Title of Invention	1H-IMIDAZOLE DERIVATIVES HAVING CB1 AGONISTIC, CB1 PARTIAL AGONISTIC OF CB1-ANTAGONISTIC ACTIVITY
Abstract	The present invention relates to a group of novel IH-imidazole derivatives, to methods for the preparation of these compounds, and to pharmaceutical compositions containing one or more of these compounds as an active component. These 1 H- imidazole derivatives are potent cannabinoid-CB<SUB>1</SUB> receptor agonists, partial agonists or antagonists, useful for the treatment of psychiatric and neurological disorders, as well as and other diseases involving cannabinoid neurotransmission. The compounds have the general formula (I) wherein R and R1-~ have the meanings given in the specification.

Title of Invention

1H-IMIDAZOLE DERIVATIVES HAVING CB1 AGONISTIC, CB1 PARTIAL AGONISTIC OF CB1-ANTAGONISTIC ACTIVITY

Abstract

The present invention relates to a group of novel IH-imidazole derivatives, to methods for the preparation of these compounds, and to pharmaceutical compositions containing one or more of these compounds as an active component. These 1 H- imidazole derivatives are potent cannabinoid-CB<SUB>1</SUB> receptor agonists, partial agonists or antagonists, useful for the treatment of psychiatric and neurological disorders, as well as and other diseases involving cannabinoid neurotransmission. The compounds have the general formula (I) wherein R and R1-~ have the meanings given in the specification.

