine, 5- [3- (1, 1-difluoro-ethyl)-4-fluoro-phenyl]-3- (2-methyl-imidazol-l-yl-methyl)- pyridazine, 5-13-(l, l-difluoro-ethyl)-4-fluoro-phellyll-3-(2-nlethyl-imidazol-l- yl-methyl)- pyridazine, 5- (4-fluoro-3-methyl-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine, 5- (4-chloro-3-methyl-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine, 5-[3-(1,1-difluoro-ethyl)-5-fluoro-phenyl]-3-(2-methyl-imida zol-1-yl-methyl)- pyridazine, 5- (3-difluoromethyl-4-fluoro-phenyl)-3- (2-ethyl-imidazol-l-ylethyl)-pyridazine or 5-(3-cyclopropyl-4-fluoro-phenyl)-3-(2-methyl-imidazol-l-yl- methyl)-pyridazine.

Further preferred are further compounds, wherein A is the group d), for example the following compound 5-benzo [b] thiophen-5-yl-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine.

A further preferred group of compounds are those, wherein A is the group k), for example the following compound 5- (3, 4-dihyd ro-naphthalen-2-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine.

The afore-mentioned compounds of formula I can be manufactured in accordance with the invention by a) reacting a compound of formula with a compound of formula to give a compound of formula

wherein A is the group a), b), c), d), e), f), g), h), i), j) or k) as described above and R is hydrogen or lower alkyl, or b) reacting a compound of formula

with a compound of formula to obtain a compound of formula

wherein A is the group a), b), c), d), e), f), g), h), i), j) or k) as described above and R is hydrogen or lower alkyl, and if desired, converting the compound of formula I obtained into a pharmaceutically acceptable salt.

In the following the preparation of compounds of formulas IA and IB are described in more detail: In accordance with the process variants, described above, and with schemes 1-5, described below, compounds of formula IA and IB may be prepared by known procedures, for example the following In the following schemes 1-5 are described processes for preparation of compounds of formula IA, starting from known compounds, from commercial products or from compounds, which can be prepared in conventional manner.

The preparation of compounds of formula IA and IB are further described in more detail in working examples 1-73 and in examples 74-180.

Scheme 1 Starting from 3-chloro-5-methoxy-pyridazine (Bryant, 1'. D.; Kunng, F. -A.; South, M. S. J. Heterocycl. Chem. (1995), 32 (5), 1473-6.), the compound of formula VII may be prepared as follwvs : 3-Chloro-5-methoxy-pyridazine, bis (triphenylphosphine) palladium dichloride and triethyl amine in ethanol are heated at about 120 °C under a 40 bar pressure of carbon monoxide for about 5 hours. Reaction mixture is cooled, filtered and

concentrated in vacuo. The residue is taken in CH, CI,, washed with H20, dried over Na. ; S04 and concentrated in vacuo to provide 5-methoxy-pyridazine-3-carboxylic acid ethyl ester (VII).

5-Methoxy-pyridazine-3-carboxylic acid ethyl ester is dissolved in ethanol under argon. Reaction mixture is cooled to 0°C and treated with NaBH4. After 10 minutes, reaction mixture is warmed to room temperature, stirred for about 1 hour and treated successively with HCI and saturated sodium bicarbonate to adjust the pH at 8. Solvent is removed in vacuo and the residue is stirred with MeOH. The suspension is filtered and the filtrate is concentrated.

The obtained (5-methoxy-pyridazin-3-yl)-methanol (VIII) is dissolved in MeCl,- under argon and a drop of DMF is added. The mixture is cooled with an icebath, thionylchloride is added dropwise and the reaction mixture was allowed to warm to room temperature. After 30 minutes stirring, the orange solution was cooled to 0°C, and saturated NaHCO3 solution is added dropwise. The aqueous layer is extracted with Mec,. The combined organic layers are dried over Na2SO4, filtered and concentrated in vacuo and treated with a appropriate imidazole (III). Reaction mixture is heated at about 100 °C for 2 hours then cooled to room temperature to provide the corresponding 5- methoxy-3- (imidazol-1-yl-methyl)-pyridazine (IX).

The 5-methoxy-3- (imidazol-1-yl-methyl)-pyridazine (IX) is dissolved in dioxane and NaOH is added. The mixture is relluxed for about 7 hours, cooled to room temperature and quenched with HCI. The pH is adjusted to 8 with saturated solution of NaHCO3. The solvent is removed in vacuo and the residue is taken in MeOH. After filtration, the solvent is removed in vacuo and diluted with MeOH to provide the corresponding 6-(imidazol-1-yl-methyl)-1H-pyridazin-4-one (X).

6- (imidazol-1-yl-methyl)-lH-pyridazin-4-one (X) is taken in phosphorus oxychloride under argon. The mixture is stirred in a 60 °C oilbath for 1.5 hour. The solvent is removed in vacuo and the residue is dissolved in water under icebath cooling.

The solution is neutralized with solid NiHCO3 and the aqueous layer is extracted with MeCl2 to provide the corresponding 5-chloro-3- (imidazol-l-yl-methyl)-pyridazine (IV A).

The compounds of formula IV B may be prepared in accordance with the above scheme, starting from Scheme 2

wherein A is the group a), b), c), d), e), t)} g),h),i),j) or k) as described above and R is hydrogen or lower alkyl. Preferred compounds are those, wherein R is methyl.

In accordance with scheme 2, compounds of formula I may be prepared as follows: The corresponding 5-chloro-3-(imidazol-1-yl-methyl)-pyridazine (IV A), a corresponding boronic acid of formula VI or of a corresponding 4, 4, 5, 5-tetramethyl- 1, 3, 2)-dioxaborolane (V), K2CO3 and tetrakis (triphenylphosphine) palladium are mixed and degassed dioxane is added. The mixture is refluxed for about 44 hours and the solvent is removed in vacuo. The residue is taken in MeCl2 filtrated and the filtrate is concentrated in vacuo and a compound of formula IA is obtained.

I n accordance with this scheme, a corresponding compound of formula IB may be obtained, using as starting material the compound of formula Scheme 3

wherein A is the group a), b), c), d), e), f), g), h), i), j) or k) as described above.

A compound of formula A-Br maybe prepared, for example as follows : 5- bromo-2-fluorobenzaldehyde in CH2Cl2 is treated at 0 °C with (diethylamino) sulfur trifluoride. The reaction mixture is refluxed overnight and then quenched with saturated solution of NaHCO). The aqueous phase is extracted with ethylacetate. The combined organic layers are washed with brine, dried over MgSO4, filtrated and concentrated in vacuo to provide 4-bromo-2-difluoromethyl-1-fluoro-benzene (a compound of formula A-Br).

Following the methods of scheme 3, compounds of formulas V and VI may be obtained.

Compounds of formula V: A compound of formula A-Br, bis (pinacolato) diboron, potassium acetate and bis (triphenylphosphine) palladium dichloride are suspense in dioxane. The suspension is flushed with argon for 30 minutes and refluxed for about 12 hours. The reaction mixture is cooled to room temperature, diluted with ethyl acetate, washed with brine, dried over Na-IS04 and concentrated in vacuo to provide a corresponding compound of formula V.

Compounds of formula Vl : A compound of formula A-Br, for example a solution of 3-bromo-1, 2-dihydro-naphtllalene (Adamczyl ;, NI. ; Watt, D. S.; Netzel, D. A.

J. OrS,. Chem. 1984,49, 4226-4237) in diethylether is cooled in a dry ice bath and tert.- butyllithium solution is added maintaining T <-65"C. At this temperature stirring is continued for 30 min, then triisopropylborate is added. The reaction mixture is brought to rt and treated with HCI. After 15 min the organic phase is dried (Na2SO4), evaporated and precipitated with pentane to provide a corresponding compound of formula VI.

Scheme 4

wherein A is the group a), b), c), d), e), f), g), h), i), j) or k) as described above and ls is hydrogen or lower alkyl.

In accordance with scheme 4, a compound of formula XI may be obtained in analogy to the following method: 3-Chloro-5-methoxy-pyridazine (Bryant, R. D.; Kunng, F.-A. ; South, M. S. J.

Hctcrocycl. Cliciti. (1995), 32 (5), 1473-6.), 3-chloro-4-fluorophenylboronic acid, Cs2CO3 and tris (dibenzylideneacetone) dipalladium chloroform complex are mixed and a solution of tri-tert-butylphosphine in degassed dioxane is added. The mixture is heated at about 90 °C for 22 hours then cooled to room temperature, ethylacetate is added, the solid is filtered and the filtrate is concentrated in vacuo to provide 3- (3-chloro-4-fluoro- phenyl)-5-methoxy-pyridazine (a compound of formula XI).

The compound of formula XI, for example 3- (3-chloro-4-fluoro-phenyl)-5- methoxy-pyridazine in HBr is heated at about 100 °C for 19 hours under argon. The solvent is removed in vacuo and the resulting solid is dissolved in MeOH. The turbid solution is filtered though decalite and the filtrate is concentrated to provide, for example, 6- (3-chloro-4-fluoro-phenyl)-pyridazin-4-ol hydrobromide (XII).

The compound of formula XII ! is prepared from a compound of formula XII in phosphorus oxychloride under argon. The mixture was stirred in a 60 °C oilbath for 1.5 hours. The solvent was removed in vacuo and the residue is dissolved in water under icebath cooling. The solution is neutralized with NaHCO, and the aqueous layer is extracted with MeCl,. The combined extracts are dried over NaIS04, filtered and the

solvent is removed in vacuo to provide a compound of formula XIII.

This compound of formula XIII and bis- (triphenylphosphine)-palladium (II)- dichloride are treated with a solution of tributyl-methoxymethoxymethyl-stannane (Sawyer J. S.; Kucerovy A. ; Macdonald T. L.; McGarvey G. J. J. Am. Chern. Soc. (1988), 110, 842-853) in DMF. The mixture is heated at about 100 °C for 4 hours then cooled to room temperature and a saturated KF solution is added. The mixture is stirred for 30 minutes at room temperature and ethyl acetate and water are added. The mixture is filtered and extracted. The combined extracts are dried over Na2SO4, filtered and the solvent is removed in vacuo to provide a compound of formula XIV.

The obtained compound is dissolved in dioxane and treated with HCI. The reaction mixture is refluxed for 1.5 hours and then cooled to room temperature. Water and ethyl acetate are added. The aqueous layer is extracted with ethyl acetate. The combined organic layers are dried over Na2SO4, filtered and concentrated in vacuo to provide a compound of formula IIA, which is then treated with a compound of formula III in thionylchloride to a corresponding compound of formula IA.

1 n accordance with scheme 4, a compound of formula IB may be prepared starting from the compound of formula Scheme 5

svherein Rt and R4 are described above.

A compound of formula XV may be obtained as follonvs : To a suspension of (methyl) triphenyl-phosphonium bromide in THF are added at-78 °C BuLi and a corresponding bromo-benzaldehyde. The reaction mixture is stirred about 18 hours at r. t. After work-up and purification by chromatography a compound of formula XV is obtained.