Full Text	1H-lmidazole derivatives having CB1 agonistic, CB-1 partial agonistic or CB-r antaqonistic activity The present invention relates to a group of novel 1H-irnidazo!e derivatives, to methods for the preparation of these compounds, and to pharmaceutical compositions containing one or more of these compounds as an active component. These 1H-imidazoie derivatives are potent cannabinoid-CB1receptor agonists, partial agonists or antagonists, useful for the treatment of psychiatric and neurological disorders, as well as and other diseases involving cannabinoid neurotransmission. Cannabinoids are present in the Indian hemp Cannabis sativa and have been used as medicinal agents for centuries (Mechoulam, R. and Feigenbaum, J. J. Prog. Med. Chem. 1987, 24, 159). However, only within the past ten years the research in the cannabinoid area has revealed pivotal information on cannabinoid receptors and their (endogenous) agonists and antagonists. The discovery and the subsequent cloning of two different subtypes of cannabinoid receptors (CB1and CB2) stimulated the search for novel cannabinoid receptor antagonists (Munro, S. et a/., Nature 1993, 365, 61. Matsuda, L A. and Bonner, T. i. Cannabinoid Receptors, Pertwee, R. G, Ed. 1995, 117, Academic Press, London). In addition, pharmaceutical companies became interested in the development of cannabinoid drugs for the treatment of diseases connected with disorders of the cannabinoid system (Consroe, P. Neurobiology of Disease 1998, 5, 534. Pop, E. Curr. Opin. In CPNS Investigational Drugs 1999, 7, 587. Greenberg, D. A. Drug News Perspect. 1999, 72, 458. Pertwee, R.G., Progress in Neurobiology 2001, 63, 569). Hitherto, several CB^ receptor antagonists are known. Sanofi disclosed their diarylpyrazole congeners as selective CB1receptor antagonists. A representative example is SR-141716A (Dutta, A.K. et a/., Med. Chem. Res. 1994, 5, 54. Lan, R. et at., J. Med Chem. 1999, 42, 769. Nakamura-Paiacios, E. M. et a/., CNS Drug Rev. 1999, 5, 43). CP-272871 is a pyrazole derivative, like SR141716A, but less potent and less CB1receptor subtype-selective than SR141716A (Meschler, J. P. et at., Biochem. Pharmacol. 2000, 60, 1315). Aminoalkylindoles have been dis-closed as CB1 receptor antagonists. A representative example is lodopravadoiine (AM-630), which was introduced in 1995. AM-630 is a moderately active CB1receptor antagonist, in some assays behaving as a weak partial agonist (Hosohata, K. et a/,, Life Sc. 1997, 61, PL115). Researchers from Eli Lilly described aryl-aroyl substituted benzofurans as selective CB1receptor antagonists (e.g. LY-320135) (Felder, C. C. et a/., J. Pharmacol. Exp. Ther. 1998, 234; 291). 3-Aikyl-5,5'-diphenylimidazolidine-diones were described as cannabinoid receptor ligands, which were indicated to be cannabinoid antagonists (Kanyonyo, M. et a/., Biorg. Med.Chem. Lett. 1999, 9, 2233). Aventis Pharma claimed diarylmethyleneazetidine analogs as CB1receptor antagonists (Mignani, S, et a/., Patent FR 2783246, 2000; Chem. Abstr 2000, 732, 236982). Tricyclic pyrazoies were claimed by Sanofi-Synthelabo as CB-i antagonists (Barth, F. et al. Patent WO 0132663, 2001; Chem. Abstr. 2001, 734, 340504). Interestingly, many CB, receptor ' antagonists have been reported to behave as inverse agonists in vitro (Landsman, R. S. et a/., Eur. J. Pharmacol. 1997, 334, R1). Pyrazole cannabinoids have also been reported as CB-i receptor partial agonists showing in vivo cannabimimetic effects (Wiley, J. L et al.,J. Pharmacol. Exp. Then 2001, 296, 1013). A number of classes of CBT receptor agonists are known such as for example the classical cannabinoids (e.g. A9-THC), non-classical cannabinoids, aminoalkylindoles and eicosanoids (e.g. anandamide). Reviews provide a nice overview of the cannabinoid research area (Mechouiam, R. et a/., Prog. Med. Chem. 1998, 35, 199. Lambert, D. M. Curr. Med. Chem. 1999, 6, 635. Mechouiam, R. et a/., Eur. J. Pharmacol. 1998, 359, 1. Williamson, E. M. and Evans, F. J. Drugs 2000, 60, 1303. Pertwee, R. G. Addiction Biology 2000, 5, 37. Robson, P. Br. J. Psychiatry 2001, 178, 107. Pertwee, R. G. Prog. Neurobiol. 2001, 63, 569. Goya, P. and Jagerovic, N. Exp. Op'm. Ther. Patents 2000, 10, 1529. Pertwee, R. G. Gut 2001, 48, 859). It has now surprisingly been found that the novel 1H-imidazole derivatives of the formula (I), prodrugs thereof and salts thereof, are potent agonists, partial agonists or antagonists on cannabinoid-CB1receptors wherein - R represents phenyl, thienyl, 2-pyridinyl, 3-pyridinyl, 4-pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl ortriazinyl, which groups may be substituted with-,1, 2, 3 or 4 substituents Y, which can be the same or different, from the group C1.3-alkyl or alkoxy, hydroxy, halogen, trifluoromethyl, trifluoromethylthio, trifiuoromethoxy, nitro, amino, mono- or dialkyi (C^-amino, mono- or dialkyl (C1.2)-amido, (C^)-alkoxycarbonyl, carboxyl, cyano, carbamoyl and acetyl, or R represents naphtyl, with the proviso that when R is 4-pyridinyl, R4 represents a halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyl, fluoroacetyl, propionyl, sulfamoyl, methanesulfonyi, methylsulfanyl or branched or unbranched d_4 alky] group, which d-4 alkyl group may be substituted with 1-3 fluoro atoms or with a bromo, chloro, iodo, cyano or hydroxy group, - R, represents phenyl or pyridinyl, which groups may be substituted with 1-4 substituents Y, which can be the same or different, wherein Y has the above mentioned meaning, or Ri represents pyrimidinyl, pyrazinyl, pyridazinyl or triazinyl, which groups may be substituted with 1-2 substituents Y, which can be the same or different or R^ represents a five-membered aromatic heterocyclic ring having one or two heteroatoms from the group (N, O, S), which heteroatoms can, be the same or different, which five-membered aromatic heterocyclic ring may be substituted with 1-2 substituents Y, which can be the same or different or Ri represents naphtyl, R2 represents H, branched or unbranched Cv8 alkyl, C3_8 cycloafkyl, C3.8 alkenyl, C5.8 cycloalkenyl which groups may contain a sulfur, oxygen or nitrogen atom, R3 represents branched or unbranched C2.8 alkyl, Cv8 alkoxy, C5.8 cycloalkyioxy, C3.3 cycloalkyl, C5-10 bicycloalkyl, C6-io tricycloalkyl, C3.8 alkenyl, C5-e cycloalkenyl, which groups may optionally contain one or more heteroatoms from the group (0, N, S) and which groups may be substituted with a hydroxy group or 1-2 Chalky) groups or 1-3 fluoro atoms, or R3 represents a benzyl or phenethyl group which aromatic rings may be substituted with 1-5 substituents Z, which can be the same or different, from the group d.3-alkyl or alkoxy, hydroxy, halogen, trifluoromethyl, trifiuoromethylthio, trifluoromethoxy, nitro, amino, mono- or dialkyl (C^-amino, mono- or dialkyl (C^-arnido, (C^-alkyfsulfonyi, dimethyl-suifamido, C^-alkoxycarbonyl, carboxyl, trifluoromethyisulfonyl, cyano, carbamoyl, sulfamoyl and acetyl, or R3 represents a phenyl or pyridinyl group, which groups are substituted with 1-4 substituents Z, wherein Z has the meaning as indicated above, or R3 represents a pyridinyl group, or R3 represents a phenyl group, with the proviso that R4 represents a halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyl, fluoroacetyl, propionyl, sulfamoyl, methanesulfonyl, methylsulfanyl or 0^4 alkyl group, which C-M alkyl group may be substituted with 1-3 fluoro atoms or with a bromo, chloro, iodo, cyano or hydroxy group, or R3 represents a group NR5R6 with the proviso that R2 represents a hydrogen atom or a methyl group, wherein R5 and R6 are the same or different and represent branched or unbranched C-M alkyl, or R5 and R6 - together with the nitrogen atom to which they are -bonded -form a saturated or unsaturated, monocyclic or bicyclic heterocyclic group having 4 to 10 ring atoms which heterocyclic group contains one or two heteroatoms from the group (N, O, S), which heteroatoms can be the same or different, which heterocyclic group may be substituted with a C^ alkyl group or a hydroxy group, or R2 and R3 - together with the nitrogen atom to which they are bonded - form a saturated or unsaturated heterocyclic group having 4 to 10 ring atoms which heterocyclic group contains one or two heteroatoms from the group (N, O, S), which heteroatoms can be the same or different, which heterocyclic group may be substituted with a Cv3 alkyl group or a hydroxy group, R4 represents a hydrogen or halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyl, fluoroacetyl, propionyl, sulfamoyl, methanesulfonyl, methylsulfanyl or branched or unbranched CM alkyl group, which C^ alkyl group may be substituted with 1-3 fluoro atoms or with a bromo, chloro, iodo, cyano or a hydroxy group, Due to the potent CB-i agonistic, partial agonistic or antagonistic activity the compounds according to the invention are suitable for use in the treatment of psychiatric disorders such as psychosis, anxiety, depression, attention deficits, memory disorders, cognitive disorders, appetite disorders, obesity, addiction, 1 appetence, drug dependence and neurological disorders such as neurodegenerative disorders, dementia, dystonia, muscle spasticity, tremor, epilepsy, multiple sclerosis, traumatic brain injury, stroke, Parkinson's disease, Alzheimer's disease, epilepsy, Huntington's disease, Tourette's syndrome, cerebral ischaemia, cerebral apoplexy, craniocerebral trauma, stroke, spinal cord injury, neuroinflammatory disorders, plaque sclerosis, viral encephalitis, demyelinisation related disorders, as well as for the treatment of pain disorders, including neuropathic pain disorders, and other diseases involving cannabinoid neurotransmission, including the treatment of septic shock, glaucoma, diabetes, cancer, emesis, nausea, gastrointestinal disorders, gastric ulcers, diarrhoea and cardiovascular disorders. The affinity of the compounds of the invention for cannabinoid CB-j receptors was determined using membrane preparations of Chinese hamster ovary (CHO) cells in which the human cannabinoid CB1receptor is stably transfected in conjunction with [3H]CP-55,940 as radioligand. After incubation of a freshly prepared cell membrane preparation with the [3H]-ligand, with or without addition of compounds of the invention, separation of bound and free ligand was performed by filtration over glassfiber filters. Radioactivity on the filter was measured by liquid scintillation counting. The cannabinoid CB1 antagonistic activity of compounds of the invention was determined by functional studies using CHO cells in which human cannabinoid CBt receptors are stably expressed. Adenylyl cyclase was stimulated using forskolin and measured by quantifying the amount of accumulated cyclic AMP. Concomitant activation of CBt receptors by CB-, receptor agonists (e.g. CP-55,940 or (R)-WIN-55,212-2) can attenuate the forskolin-induced accumulation of cAMP in a concentration-dependent manner. This CB1receptor-mediated response can be antagonized by CB-i receptor antagonists such as the compounds of the invention. Cannabinoid agonistic of partial agonistic activity of compounds of the invention can be determined according to published methods, such as assessment of//? vivo cannabimimetic effects (Wiley, J. L et a/., J. Pharmacol. Exp. Ther. 2001, 296, 1013). The invention relates both to racemates, mixtures of diastereomers and the individual stereoisomers of the compounds having formula (I). The compounds of the invention can be brought into forms suitable for administration by means of usual processes using auxiliary substances and/or liquid or solid carrier materials. Suitable synthetic routes for the compounds of the invention are the following: Synthetic route A Step 1: ester hydrolysis of a compound having formula (II) wherein R7 represents a branched or unbranched aikyl group (C^) or benzyl group This reaction gives a compound having formula (111) wherein R, R-j and R4 have the meanings as described above. Intermediates having formula (ll), wherein R7 represents a branched or unbranched aikyl group (C^) or benzyl group can be obtained according to methods known, for example: a) I. K. Khanna et aiM J. Med. Chem. 2000, 43, 3168-3185 b) N. Kudo et al., Chem. Pharm. Bull. 1999, 47y 857-868 c) K. Tsuji et a!., Chem. Pharm. Bull. 1997, 45, 987-995 d) I. K. Khanna et a!., J. Med. Chem. 1997, 40, 1634-1647 e) M. Guiliemet et al., Tetrahedron Lett 1995, 36, 547-548 Step 2 : reaction of a compound having formula (111) with a compound having formula R2R3NH wherein R2 and R3 have the meanings as described above via activating and coupling methods such as formation of an active ester, or in the presence of a coupling reagent such as DCC, HBTU, BOP or similar reagents. This reaction gives a desired 1H-imidazole derivative having formula (I). (For more information on activating and coupling methods see: M. Bodanszky and A Bodanszky: The Practice of Peptide Synthesis, Springer-Veriag, Nevs York, 1994; ISBN: 0-387-57505-7). Alternatively, a compound having formula (Id) is reacted with a hafogenating agent, for example thionyl chloride (SOCI2). This reaction gives the corresponding carbonyl chloride (IV). Reaction of a compound having formula (IV) with a compound having formula R2R3NH wherein R2 and R3 have the meanings as described above, yields a 1H-imidazole derivative having formula (I). This reaction is preferably carried out in the presence of an organic base such as for example diisopropylethylamine (DIPEA) or triethylamine. Alternatively, a compound having formula (II) is reacted in an amidation reaction with a compound having formula R2R3NH wherein R2 and R3 have the meanings as described above to give a 1H-imidazole derivative having formula (I). Synthetic route B Reaction of a compound having formula (II), wherein R4 represents hydrogen and wherein R, R1 and R7 have the meanings as described above for compound (II), with a compound having general formula R4'-X, wherein X represents a leaving group and R4' represents a d.4 alkyl group, which alkyi group may be substituted with 1-3 fluoro atoms or wherein R/ represents a cyano, formyl, acetyl, trifluoroacetyl, fluordacetyi, methyisuifanyl or propionyl moiety, or a halogen atom. This reaction is carried out in the presence of a strong non-nucleophific base such as lithium diisopropylamide (LDA), preferably under anhydrous conditions in an inert organic solvent, for example tetrahydrofuran, and yields a compound having formula (II) wherein R, R^ and R7 have the meanings as described hereinabove and R4 represents a CM alkyl group, which alkyl group may be substituted with 1-3 fluoro atoms or wherein R4 represents a cyano, formyl, acetyl, trifluoroacetyl, fiuoroacetyl, methyisuifanyl or propionyl group, or a halogen atom. Compounds of general formula (II) which have been obtained according to synthesis route B can be converted to compounds of general formula (I) analogously to the procedures described in synthesis route A, step 1 of route A or step 2 of route A (see above). Synthetic route C wherein R4 represents a branched or unbranched C-M alkyl group, which CM alky! group may be substituted with 1-3 fiuoro substituents and wherein R, R., have the meanings given above and R7 represents a branched or unbranched alkyl group (C-t. : 4) or benzyl group can be synthesized by reacting a compound having formula (V) or its tautomer wherein R and Rt have the meanings given above, with a compound having formula (VI) wherein R4 represents a branched or unbranched C-M alkyl group, which CV4 alkyl group may be substituted with 1-3 fiuoro atoms and R8 represents a leaving group, for example a bromo substituent, and R7 represents a branched or unbranched alkyl group (C1.4) or benzyl group. The reaction is preferably carried out in an organic solvent, for example in 2-propanol or in N-methyI-2-pyrrolidinone (NMP). The addition of an acid like trifluoroacetic acid (TFA) during the reaction may enhance the formation of the compounds having formula (II). (For more information on the leaving group concept see: M, S. Smith and J. March: Advanced organic chemistry, p. 275, 5th ed.} (2001) John Wiley & Sons, New York, ISBN: 0-471-58589-0). Compounds of general formula (II) which have been obtained according to synthesis route C can be converted to compounds of general formula (I) analogously to the procedures described in synthesis route A, step 1 of route A or step 2 of route A (see above). Compounds of the invention having formula (VI) can be obtained according to methods known, for example: P. Seifert etai, He/v. Chim. Acta, 1950, 33, 725. Synthetic route D Reaction of a compound having formula (li) wherein R4 represents a methyl group and R, Rt have the meanings given above and R7 represents a branched or unbranched alkyl group (C^) or benzyl group with a regioselective brominating compound such as N-bromo-succinimide (NBS) in an organic solvent such as CC)4 in the presence of a free-radical initiator like dibenzoyi peroxide gives a compound of formula (VII) wherein R, R^ and R7 have the meanings given above. Reaction of a compound having formula (VII) (analogous to the method described in Mathews, W.B. et a/., J. Label. Compds. Radiopharm., 1999, 42, 589) with for example KCI, Kl, KF or KCN gives a compound of formula (VIII) wherein R, R-, and R7 have the meanings given hereinabove and Nu represents a chloro, iodo, fluoro or cyano group. The reaction is preferably carried out in the presence of a weak base like NaHC03 or in the presence of a crown ether ov a cryptand. (For more information on crown ethers and cryptands see: M. B. Smith and J. March: Advanced organic chemistry, p. 105, 5th ed, (2001) John Wiley & Sons, New York, ISBN: 0-471-58589-0). Compounds of general formula (VII) or (VII!) which have been obtained according to synthesis route D can be converted to compounds of general formula (I) analogously to the procedures described in synthesis route A, step 1 of route A, or step 2 of route A (see above). Example 1 Part A: To a 1M solution of sodium bis(trimethylsilyl) amide in THF (70 mL) is added dropwise a solution of 4-chloroaniline (8.86 gram, 69.5 mmol) in anhydrous THF in a nitrogen atmosphere. After the mixture is stirred for 20 minutes a solution of 2,4-dichlorobenzonitrile (12 gram, 70 mmol) in THF is added. The resulting mixture is stirred overnight, poured into ice-water (400 mL) and extracted with dichloromethane, dried over Na2S04 and concentrated in vacuo to give a yellow oil (15.7 gram). Crystallisation from a dichloromethane/heptane mixture, and subsequent washing with methyl-t-butyl ether gives N-(4-chlorophenyl)-2,4-dichiorobenzenecarboxamidine (8.66 gram, 42% yield) as a yellow solid. Melting point (MP): 93-95 °C. Analogously was prepared: - N-(4-bromophenyl)~2,4-dichiorobenzenecarboxamidine. MP: 117-119 °C. Part B: A mixture of N-(4-chIorophenyl)-2]4-dichiorobenzenecarboxamidine (2.00 gram, 6.68 mmol), ethyl 3-bromo-2-oxopropanoate (2.65 gram, 13.6 mmol) and NaHCOz (1.12 gram, 13.3 mmol) in 2-propanol is stirred at reflux temperature for 20 hours. After cooling to room temperature the mixture is concentrated in vacuo and the residue suspended in dichloromethane, washed with water (3 x 50 mL) and brine (3 x 50 mL). The aqueous layers are extracted with dichloromethane. The combined organic layers are dried over Na2S04 and concentrated in vacuo to afford crude brown product (2.0 gram). This product is further purified by column chromatography (silicagel, heptane/EtOAc = 90/10 (v/v)) to yield ethyl 1-(4-chlorophenyl)-2-(2,4-dichIorophenyI)-1H-imidazole-4-carboxylate (0.759 gram, 29 % yield) as a yellow oil which slowly solidifies on standing. Melting point: 150-152 °C; MS: 395 (MH+). 1H-NMR (400 MHz, CDCI3): 5 7.91 (s, 1H), 7.49 (dd, J = 8 Hz: J = 2 Hz, 1H), 7.29-7.36 (m, 4H), 7.07 (dt, J = 8 Hz, J= 2 Hz, 2H), 4.44 (q, J = 7 Hz, 2H), 1.42 (t, J =7 Hz, 3H). Part C: Ethyl 1-(4-chlorophenyl)-2-(2,4-dichIorophenyl)-1H-imidazole-4-carboxylate (0.810 gram, 2.06 mmol) and LiOH (0.173 g, 7.20 mmol) are dissolved in a H20/THF (20 mL/20 mL) mixture and stirred at 50 °C for 16 hours. The mixture is concentrated in vacuo to give 1-(4-chlorophenyi)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylic acid. Thionyl chloride (60 mL) is added and the mixture is heated at reflux temperature for 1 hour and concentrated in vacuo to give crude 1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1 H-imidazole-4-carbonyl chloride. Part D: Crude 1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carbonyI chloride (919 mg, -2.39 mmol), 1-aminopiperidine (0.469 g, 4.69 mmol) and triethylamine (0.363 g, 3.59 mmol) are dissolved in dichloromethane and stirred for one hour at room temperature. The mixture is washed with a saturated aqueous NaHC03 solution (3 x 20 ml_), dried oyer Na2S04 and concentrated in vacuo and further purified by column chromatography (ethyl acetate, silicagei) to give 1-(4-chlorophenyl)-2-(2I4-dichlorophenyl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide (356 mg, 26 % yield (based on ethyl 1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylate). Mass Spectrometry (MS): 449. Analogously were prepared: 2. 1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-N-(pyrrolidin-1-yl)-1H-imidazole-4-carboxamide; MS: 435. 3. N-(t-Butoxy)-1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxamide; MS: 438. 4. 1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-N-phenyl-1H-imidazole-4-carboxamide; MS: 442. 5. 1-(4-Chlorophenyl)-N-cyclohexyl-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxamide; MS: 448. 6. N-(Benzyl)-1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-N-methyl-1H-imidazole-4-carboxamide; MS: 470. 7. 1-[1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-4-(1H-imidazolyl)carbonyi] hexahydro-1H-azepine; MS: 448. 8. 2-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide (prepared from 2,4-dichloroaniline and 4-chlorobenzo-nitriie); MS: 449. 9. N-(t-Butoxy)-2-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-1H-imidazoie-4-carboxamide (prepared from 2,4-dichloroaniline and 4-chlorobenzonitrile); MS: 438. Example 10 Part A: Diisopropyiamine (2.30 gram, 22.8 mmol) is added dropwise to anhydrous THF (100 mL) in a nitrogen atmosphere at 0 °C. n-BuLi is added dropwise (7.34 mL, 2.5 M solution in hexane, 18.4 mmol). The resulting solution is cooled to - 78 °C. A solution of ethyl 2-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylate (6.0 gram, 15.2 mmol) in anhydrous THF is added dropwise. The colour of the mixture changes from yellow to purple brown. The stirred mixture is warmed to - 40 °C and cooled to - 78 °C and allowed to stand for 30 minutes. Methyl iodide (5.44 gram, 45.4 mmol) is added dropwise and the resulting solution is stirred for 30 min at - 78 °C and then allowed to attain room temperature. The resulting solution is quenched with an aqueous NH4CI solution, diethyl ether is added and the organic layer is dried over MgS04l filtered and concentrated in vacuo to give an oil (6.4 gram). This oil is purified by column chromatography (toluene/EtOAc = 10/2 (v/v), silicagel) to give pure ethyl 2-(4-chlorophenyl)-1-(2(4-dichiorophenyi)-5-methyl-1H-imidazole-4-carboxylate (5,3 gram, 85 % yield) as a yellow oil. Part B: Ethyl 2-(4-chlorophenyl)-1-(2,4-dichiorophenyl)-5-methyi-1 H-imidazole-4-carboxylate (0.250 gram, 0.51 mmol) and LiOH (Q.052 gram, 2.17 mmol) are dissolved in H2OrTHF (1:1 (v/v); 50 mL) and stirred at 50 °C for one hour. The mixture is concentrated to give crude 2-(4-chlorophenyl)-1-(2,4-dicMorophenyl)-5-methyl- 1H-imidazole-4-carboxy!ic acid. To this mixture is added SOCI2 (50 mL) and the resulting mixture is heated at reflux temperature for 1 hour. The mixture is concentrated to give 2-(4-chlorophenyl)-1-(2J4-dichlorophenyl)-5-methyl-1H-imidazoie-4-carbonyl chloride. Part C: 2-(4-Ch]orophenyI)-1-(2,4-dichlorophenyl)-5-methyMH-imidazole-4-carbonyl chloride (1.5 gram, 3.75 mmol), 1-aminopiperidine (0.725 gram, 7.25 mmol) and triethylamine (0.549 gram, 5.44 mmo!) are dissolved in dichloromethane and stirred for one hour at room temperature. The mixture is washed with a saturated aqueous NaHC03 solution, dried over Na2S04 and concentrated in vacuo and further purified by column chromatography (heptane/ethyl acetate = 1/1 (v/v), siiicagei) to give 2-(4-chlorophenyl)-1-(2J4-dichlorophenyl)-5-methyl-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide (0.220 gram, 13 % yield) as a white foam. MS: 463. Analogously were prepared: 11. N~(t-Butoxy)-2-(4-chiorophenyl)-1 -(2J4-dichlorophenyl)-5-methyl-1 H-imidazoIe-4- carboxamide: MS: 452. 12.1-(4-Chiorophenyl)-2-(2l4-dichlorophenyl)-5-methyl-N-(piperidin-1-yl)-1H- imidazole-4-carboxamide: MS: 463; Melting point: 165-167 °C. 13. N-(t-Butoxy)-2-(2,4~dichiorophenyl)-1 -(4-chlorophenyl)-5-methyl-1 H-imidazole-4- carboxamide: MS: 452. 14. N-(t-Butoxy)-1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-5-ethyl-1H-irnidazole-4- carboxamide: Amorphous. MS: 468. 15.1-(4-Chlorophenyi)-2"(2,4-dichlorophenyl)-5-ethyl-N-(piperidin-1-y()-1H-imidazole- 4-carboxamide: MS: 477. 15. 1 -(4-Bromophenyl)-N-(t-butoxy>2-(2l4-dichlorophenyl)-5-methyl-1 H-imidazoie-4- carboxamide: Amorphous. 17. 1 -(4-Bromophenyl)-2-(2l4-dichlorophenyl)-5-methyl-N-(piperidin-1 -yl)-1 H- imidazole-4-carboxamide: MP: > 204 °C. TLC (Silicagel, EtOAc) Rf = 0.3. 18.1 -(4-Bromophenyl)-N-(t-butoxy)-2-(2,4-dichlorophenyl)-5-ethyi-1 H-imidazo!e-4- carboxamide: Amorphous. TLC (Silicagel, CH2CI2/acetone = 9/1 (v/v)) Rf = 0.45. 19. 1 -(4-Bromophenyl)-2-(2>4-dichIorophenyl)-5-ethyl-N-(pfperidin--1 -yl)-1 H-imidazoIe- 4-carboxamide: MP: > 140 °C. TLC (Silicagei, EtOAc) Rf = 0.4. 20. 1-(4-Bromophenyi)-N-cyciohexyl-2-(2/^ carboxamide; Melting point > 135-140 °C. 21. 1-(4-Bromophenyl)-2-(2,4 carboxamide; Syrup. TLC (Silicagei, CH2CI2/acetone = 19/1 (v/v)) Rf = 0.4. Example 22 Part A: To a stirred solution of ethyl 1-(4-bromophenyl)-2-(2,4-dichiorophenyl)-1H-imidazole-4-carboxy)ate (6.10 gram, 0.0139 mol) in THF (70 mL) is added UOH (0.67 gram, 0.0278 mol) and water (70 mL). The resulting mixture is stirred for 16 hours at 50 °C to give a clear solution. After cooling to room temperature, HCI (1N solution, 28 mL) is added to give an oily precipitate which completely solidifies on continued stirring and addition of water (70 mL). The precipitate is collected by filtration, washed with water and dried in vacuo to give 1-(4-bromophenyi)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylic acid (4.92 gram, 86 % yield). Melting point: 138-142 °C. Part B: To a stirred suspension of 1-(4-bromophenyI)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylic acid (1.23 gram, 2.99 mmol) in dry acetonitrile (40 mL) is successively added diisopropylethylamine (DIPEA) (1.15 mL, 6.6 mmol), O-benzotriazol-1-yl-N, N, 1ST, N'-tetramethyluronium hexafluorophos-phate (HBTU) (1.36 gram, 3.6 mmol) and 1-aminopiperidine (0.39 mL, 3.6 mmol). After stirring for 16 hours, the resulting mixture is concentrated in vacuo. The residue is dissolved in ethylacetate and an aqueous NaHC03 solution is added. The ethyiacetate layer is collected, washed with water and brine, dried over Na2SO^f filtered and concentrated in vacuo to give a crude solid. This solid is further purified by recrystallisation from acetonitrile to give 1-(4-bromophenyl)-2-(2,4-d/chlorophenyl)-N-(piperidin-'}7yI)-1H-imidazole-4-carboxamide (830 mg, 56 % yield). Melting point: 219-221 °C. Analogously were prepared: 23. N-(t-Butoxy)-1-(4-bromophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxamide. Amorphous. TLC (Silicagei, Et20) Rf = 0.3. 24. 1-(4-Bromophenyl)-2-(2,4-dichIorophenyI)-N-(pyrrolidin-1-yl)-1H-irnidazoIe-4-carboxamide. Melting point: 238-240 °C. 25. N-(Azepan-1-yi)-1-(4-bromophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxamide. Melting point: 201-204 °C. 26. 1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-N-(hexahydrocyclopenta[c]pyrrol 2(1H)«yl)-lH-imidazole-4-carboxamide. MS: 475. 27. 1 -(4-Chlorophenyi)-2-(2,4-dichlorophenyl)-N-(4-fluorobenzyl)-1 H-imidazole-4-carboxamide. MS: 474. 28. 1-(4-ChIorophenyO-2-(2-methoxy-4-chlorophenyl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: 220 °C. 29. 1 -(4-Chlorophenyl)-N-cyclohexyl-2-(2-methoxy-4-chlorophenyl)-1 H-imidazole-4-carboxamide. Melting point: 177-179 °C. 30. 1 -(4-Chlorophenyl)-2-(2-fluoro-4-chlorophenyl)-N-(piperidin-1 -yl)-1 H-imidazole-4-carboxamide. Melting point: 217-218 °C. 31. 