The compound of formula XV, bis (pinacolato) diboron, potassium acetate and bis (triphenylphosphine) palladium dichloride are suspense in dioxane. The suspension is flushed with argon for 30 minutes and refluxed for 12 hours. The reaction mixture is cooled to room temperature, diluted with ethyl acetate, washed with brine, dried over Na2SO4 and concentrated in vacuo to provide a compound of formula XVI.

To a corresponding solution of 4, 4,5, 5-tetramethyl-2- (3-vinyl-phenyl)- 1, 3,2] dioxaborolane (XVI) in toluene are added a diethylxink solution and diiodomethane. The reaction mixture is stirred for 1 hour at room temperature and then refluxed for 3 hours. The reaction mixture is poured on sat. NH4CI solution and is extracted with ethylacetate. The combined organic layers are washed with brine, dried over M', S04, filtrated and concentrated to provide a corresponding cyclopropyl- substituted compound of formula XVII.

Pharmaceutically acceptable salts can be manufactured according to methods which are known per se and familiar to any person skilled in the art. The acid addition salts of compounds of formulas IA or Ili are especially well suited for pharmaceutical use.

As mentioned earlier, the compounds of formula IA and IB and their pharmaceutically usable acid addition salts possess valuable pharmacodynamic properties. They are NMDA-receptor subtype 2B selective blockers, which have a key function in modulating neuronal activity and plasticity which makes them key players in mediating processes underlying development of CNS as well as learning and memory formation.

The compounds were investigated in accordance with the test given hereinafter.

Test method 3H-Ro 25-6981 binding (Ro 25-6981 is [R-(R*,S*)]-α-(4-hydroxy-phenyl)-ß-methyl-4- (phenyl-methyl)-1-piperidine propanol) Male Füllinsdorf albino rats weighing betcveen 150-200 g were used. Membranes were prepared by homogenization of the whole brain minus cerebellum and medulla oblongata with a Polytron (10.000 rpm, 30 seconds), in 25 volumes of a cold Tris-HCI 50 mM, EDTA 10 mM, pH 7.1 buffer. The homogenate was centrifuged at 48,000 g for 10 minutes at 4 °C. The pellet was resuspended using the Polytron in the same volume of buffer and the homogenate was incubated at 37 °C for 10 minutes. After centrifugation the pellet was homogenized in the same buffer and frozen at-80 °C for at least 16 hours but not more than 10 days. For the binding assay the homogenate was thawed at 37 °C, centrifuged and the pellet was washed three times as above in a Tris-HCI 5 mM, pH 7.4 cold buffer. The final pellet was resuspended in the same buffer and used at a final concentration of 200 mg of protein/ml.

#H-Ro 25-6981 binding experiments were performed using a Tris-HCl 50 mM, pH 7.4 buffer. For displacement experiments 5 IN,, of 3H-Ro 25-6981 were used and non specific binding was measured using 1 () oftetrahydroisoquinoline and usually it accounts for 10% of the total. The incubation time was 2 hours at 4 °C and the assay was stopped by filtration on Whatmann GF/13 glass fiber filters (Unifilter-96, Packard, Zurich, Switzerland). The filters were washed 5 times with cold buffer. The radioactivity on the filter was counted on a Packard'Top-count microplate scintillation counter after addition of 40 mL of microscint 40 (Canberra Packard S. A., Zürich, Switzerland).

The effects of compounds were measured using a minimum of 8 concentrations and repeated at least once. The pooled normalized values were analyzed using a non-linear regression calculation program which provide 1C ;, ;) with their relative upper and lower 95% confidence limits.

The IC50 (µM) of preferred compounds of formula I, tested in accordance with the above mentioned method, is <0,1 µM.

Examples of such compounds are: Example-No. IC50 (µM) Example-No. IC5o (µM) 1 0. 021 31 0.031 3 0. 038 34 0. 068 4 0. 027 35 0. 025 0.017 36 0. 077 9 0. 034 38 0.054 11 0. 029 39 0. 024 12 0. 022 41 0. 041 13 0. 011 42 0. 048 14 0. 02 45 0.057 15 (). () 16 48 0. 035 16 0.01 49 0. 034 24 0. 047 50 0.029 25 0. 058 52 0. 026 26 0. 012 58 0. 037 27 0. 044 68 0.027 30 0. 007

The compounds of formula IA and IB and their salts, as herein described, can be incorporated into standard pharmaceutical dosage forms, for example, for oral or parenteral application with the usual pharmaceutical adjuvant materials, for example, organic or inorganic inert carrier materials, such as, water, gelatin, lactose, starch,

magnesium stearate, talc, vegetable oils, gums, polyalkylene-glycols and the like. The pharmaceutical preparations can be employed in a solid form, for example, as tablets, suppositories, capsules, or in liquid form, for example, as solutions, suspensions or emulsions. Pharmaceutical adjuvant materials can be added and include preservatives stabilizers, wetting or emulsifying agents, salts to change the osmotic pressure or to act as buffers. The pharmaceutical preparations can also contain other therapeutically active substances.

The dosage can vary within wide limits and will, of course, be fitted to the individual requirements in each particular case. In the case of oral administration the dosage lies in the range of about 0. 1 mg per dosage to about 1000 mg per day of a compound of general formula I although the upper limit can also be exceeded when this is shown to be indicated.

The following examples illustrate the present invention in more detail. However, they are not intended to limit its scope in any manner. All temperatures are given in degree Celsius.

Example 1 5- (3-Chloro-4-fluoro-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride 5-Chloro-3- (2-methyl-imidazol-l-yl-methyl)-pyridazine (0. 07g, 0. 34 mmol), 3-chloro- 4-iluorophenylboronic acid (0. 076 g, (). 44 mmol), K2CO3 (0.09 g, 0. 67 mmol) and tetrakis (triphenylphosphine) palladium (0. 04 g, 0. 034 mmol) were mixed and degassed dioxane (1.4 ml) was added. The mixture was refluxed for 44 hours and the solvent was removed in vacuo. The residue was talien in MeCI., filtrated and the filtrate was concentrated in vacuo. The residue was chromatographed over silica gel (CH2CI2-MeOH 98 : 02) to provide a white foam which was dissolved in MeOH (2 ml). HCI-Et2O was added to provide 5- (3-chloro-4-fluoro-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)- pyridazine hydrochloride (0.1 g, 77 %) as an off white solid, MS : m/e = 302.7 (M F).

Following the general method of Example 1, the compounds of Examples 2 to Example 67 were prepared.

Example 2 3- (2-Methyl-imidazol-1-yl-methyl)-5- (3-trifluoromethyl-phenyl)-pyridazine hydrochloride

The title compound, MS: m/e = 319.4 (M+H+), was prepared from 3- trifluoromethylbenzeneboronic acid (commercially available) and 5-chloro-3- (2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 3 5- (4-Fluoro-3-trifluoromethyl-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 337.2 (M+H+), was prepared from 2- (4-fluoro-3- tifluoromethyl-phenyl)-4, 4,5, 5-tetramethyl-[1, 3, 2Jdioxaborolane and 5-chloro-3-(2- methyl-imidazol-1-ylmethyl)-pyridazine.

Example 4 5- (4-Chloro-3-trifluoromethyl-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 353.3 (M+H+), was prepared from 2- (4-chloro-3- trifluoromethyl-phenyl)-4, 4,5, 5-tetramethyl-[1, 3, 21 dioxaborolane and 5-chloro-3-(2- methyl-imidazol-1-ylmethyl)-pyridazine.

Example 5 5- (4-Chloro-3-fluoro-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 303.3 (M+H+), was prepared from 2- (4-chloro-3-fluoro- phenyl)-4, 4,5, 5-tetramethyl-[1, 3, 2]dioxaborolane and 5-chloro-3-(2-methyl-imidazol-1- yl-methyl)-pyridazine.

Example 6 5- (3-Difluoromethyl-4-fluoro-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 319.4 (i\I+H+), was prepared from 2- (3-difluoromethyl- 4-fluoro-phenyl)-4, 4,5, 5-tetramethyl-[1,3,2]dioxaborolane and 5-chloro-3- (2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 7 <BR> <BR> <BR> 5- (3-Fluoro-5-trifluoromethyl-phenyl)-3-(2-methyl-imidazol-1-y l-methyl)-pyridazine hydrochloride The title compound, AvIS : m/e = 337.2 (M+H+), was prepared from 2- (3-fluoro-5- trifluoromethyl-phenyl)-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborulane and 5-chloro-3- (2- methyl-imidazol-1-yl-methyl)-pyridaiine.

Example 8 3- (2-Methyl-imidazol-1-yl-methyl)-5-phenyl-pyridazine hydrochloride The title compound, MS: m/e = 251. 2 (M+H+), was prepared from phenylboronic acid and 5-chloro-3- (2-methyl-imidazol-1-ylmethyl)-pyridazine.

Example 9 5- [3- (1, I-Difluoro-ethyl)-phenyl]-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 315.4 (M+H+), was prepared from 2- [3- (1, 1-difluoro- ethyl)-phenyl]-4, 4,5, 5-tetramethyl-[1,3,2]dioxaborolane and 5-chloro-3- (2-methyl- imidazol-1-ylmethyl)-pyridazine.

Example 10 5- (4-Chloro-phenyl)-3-(2-methyl-imidazol-1-yl-methyl)-pyridazi ne hydrochloride The title compound, MS: m/e = 285.2 (M+H+), was prepared from 4- chlorophenylboronic (commercial available) and 5-chloro-3-(2-methyl-imidazol-1-yl- methyl)-pyridazine.

Example 11 5- [3- (1, 1-Difluoro-ethyl)-4-fluoro-phenyl]-3- (2-methyl-imidazol-1-yl-methyl)- pyridazine hydrochloride The title compound, MS : m/e = 333.3 (M+H+), was prepared from 2- [3- (l, l-difluoro- ethyl)-4-fluoro-phenyl]-4, 4,5, 5-tetramethyl- [1, 3, 2]dioxaborolane and 5-chloro-3-(2- methyl-imidaiol-1-yl-methyl)-pyridaiine.

Example 12 3- (2-Methyl-imidazol-1-ylmethyl)-5-naphthalen-2-yl-pyridazine- hydrochloride The title compound, MS: m/e = 301.3 (M+H+), was prepared from naphtylboronic acid and 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine.

Example 13 5- (3,4-Dichloro-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 319. 2 was prepared from 3, 4- dichlorophenylboronic acid and 5-chloro-3- (2-methyl-imidazol-l-yl-methyl)- pyridazine.

Example 14 5- (3-Cyclopropyl-phenyl)-3- (2-method hydrochloride

The title compound, MS: m/e = 291.3 (M+H+), was prepared from 2- (3-cyclopropyl- phenyl) -4,4, 5, 5-tetramethyl- [1, 3, 2] dioxaborolane and 5-chloro-3- (2-methyl-imidazol-l- yl-methyl)-pyridazine.

Example 15 5-Benzo [b] thiophen-5-yl-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 307.3 (M+H), was prepared from 2-benzo [b] thiophen- 5-yl-4, 4,5, 5-tetramethyl- [1, 3, 21 dioxaborolane and 5-chloro-3-(2-methyl-imidazol-1-yl- methyl)-pyridazine.