2-(2,4-Dichlorophenyl)-1-(4-fluorophenyl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: 175-176 °C. 32. N-Cyclohexyl-2-(2,4-dichiorophenyl)-1 -(4-fluoropheny])-1 H-imidazole-4-carboxamide. Melting point: 184-185 °C. 33. N-Cyclohexyl-2-(2-fluoro-4-chlorophenyl)-1-(4-chlorophenyl)-1H-imidazole-4-carboxamide. Melting point: 157-159 °C. 34. 1 -(4-Chlorophenyl)-2-(2-methoxy-4-chlorophenyl)-N-(n-pentyl)-1 H-imidazole-4-carboxamide. Melting point: 115 °C. 35. 2-(2,4-Dichlorophenyl)-1-(4-methoxyphenyf)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: 178-179 °C. 36. N-Cyclohexyl-2-(2,4-dichlorophenyl)-1 -(4-methoxyphenyl)-1 H-imidazoie-4-carboxamide. Melting point: 175-176 °C. 37. 1-(4-Chlorophenyl)-2-(2,4-dichloropheny[)-N,N-diethyl-1H-imidazole-4- carboxamide. Melting point: 177-179 °C. 38. 1 -(4-Chlorophenyl)-N-cyclohexyl-2-(2-trifluoromethyl-4-chlorophenyl)-1 H- imidazole-4-carboxamide. Melting point: 172 °C. 39. 1-(4-Chlorophenyl)-N-(piperidin-1-yl)-2-(24rifluoromethyl-4-chlorophenyl)-1H- imidazoie-4-carboxamide. Melting point: 219°C. 40. N-(1-Adamantyl)-1-(4-chlorophenyl)-2-(2-trifluoromethyl-4-chloropheny!)-1H- imidazole-4-carboxamide. Melting point: 288 °C. 41. 1-(4-Chloropheny!)-N-(2t2l2-trifluoroethyl)-2-(2-trifluoromethyl-4-chloroph^ 1H-imidazole-4-carboxamide. Melting point: 149 °C. 42. 2-(2,4-Dichlorophenyl)-1-(pyridin-3-yl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: 165-170 °C. 43. N-Cyciohexyl-2-(2l4-dichlorophenyl)-1-(pyridin-3-yl)-1H-imidazole-4-carboxamide.Melting point: 195 °C. 44. 2-(2,4-Dichlorophenyl)-1 -(pyridin-3-yl)-N-(n-pentyl)-1 H-imidazole-4-carboxamide. Melting point: 117°C. Example 45 Part A: 2,4-Dichlorobenzoyl chloride (40.0 g, 0.19 mol) is dissolved in tetrahydrofuran (1 L). To the resulting stirred solution is successively added diisopropylethylamine (DIPEA) (73.4 mL, 2.2 molar equivalent) and 4-(trifluoromethyl)phenylamine (30.7 g, 0.19 mol). After one hour the mixture is concentrated in vacuo to give an oil. This oil is crystallised from ethanol to give pure 2,4-dichloro-N-(4-(trifluoromethyl)phenyl)benzamide (53.2 g, 83 % yield). 1H-NMR (200 MHz, DMSO-d6): 5 10.90 ( br s, 1H), 7.91 (br d, J = 8 Hz, 2H), 7.63-7.77 (m, 4H), 7.57 (dt, J = 8 Hz, J= 2 Hz, 1H). Part B: 2,4"Dich!oro-N-(4-(trifluoromethyl)phenyl)benzamide (19.0 g, 0.057 mol) is dissolved in benzene (150 mL) and PCI5 (13.0 g, 1.1 molar equivalent) is added. The resulting mixture is heated at reflux temperature for two hours, allowed to attain room temperature and concentrated in vacuo to give a residue. The residue is dissolved in anhydrous THF, cooled to 0 °C and transferred into an autoclave. Excess NH3 is quickly added from a lecture bottle and the mixture is stirred at room temperature for 50 hours. A mixture of ethylacetate and aqueous NaHC03 is added. The ethylacetate layer is collected, dried over Na2S04, filtered and concentrated in vacuo. The resulting oil is purified by column chromatography (diethyl ether/petroleum ether = 1/1 (v/v), silicagel) to give pure 2]4-dichIoro-N-(4-(trifIuoromethy[)phenyl)benzene-carboxamidine (16.9 g, 89 % yield). Melting point: 108-109 °C. Part C: 2I4-Dichloro-N-(4-(trifluoromethyl)phenyl)benzenecarboxamidine (15.0 g, 0.0450 mol) is dissolved in 2-propanol and ethyl 3-bromo-2-oxobutanoate (20.8 g, 2 molar equivalent) and NaHC03 are successively added. The resulting mixture is heated at reflux temperature for 40 hours and allowed to attain room temperature. The 2-propanoi is removed in vacuo, ethyl acetate is added to the residue and the resulting organic layer is washed with NaHC03 (5 % aqueous solution). The ethylacetate layer is collected, dried over Na2S04, filtered and concentrated in vacuo. The resulting oil is purified by column chromatography (diethyl ether/petroleum ether - 1/3 (v/v), silicagel) and further purified by crystallisation from cyclohexane to give ethyl 2-(2l4-dichlorophenyi)-5-methyl-1-(4-(trifluoromethyl)phenyl)-1H-imidazoie-4-carboxylate (10.45 g, 52 % yield) as a yellow solid. Melting point: 160-162 °C. Part D: The formed ethyl 2-(2,4-dichlorophenyI)-5-methyl-1-(4-(trifluoromethyl) phenyi)-1H-fmidazole-4-carboxy!ate is converted to 2-(2,4-dichlorophenyl)-5-methyl-1-(4-(trif[uoromethyl)phenyl)-1H-imidazole-4-carboxylic acid (melting point: -224-226 °C), which carboxylic acid is converted to 2-(2,4-dichlorophenyl)-5-methyl-N-(piperidin-1-yl)-1-(4-(trifiuoromethyl)phenyl)-1H-imidazole-4-carboxamide (melting point: 173-174 °C) according to the procedure described in example 22 above. Analogously were prepared 46. 2-(2t4-dichlorophenyl)-N-(piperidin-1-yl)-1-(4-(trifluoromethyl)phenyl)-1H-imidazole-4-carboxamide. Melting point >200 °C (decomposition). 47. N-Cyclohexyl-2-(2)4-dlchlorophenyl)-5-methyl-1-(4-(trif!uoromethyI) phenyl)-1H-imidazole-4-carboxamide. Melting point: 178-179 °C. 48. N-Cyclohexyl-2-(2,4-dichlorophenyl)-1-(4-(tnfluoromethyl)phenyl)-1H-imidazo!e-4-carboxamide. Melting point: 199-200 °C. Example 49 Part A: N-(4-methoxyphenyl)-2J4-dichlorobenzenecarboxamidine (15.0 gram, 50.8 mmol) is dissolved in 2-propanol and ethyl 3-bromo-2-oxobutanoate (23.5 g, 2 molar s equivalents) and NaHC03 (8.5 gram, 2 molar equivalents) are successively added. The resulting mixture is heated at reflux temperature for 40 hours and allowed to attain room temperature. The 2-propanol is removed in vacuo, ethyl acetate is added to the residue and the resulting organic layer is washed with NaHC03 (5 % aqueous solution). The ethylacetate layer Is collected, dried over Na2S04, filtered and concentrated in vacuo. The resulting oil is purified by column chromatography (diethyl ether/petroleum ether = 1/3 (v/v), silicagel) to give ethyl 2-(2,4-dichiorophenyl)"5-methyl-1«(4-methoxy-phenyI)-1H-imidazole-4-carboxyIate (8.61 g, 42 % yield) as a solid. 1H-NMR (200 MHz, CDCI3): 5 7.33 (d, J = 8 Hz, 1H), 7.27 (d, J = 2 Hz, 1H), 7.18 (dd, J = 8 Hz, J = 2 Hz, 1H), 7.03 (dt, J = 8 Hz, J = 2 Hz, 2H), 6.85 (dt, J = 8 Hz, J = 2 Hz, 2H), 4.42 (q, J = 7 Hz, 2H), 3.80 (s, 3H), 2.43 (s, 3H), 1.43 (t, J =7 Hz, 3H). Part B: To a stirred solution of ethyl 2-(2,4-dichlorophenyl)-5-methyl-1 -(4-methoxyphenyl)-1H-imidazole-4-carboxylate (8.00 gram, 0.0198 mol) in THF (80 mL) is added LiOH (0.59 gram, 2 molar equivalents) and water (80 mL). The resulting mixture is stirred for 16 hours at 80 °C. After cooling to room temperature, HCI (2N solution, 12.3 mL) is added to give an oily precipitate. After addition of water and extraction with ethylacetate, the ethylacetate layer is collected, dried over Na2S04, filtered and concentrated in vacuo. The residue is crystallised from diisopropyl ether and dried to give 2-(2,4-dichlorophenyl)-5-methyl-1-(4-methoxyphenyl)-1H-irnidazole-4-carboxyiic acid (4.04 gram, 87 % yield) as a pale grey solid. Melting point: 189-191 CC. Part C: To 2-(2,4-dichlorophenyl)-5-methyl-1 -(4-methoxyphenyl)-1 H-imidazole-4-carboxyiic acid (1.00 gram, 2.65 mmol) in dry acetonitrile (25 mL) is successively added diisopropyiethylamine (DIPEA) (1.02 mL, 2.2 molar equivalents), O-benzotriazol-1-yl-N, N, N', N'-tetramethyluronium hexafluoro-phosphate (HBTU) (1.21 gram, 1.2 molar equivalents) and the resulting solution is stirred for 15 minutes. Cyclohexylamine (0.36 mL, 1.2 molar equivalents) is added. After stirring for 50 hours, the resulting mixture is concentrated in vacuo. The residue is dissolved in dichloromethane and an aqueous NaHC03 solution is added. The dichloromethane layer is collected, dried over Na2S04l filtered and concentrated in vacuo. The residue is further purified by column chromatography (gradient: dichloromethane => dichloromethane/methanol = 99/1 (v/v), silicagel) to give N-(1-cyclohexyI)-2-(2,4-dichlorophenyl)-5-methyl-1-(4-methoxyphenyl)-1H-imidazole-4-carboxamide (1.03 gram, 85 % yield). Melting point: 160-161 °C. Analogously were prepared: 50. 1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-N,N,5-trimethyl-1H-imidazoie-4-carboxamide. Melting point: 101-104 °C. 51. 1-(4-Chioropyridin-2-yl)-2-(2)4-dichlorophenyl)-5-methyl-N-(piperidin-1--yl)-1H-imidazole-4-carboxamide. MS: 464 (MH+). 52. 1-(4-Chloropyridin-2-y[)-2-(2,^ imidazole-4-carboxamide. MS: 466 (MH+). 53. N-(1-Azepanyl)-1-(4-Chloropyridin-2-yl)-2-(2,4-dichlorophenyl)-5-methyl-1H^ imidazole-4-carboxamide. MS: 478 (MH+). 54. 1-(4-Chioropyridin-2-yl)-N-cyclohexyl-2-(2,4-dichlorophenyI>5-methyl^ imidazole-4-carboxamide. MS: 463. 55. 1-(4-Chloropyridin-2-yl^ imidazole-4-carboxamide. MS: 451. 55. 1 -(4-Ch!oropyridin-2-yl)-2-(2,4-dichlorophenyi)-N-(4~fluorobenzyI)-5-methyl-1 H-imidazole-4-carboxamide. MS: 489. Melting point: 123-126 °C. 57. 1-(4-Chloropheny!)-N-cyclohexyl-5-methyl-2-(2-trffluoromethyl-4-chlorophenyl)-1H-imidazole-4-carboxamide. Melting point: 212 °C. 53. 1 -(4-Chlorophenyl)-5-methyI-N-(piperidin-1 -yl)-2-(2-trifiuoromethyl-4-chlorophenyl)-1H-imidazole-4-carboxamide. Melting point: 165 °C. 59. 1-(4-ChlorophenyO-2-(2-methoxy-4-chIorophenyi)-5-methyl-N-(n-pentyi)-1H-imidazole-4-carboxamide. Melting point 131 °C. 60. 1-(4-Chlorophenyl)-2-(2-methoxy-4-chloropheny^ imidazole-4-carboxamide. Melting point: > 256 °C. 61. N-Cyclohexyl-1-(4-chlorophenyl)-2-(2-methoxy-4-chlorophenyl)~5-methyl-1H-imidazole-4-carboxamide. Melting point: 201 °C. 62. 2-(2,4-Dfchlorophenyl)-1-(4-fliJorophenyl)-5-methyl-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: 223-224 °C. 63. 2-(2I4-Dichlorophenyl)-5-methyl-1-(4-methoxyphenyl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: > 90 °C (decomposition). 64. N-Cyclohexyl-1-(4-fiuorophenyl)-2-(2,4-dichlorophenyl)-5-methyl-1H-imidazole-4-carboxamide. Melting point: 229-230 °C. 65. 1-(4-Chloropheny!)-5-methyl-N-^ imidazole-4-carboxamide. Amorphous. 66. 1-(4-ChlorophenyO-2-(2-fluoro-4-chlorophenyl)-5-methyl-N-(piperidin-1-y[)-1H-imidazole-4-carboxamide. Melting point: 195 °C. 67. 1-(4-Chiorophenyl)-2-(2-fluoro-4-chlorophenyl)-5-methyl-N-(n-pentyl)--1H-imidazole-4-carboxamide. Melting point: 115°C. 68. 1 -(4-Chlorophenyl)-N-(cyciohexy[)-2-(2-fiuoro-4-chlorophenyl)-5-methyl-1 H-imidazole-4-carboxamide. Melting point: 188 °C. 69. 1-(4-Chlorophenyl)-N-(cyclohexyl)-2-(1,5-dimethyl-1H-pyrrol-2-yl)-5-methyl-1H-imidazole-4-carboxamide. Melting point: 183-189 °C. 70. 1-(4-ChIoropheny!)-2-(1,5-dime^ imidazole-4-carboxamide. Melting point: 208-210 °C. 71. 2-(2-Chlorophenyl)-1-(3-fluorophenyl)-5-methyl-N-(piperidin-1-yl)-1H-imidazo!e-4-carboxamide. Melting point: 236-238 °C. 72. 2-(2-Chlorophenyl)-1-(3-fluorophenyl)-5-methyl-N-(n-pentyl)-1H-imidazo!e-4-carboxamide. Melting point: 97-102 °C. 73. 2-(2-Chlorophenyl)-N-cyclohexyl-1-(3-fluorophenyl)-5-methyN1H-imidazoIe-4-carboxamide. Melting point: 180-182.5 °C. 74. 2-(2-Chiorophenyl)-1 -(3-fluorophenyi)-N-(2-(4-fluorophenyl)ethyi)-5-methyl-1 H-imidazole-4-carboxamide. Melting point: 123.5-126 °C. 75. 1-(4-CNoropyridin-2-yl)-2-(2,4-d^ imidazofe-4-carboxamide. Melting point: 146 CC. 76.. 1 -(4-Chloropyridin-2-yl)-2-(2,^ H- imidazole-4-carboxamide. Melting point: 223 °C. 77. N-(1-Azepanyl)-1-(4-Ch!oropyridin-2-yl)-2-(2I4-dichlorophenyl)-5-ethyi-1H-imidazole-4-carboxamide. Melting point: 177 °C. 78. 1-(4-Chloropyridin-2-yI)-N-cyc!ohexyl-2-(2f4-dichlorophenyl)-5-ethyl-1H-imidazole-4-carboxamide. Melting point: 149 °C. 79. 1 -(4-Chloropyridin-2-yi)-2-(2,4-dichlorophenyl)-5-ethyl-N-(n-penty i)-1 H-imidazo(e-4-carboxamide. Melting point: Oil. 80. 1-(4-Chioropyridin-2-yl)-2-(2)4-dichlorophenyl)-5-ethyl-N-(4-fiuorophenylmethyi)-1H-imidazoie-4-carboxamide. MP: amorphous. 81. 1 -(4-Chiorophenyl)-2-(2,4-dichlorophenyl)-N-(hexahydrocyclopenta"[c]pyrroi-2(1H)-yl)-5-methyl-1H-imidazoie-4-carboxamide. MP: 143-146 °C. 82. 1 -(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyi-N-phenyl-1 H-imidazole-4-carboxamide. Melting point: 91-95 °C. 83. 1-(4-Chiorophenyl)-2-(2,4^ichloro^ yioxy)-1H-imidazole-4-carboxam(de. Melting point: 128-133 °C. 84. N-(Exo-bicycio[2.2.1]hept-2-yl)-1-(4-chlorophenyl)-2-(2,4-dichlorophenyi)-5-methyi-lH-imidazole-4-carboxamide. Melting point: 194-195 °C. 85. 1 -(4-Chloropheny l)-2-(2,4-dich!orophenyl)-N-(2-fiuoroethy l)-5-methyl-1 H-imidazoIe-4-carboxamide. Melting point: 128-133 °C. 85. 1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-N-(trans-4-hydroxycyclohexyl)-5-methyl-1H-imidazole-4-carboxamide. Melting point: 160 °C (dec). 87. 1 -{[1 -(4-Chlorophenyl)-2-(2,4-dichlorophenyi)-5-methyi-1 H-imidazol-4-yl]carbonyl}-4-hydroxypiperidine. Melting point: Amorphous. 88. 1-{E1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyi-1H-imidazol-4-ylJcarbonylJ-I^.S^-tetrahydrofsoquinoline. Melting point: 143-146 °C. 89. N-(Endo-bicyclo[2.2.1]hept-2-yl)-1-(4-chlorophenyl)-2-(2l4-dichiorophenyl)-5-methyl-1H-imidazole-4-carboxamide. Melting point: 194-195 °C. 90. 1 -(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-N-(4-fluorobenzyl)-5-methyl-1 H-imidazole-4-carboxamide. Melting point: 165-166 °C. 91. 1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyi-N-(n-pentyl)-1H-imidazole-4-carboxamide. Oil. 92. N-(Azepan-1-yl)-1-(4-ch[oropheny!)-2-(2,4-dichlorophenyl)-5-methyl-1H-imidazole-4-carboxamide. Melting point: 147-149 °C. 93. 1 -(4-Chlorophenyi)-2-(2,4-dichloropheny l)-5-methyl-N-(py rrolidin-1 -yi)-1 H-imidazole-4-carboxamide. Melting point: 205-206 °C. 94. l^-ChlorophenyO^^^-dichlorophenyQ-S-methyl-N^morpholin^-yO-IH-imidazote-4-carboxamide. Melting point: 225 °C (dec). 95. 2-(2,5-Dichlorophenyl)-5-methyi-1-phenyl-N-(piperidin-1-yi)-1H-imidazo!e-4-carboxamide. Melting point: 227 °C. 96. N-Cyclohexy!-2-(2,5-dichlorophenyl)-5-methyl-1-phenyl-1H-imidazole-4-carboxamide. Melting point: 236 °C. 97. N-Cyclohexyl-2-(2(4-dichiorophenyl)-1-(2,5-difluorophenyl)-5-ethyl-1H-imidazole-4-carboxamide. Melting point: 144-146 CC. 98. N-Cyclohexyl-2-(2I4-dichlorophenyl)-1-(2,5-difluorophenyl)-5-methyl-1H-imidazole-4-carboxamide. Melting point: 206-208 °C. 99. N-Cyclohexyl-2-(1,5-dimethyM H-pyrrol-2-yl)-5-ethyl-1-phenyl-1 H-imidazole-4-carboxamide. Melting point: 195-196 °C. 100. N-Cyclohexyl-2-(2,5-dichlorophenyl)-5-ethyl-1-phenyl-1H-imidazole-4-carboxamide. Melting point: 198-199 °C. 101. 