Example 16 5- (4-Fluoro-3-methyl-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 283.1 (M+H), was prepared from 4-fluoro-3- methylphenylboronic acid (commercially available) and 5-chloro-3- (2-methyl-imidazol- 1-yl-methyl)-pyridazine.

Example 17 5- (4-Methoxy-phenyl)-3-(2-methyl-imidazol-1-yl-methyl)-pyridaz ine hydrochloride The title compound, MS: m/e = 281. 2 (M+H+), was prepared from 4- methoxybenzeneboronic acid and 5-chloro-3- (2-methyl-imidazol-1-yl-methyl)- pyridazine.

Example 18 3- (2-Methyl-imidazol-I-yl-methyl)-5-p-tolyl-pyridazine hydrochloride The title compound, MS: m/e = 265. 3 (M+H+), was prepared from p-tolylboronic acid and 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine.

Example 19 5- (2-Chloro-phenyl) -3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 285. 2 (i\I+H+), was prepared from 2- chlorophenylboronic acid and 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine.

Example 20 5- (3-Chloro-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 285. 2 (M+H+), was prepared from 3- chlorophenylboronic acid and 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine.

Example 21 5- (3, 4-Difluoro-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 287.2 (M+H+), was prepared from 3,4- difluorobenzeneboronic acid and 5-chloro-3- (2-methyl-imidazol-l-yl-methyl)- pyridazine.

Example 22 5- (3, 5-Dichloro-phenyl)-3-(2-methyl-imidazol-1-yl-methyl)-pyridaz ine hydrochloride The title compound, MS : m/e = 319. 3 (M+H+), was prepared from 3,5- dichlorobenzeneboronic acid and 5-chloro-3-(2-methyl-imidazol-1-ylmethyl)- pyridazine.

Example 23 5-Benzo [b] thiiophen-2-yl-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 307.3 (M+H), was prepared from benzo [B] thiophene- 2-boronic acid and 5-chloro-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine.

Example 24 5- (3-Difluoromethyl-5-fluoro-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 319. 3 (M+H+), was prepared from 2- (3-difluoromethyl- 5-fluoro-phenyl)-4, 4,5, 5-tetramethyl-[1,3,2]dioxaborolane and 5-chloro-3-(2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 25 5- (3-Difluoromethyl-phenyl)-3- (2-methvl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 301. 3 (M+H+), was prepared from 2- (3-difluoromethyl- phenyl)-4, 4, 5, 5-tetramethyl- [1, 3,2] dioxaborolane and 5-chloro-3-(2-methyl-imidfazol-1- yl-methyl)-pyridazine.

Example 26 5- (4-Chloro-3-difluoromethyl-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 335.3 (M+H+), was prepared from 2- (4-chloro-3- difluoromethyl-phenyl)-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaboro) ane and 5-chloro-3- (2- methyl-imidazol-1-yl-methyl)-pyridazine.

Example 27 5- (6-Methoxy-naphthalen-2-yl) -3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 331. 4 WI+H'), was prepared from 2- (6-methoxy- naphthalen-2-yl)-4, 4,5, 5-tetramethyl-[1,3, 2] dioxaborolane and 5-chloro-3- (2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 28 5- (6-Difluoromethyl-naphthalen-2-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 351.4 (M+Ht), was prepared from 2- (6-difluoromethyl- naphthalen-2-yl)-4, 4,5, 5-tetramethyl-[1,3,2]dioxaborolane and 5-chloro-3-(2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 29 3- (2-Mekthyl-imidazol-1-yl-methyl)-5-(3-trifluoromethoxy-pheny l)-pyridazine hydrochloride The title compound, MS: m/e = 335.3 (M+H+), was prepared from 3- (trifluoromethoxy) phenylboronic acid and 5-chloro-3- (2-methyl-imidazol-l-yl-methyl)- pyridazine.

Example 30 5- (4-Chloro-3-methyl-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 299. 3 (M+H+), was prepared from 2- (4-chloro-3- methyl-phenyl)-4, 4,5, 5-tetramethyl-[1,3,2]dioxaborolane and 5-chloro-3- (2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 31 5- [3- (l, l-Difluoro-ethyl)-5-fluoro-phenyl]-3- (2-methyl-imidazol-l-yl-methyl)- pyridazine hydrochloride The title compound, MS: m/e = 333.3 (M+H+), was prepared from 2- [3- (1, 1-difluoro- ethyl)-5-fluoro-phenyl]-4, 4,5, 5-tetramethyl-[1,3,2]dioxaborolane and 5-chloro-3- (2- methyl-imidazol-l-yl-methyl)-pyridarine.

Example 32 5- (5-Difluoromethyl-thiophen-3-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride

The title compound, MS: m/e = 307.2 (M+H+), was prepared from 2- (5-difluoromethyl- <BR> <BR> <BR> thiophen-3-yl) -4, 4, 5,5-tetramethyl- [1,3,2]dioxaborolane and 5-chloro-3-(2-methyl-<BR> <BR> <BR> <BR> <BR> <BR> imidazol-1-yl-methyl)-pyridazine.

Example 33 5-Biphenyl-4-yl-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 327.4 (M+H+), was prepared from 4-biphenylboronic acid and 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine.

Example 34 5- (3-tert-Butyl-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 307.3 (M+H+), was prepared from 2- (3-tert-butyl- phenyl)-4, 4,5, 5-tetramethyl-[1,3, 2] dioxaborolane and 5-chloro-3-(2-methyl-imidazol-1- yl-methyl)-pyridazine.

Example 35 3- (2-Methyl-imidazol-1-yl-methyl)-5-naphthalen-1-yl-pyridazine hydrochloride The title compound, MS: m/e = 301. 3 (M+H+), was prepared from 1-naphtylboronic acid and 5-chloro-3- (2-methyl-imidazol-l-yl-methyl)-pyridazine.

Example 36 5- (5-Methoxy-naphthalen-1-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 331.4 (s\I+H), was prepared from 2- (5-methoxy- naphthalen-1-yl)-4, 4,5, 5-tetramethyl-[1, 3, 2Jdioxaborolane and 5-chloro-3- (2-methyl- imidazol-l-yl-methyl)-pyridazine.

Example 37 5-Biphenyl-3-yl-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 327.3 (M+H+), was prepared from 3-biphenylboronic acid and 5-chloro-3- (2-methyl-imidizol- I-ylmethyl)-pyridazine.

Example 38 5- (3-Methoxy-5-trifluoromethyl-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 349. 4 (M+H+), was prepared from 2- (3-methoxy-5- trifluoromethyl-phenyl)-4,4, 5, 5-tetramethyl- (1, 3, 2]dioxaborolane and 5-chloro-3- (2- methyl-i midazol-1-yl-methyl)-pyridazi ne.

Example 39 5-[4-Chloro-3-(1,1-difluoro-ethyl)-phenyl]-3-(2-methyl-imida zol-1-yl-methyl)- pyridazine hydrochloride The title compound, MS: m/e = 349.4 (M+H+), was prepared from 2-[4-chloro-3-(1,1- difluoro-ethyl)-phenyl]-4, 4,5, 5-tetramethyl-[1, 3, 2]dioxaborolane and 5-chloro-3- (2- methyl-imidazol-l-yl-methyl)-pyridarine.

Example 40 <BR> <BR> <BR> 5- (7-Difluoromethyl-naphthalen-2-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 351.3 (M+H+), was prepared from 2- (7-difluoromethyl- naphthalen-2-yl)-4, 4,5, 5-tetramethyl-[1,3, 2] dioxaborolane and 5-chloro-3- (2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 41 5- (4-Chloro-3-methoxy-phenyl) -3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 315.3 (M+H+), was prepared from 2- (4-chloro-3- methoxy-phenyl)-4, 4,5, 5-tetramethyl- ( 1, 3, 2]dixoaborolane and 5-chloro-3-(2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 42 5- (3-Isopropyl-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 293.3 (M+H+), was prepared from 2- (3-isopropyl- phenyl)-4, 4,5, 5-tetramethyl- 1, 3,2] dioxaborolane and 5-chloro-3- (2-methyl-imidazol-l- yl-methyl)-pyridazine.

Example 43 5- (7-Ethoxy-naphthalen-2-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 345.4 (M+H+), was prepared from 2- (7-ethoxy- naphthalen-2-yl)-4, 4,5, 5-tetramethyl-[1,3,2]dioxaborolane and 5-chloro-3- (2-methyl- imidazol-1-ylmethyl)-pyridazine.

Example 44 5- (4-Methoxy-naphthalen-1-yl)-3- (2-methyl-imidazol-l-yl-methyl)-pyridazine hydrochloride

The title compound, MS: m/e = 331. 3 (M+H+), was prepared from 2- (4-methoxy- naphthalen-1-yl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane and 5-chloro-3- (2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 45 5-Acenaphthen-5-yl-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 327.3 (M+H+), was prepared from 2-acenaphthen-5-yl- 4,4, 5, 5-tetramethyl-[1, 3,2] dioxaborolane and 5-chloro-3- (2-methyl-imidazol-1-yl- methyl)-pyridazine.

Example 46 3- (2-Methyl-imidazol-1-yl-methyl)-5- (2-methyl-naphthalen-1-yl)-pyridazine hydrochloride The title compound, MS: m/e = 315.3 (M+H+), was prepared from 4,4, 5, 5-tetramethyl- 2-(2-methyl-naphthalen-1-yl)-[1, 3,2] dimaborolane and 5-chloro-3- (2-methyl-imidazol- 1-yl-methyl)-pyridazine.

Example 47 5- (2-Methoxy-naphthalen-1-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 331. 3 (M+H+), was prepared from 2-(2-methoxy- naphthalen-1-yl)-4, 4,5, 5-tetramethyl-[1,3,2]dioxaborolane and 5-chloro-3- (2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 48 5- (7-Methoxy-naphthalen-2-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 331.3 (hI+H+), was prepared from 2- (7-methoxy- naphthalen-2-yl)-4, 4,5, 5-tetramethyl-[1,3,2]dioxaborolane and 5-chloro-3-(2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 49 5- (3-Methoxy-naphthalen-1-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 331.3 (M+H+), was prepared from 2- (3-methoxy- naphthalen-1-yl)-4, 4,5, 5-tetramethyl- I 3, dioxaborolane and 5-chloro-3-(2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 50 5- (4-Fluoro-naphthalen-1-yl)-3- (2-methyl-imidazol-l-yl-methyl)-pyridazine hydrochloride The title compound, MS: m/e = 319. 3 (M+H+), was prepared from 2- (4-fluoro- naphthalen-1-yl)-4, 4,5, 5-tetramethyl-[1, 3,2] dioxaborolane and 5-chloro-3- (2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 51 5- (3-Difluoromethyl-4-fluoro-phenyl)-3-imidazol-l-yl-methyl-py ridazine hydrochloride The title compound, MS: m/e = 305.2 (M+H), was prepared from 2- (3-difluoromethyl- 4-fluoro-phenyl)-4, 4,5, 5-tetramethyl-[1, 3, 2] dioxaborolane and 5-chloro-3-imidazol-1- yl-methyl-pyridazine.

Example 52 5- (3-Difluoromethyl-4-fluoro-phenyl)-3- (2-ethyl-imidazol-1-ylethyl)-pyridazine hydrochloride The title compound, MS: m/e = 333.3 (M+H*), was prepared from 2- (3-difluoromethyl- 4-fluoro-phenyl)-4, 4,5, 5-tetramethyl-[1,3, 2] dioxaborolane and 5-chloro-3- (2-ethyl- imidazol-1-ylethyl)-pyridazine.

Example 53 5- (7-Methoxy-naphthalen-1-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine The title compound, MS : m/e = 331. 4 (M+H+), was prepared from 2- (7-methoxy- naphthalen-1-yl)-4, 4,5, 5-tetramethyl-[1,3, 2] dloxaborolane and 5-chloro-3- (2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 54 5- (6-Methoxy-naphthalen-1-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine The title compound, MS: m/e = 331.4 (M+H+), was prepared from 2- (6-methoxy- naphthalen-1-yl)-4, 4,5, 5-tetramethyl-[1,3,2]dioxaborolane and 5-chloro-3-(2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 55 3- (2-Methyl-imidazol-1-yl-methyl)-5- (4-methyl-naphthalen-2-yl)-pyridazine hydrochloride

The title compound, MS: m/e = 351. 8 (M+H+), was prepared from 4,4, 5, 5-tetramethyl- 2- (4-methyl-naphthalen-2-yl)- [1, 3,2] dioxaborolane and 5-chloro-3- (2-methyl-imidazol- 1-yl-methyl)-pyridazine.

Example 56 5- (5-Methoxy-mnaphthalen-2-yl)-3-(2-methyl-imidazol-1-yl-methy l)-pyridazine The title compound, MS : m/e = 331.4 (M+H+), was prepared from 2- (5-methoxy- naphthalen-2-yl)-4, 4,5, 5-tetramethyl-[1,3,2] dioxaborolane and 5-chloro-3- (2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 57 5- (1-Methoxy-naphthalen-2-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine The title compound, MS: m/e = 331.4 (M+H+), was prepared from 2- (1-methoxy- naphthalen-2-yl)-4, 4,5, 5-tetramethyl-[1,3,2]dioxaborolane and 5-chloro-3- (2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 58 5- (2-Fluoro-3-trifluoromethyl-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 337.4 (M+H+), was prepared from 2- (2-fluoro-3- trifluoromethyl-phenyl)-4, 4,5, 5-tetramethyl-[1, 3,2] dioxaborolane and 5-chloro-3- (2- methyl-imidazol-1-yl-methyl)-pyridazine.

Example 59 3- (2-Methyl-imidazol-1-yl-methyl)-5- (4-methyl-naphthalen-1-yl)-pyridazine hydrochloride The title compound, MS: m/e = 351.9 (M+H+), was prepared from 4,4, 5,5-tetramethyl- 2- (4-methyl-naphthalen-1-yl)- [1, 3, 2] dioxaborolaneand 5-chloro-3- (2-methyl-imidazol- 1-ylmethyl)-pyridazine.

Example 60 3- (2-Methyl-imidazol-1-ylmethyl)-5-phenanthren-9-yl-pyridazine The title compound, MS: m/e = 351. 4 (M+H+), was prepared from 4,4, 5, 5-tetramethyl- 2-phenanthren-9-yl- [1, 3,2] dioxaborolane and 5-chloro-3- (2-methyl-imidazol-1-yl- methyl)-pyridazine.

Example 61 5- (3-Cyclopropyl-5-fluoro-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine

The title compound was prepared from 2- (3-cyclopropyl-5-fluoro-phenyl)-4, 4,5, 5- tetramethyl- [1, 3, 2] dioxaborolane and 5-chloro-3- (2-methyl-imidazol-1-yl-methyl)- pyridazine. (1H-NMR (300MHz, CDCt. ) 5 = 9.38 (s, 1H), 6. 80-7. 55 (m, 6H), 5.50 (s, 2H), 2.41 (s, 3H), 1.92-2. 02 (m, 1H), 1. () 2-1. 14 (m, 2H), 0. 68-0. 78 (m, 2H)) Example 62 5- (3-Cyclopropyl-4-fluoro-phenyl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine The title compound, MS: m/e = 309.4 (M+H), was prepared from 2- (3-cyclopropyl-4- fluoro-phenyl)-4,4,5,5-tetramethyl-[1,3,2] dioxaborolane and 5-chloro-3-(2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 63 5- (7-Fluoro-naphthalen-2-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine The title compound, MS: m/e = 319 (M+H+), was prepared from 7-fluoro-naphthalene- 2-boronic acid and 5-chloro-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine.

Example 64 5- (5-Fluoro-naphthalen-2-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine The title compound, MS : m/e = 319.4 (M+H), was prepared from 5-fluoro- naphthalene-2-boronic acid and 5-chloro-3- (2-methyl-imidazol-1-yl-methyl) pyridazine.

Example 65 5- (8-Fluoro-naphthalen-2-yl)-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine The title compound, MS : m/e = 319 (M+H+), was prepared from 8-fluoro-naphthalene- 2-boronic acid and 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine.

Example 66 5-Indan-5-yl-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine hydrochloride The title compound, MS : m/e = 291. 3 (M+H+), was prepared from (2, 3-dihydro-lH- inden-5-yl) boronic acid (Dack, K. N.; Whitlock, G. A. PCT Int. Appl. WO 9929667, 1999 ; Chem Abstr. 1999, 131, 44740) and 5-chloro-3- (2-methyl-imidazol-1-yl-methyl)- pyridazine.

Example 67 3-(2-Methyl-imidazol-1-yl-methyl)-5- (5, 6, 7,8-tetrahydro-naphthalen-2-yl)-pyridazine hydrochloride

The title compound, MS: m/e = 305.3 (M+H+), was prepared from 4,4, 5,5-tetramethyl- 2- (5, 6,7, 8-tetrahydro-naphthalen-2-yl)-[1, 3, 21dioxaborolane and 5-chloro-3- (2-methyl- imidazol-1-yl-methyl)-pyridazine.

Example 68 5- (3, 4-Dihydro-naphthalen-2-yl)-3-(2-methyl-imidazol-1-yl-methyl) -pyridazine hydrochloride Tetrakis (triphenylphosphine) palladium (0. 02 g, 0.017 mmol), biphenyl-2-yl- dicyclohexyl-phosphane (0.005 g, 0. 014 mmol), K3PO4 (0. 21, 1 mmol) and 3,4- dihydro-naphthalene-2-boronic acid (0.13 g, 0.7 mmol) were mixed in degassed toluene (2 ml). 5-Chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine (0.1 g, 0.48 mmol) was added and the mixture was refluxed for 24 hours. After further addition of tetrakis (triphenylphosphine) palladium (0. 02 g, 0. 017 mmol), biphenyl-2-yl- dicyclohexyl-phosphane (0.005 g, 0. 014 mmol) and 3, 4-dihydro-naphthalene-2-boronic acid (0.13 g, 0. 7 mmol) reflux was continued for another 12 hours. After removal of the solvent in vncno the residue was dissolved in AcOEt, washed with HO, dried (Na2SO4) and concentrated in vacuo. The residue was chromatographed over silica gel [gradient CH : C12 to 40 % (CH2Cl2-MeOH-NH40H 90: 10: 1)] to provide a white foam which was dissolved in MeOH (2 ml). HCl-Et2O was added to provide the title compound (0.098 g, 40 (Yo) as a light yellow solid, MS: m/e = 303. 3 (M+).

Following the general method of Example 68, the compounds of Example 69 to Example 72 were prepared.

Example 69 5- (7-Methoxy-3, 4-dihydro-naphthalen-2-yl) -3- (2-methyl-imidazol-1-yl-methyl)- pyridazine hydrochloride The title compound, MS: m/e = 333.3 (M+H), was prepared from 7-methoxy-3, 4- dihydro-naphthalene-2-boronic acid and 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)- pyridazine.

Example 70 5- (5, 7-Dimethyl-3,4-dihydro-naphthalen-2-yl)-3-(2-methyl-imidazol -1-yl-methyl)- pyridazine hydrochloride

The title compound, MS: m/e = 331.3 (M+HF), was prepared from 5, 7-dimethyl-3, 4- dihydro-naphthalene-2-boronic acid and 5-chloro-3- (2-methyl-imidazol-1-yl-methyl)- pyridazine.

Example 71 5- (5,8-Dimethyl-3, 4-dihydro-naphthalen-2-yl)-3-(2-methyl-imidazol-1-yl-methyl) - pyridazine hydrochloride The title compound, MS: m/e = 331.3 (M+H+), was prepared from 5,8-dimethyl-3, 4- dihydro-naphthalene-2-boronic acid and 5-chloro-3-(2-methyl-imidzol-1-yl-methyl)- pyridazine.

Example 72 5- (5-Methoxy-3, 4-dihydro-naphthalen-2-yl) -3- (2-methyl-imidazol-1-yl-methyl)- pyridazine hydrochloride The title compound, MS: m/e = 333.3 (M+H+), was prepared from 5-methoxy-3, 4- dihydro-naphthalene-2-boronic acid and 5-chloro-3- (2-methyl-imidazol-1-yl-methyl)- pyridazine.

Example 73 3- (3-Chloro-4-fluoro-phenyl)-5- (2-methyl-imidazol-1-yl-methyl)-pyridazine [6- (3-Chloro-4-fluoro-phenyl)-pyridazin-4-yl]-methanol (13 mg, 0.054 mmol) was dissolved in MeCI, (1 ml) under argon and a drop of DMF was added. The mixture was cooled with an icebath, thionylchloride (0. 02 ml, 0.27 mmol) was added dropwise and the reaction mixture was allowed to warm to room temperature. After 30 minutes the reaction mixture was concentrated in vacuo. The residue was dissolved in ethanol and treated with 2-methylimidazole (22.3 mg, 0.27 mmol). The reaction mixture was refluxed for 12 hours then cooled to room temperature and concentrated. Ethyl acetate and a saturated NaHCO3 solution were added.'I'he aqueous layer was extracted twice with ethyl acetate. The combined organic layers were dried over Na. ; SO. t, filtered and concentrated in vacuo. The residue was chromatographed over silica gel (CH2CI-MeOH 19: 1) to provide 3- (3-chloro-4-fluoro-phenyl)-5- (2-methyl-imidazol-1-yl-methyl)-pyridazine (4 mg, 24 %) as a light brown oil, MS: m/e = 303.2 (MI+H+).

Preparation of intermediates Example 74 5-Chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine (i- (2-Methyl-imidazol-1-ylmethyl)-lH-pyridazin-4-one (3. 9 g, 20.5 mmol) ) was treated

with phosphorus oxychloride (18 ml, 205 mmol) under argon. The mixture was stirred in a 60 °C oilbath for 1.5 hours. The solvent was removed in vacuo and the residue was dissolved in water (100 ml) under icebath cooling. The brown solution was neutralized with solid NaHCO3 and the aqueous layer was extracted with MIeCI, (6x50 ml). The combined extracts were dried over Na2SO4, filtered and the solvent was removed in vacuo to provide 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine (3.1 g 73 %) as a brown solid, MS : m/e = 209.3 (NI+H').