2-(2J5-Dichlorophenyl)-5-ethyl-1-phenyl-N-(piperidin-1-yl)-1H-innidazole-4-carboxamide. Melting point: 207-208 °C. 102.1-(4-Chlorophenyl)-5-methyl-2-(3-methylpyridin-2-yl)-N-(piperidin-1-yl)-1H- imidazole-4-carboxamide. Melting point: 211-213 °C. 103.1 -(4-Chlorophenyl)-N-cyclohexyl-5-methyl-2-(3-methylpyridin-2-yl)-1 H- imidazoIe-4-carboxamide. Melting point: 188-190 °C. 104.1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyl-N-(3- (trifluoromethyl)phenyl)-1H-imidazole-4-carboxamide. Melting point: 177°C. 105.1-(4-Chlorophenyl)-2-(2l4-dichlorophenyl)-5-methyl-N-(3- (trifluoromethyl)benzyI)-1H-imidazole-4-carboxamide. Melting point: 138-140 °C. 106.1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyl-N-(4- (trifluoromethyl)benzyl)-1H-imidazole-4-carboxamide. Melting point: 232 °C. 107.1-(4-Chlorophenyl)-N-cyclopentyl-2-(2,4-dichlorophenyl)-5-methyl-1H-imfdazole- 4-carboxamide. Melting point: 172 °C. 108.1-(4-Chlorophenyl)-N-cycloheptyl-2-(2I4-dichlorophenyl)-5-methyl-1H-imidazole- 4-carboxamide. Melting point: 154-156 °C. Example 109 Part A: Ethyl 1 -(4-bromophenyl)-2-(2,4-dichlorophenyl)-1 H-imidazole-4-carboxylate is converted to ethyl 1-(4-bromophenyl)-5-chloro-2-(2,4-dichlorophenyl)-1H- imidazole-4-carboxylate analogously to a published procedure (N. Kudo et al.T Chern. Pharm. Bull. 1999, 47, 857-868) using excess of S02CI2 in dichloroethane at reflux temperature for 50 hours. Part B: Ethyl 1-(4-bromophenyl)-5-chloro-2-(2,4-dichlorophenyl)-1H-imidazole-4- carboxylate is converted to 1 -(4-bromophenyl)-5-chloro-2-(2,4-dichloro-phenyl)-N- (piperidin-1-yl)-1H-imidazole-4-carboxamide (melting point: > 150 °C; Rf (Silicagel, EtOAc) - 0.35) analogously to the procedure described in example 22 above. 1H- NMR (400 MHz, CDCI3): 5 7.85 (br s, 1H)T 7.52 (dt, J = 8 Hz; J = 2 Hz, 2H), 7.26-7.36, (m, 3H), 7.01 (dt, J = 8 Hz, J = 2 Hz, 2H), 2.85-2.92 (m, 4H), 1.72-1.80 (m, 4H), 1.40 -1.44(m, 2H). Example 110 Part A: To a stirred solution of 1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylic acid (18.38 gram, 50 mmol) in toluene (200 mL) in a nitrogen atmosphere is added N,N-dimethylformamide di-tert-butyl acetal (50 mL) and the resulting mixture is heated at 80 °C for 4 hours. After cooling to room temperature the reaction mixture is concentrated and diethyl ether is added. The resulting solution is twice washed with water, dried over MgS04p filtered and concentrated in vacuo. The residue is crystallised from diisopropyl ether to give pure tert-butyl 1-(4-chlorophenyl)-2-(2,4-dichlorophenyI)-1H-imidazoie-4-carboxylate (10.35 gram, 49 % yield). Melting point: 179-181 °C. PartB: Lithium diisopropyl amide (LDA) (5.25 mL of a 2 M solution in THF, 0.0105 mol) is added dropwise to a cooled solution (-70 °C) of tert-butyl 1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylate (4.24 gram, 0.010 mol) in anhydrous THF (80 mL) in a nitrogen atmosphere and the resulting mixture is stirred for one hour. A solution of p-toluenesulfonyl cyanide (1.88 gram, 0.011 mol) in anhydrous THF (20 mL) is added dropwise and the resulting red solution is stirred for one hour at - 70 °C and then allowed to attain room temperature. Diethyl ether is added and the resulting solution is quenched with water and filtered over hyflo. The organic layer is collected and washed with water, dried over MgS04, filtered and concentrated in vacuo to give an oil. This oil is purified by column chromatography (dichloromethane, silicagel) to give 3.4 gram of tert-butyl 1 -(4-chlorophenyl)-5~cyano-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylate. Recrystallisation from diisopropyl ether gave crystalline tert-butyl 1-(4-chlorophenyl)-5-cyano-2-(2,4-dichlorophenyl)-1H-imidazoie-4-carboxyIate (2.57 gram, 57 % yield). Melting point: 210-212 °C. Analogously was prepared: - Tert-butyl 1 -(4-chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyl-1 H-imidazole-4-carboxylate. 1H-NMR (400 MHz, CDCI3): 5 7.38 (d, J = 8 Hz, 1H), 7.34 (dt, J = 8 Hz, J = 2 Hz, 2H), 7.27 (d, J = 2 Hz, 1H), 7.22 (dd, J = 8 Hz, J = 2 Hz, 1H), 7.03 (dt, J = 8 Hz, J = 2 Hz, 2H), 2.40 (s, 3H), 1.63 (s, 9H). PartC: To a solution of tert-butyl 1 -(4-chlorophenyl)-2-(2,4-dichlorophenyl)-5-cyano-1 H-imidazoie-4-carboxylate (2.57 gram, 5.73 mmol) in dichloromethane (40 mL) is added trifluoroacetic acid and the resulting solution is stirred at room temperature for 20 hours and concentrated in vacuo. The residue is crystallised from diisopropyl ether to give pure 1 -(4-chlorophenyl)-5-cyano-2-(2,4-dichlorophenyl)-1 H-imidazole-4-carboxylic acid (1.95 gram, 87 % yield). Melting point: 200-202 °C (dec). PartD: 1-(4-Chlorophenyl)-5-cyano-2-(2,4-dichloropheny!)-1 H-imidazole-4-carboxylic acid is converted to 1-(4-chlorophenyl)-5-cyano-2-(2,4-dichlorophenyl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide in 60 % yield, analogously to the procedure described in example 22, part B herein above. Melting point: 231-233.5 °C. Analogously were prepared: 111. 1-(4-Chlorophenyl)-2-(2,4-dichIorophenyl)-5-iodo-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: 1S6-201 °C. 112.1-(4-Chlorophenyl)-N-cyclohexyl-2-(2,4-dichlorophenyl)-5-iodo-1 H-imidazole-4- carboxamide. Melting point: 226-230 °C. 113.1 -(4-Chlorophenyl)-5-cyano-N-cyclohexyl-2-(2,4-dichlorophenyl)-1 H-imidazole- 4-carboxamide. Melting point: 157-158 °C. wherein R represents phenyl, thienyl, 2-pyridinyI, 3-pyridinyl, 4-pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl or triazinyl, which groups may be substituted with 1, 2, 3 or 4 substituents Y, which can be the same or different, from the group d-3-alkyl or aikoxy, hydroxy, halogen, trifluoromethyl, trifluoromethylthio, trifluoromethoxy, nitro, amino, mono- or dialkyJ (d^-amino, mono- or dialkyi (C^-amido, (d-3)-aikoxycarbonyl, carboxyl, cyano, carbamoyl and acetyl, or R represents naphtyl, with the proviso that when R is 4-pyridinyl, R4 represents a halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyf, fluoroacetyl, propionyl, sulfamoyl, methanesulfonyl, methylsulfanyl or branched or unbranched d-4 alkyl group, which d-4 alkyl group may be substituted with 1-3 fluoro atoms or with a bromo, chloro, iodo, cyano or hydroxy group, R! represents phenyl or pyridinyl, which groups may be substituted with 1-4 substituents Y, which can be the same or different, wherein Y has the above mentioned meaning, or R1 represents pyrimidinyl, pyrazinyl, pyridazinyl or triazinyl, which groups may be substituted with 1-2 substituents Y, which can be the same or different or R1 represents a five-membered aromatic heterocyclic ring having one or two heteroatoms from the group (N, O, S), which heteroatoms can be the same or different, which five-membered aromatic heterocyclic ring may be substituted with 1-2 substituents Y, which can be the same or different or Rt represents naphtyl, R2 represents H, branched or unbranched d-s alkyl, d-3 cycloalkyl, C3-3 alkenyl, C5-8 cycloalkenyl which groups may contain a sulfur, oxygen or nitrogen atom, R3 represents branched or unbranched C2-e alkyl, d-s aikoxy, C5.s cycloalkyloxy, C3-3 cycloalkyl, C5.10 bicycloalkyl, Cs_10 tricycloalkyl, C3.5 alkenyl, d-s cycloalkenyl, which groups may optionally contain one or more heteroatoms from the group (O, N, S) and which groups may be substituted with a hydroxy group or 1-2 d-3 alkyl groups or 1-3 fiuoro atoms, or R3 represents a benzyl or phenethyl group which aromatic rings may be substituted with 1-5 substituents Z; which can be the same or different, from the group C1-3-alkyl or aikoxy, hydroxy, halogen, trifluoromethyl, trifluoromethylthio, trifluoromethoxy, nitro, amino, mono- or dialkyi (C1-2)-amino, mono- or dialkyi (C1-2)-amido, (C1-3-alkylsulfonyl, dimethyl-sulfamido, C1-3- alkoxycarbonyl, carboxyl, trifluoromethylsulfonyl, cyano, carbamoyl, sulfamoyl and acetyl, or R3 represents a phenyl or pyridinyl group, which groups are substituted with 1-4 substituents Z, wherein Z has the meaning as indicated above, or R3 represents a pyridinyl group, or R3 represents a phenyl group, with the proviso that R4 represents a halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyi, fluoroacetyl, propionyl, sulfamoyl methanesulfonyl, methylsulfanyl or d.4 alkyl group, which C1-4alkyl group may be substituted with 1-3 fluoro atoms or with a bromo, chloro, iodo, cyano or hydroxy group, or R3 represents a group NR5R5 with the proviso that R2 represents a hydrogen atom or a methyl group, wherein R5 and R6 are the same or different and represent branched or unbranched C^ alkyl, or R5 and R6 - together with the nitrogen atom to which they are bonded -form a saturated or unsaturated, monocyclic or bicyclic heterocyclic group having 4 to 10 ring atoms which heterocyclic group contains one or two heteroatoms from the group (N, O, S), which heteroatoms can be the same or different, which heterocyclic group may be substituted with a Ci_3 alkyl group or a hydroxy group, or R2 and R3 - together with the nitrogen atom to which they are bonded - form a saturated or unsaturated heterocyclic group having 4 to 10 ring atoms which heterocyclic group contains one or two heteroatoms from the group (N, O, S), which heteroatoms can be the same or different, which heterocyclic group may be substituted with a C-i_3 alkyl group or a hydroxy group, R4 represents a hydrogen or halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyi, fluoroacetyl, propionyl, sulfamoyl, methanesulfonyl, methylsulfanyl or branched or unbranched C1-4 alkyl group, which C-M alkyl group may be substituted with 1-3 fluoro atoms or with a bromo, chloro, iodo, cyano or a hydroxy group, and prodrugs, stereoisomers and salts thereof. Pharmaceutical compositions containing a pharmacologically active amount of at least one compound as claimed in 1 as an active component. Method of preparing pharmaceutical compositions as claimed in claim 2 characterised in that a compound as claimed in claim 1 is brought in a form suitable for administration. Process for the preparation of compounds having formula (I), characterised in that a compound is prepared wherein R, RrR3 have the meanings given in claim 1 and R4 represents a hydrogen or halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyi, propionyl, sulfamoyl, methanesulfonyl, methylsulfanyl or C1-4 alkyl group, which C1-4 alkyl group may be substituted with 1-3 fluoro atoms, ,t by reacting a compound having formula (II), (III) or (IV) with a compound of formula R2R3NH. 5. Process for the preparation of compounds having formula (II) wherein R4 represents a C1-4alkyl group, which C-\|.4 alkyl group may be substituted with 1-3 fluoro substituents, or wherein R4 represents a halogen atom or a cyano, formyl, acetyl, trifluoroacetyl, fluoroacetyl, methylsulfanyl or propionyl group, characterized in that a compound is prepared wherein R and R1 have the meanings given in claim 1 and R7 represents a branched or unbranched alkyl group (C1-4) or benzyl group, by reacting a compound having formula (II) wherein R4 is a hydrogen atom with a compound having formula R4'-X, wherein X represents a leaving group and R4' represents a C1-4 alkyl group, which CV4 alkyl group may be substituted with 1-3 fluoro substituents, or wherein R4' represents a halogen atom or a cyano, formyl, acetyl, trifluoroacetyl, fluoroacetyl, methylsulfanyl or propionyl group, in the presence of a strong non-nucleophilic base. 6. Process for the preparation of a compound having formula (II) wherein R4 represents a branched or unbranched C-1-4 alkyl group, which C1-4 alkyi group may be substituted with 1-3 fluoro substituents, characterized in that a' compound is prepared wherein R, R1 have the meanings given in claim 1 and R7 represents a branched or unbranched alkyl group (C1-4) or benzyl group, by reacting a compound having formula (V) or its tautomer wherein R and R-, have the meanings given in claim 1, with a compound having formula (V!) wherein R4 represents a branched or unbranched C1-4 alkyl group, which C1-4 alkyl group may be substituted with 1-3 fluoro atoms and R8 represents a so-called leaving group and R7 represents a branched or unbranched alkyl group (C1-4) or benzyl group. 7. Compounds of formula (IX) wherein R and R4 have the meanings given in claim 1 and wherein R1 represents a phenyl or pyridinyl group, which groups are substituted with 1-4 substituents Y, which can be the same or different, or R^ represents a pyrimidinyl, pyrazinyl, pyridazinyl or triazinyi group, which groups are substituted with 1-2 substituents Y, which can be the same or different or RT represents a five-membered aromatic heterocyclic moiety having one or two heteroatoms from the group (N, 0, S), which heteroatoms can be the same or different, which five-membered "aromatic heterocyclic moiety may be substituted with 1-2 substituents Y, which can be the same or different or R^ represents naphtyi and R9 represents a hydroxy group, a branched or unbranched alkoxy (C1-4) group, a benzyloxy group or a chloro substituent. 8. Compounds of formula (X) and tautomers thereof wherein R represents a 4-chlorophenyl group, a 4-bromophenyl group or a 4-(trifluoromethyl)phenyl group. 9. Use of a compound as claimed in claim 1 for the preparation of a pharmaceutical composition for the treatment of disorders involving cannabinoid neurotransmission. 10. Use as claimed in claim 9 characterised in that said disorders are psychiatric disorders such as psychosis, anxiety, depression, attention deficits, memory disorders, cognitive disorders, appetite disorders, obesity, addiction, appetence, drug dependence and neurological disorders such as neurodegenerative disorders, dementia, dystonia, muscle spasticity, tremor, epilepsy, multiple sclerosis, traumatic brain injury, stroke, Parkinson's disease, Alzheimer's disease, epilepsy, Huntington's disease, Tourette's syndrome, cerebral' ischaemia, cerebral apoplexy, craniocerebral trauma, stroke, spinal cord injury, neuroinfiammatory disorders, plaque sclerosis, viral encephalitis, demyelinisation related disorders, as well as for the treatment of pain disorders, including neuropathic pain disorders, and other diseases involving cannabinoid neurotransmission, including the treatment of septic shock, glaucoma, cancer, diabetes, emesis, nausea, asthma, respiratory diseases, gastrointestinal disorders, gastric ulcers, diarrhoea and cardiovascular disorders. 11. Pharmaceutical compositions substantially as hereinabove described and exemplified. 12. Method of preparing pharmaceutical compositions substantially as hereinabove described and exemplified.