Following the general method of example 74, the compounds of examples 75 and 76 were prepared.

Example 75 5-Chloro-3-imidazol-1-yl-methyl-pyridazine The title compound, MS: m/e = 195.2 (M+H), was prepared from 6-imidazol-1-yl- methyl-1H-pyridazin-4-one.

Example 76 5-Chloro-3- (2-ethyl-imidazol-1-yl-methyl)-pyridazine The title compound, MS: m/e = 223.2 (NI+H+), was prepared from 6-(2-ethyl-imidazol-1- yl-methyl)-1 H-pyridazin-4-one.

Example 77 6- (2-Methyl-imidazol-1-yl-methyl)-1H-pyridazin-4-one 5-Methoxy-3- (2-methyl-imidazol-1-yl-methyl)-pyridazine (4. 25 g, 21 mmol) was dissolved in dioxane (65 ml) and 2N NaOH (42 ml) was added. The mixture was refluxed for 7 hours, cooled to room temperature and quenched with 2N HCI (65 ml). The pH was adjusted to 8 with saturated solution of NaHCO. The solvent was removed in vacuo and the residue was taken in MeOH (100 ml). After filtration, the solvent was removed in vacuo and diluted with MeOH (50 ml). Silicagel (10 g) was added and the solvent was evaporated. The residue was chromatographed over silica gel (CH2Cl2-MeOH 9: 1,4 : 1,2 : 1) to provide 6-(2-methyl-imidazol-1-methyl)-1h-pyridazin-4-one (4.1 g, 100 %) as a pale yellow solid, MS: m/e = 191. 3 (M+H+).

Following the general method of example 77 the compounds of examples 78 and 79 were prepared.

Example 78 6-Imidazol-1-yl-methyl-1 H-pyridazin-4-one The title compound, MS : m/e = 177.1 (hI+H*), was prepared from 3-imidazol-1-yl- methyl-5-methoxy-pyridazine.

Example 79 6- (2-Ethyl-imidazol-1-yl-methyl)-1H-pyridazin-4-one The title compound. N'IS : m/e = 205. 2 (M+H'), was prepared from 3- (2-ethyl- imidazol-1-yl-methyl)-5-methoxy-pyridazine.

Example 80

5-Methoxy-3-(2-methyl-imidazol-l-yl-methyl)-pyridazine (5-methoxy-pyridazin-3-yl)-methanol (5. 7 g, 40 mmol) was dissolved in MeC ! 2 (115 ml) under argon and a drop of DMF was added. The mixture was cooled with an icebath, thionylchloride (3.6 ml, 49 mmol) was added dropwise and the reaction mixture was allowed to warm to room temperature. After 30 minutes the orange solution was cooled to 0 °C, and saturated NaHCO3 solution (I 50 ml) was added dropwise. The aqueous layer was extracted twice with MeCl2, The combined organic layers were dried over Na, S04, filtered and concentrated in vacuo to provide 5.85 goda brown oil which was dissolved in dioxane (60 ml) and treated with 2-methylimidazole (6. 1 g, 74 mmol). The reaction mixture was heated at 100 °C for 2 hours then cooled to room temperature. The solvent was evaporated, and the residue was chromatographed over silica gel (CH2CI2-MeOH 19 : 1) to provide 5-methoxy-3-(2-methyl-imidazol-1-ylmethyl)-pyridazine (4.6 g, 62 %) as a light brown solid, MS: m/e = 205.3 (M+H').

Following the general method of example HO the compounds of examples 81 and 82 were prepared.

Example 81 3-Imidazol-1-yl-methyl-5-methoxy-pyridazine The title compound, MS: m/e = 191. 2 (M+H), was prepared from (5-methoxy-pyridazin- 3-yl)-methanol and imidazole.

Example 82 3- (2-Ethyl-imidazol-l-yl-methyl)-5-methoxy-pyridazine The title compound, MS: m/e = 219. 3 (M+H+), was prepared from (5-methoxy-pyridazin- 3-yl)-methanol and 2-ethylimidazole.

Example 83 (5-Methoxy-pyridazin-3-yl)-methanol 5-Methoxy-pyridazine-3-carboxylic acid ethyl ester (8. 1 g, 44. 5 mmol) was dissolved in ethanol (105 ml) under argon. The reaction mixture was cooled to 0 °C and treated with Nabi ; (3.5 g"89 mmol). After 10 minutes, the reaction mixture was warmed to room temperature, stirred for 1 hour and treated successively with 2N HCl and saturated sodium bicarbonate to adjust the pH at 8. The solvent was removed in vacuo and the residue was stirred with MeOH (100 m !). The suspension was filtered and the filtrate was concentrated. The residue was chromatographed over silica gel (CH2Cl2-MeOH 19: 1) to provide (5-methoxy-pyridazin-3-yl)-methanol (5. 2 g, 83 %) as a light brown solid, MS: m/e= = 140 (M+).

Example 84 5-Methoxy-pyridazine-3-carboxylic acid ethyl ester 3-Chloro-5-methoxy-pyridazine (Bryant, R. D.; Kunng, F. -A.; South, M. S. J. Heterocycl.

Cliciti. (1995), 32 (5), 1473-6.) (21 g, 0.145 mol), bis(triphenylphosphine) palladium dichloride (10. 2 g, 14. 5 mmol) and triethylamine (30. 5 ml, 0. 218 mol) in ethanol (420 ml)

were heated at 120 °C under a 40 bar pressure of carbon monoxide for 5 hours. The reaction mixture was cooled, filtered and concentrated in vacuo. The residue was taken in CH, C12 (200 ml), washed with H2O (twice), dried over Na, SO4 and concentrated in vacuo.

The crude solid was stirred in Et2O and filtered to provide 22.1 g of a light brown solid which was chromatographed over silica gel (hexane-ethylacetate 99 : 1 to 50: 50) to provide 5-methoxy-pyridazine-3-carboxylic acid ethyl ester (21.1 g, 80 %) as a pale yellow solid, MS : m/e = 183. 2 (M+H+).

Example 85 [6- (3-Chloro-4-fluoro-phenyl)-pyridazin-4-yl]-methanol 3-(3-Chloro-4-fluoro-phenyl)-5-methoxymethoxymethyl-pyridazi ne (0. 06 g, 0.21 mmol) was dissolved in dioxane (2 ml) and treated with 1N HCI (0.2 ml, 0.2 mmol). The reaction mixture was refluxed for 1.5 hours then cooled to room temperature. Water and ethyl acetate were added. The aqueous layer was extracted twice with ethyl acetate. The combined organic layers were dried over Na ; ; S04, filtered and concentrated in vacuo. The residue was chromatographed over silica gel (hexane-ethylacetate 1: 1 then 2: 8) to provide [6-(3-chloro-4-fluoro-phenyl)-pyridazin-4-yl]-methanol (13 mg, 26 %) as a light yellow solid, MS : m/e = 239. 2 (M+H F).

Example 86 3- (3-Chloro-4-fluoro-phenyl)-5-methoxymethoxymethyl-pyridazine 5-Chloro-3- (3-chloro-4-fluoro-phenyl)-pyridazine (535 mg, 2.2 mmol) and bis- (triphenylphosphine)-palladium (II)-dichloride (145 mg, 0. 22 mmol) were treated with a solution of tributyl-methoxymethoxymethyl-stannane (Sawyer J. S.; Kucerovy A. ; Macdonald T. L. ; McGarvey G. J. J. Am. Chem. Soc. (1988), 110, 842-853) (964 mg, 2. 64 mmol) in DMF (5.3 ml). The mixture was heated at 100 °C for 4 hours then cooled to room temperature and a saturated KF solution (5.') ml) was added. The mixture was stirred for 30 minutes at room temperature and ethyl acetate and water were added. The mixture was filtered and extracted 3 times with ethyl acetate. The combined extracts were dried over Na, SO4, filtered and the solvent was removed in vacuo. The residue was chromatographed over silica gel (hexane-ethylacetate 7: 3) to provide 3- (3-chloro-4-fluoro- phenyl)-5-methoxymethocymethyl-pyridaiine (370 mg, 60 %) as a pale yellow solid, MS: m/e = 283.0 (M+H+).

Example 87 5-Chloro-3- (3-chloro-4-fluoro-phenyl)-pyridazine The title compound, MS : m/e = 243.2 (M+), was prepared from 6- (3-chloro-4-fluoro- phenyl)-pyridazin-4-ol hydrobromide following the procedure described in example 74.

Example 88 6- (3-Chloro-4-fluoro-phenyl)-pyridazin-4-ol hydrobromide

3- (3-Chloro-4-fluoro-phenyl)-5-methoxy-pyridazine (365 mg, 1.53 mmol) in aqueous HBr (48 O/o, 3. 6 ml) was heated at 100 °C for 19 hours under argon. The solvent was removed in vacuo and the resulting solid was dissolved in MeOH. The turbid solution was filtered though decalite and the filtrate was concentrated. The crude solid was stirred in MeCl2, filtered and dried to provide (-(3-chloro-4-fluoro-phenyl)-pyridazin-4-ol hydrobromide (375 mg, 80 %) as a beige solid, MS : m/e = 225.1 (M+H+).

Example 89 3- (3-Chloro-4-fluoro-phenyl)-5-methoxy-pyridazine 3-Chloro-5-methoxy-pyridazine (Bryant, R. D.; Kunng, F.-A. ; South, MI. S. J. Heterocycl.

Cliciti. (1995), 32 (5), 1473-6.) (300 mg, 2. 08 mmol), 3-chloro-4-fluorophenylboronic acid (724 mg, 4.15 mmol), Cs2CO3 (2 g, 6. 2 mmol) and tris (dibenzylideneacetone)dipalladium chloroform complex (96. 7 mg, 0.093 mmol) were mixed and a solution of tri-tert-butylphosphine (45, 4 mg, 0.22 mmol) in degassed dioxane (6 ml) was added. The mixture was heated at 90 °C for 22 hours then cooled to room temperature, ethylacetate was added, the solid was filtered and the filtrate was concentrated in vacuo. The residue was chromatographed over silica gel (hexane-ethyl acetate 4: 1) to provide 3-(3-chloro-4-fluoro-phenyl)-5-methoxy-pyridazine (330 mg, 67 %) as an orange solid, MS: m/e = 239.3 (M+H+).

Example 90 2- (4-Chloro-3-fluoro-phenyl)-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborolane 1-13romo-4-chloro-3-fluorulbenzene (1 g, 4. 8 mmol), bis (pinacolato) diboron (1.33 g, 5. 3 mmol), potassium acetate (1. 4 g, 14. 3 mmol) and bis (triphenylphosphine) palladium dichloride (0.2 g, 0. 29 mmol) were suspense in dioxane (20 ml). The yellow suspension was flushed with argon for 30 minutes and refluxed for 12 hours. The reaction mixture was cooled to room temperature, diluted with ethyl acetate, washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was chromatographed over silica gel (hexane-ethyl acetate 99: 1) to provide 2- (4-chloro-3-fluoro-phenyl)-4, 4,5, 5-tetramethyl- [1, 3, 2 dioxaborolane (0. 7 g, 59 %) as a colorless oil, MS : m/e = 256.2 (M).