Full Text

1H-lmidazole derivatives having CB1 agonistic, CB-1 partial agonistic or CB-r antaqonistic activity
The present invention relates to a group of novel 1H-irnidazo!e derivatives, to methods for the preparation of these compounds, and to pharmaceutical compositions containing one or more of these compounds as an active component.
These 1H-imidazoie derivatives are potent cannabinoid-CB1receptor agonists, partial agonists or antagonists, useful for the treatment of psychiatric and neurological disorders, as well as and other diseases involving cannabinoid neurotransmission.
Cannabinoids are present in the Indian hemp Cannabis sativa and have been used as medicinal agents for centuries (Mechoulam, R. and Feigenbaum, J. J. Prog. Med. Chem. 1987, 24, 159). However, only within the past ten years the research in the cannabinoid area has revealed pivotal information on cannabinoid receptors and their (endogenous) agonists and antagonists. The discovery and the subsequent cloning of two different subtypes of cannabinoid receptors (CB1and CB2) stimulated the search for novel cannabinoid receptor antagonists (Munro, S. et a/., Nature 1993, 365, 61. Matsuda, L A. and Bonner, T. i. Cannabinoid Receptors, Pertwee, R. G, Ed. 1995, 117, Academic Press, London). In addition, pharmaceutical companies became interested in the development of cannabinoid drugs for the treatment of diseases connected with disorders of the cannabinoid system (Consroe, P. Neurobiology of Disease 1998, 5, 534. Pop, E. Curr. Opin. In CPNS Investigational Drugs 1999, 7, 587. Greenberg, D. A. Drug News Perspect. 1999, 72, 458. Pertwee, R.G., Progress in Neurobiology 2001, 63, 569). Hitherto, several CB^ receptor antagonists are known. Sanofi disclosed their diarylpyrazole congeners as selective CB1receptor antagonists. A representative example is SR-141716A (Dutta, A.K. et a/., Med. Chem. Res. 1994, 5, 54. Lan, R. et at., J. Med Chem. 1999, 42, 769. Nakamura-Paiacios, E. M. et a/., CNS Drug Rev. 1999, 5, 43). CP-272871 is a pyrazole derivative, like SR141716A, but less potent and less CB1receptor subtype-selective than SR141716A (Meschler, J. P. et at., Biochem. Pharmacol. 2000, 60, 1315). Aminoalkylindoles have been dis-closed as CB1 receptor antagonists. A representative example is lodopravadoiine (AM-630), which was introduced in 1995. AM-630 is a moderately active CB1receptor antagonist, in some assays behaving as a weak partial agonist (Hosohata, K. et a/,, Life Sc. 1997, 61, PL115). Researchers from Eli Lilly described aryl-aroyl substituted benzofurans as selective CB1receptor antagonists (e.g. LY-320135) (Felder, C. C. et a/., J. Pharmacol. Exp. Ther. 1998, 234; 291). 3-Aikyl-5,5'-diphenylimidazolidine-diones were described as cannabinoid receptor ligands, which were indicated to be cannabinoid antagonists (Kanyonyo, M. et a/., Biorg. Med.Chem. Lett. 1999, 9, 2233). Aventis Pharma claimed diarylmethyleneazetidine analogs as CB1receptor antagonists (Mignani, S, et a/., Patent FR 2783246, 2000; Chem. Abstr 2000, 732, 236982). Tricyclic pyrazoies were claimed by Sanofi-Synthelabo as CB-i antagonists (Barth, F. et al. Patent WO 0132663, 2001; Chem. Abstr. 2001, 734, 340504). Interestingly, many CB, receptor '

antagonists have been reported to behave as inverse agonists in vitro (Landsman, R. S. et a/., Eur. J. Pharmacol. 1997, 334, R1). Pyrazole cannabinoids have also been reported as CB-i receptor partial agonists showing in vivo cannabimimetic effects (Wiley, J. L et al.,J. Pharmacol. Exp. Then 2001, 296, 1013). A number of classes of CBT receptor agonists are known such as for example the classical cannabinoids (e.g. A9-THC), non-classical cannabinoids, aminoalkylindoles and eicosanoids (e.g. anandamide). Reviews provide a nice overview of the cannabinoid research area (Mechouiam, R. et a/., Prog. Med. Chem. 1998, 35, 199. Lambert, D. M. Curr. Med. Chem. 1999, 6, 635. Mechouiam, R. et a/., Eur. J. Pharmacol. 1998, 359, 1. Williamson, E. M. and Evans, F. J. Drugs 2000, 60, 1303. Pertwee, R. G. Addiction Biology 2000, 5, 37. Robson, P. Br. J. Psychiatry 2001, 178, 107. Pertwee, R. G. Prog. Neurobiol. 2001, 63, 569. Goya, P. and Jagerovic, N. Exp. Op'm. Ther. Patents 2000, 10, 1529. Pertwee, R. G. Gut 2001, 48, 859).
It has now surprisingly been found that the novel 1H-imidazole derivatives of the formula (I), prodrugs thereof and salts thereof, are potent agonists, partial agonists or antagonists on cannabinoid-CB1receptors

wherein
- R represents phenyl, thienyl, 2-pyridinyl, 3-pyridinyl, 4-pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl ortriazinyl, which groups may be substituted with-,1, 2, 3 or 4 substituents Y, which can be the same or different, from the group C1.3-alkyl or alkoxy, hydroxy, halogen, trifluoromethyl, trifluoromethylthio, trifiuoromethoxy, nitro, amino, mono- or dialkyi (C^-amino, mono- or dialkyl (C1.2)-amido, (C^)-alkoxycarbonyl, carboxyl, cyano, carbamoyl and acetyl, or R represents naphtyl, with the proviso that when R is 4-pyridinyl, R4 represents a halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyl, fluoroacetyl, propionyl, sulfamoyl, methanesulfonyi, methylsulfanyl or branched or unbranched d_4 alky] group, which d-4 alkyl group may be substituted with 1-3 fluoro atoms or with a bromo, chloro, iodo, cyano or hydroxy group,
- R, represents phenyl or pyridinyl, which groups may be substituted with 1-4 substituents Y, which can be the same or different, wherein Y has the above mentioned meaning, or Ri represents pyrimidinyl, pyrazinyl, pyridazinyl or triazinyl, which groups may be substituted with 1-2 substituents Y, which can be the same or different or R^ represents a five-membered aromatic heterocyclic ring having one or two heteroatoms from the group (N, O, S), which heteroatoms can*,

be the same or different, which five-membered aromatic heterocyclic ring may be substituted with 1-2 substituents Y, which can be the same or different or Ri represents naphtyl,
R2 represents H, branched or unbranched Cv8 alkyl, C3_8 cycloafkyl, C3.8 alkenyl, C5.8 cycloalkenyl which groups may contain a sulfur, oxygen or nitrogen atom, R3 represents branched or unbranched C2.8 alkyl, Cv8 alkoxy, C5.8 cycloalkyioxy, C3.3 cycloalkyl, C5-10 bicycloalkyl, C6-io tricycloalkyl, C3.8 alkenyl, C5-e cycloalkenyl, which groups may optionally contain one or more heteroatoms from the group (0, N, S) and which groups may be substituted with a hydroxy group or 1-2 Chalky) groups or 1-3 fluoro atoms, or R3 represents a benzyl or phenethyl group which aromatic rings may be substituted with 1-5 substituents Z, which can be the same or different, from the group d.3-alkyl or alkoxy, hydroxy, halogen, trifluoromethyl, trifiuoromethylthio, trifluoromethoxy, nitro, amino, mono- or dialkyl (C^-amino, mono- or dialkyl (C^-arnido, (C^-alkyfsulfonyi, dimethyl-suifamido, C^-alkoxycarbonyl, carboxyl, trifluoromethyisulfonyl, cyano, carbamoyl, sulfamoyl and acetyl, or R3 represents a phenyl or pyridinyl group, which groups are substituted with 1-4 substituents Z, wherein Z has the meaning as indicated above,
or R3 represents a pyridinyl group, or R3 represents a phenyl group, with the proviso that R4 represents a halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyl, fluoroacetyl, propionyl, sulfamoyl, methanesulfonyl, methylsulfanyl or 0^4 alkyl group, which C-M alkyl group may be substituted with 1-3 fluoro atoms or with a bromo, chloro, iodo, cyano or hydroxy group, or R3 represents a group NR5R6 with the proviso that R2 represents a hydrogen atom or a methyl group, wherein
R5 and R6 are the same or different and represent branched or unbranched C-M alkyl, or R5 and R6 - together with the nitrogen atom to which they are -bonded -form a saturated or unsaturated, monocyclic or bicyclic heterocyclic group having 4 to 10 ring atoms which heterocyclic group contains one or two heteroatoms from the group (N, O, S), which heteroatoms can be the same or different, which heterocyclic group may be substituted with a C^ alkyl group or a hydroxy group, or R2 and R3 - together with the nitrogen atom to which they are bonded - form a saturated or unsaturated heterocyclic group having 4 to 10 ring atoms which heterocyclic group contains one or two heteroatoms from the group (N, O, S), which heteroatoms can be the same or different, which heterocyclic group may be substituted with a Cv3 alkyl group or a hydroxy group,
R4 represents a hydrogen or halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyl, fluoroacetyl, propionyl, sulfamoyl, methanesulfonyl, methylsulfanyl or branched or unbranched CM alkyl group, which C^ alkyl group may be substituted with 1-3 fluoro atoms or with a bromo, chloro, iodo, cyano or a hydroxy group,

Due to the potent CB-i agonistic, partial agonistic or antagonistic activity the compounds according to the invention are suitable for use in the treatment of psychiatric disorders such as psychosis, anxiety, depression, attention deficits, memory disorders, cognitive disorders, appetite disorders, obesity, addiction, 1 appetence, drug dependence and neurological disorders such as neurodegenerative disorders, dementia, dystonia, muscle spasticity, tremor, epilepsy, multiple sclerosis, traumatic brain injury, stroke, Parkinson's disease, Alzheimer's disease, epilepsy, Huntington's disease, Tourette's syndrome, cerebral ischaemia, cerebral apoplexy, craniocerebral trauma, stroke, spinal cord injury, neuroinflammatory disorders, plaque sclerosis, viral encephalitis, demyelinisation related disorders, as well as for the treatment of pain disorders, including neuropathic pain disorders, and other diseases involving cannabinoid neurotransmission, including the treatment of septic shock, glaucoma, diabetes, cancer, emesis, nausea, gastrointestinal disorders, gastric ulcers, diarrhoea and cardiovascular disorders.
The affinity of the compounds of the invention for cannabinoid CB-j receptors was determined using membrane preparations of Chinese hamster ovary (CHO) cells in which the human cannabinoid CB1receptor is stably transfected in conjunction with [3H]CP-55,940 as radioligand. After incubation of a freshly prepared cell membrane preparation with the [3H]-ligand, with or without addition of compounds of the invention, separation of bound and free ligand was performed by filtration over glassfiber filters. Radioactivity on the filter was measured by liquid scintillation counting.
The cannabinoid CB1 antagonistic activity of compounds of the invention was determined by functional studies using CHO cells in which human cannabinoid CBt receptors are stably expressed. Adenylyl cyclase was stimulated using forskolin and measured by quantifying the amount of accumulated cyclic AMP. Concomitant activation of CBt receptors by CB-, receptor agonists (e.g. CP-55,940 or (R)-WIN-55,212-2) can attenuate the forskolin-induced accumulation of cAMP in a concentration-dependent manner. This CB1receptor-mediated response can be antagonized by CB-i receptor antagonists such as the compounds of the invention.
Cannabinoid agonistic of partial agonistic activity of compounds of the invention can be determined according to published methods, such as assessment of//? vivo cannabimimetic effects (Wiley, J. L et a/., J. Pharmacol. Exp. Ther. 2001, 296,
1013).
The invention relates both to racemates, mixtures of diastereomers and the individual stereoisomers of the compounds having formula (I).

The compounds of the invention can be brought into forms suitable for administration by means of usual processes using auxiliary substances and/or liquid or solid carrier materials.
Suitable synthetic routes for the compounds of the invention are the following: Synthetic route A
Step 1: ester hydrolysis of a compound having formula (II) wherein R7 represents a branched or unbranched aikyl group (C^) or benzyl group

This reaction gives a compound having formula (111)

wherein R, R-j and R4 have the meanings as described above.
Intermediates having formula (ll), wherein R7 represents a branched or unbranched aikyl group (C^) or benzyl group can be obtained according to methods known, for example:
a) I. K. Khanna et aiM J. Med. Chem. 2000, 43, 3168-3185
b) N. Kudo et al., Chem. Pharm. Bull. 1999, 47y 857-868
c) K. Tsuji et a!., Chem. Pharm. Bull. 1997, 45, 987-995
d) I. K. Khanna et a!., J. Med. Chem. 1997, 40, 1634-1647
e) M. Guiliemet et al., Tetrahedron Lett 1995, 36, 547-548
Step 2 : reaction of a compound having formula (111) with a compound having formula R2R3NH wherein R2 and R3 have the meanings as described above via activating and coupling methods such as formation of an active ester, or in the presence of a coupling reagent such as DCC, HBTU, BOP or similar reagents. This reaction gives a desired 1H-imidazole derivative having formula (I).
(For more information on activating and coupling methods see: M. Bodanszky and A Bodanszky: The Practice of Peptide Synthesis, Springer-Veriag, Nevs York, 1994; ISBN: 0-387-57505-7).