Following the general method of example 90, the compounds of examples 91 to example 133 were prepared.

Example 91 2- (4-Fluoro-3-trifluoromethyl-phenyl)-4, 4,5, 5-tetramethyl-[1, 3, 2] dioxaborolane

The title compound, MS: m/e = 290.1 (M+), was prepared from 5-brom-2- fluorobenzotrifluoride.

Example 92 2- (4-Chloro-3-trifluoromethyl-phenyl)-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborolane The title compound, MS : m/e = 306. 1 (M+), was prepared from 5-bromo-2- chlorobenzotrifluoride.

Example 93 2-(3-Difluoromethyl-4-fluoro-phenyl)-4, 4,5, 5-tetramethyl- [ 1, 3,2] dioxaborolane The title compound, MS: m/e = 272.1 (M+), was prepared from 4-bromo-2- difluoromethyl-1-fluoro-benzene.

Example 94 2- (3-Fluoro-5-trifluoromethyl-phenyl)-4, 4,5, 5-tetramethyl- [ 1, 3,2] dioxaborolane The title compound, MS: m/e = 290. 1 (M+), was prepared from 3-bromo-5- fluorobenzotrifluoride.

Example 95 2- [3-(1,1-Difluoro-ethyl)-phenyl]-4, 4,5, 5-tetramethyl-[1, 3, 2] dioxaborolane The title compound, MS: m/e = 268, 2 (M+), was prepared from 1-bromo-3- (l, l- difluoro-ethyl)-benzene.

Example 96 2-Benzo [b]thiophen-5-yl-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborolane The title compound, MS : m/e = 260. 1 (1\1'), was prepared from 5-bromo- benzo[b]thiophene(Ple, P. A.; Marnett, L. J. J. Hetecocycl. Chem. (1988), 25 (4), 1271-2).

Example 97 2- (3-Difluoromethyl-phenyl)-4, 4,5, 5-tetramethyl- [ 1, 3, 2] dioxaborolane

The title compound, MS: m/e = 254.2 (M+), was prepared from l-bromo-3- difluoromethyl-benzene.

Example 98 2- (4-Chloro-3-methyl-phenyl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS : m/e = 252.1 (M'), was prepared from 5-bromo-2- chlorotoluene.

Example 99 2- (3-Methoxy-5-trifluoroemthyl-phenyl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS: m/e = 302.1 was prepared from 1-bromo-3-methoxy-5- trifluoromethyl-benzene.

Example 100 2- [4-Chloro-3-(1,1-difluoro-ethyl)-phenyl]-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborolane The title compound, MS: m/e = 302.1 was prepared from 4-bromo-1-chloro-2- (1, 1-difluoro-ethyl)-benzene.

Example 101 2- (4-Chloro-3-methoxy-phenyl) -4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborolane The title compound, MS : m/e = 268. 1 (\1'), was prepared from 4-bromo-1-cloro-2- methoxy-benzene.

Example 102 2- (3-Isopropyl-phenyl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS : m/e = 246.2 was prepared from 1-brom-3- isopropylbenzene.

Example 103 2- (7-Methoxy-naphthalen-1-yl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane

The title compound, MS: m/e = 284. 2 (M''), was prepared from 1-bromo-7-methoxy- naphthalene.

Example 104 2- [3- (1, 1-Difluoro-ethyl)-4-fluoro-phenyl]-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, hIS : m/e = 2S6. 2 (M+), was prepared from 4-bromo-2-(1, 1- difluoro-ethyl)-1-fluoro-benzene (prepared according to EP Application No.

01101947. 8).

Example 105 4,4, 5,5-Tetramethyl-2- (3-vinyl-phenyl)- [ 3, 2] dioxaborolane The title compound, MS : m/e = 230.2 (M+), was prepared from 3-bromostryene.

Example 106 2- (3-Fluoro-5-vinyl-phenyl) -4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compoundwas prepared from 3-bromo-5-fluoro-stryene. 1H-NMR (300MHz, CECI) : # = 7.6 (s, 1H), 7.32-7. 40 (m, 1 H), 7. 16-7. 26 (m, 1H), 6.70 (dd, 1H), 5. 82 (d, 1H), 5.29 (d, 1H), 1.35 (s, 12H).

Example 107 2- (4-Fluoro-3-vinyl-phenyl)-4, 4,5, 5-Tetramethyl- [1, 3, 2] dioxaborolane The title compound was prepared from 3-bromo-6-fluoro-stryene. 1H-NMR (300MHz, CECI.) : # = 7.90-7.96 (m, 1H), 7. 64-7. 70 (m, 1H), 7.03 (dd. 1H), 6.85 (dd, 1H), 5.82 (d, 1H), 5.28 (d, lH), 1. 35 (s, 12H).

Example 108 2- (3-Difluoromethyl-5-fluoro-phenyl)-4,4, 5,5-tetramethyl- [1, 3,2] dioxaborolane The title compound, hIS : m/e = 272 (M+), was prepared from l-bromo-3- difluoromethyl-5-fluorobenzene.

Example 109 2-(4-Chloro-3-difluoromethyl-phenyl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS: m/e = 288. 1 (M+), was prepared from 4-bromo-1-chloro-2- difluoromethyl-benzene.

Example 110 2- (6-Methoxy-naphthalen-2-yl) -4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS: m/e = 284.2 was prepared from 2-bromo-6-methoxy- naphthalene (commercially available).

Example 111 2-(6-Difluoromethyl-naphthalen-2-yl)-4,4,5,5-tetramethyl-[1, 3,2] dioxaborolane The title compound, MS: m/e = 304.2 (M'), was prepared from 2-bromo-6- difluoromethylnaphthalene.

Example 112 2- [3- (1, 1-Difluoro-ethyl)-5-fluoro-phenyl]-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborolane The title compound, MS : m/e = 286.2 (M+), was prepared from 1-bromo-3- (l, l- ditluoro-ethyl)-5-fluoro-benzene.

Example 113 2- (5-Difluoromethyl-thiophen-3-yl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS: m/e = 260.3 (M'), was prepared from 4-bromo-2- dinuoromethyl-thiophene.

Example 114 2- (3-tert-Butyl-phenyl)-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborolane The title compound, MS : m/e = 260 (MI'), was prepared from 2-bromo-3-tert- butylbenzene (prepared according to patent EP 627400).

Example 115 2- (5-Methoxy-naphthalen-1-yl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS: m/e = 284. 2 (M'), was prepared from 1-bromo-5-methoxy- naphthalene.

Example 116 2- (7-Difluoromethyl-naphthalen-2-yl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS: m/e = 304 (M+), was prepared from 2-brom-7- difluoromethylnaphthalene.

Example 117 2- (7-Ethoxy-naphthalen-2-yl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS: m/e = 298 (M+), was prepared from 2-bromo-7- ethoxynaphthalene.

Example 118 2- (4-Methoxy-naphthalen-1-yl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS : m/e = 284 (M'), was prepared from 1-bromo-4-methoxy- naphthalene.

Example 119 2-Acenaphthen-5-yl-4,4, 5,5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS : m/e = 280 (M+), was prepared from 5-bromoacenaphthalene.

Example 120 4,4, 5, 5-Tetramethyl-2-(2-methyl-naphthalen-1-yl)-[1, 3,2] dioxaborolane The title compound, MS : m/e = 286 (M'). was prepared from 1-bromo-2-methyl- naphthalene.

Example 121 2- (2-Methoxy-naphthalen-1-yl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS : m/e = 284 (M+), was prepared from 1-bromo-2-methoxy- naphthalene.

Example 122 2- (7-Methoxy-naphthalen-2-yl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS: m/e = 284 (M'). was prepared from 2-bromo-7- methoxynaphthalene.

Example 123 2-(3-Methoxy-naphthalen-1-yl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS: m/e = 284 (M'), was prepared from 1-bromo-3-methoxy- naphthalene.

Example 124 2-(4-Fluoro-naphthalen-1-yl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS : m/e = 272 (M+), was prepared from 1-brom-4- fluoronaphalene Example 125 2- (7-Methoxy-naphthalen-1-yl)-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborolane The title compound was prepared from l-bromo-7-methoxynaphalene. 1H-NMR (300MHz, CDCl3) : 8 = 8.22 (s, 1H), 8. () 2 (d, 1H), 7. 84 (d, 1H), 7.72 (d, 1H), 7.33 (t, 1H), 7. 16 (s, 1H), 3. 94 (s, 3H), 1.42 (s, 12H).

Example 126 2- (6-Methoxy-naphthalen-1-yl)-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborolane The title compound was prepared from 1-Uromo-6-methovynaphalene (prepared according to patent WO 9000164A1). 1H-NMR (300MHz, CDCl3) : # = 8. 67 (d, 1H), 7.91

(d, 1H), 7.82 (d, 1H), 7.73 (d, 1H), 7.43 (t, 1H), 7.10-7. 22 (m, 1H), 3.92 (s, 3H), 1.42 (s, 12H).

Example 127 4,4, 5, 5-Tetramethyl-2- (4-methyl-naphthalen-2-yl)- [1, 3,2] dioxaborolane The title compound, MS : m/e = 268 (M+), was prepared from 2-bromo-6- methylnaphalene (prepared according to patent WO 0064891A1).

Example 128 2- (5-Methoxy-naphthalen-2-yl)-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborolane The title compound, MS : m/e = 284 (M'), was prepared from 2-bromo-5- methoxynaphalene (prepared according to patent WO 0064891A1).

Example 129 2- (1-Methoxy-naphthalen-2-yl)-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborolane The title compound, MS : m/e = 284 (M+), was prepared from 2-brom-1- methoxynaphalene.

Example 130 2- (2-Fluoro-3-trifluoromethyl-phenyl)-4, 4,5, 5-tetramethyl- [1, 3,2] dioxaborolane The title compound, MS : m/e = 290 (M+), was prepared from 3-bromo-2- tluorobenzotrifluoride (commercially available).

Example 131 4,4, 5, 5-Tetramethyl-2-(4-methyl-naphthalen-1-yl)-[1, 3,2] dioxaborolane The title compound, MS : m/e = 268 (M+), was prepared from l-bromo-4- methylnaphthalene (commercial available).

Example 132 4,4, 5,5-Tetramethyl-2-phenanthren-9-yl- [1, 3,2] dioxaborolane

The title compound, MS: m/e = 304 (MF), was prepared from 9-bromophenanthrene (commercially available).

Example 133 4,4, 5, 5-Tetramethyl-2- (5, 6,7, 8-tetrahydro-naphthalen-2-yl)- [1, 3, 2] dioxaborolane The title compound, MS : m/e = 258.3 (1\1), was prepared from trifluoro- methanesulfonic acid 5,6, 7, 8-tetrahydro-naphthalen-2-yl ester (Han, X.; Stoltz, B. M. ; Corey, E. J. J. Am. Chem. Soc. 1999, 121, 7600-7605).

Example 134 2- (3-Cyclopropyl-phenyl) -4, 4,5, 5-tetramethyl-[1, 3, 2] dioxaborolane To a solution of4, 4,5, 5-tetramethyl-2- (3-vinyl-phenyl)- [1, 3, 2] dioxaborolane (300 mg, 1.3 mmol) in toluene (10 ml) were added diethylzinc solution (1.1 N in toluene, 5.22 ml, 5.74 mmol) and diiodomethane (8. 7 ml, 33 mmol). The reaction mixture was stirred for 1 hour at room temperature and then refluxed for 3 hours. The reaction mixture was poured on sat. NH4Cl solution (20 ml) and was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo to provide 2- (3-cyclopropyl-phenyl)-4, 4,5, 5-tetramethyl- [L3, 2] dioxaborolane (69 % yield), 1H-NMR (300 MHz, CDCl3) : 5 = 7.12-7. 82 (m, 4H), 1.35 (s, 12H), 1.28 (t, lH), 0. 90-0. 96 (m, 2H), 0. 72-0. 78 (m, 2H).

Following the general method of example 134 the compounds of examples 135 and 136 were prepared.

Example 135 2- (3-Cyclopropyl-4-fluoro-phenyl)-4, 4,5, 5-tetramethyl- [1, 3, 2] dioxaborolane The title compound, MS: m/e = 262 (M'). was prepared from 2- (4-fluoro-3- vinylphenyl)-4, 4,5, 5-tetramethyl-[1,3,2]dioxaborolane following the procedure described in example 134.

Example 136 2- (3-Cyclopropyl-5-fluoro-phenyl)-4, 4, 5, 5-tetramethyl- [ 1, 3,2] dioxaborolane

The title compound, MS: m/e = 262 (A4F), was prepared from 2- (5-fluoro-3- vinylphenyl) -4,4, 5, 5-tetramethyl- [1, 3, 2]dioxaborolane following the procedure described in example 134.

Example 137 3, 4-Dihydro-naphthalene-2-boronic acid A solution of 3-bromo-1, 2-dihydro-naphthalene (7. 7g, 37 mmol) (Adamczyk, M.; Watt, D. S.; Netzel, D. A. J. Org. Chem. 1984, 49, 4226-4237) in diethylether (370 ml) was cooled in a dry ice bath and tert.-butyllithium solution (50 ml of a 1.5 M solution in pentane) was added maintaining T < -65 °C. At this temperature stirring was continued for 30 min, then triisopropylborate (17.3 ml, 75 mmol) was added. The reaction mixture was brought to rt and treated with 3N HCI (100 ml). After 15 min the organic phase was dried (Na2SO4), evaporated and precipitated with pentane to provide the title compound (3.83 g. 60 O/o) as a white solid material. hIS : m/e= 173 (M-H-).

Following the general method of Example 137 the compounds of Examples 138 to Example 144 were prepared.

Example 138 5-Fluoro-naphthalene-2-boronic acid The title compound was obtained by reaction of 2-bromo-5-fluoro-naphthalene with tert.-butyllithium solution followed by triisopropylborate and HCI. MS: m/e = 189 (M').

Example 139 8-Fluoro-naphthalene-2-boronic acide The title compound was obtained by reaction of2-bromo-8-fluoro-naphthalene with tert.-butyllithium solution followed by triisopropylborate and HCI. MS: m/e = 189 (M-).

Example 140 7-Fluoro-naphthalene-2-boronic acid The title compound was obtained by reaction of 2-bromo-7-fluoro-naphthalene with tert.-butyllithium solution followed by triisopropylborate and HCI. 1H-NMR (300 MHz, DMSO) : # = S. 35 (s, 1H), 8.22 (br. s, 2H), 7. 82-8. 04 (m, 3H), 7.69 (d, 1H), 7.44 (t, 1H).

Example 141 7-Methoxy-3,4-dihydro-naphthalene-2-boronic acid The title compound was obtained as a white solid material by reaction of 3-bromo-6- methoxy-l, 2-dihydro-naphthalene with tert.-butyllithium solution followed by triisopropylborate and 3N HCI. MS: m/e= 263 (MI+OAc-).

Example 142 5,7-Dimethyl-3, 4-dihydro-naphthalene-2-boronic acid The title compound was obtained as a white solid material by reaction of 3-bromo-6, 8- dimethyl-1, 2-dihydro-naphthalene with tert.-butyllithium solution followed by triisopropylborate and 3N HCI. MS : m/e= 261 (M+OAc-).

Example 143 5, 8-Dimethyl-3, 4-dihydro-naphthalene-2-boronic acid The title compound was obtained as a white crystalline material by reaction of 3-bromo- 5, 8-dimethyl-1, 2-dihydro-naphthalene with tert.-butyllithium solution followed by triisopropylborate and 3N HCI. hIS : m/e= 261 (M+OAc).

Example 144 5-Metho. xy-3, 4-dihydro-naphthalene-2-lroronic acid The title compound was obtained as a white crystalline material by reaction of 3-bromo- 8-methoxy-1, 2-dihydro-naphthalene with tert.-butyllithium solution followed by triisopropylborate and 3N HCI. MS : m/e= 203 M-H-).

Example 145 4-Bromo-2-difluoromethyl-l-flloro-benzene 5-Bromo-2-fluorobenzaldehyde (2 g, mmol) in CH2Cl2 (50 ml) was treated at 0 °C with (diethylamino) sulfur trifluoride (2 ml, 14.8 mmol). The reaction mixture was refluxed overnight and then quenched with saturated solution of NaHCOx. The aqueous phase was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4, tìltered and concentrated in vacuo. The residue was chromatographed over silica gel (hexane-ethyl acetate 99 : 01) to provide 4-bromo-2-

difluoromethyl-1-fluoro-benzene (1. 55 g, 70 %) as a colorless oil, MS: m/e = 226.0 (M+H+).

Following the genera ! method of Example 145 the compounds of Examples 146 to Example 152,157 and 159, were prepared.

Example 146 l-Bromo-3-(1, 1-difluoro-ethyl)-benzene The title compound, MS : m/e = 221. 0 (M'), was prepared from 3-bromoacetophenone (commercially available).

Example 147 1-Bromo-3-difluoromethyl-benzene The title compound, MS: m/e = 207. 0 (M), was prepared from 3-bromo-benzaldehyde (commercially available).

Example 148 4-Bromo-1-chloro-2- (1, 1-difluoro-ethyl)-benzene The title compound, MS : m/e = 255.4 (M+), was prepared from 1-(5-bromlo-2-chloro- phenyl)-ethanone (prepared according to patent : DD 236726).

Example 149 1-Bromo-3-difluoromethyl-5-fluorobenzene The title compound, MS: m/e = 272 (M+), was prepared from 3-bromo-5-fluoro- benzaldehyde (prepared according to patent WO 0066556).

Example 150 4-Bromo-2-difluoromethyl-thiophene The title compound, MS : m/e = 214. 0 (M+H+), was prepared from 4-bromothiophen-2- carbaldehyde (commercially available).

Example 151 2-bromo-6-difluoromethylnaphthalene The title compound, MS: m/e = 258 I+Hi), was prepared from 2-bromo-6- carbaldehyde-naphthalene (prepared according to patent WO 9833778).

Example 152 1-B romo-3- (1, 1-difluoro-ethyl)-5-fluoro-benzene The title compound was prepared from l- (3-bromo-5-fluoro-phenyl)-ethanone. 1H- NMR (300MHz, CDCIs) : # = 7.44 (s, 1H), 7.31 (d, 1H), 7.16 (d, 1H), 1.90 (t, 3H).

Example 153 1- (3-Bromo-5-fluoro-phenyl)-ethanone To a solution of 1- (3-bromo-5-fluoro-phenyl)-ethanol (2.9 g, 13. 2 mmol) in methylene chloride (150 ml) was added at room temperature pyridinium dichromate (3.98 g). The reaction mixture was stirred for 4 hours at room temperature and the solvent was removed in the presence of silica gel. The crude product was purified by chromatography over silica gel to provide 1-(3-bromo-5-fluoro-phenyl)-ethanone (1.39 g, 45 %) as a light yellow solid, MS : m/e = 216. 1 (Mi).

Example 154 1- (3-Bromo-5-fluoro-phenyl)-ethanol To a solution of3-bromo-5-nuorobenxaldehyde (6. 0 g, 29. 6 mmol, prepared according to patent WO 0066556) in THF (100 ml) was added dropwise at 0 °C methylmagnesiumchloride (3N in THF, 12 ml). The reaction mixture was stirred for 3 hours at room temperature and then sat. NH4CI solution was added. The aqueous phase was extracted twice with ethyl acetate. The combined organic layers were washed with water, dried over MgSO.,, filtered and the solvent was removed in vacuo. The crude product was purified by chromatography over silica gel to yield 1- (3-bromo-5-fluoro- phenyl)-ethanol (2.9 g, 45 %), 1H-NMR (300MHz, CDCl3): # = 7.31 (s, 1H), 7.14 (d, lH), 7.04 (d, 1H), 4. 82-4. 94 (m, 1H), 1.51 (d, 3H).

Example 155 4-Bromo-1-chloro-2-difluoromethyl-benzene To a solution of NaNO2 0. 59 g, 8.6 mmol) in sulfuric acid (6 mi) and acetic acid (7 ml) was added portionwise under cooling 4-chloro-3-difluoromethyl-phenylamine (1.5 g, 8. 4 mmol). This mixture was added dropwise to a vigorously stirred solution of CuBr in HBr at 0 °C. The mixture was stirred for 45 min at room temperature and then poured on ice- water. The aqueous phase was extraction with CH2Cl3. The combined organic layers were dried over MgSO4, the solvent was removed under reduced pressure to provide 4-bromo- l-chloro-2-difluoromethyl-benzene (64 %), MS : m/e = 242. 0 (MI+1).

Example 156 4-Chloro-3-difluoromethyl-phenylamine To a suspension of iron powder (16 g) in acetic acid (95 ml) was added 1-chloro-2- difluoromethyl-4-nitro-benzene (5. 1 g, 15 mmol) and the reaction mixture was heated to 115 °C for 15 minutes. The mixture was filtered and the residue was washed with acetic acide and CH2Cl2. Evaporation of the solvent gave the crude product. It was further purified by chromatography over silica gel to give 4-chloro-3-difluoromethyl- phenylamine (76%). MS : m/e = 177.1 (M+).

Example 157 I-Chloro-2-difluoromethyl-4-nitro-benzene The title compound, MS : m/e = 207. 0 (M+), was prepared from 2-chloro-5- nitrobenxaldehyde following the procedure described in example 145.

Example 158 1-Bromo-5-methoxy-naphthalene A suspension of l-bromo-5-hydroxy-n. lphthalene (1. 56 g. 7.0 mmol, prepared according to patent WO0146181), K2CO3 (1.45 g. 10. 5 mmol), tetrabutylammonium chloride (15 mg. 0. 05 mmol) and dimethyl sulfate (1. s2 ml, 10.5 mmol) i MeCN was refluxed for 1 hour. After the addition of water, the aqueous phase was extracted three times with CH2Cl2. The combined organic layers were washed with water, dried over MgSO4, filtered and the solvent was removed under reduced to provide 1-bromo-5-methoxy- naphthalene (1. 05 g, 64 %) as a white solid, MS : m/e = 236 (M+).

Example 159 2-bromo-7-difluoromethyl-naphthalene The title compound, MS: m/e = 256 (M+), was prepared from 7-bromo-2-naphthalene- carbaldehyde following the procedure described in example 145.

Example 160 7-Bromo-2-naphthalene-carbaldehyde To a solution of 7-bromo-naphthalene-2-yl) methanol (1.37 g, 5. 8 mmol) in CH2Cl2 was reacted (according to A. J. Mancuso and D. Swern, Synthesis, 1981,165) with oxalylchloride (0. 55 ml, 6 mmol), DMSO (0.9 ml, 13 mmol) and NEts (0. 73 ml, 29 mmol) to provide 7-bromo-2-naphthalene-carbaldehyde (quantitative yield), MS: m/e = 234 (M').

Example 161 7-Bromo-naphthalene-2-yl-methanol To a solution of 7-bromo-naphthalene-2-carboxylic acid methyl ester (1.4 g, 5.3 mmol, prepared according to patent EP 483667 A2) in THF (50 ml) was added DIBAL-H (15.8 ml, 1 M solution in THF) and the reaction mixture was stirred for I hour. After workup, 7-bromo-naphthalene-2-yl-methanol was ontained in quantitative yield, MS: m/e = 236 (1\v1') Example 162 2-Bromo-7-ethoxynaphthalene To a solution of 7-bromo-naphth-2-ol (1.0 g. 4. 5 mmol, prepared according to patent WO 0146187 Al) in acetonitrile (10 ml) was added diethyl sulfate (1.04 g, 6. 7 mmol), KCO (0. 92 g) and tetrabutylammonium bromide (10 mg). The reaction mixture was refluxed for 1 hour, poured on water and extracted with CH2Cl2 The combined organic layers were dried over MgSO4, filtered and the solvent was removed under reduced pressure to provide 2-bromo-7-ethoxynaphthalene (89 %), MS : m/e = 252 (M+).

Example 163 2-Bromo-7-methoxynaphthalene The title compound, MS : m/e = 236 (M'), was prepared from 7-bromo-naphth-2-ol and dimethylsulfate following the procedure described in example 162.

Example 164 1-Bromo-3-methoxy-5-trifluoromethyl-benzene The title compound, MS: m/e = 254 (M1 +), was prepared from 5-methoxy-3- (trifluoromethyl)-aniline following the procedure described in example 155.

Example 165 2-Bromo-8-fluoro-naphthalene To a solution of BF-etherate (0. 86 ml, l. 25 M in THF, 6. 5 mmol) in 12 ml dimethoxyethane was added at-5 °C a solution of 8-amino-2-bromo-naphthalene (1.20 g, 5. 4 mmol) in dimethoxyethane (12 ml) over a periode of 35 min. After 1 hour a solution of tert-butylnitrite (0.62 ml, 5.4 mmol) in dimethoxyethane (24 ml) was added and the mixture was stirred for two hours at r. t. and the solvent was removed under reduced pressure. Chlorbenzene (120 ml) was added and the reaction mixture was refluxed for 50 min and the mixture was concentrated. The solid was diluted in methylene chloride and washed with NaHCO. The organic phase was dried over MgSO4, filtered and reduced to give the crude product. Chromatography on silica gel (hexane) afforded 721 mg (59 %) of the product as a brown oil. MS : m/e = 242 (M+).

Example 166 8-Amino-2-bromo-naphthalene To a suspension of iron powder (1. 6wog) in 25 ml water and 25% HCL (1.7 ml) was added 2-bromo-8-nitro-naphthalene (2.15 g, dz 5 mmol) and the reaction mixture was refluxed for 2 hours. The aqueous phase was extracted with ethyl acetate to give the crude product. Chromatography on silica gel (hexane/ethyl acetate 1/9 to 2/3) afforded 1.17 g (62'po) of the product as brown oil. MS : m/e = 222.2 (M+).

Example 167 2-Bromo-8-nitro-naphthalene A solution of 2-bromonaphthalene (11. 4 g, 55mmol) in nitric acide (40 ml) and acetic acide (40 ml) was heated to 60 °C for 2 hours and then poured on ice. The mixture was filtered and a yellow solid was obtained. The mixture of mono-nitrated products was separated by chromatography on silica gel (hexane: toluene 95 : 5) to give 2.15 g (15 %) of the title product as yellow solid, MS : m/e = 251 (M+). <BR> <BR> <BR> <P> Example 168<BR> <BR> <BR> <BR> 2-Bromo-5-fluoro-naphthalene

The title compound, MS: m/e = 224 (M"), was prepared from 5-amino-2-bromo- naphthalene following the procedure described in example 165.

Example 169 5-Amino-2-bromo-naphthalene The title compound, MS: m/e = 222 (M+), was prepared from 2-bromo-5-nitro- naphthalene following the procedure described in example 166.

Example 170 2-Bromo-5-nitro-naphthalene The title compound, MS: m/e = 251 (M+), was prepared from 2-bromo-naphthalene following the procedure described in example 167.

Example 171 2-Bromo-7-fluoronaphthalene The title compound, MS : m/e = 224 (M'). was prepared from 7-amino-2-bromo- naphthalene following the procedure described in example l f 5.

Example 172 7-Amino-2-bromo-naphthalene The title compound was prepared from 2-bromo-7-nitro-naphthalene following the procedure described in example 166. 1 H-NMR (300 MHz, CDCh) : 8 = 7.72 (s, 1H), 7.61 (d, 1H), 7.54 (d, 1H), 7.27 (d, 1H), 6. 93 (d. 1H), 6. 86 (s, IH), 3. 90 (br. s, 2H).

Example 173 2-Bromo-7-nitro-naphthalene To a solution of NaN2 (1.1 g, 24mmol) in sulfuric acid (8.4 ml) was added at 0 °C acetic acid (8.9 ml) and 7-amino-2-nitro-naphthalene (2.1 g, 11 mmol). This solution was added to a suspension of CuBr (2. 5 g, 39mmol) in conc. HBr (16 ml) at 0 °C and the mixture was stirred for 1 hour. The mixture was poured on ice and the aqueous phase was extracted with methylene chloride. The crude product was purified by

chromatography to give 1. 9 g (7.4 mmol, 51 %) of the title compound, MS: m/e = 251.2 (M+).

Example 174 7-Amino-2-nitro-naphthalene A suspension of 2,7-dinitro-naphthalene in ethylacetate (400ml) and DMF (4 ml) was hydrogenated over P/C at 50 °C for 2 hours. After work-up and purification by chromatography 2.1 g (11. 2 mmol, 24''o) of the title compound, hIS : m/e = 251 (Mt) was obtained.

Example 175 4-Bromo-1-fluoro-2-vinylbenzene To a suspension of methyl (triphenyl)-phosphonium bromide (15.5 g, 43 mmol) in THF (60 ml) were added at-78 °C BuLi (27 ml, 1. 6 NI in hexane, 43. 2 mmol) and 5-bromo- 2-fluoro-benraldehyde (877mg, 43 mmol). The reaction mixture was stirred 18 hours at r. t. After work-up and purification by chromatography (hexane/ethyl acetate 9/1 to 4/1) 5. 7 (28. 5 mmol, 72 %) of the title compound were obtained, 1H-NMR (300 MHz, CDCb) : 5 = 7. 62 (dd, 1H), 7. 26-7. 36 (m, 1H), 6.93 (t, 1H), 6.79 (dd, 1H), 5.82 (d, 1H), 5.42 (d, 1H).

Example 176 5-Bromo-1-fluoro-3-vinylbenzene The title compound, MS: m/e = 200 (M+). was prepared from 5-bromo-3- fluorobenzaldehyde following the procedure described in example 175.

Example 177 3-Bromo-6-methoxy-1, 2-dihydro-naphthalene Following the Adamcyk-Netzel protocol (Adamczyk, M. ; Watt, D. S.; Netzel, D. A. J.

Org. Clietit. 1984, 49, 4226-4237), the title compound was obtained as a colorless oil by reaction of 7-methoxy-1-tetralone first with bromine, then with sodium borohydride and finally with p-toluenesulfonic acid. 1H-Nmr (250 MHz, CDCl3) : 8 = 2.76 and 2.86 each:

(mc, 2H, CH2), 3.76 (s, OCH3), 6.54 (d,/= 3 Hz, 1H, arom-H), 6.68 (dd, J = 8 Hz, J = 3 Hz, 1H, arom-H), 6.75 (s, 1H, CH=CBr), 7.00 (d, J = 8Hz, 1H, arom-H).

Following the general method of Example 177, the compounds of Examples 178 to 180 were prepared.

Example 178 3-Bromo-6, 8-dimethyl-1, 2-dihydro-naphthalene The title compound was obtained as a colorless oil by reaction of 5, 7-dimethyl-1- tetralone with bromine, sodium borohydride and p-toluenesulfonic acid. MS: m/e= 236 (M+).

Example 179 3-Bromo-5, 8-dimethyl-1, 2-dihydro-naphthalene The title compound was obtained as a colorless oil by reaction of 5, 8-dimethyl-1- tetralone with bromine, sodium borohydride and p-toluenesulfonic acid. MS: m/e= 236 (M+).

Example 180 3-Bromo-8-methoxy-1, 2-dihydro-naphthalene The title compound was obtained as a colorless oil by reaction of 5-methoxy-1-tetralone with bromine, sodium borohydride and p-toluenesulfonic acid.'H-Nmr (250 MHz, CECI,) : # = 2.74 and 2.94 each: (mc, 2H, CH2), 3. 82 (s, 3H, OCH3), 6.62 (d, J = 8 Hz, 1 H, arom-H), 6. 75 (s, 1H, CH=CBr), 6.76 (d, J = 8 Hz, 1H, arom-H), 7.11 (t, J = 8Hz, 1 H, arom-H).

Example A Tablet Formulation (Wet Granulation) Item Ingredients mg/tablet 5 mg 25 mg 100mg 500mg 1. Compound of formula 1 5 25 100 500 2. Lactose Anhydrous DTG 125 105 30 150 3. Sta-Rxl500 6 6 6 30 4. Microcrystalline Cellulose 30 30 30 150 5. Magnesium Stearate 1 1 1 1 Total 167 167 167 831 Manufacturing Procedure Mix items 1,2, 3 and 4 and granulate with purified water.

2. Dry the granulation at 50 °C.

3. Pass the granlation through suitable milling equipment.

4. Add item 5 and mix for three minutes ; compress on a suitable press.

Example B Capsule Formulation Item Ingredients mg/capsule 5 mg 25mg 100mg 500mg 1. Compound of formula 1 5 25 100 500 2. Hydrous Lactose 159 123 14S--- 3. Corn Starch 25 35 40 70 4. Talc 10 15 10 25 5. Magnesium Stearate 1 2 2 5 Total 200 200 300 600 Manufacturing Procedure 1 Mix items 1,2, and 3 in a suitable mixer for 30 minutes.

2. Add items 4 and 5 and mix for 3 minutes.

3. Fill into a suitable capsule.

4. Add item 5 and mix for three minutes; compress on a suitable press.