Alternatively, a compound having formula (Id) is reacted with a hafogenating agent, for example thionyl chloride (SOCI2). This reaction gives the corresponding carbonyl chloride (IV).

Reaction of a compound having formula (IV) with a compound having formula R2R3NH wherein R2 and R3 have the meanings as described above, yields a 1H-imidazole derivative having formula (I). This reaction is preferably carried out in the presence of an organic base such as for example diisopropylethylamine (DIPEA) or triethylamine.
Alternatively, a compound having formula (II) is reacted in an amidation reaction with a compound having formula R2R3NH wherein R2 and R3 have the meanings as described above to give a 1H-imidazole derivative having formula (I).
Synthetic route B
Reaction of a compound having formula (II), wherein R4 represents hydrogen and wherein R, R1 and R7 have the meanings as described above for compound (II), with a compound having general formula R4'-X, wherein X represents a leaving group and R4' represents a d.4 alkyl group, which alkyi group may be substituted with 1-3 fluoro atoms or wherein R/ represents a cyano, formyl, acetyl, trifluoroacetyl, fluordacetyi, methyisuifanyl or propionyl moiety, or a halogen atom. This reaction is carried out in the presence of a strong non-nucleophific base such as lithium diisopropylamide (LDA), preferably under anhydrous conditions in an inert organic solvent, for example tetrahydrofuran, and yields a compound having formula (II)

wherein R, R^ and R7 have the meanings as described hereinabove and R4 represents a CM alkyl group, which alkyl group may be substituted with 1-3 fluoro atoms or wherein R4 represents a cyano, formyl, acetyl, trifluoroacetyl, fiuoroacetyl, methyisuifanyl or propionyl group, or a halogen atom.

Compounds of general formula (II) which have been obtained according to synthesis route B can be converted to compounds of general formula (I) analogously to the procedures described in synthesis route A, step 1 of route A or step 2 of route A (see above).

Synthetic route C

wherein R4 represents a branched or unbranched C-M alkyl group, which CM alky! group may be substituted with 1-3 fiuoro substituents and wherein R, R., have the meanings given above and R7 represents a branched or unbranched alkyl group (C-t. : 4) or benzyl group can be synthesized by reacting a compound having formula (V) or its tautomer
wherein R and Rt have the meanings given above, with a compound having formula (VI)
wherein R4 represents a branched or unbranched C-M alkyl group, which CV4 alkyl group may be substituted with 1-3 fiuoro atoms and R8 represents a leaving group, for example a bromo substituent, and R7 represents a branched or unbranched alkyl group (C1.4) or benzyl group. The reaction is preferably carried out in an organic solvent, for example in 2-propanol or in N-methyI-2-pyrrolidinone (NMP). The addition of an acid like trifluoroacetic acid (TFA) during the reaction may enhance the formation of the compounds having formula (II).
(For more information on the leaving group concept see: M, S. Smith and J. March: Advanced organic chemistry, p. 275, 5th ed.} (2001) John Wiley & Sons, New York, ISBN: 0-471-58589-0).
Compounds of general formula (II) which have been obtained according to synthesis route C can be converted to compounds of general formula (I) analogously to the

procedures described in synthesis route A, step 1 of route A or step 2 of route A (see above).
Compounds of the invention having formula (VI) can be obtained according to methods known, for example: P. Seifert etai, He/v. Chim. Acta, 1950, 33, 725.
Synthetic route D
Reaction of a compound having formula (li)

wherein R4 represents a methyl group and R, Rt have the meanings given above and R7 represents a branched or unbranched alkyl group (C^) or benzyl group with a regioselective brominating compound such as N-bromo-succinimide (NBS) in an organic solvent such as CC)4 in the presence of a free-radical initiator like dibenzoyi peroxide gives a compound of formula (VII)

wherein R, R^ and R7 have the meanings given above. Reaction of a compound having formula (VII) (analogous to the method described in Mathews, W.B. et a/., J. Label. Compds. Radiopharm., 1999, 42, 589) with for example KCI, Kl, KF or KCN gives a compound of formula (VIII)

wherein R, R-, and R7 have the meanings given hereinabove and Nu represents a chloro, iodo, fluoro or cyano group. The reaction is preferably carried out in the presence of a weak base like NaHC03 or in the presence of a crown ether ov a cryptand. (For more information on crown ethers and cryptands see: M. B. Smith and

J. March: Advanced organic chemistry, p. 105, 5th ed, (2001) John Wiley & Sons, New York, ISBN: 0-471-58589-0).
Compounds of general formula (VII) or (VII!) which have been obtained according to synthesis route D can be converted to compounds of general formula (I) analogously to the procedures described in synthesis route A, step 1 of route A, or step 2 of route A (see above).
Example 1
Part A: To a 1M solution of sodium bis(trimethylsilyl) amide in THF (70 mL) is added dropwise a solution of 4-chloroaniline (8.86 gram, 69.5 mmol) in anhydrous THF in a nitrogen atmosphere. After the mixture is stirred for 20 minutes a solution of 2,4-dichlorobenzonitrile (12 gram, 70 mmol) in THF is added. The resulting mixture is stirred overnight, poured into ice-water (400 mL) and extracted with dichloromethane, dried over Na2S04 and concentrated in vacuo to give a yellow oil (15.7 gram). Crystallisation from a dichloromethane/heptane mixture, and subsequent washing with methyl-t-butyl ether gives N-(4-chlorophenyl)-2,4-dichiorobenzenecarboxamidine (8.66 gram, 42% yield) as a yellow solid. Melting point (MP): 93-95 °C.
Analogously was prepared:
- N-(4-bromophenyl)~2,4-dichiorobenzenecarboxamidine. MP: 117-119 °C.
Part B: A mixture of N-(4-chIorophenyl)-2]4-dichiorobenzenecarboxamidine (2.00 gram, 6.68 mmol), ethyl 3-bromo-2-oxopropanoate (2.65 gram, 13.6 mmol) and NaHCOz (1.12 gram, 13.3 mmol) in 2-propanol is stirred at reflux temperature for 20 hours. After cooling to room temperature the mixture is concentrated in vacuo and the residue suspended in dichloromethane, washed with water (3 x 50 mL) and brine (3 x 50 mL). The aqueous layers are extracted with dichloromethane. The combined organic layers are dried over Na2S04 and concentrated in vacuo to afford crude brown product (2.0 gram). This product is further purified by column chromatography (silicagel, heptane/EtOAc = 90/10 (v/v)) to yield ethyl 1-(4-chlorophenyl)-2-(2,4-dichIorophenyI)-1H-imidazole-4-carboxylate (0.759 gram, 29 % yield) as a yellow oil which slowly solidifies on standing. Melting point: 150-152 °C; MS: 395 (MH+). 1H-NMR (400 MHz, CDCI3): 5 7.91 (s, 1H), 7.49 (dd, J = 8 Hz: J = 2 Hz, 1H), 7.29-7.36 (m, 4H), 7.07 (dt, J = 8 Hz, J= 2 Hz, 2H), 4.44 (q, J = 7 Hz, 2H), 1.42 (t, J =7 Hz, 3H). Part C: Ethyl 1-(4-chlorophenyl)-2-(2,4-dichIorophenyl)-1H-imidazole-4-carboxylate (0.810 gram, 2.06 mmol) and LiOH (0.173 g, 7.20 mmol) are dissolved in a H20/THF (20 mL/20 mL) mixture and stirred at 50 °C for 16 hours. The mixture is concentrated in vacuo to give 1-(4-chlorophenyi)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylic acid. Thionyl chloride (60 mL) is added and the mixture is heated at reflux

temperature for 1 hour and concentrated in vacuo to give crude 1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1 H-imidazole-4-carbonyl chloride.
Part D: Crude 1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carbonyI chloride (919 mg, -2.39 mmol), 1-aminopiperidine (0.469 g, 4.69 mmol) and triethylamine (0.363 g, 3.59 mmol) are dissolved in dichloromethane and stirred for one hour at room temperature. The mixture is washed with a saturated aqueous NaHC03 solution (3 x 20 ml_), dried oyer Na2S04 and concentrated in vacuo and further purified by column chromatography (ethyl acetate, silicagei) to give 1-(4-chlorophenyl)-2-(2I4-dichlorophenyl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide (356 mg, 26 % yield (based on ethyl 1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylate). Mass Spectrometry (MS): 449.
Analogously were prepared:
2. 1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-N-(pyrrolidin-1-yl)-1H-imidazole-4-carboxamide; MS: 435.
3. N-(t-Butoxy)-1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxamide; MS: 438.
4. 1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-N-phenyl-1H-imidazole-4-carboxamide; MS: 442.
5. 1-(4-Chlorophenyl)-N-cyclohexyl-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxamide; MS: 448.
6. N-(Benzyl)-1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-N-methyl-1H-imidazole-4-carboxamide; MS: 470.
7. 1-[1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-4-(1H-imidazolyl)carbonyi] hexahydro-1H-azepine; MS: 448.
8. 2-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide (prepared from 2,4-dichloroaniline and 4-chlorobenzo-nitriie); MS: 449.
9. N-(t-Butoxy)-2-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-1H-imidazoie-4-carboxamide (prepared from 2,4-dichloroaniline and 4-chlorobenzonitrile); MS: 438.
Example 10
Part A: Diisopropyiamine (2.30 gram, 22.8 mmol) is added dropwise to anhydrous THF (100 mL) in a nitrogen atmosphere at 0 °C. n-BuLi is added dropwise (7.34 mL, 2.5 M solution in hexane, 18.4 mmol). The resulting solution is cooled to - 78 °C. A solution of ethyl 2-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylate (6.0 gram, 15.2 mmol) in anhydrous THF is added dropwise. The colour of the mixture changes from yellow to purple brown. The stirred mixture is warmed to - 40 °C and cooled to - 78 °C and allowed to stand for 30 minutes. Methyl iodide (5.44 gram, 45.4 mmol) is added dropwise and the resulting solution is stirred for 30

min at - 78 °C and then allowed to attain room temperature. The resulting solution is quenched with an aqueous NH4CI solution, diethyl ether is added and the organic layer is dried over MgS04l filtered and concentrated in vacuo to give an oil (6.4 gram). This oil is purified by column chromatography (toluene/EtOAc = 10/2 (v/v), silicagel) to give pure ethyl 2-(4-chlorophenyl)-1-(2(4-dichiorophenyi)-5-methyl-1H-imidazole-4-carboxylate (5,3 gram, 85 % yield) as a yellow oil. Part B: Ethyl 2-(4-chlorophenyl)-1-(2,4-dichiorophenyl)-5-methyi-1 H-imidazole-4-carboxylate (0.250 gram, 0.51 mmol) and LiOH (Q.052 gram, 2.17 mmol) are dissolved in H2OrTHF (1:1 (v/v); 50 mL) and stirred at 50 °C for one hour. The mixture is concentrated to give crude 2-(4-chlorophenyl)-1-(2,4-dicMorophenyl)-5-methyl- 1H-imidazole-4-carboxy!ic acid. To this mixture is added SOCI2 (50 mL) and the resulting mixture is heated at reflux temperature for 1 hour. The mixture is concentrated to give 2-(4-chlorophenyl)-1-(2J4-dichlorophenyl)-5-methyl-1H-imidazoie-4-carbonyl chloride.
Part C: 2-(4-Ch]orophenyI)-1-(2,4-dichlorophenyl)-5-methyMH-imidazole-4-carbonyl chloride (1.5 gram, 3.75 mmol), 1-aminopiperidine (0.725 gram, 7.25 mmol) and triethylamine (0.549 gram, 5.44 mmo!) are dissolved in dichloromethane and stirred for one hour at room temperature. The mixture is washed with a saturated aqueous NaHC03 solution, dried over Na2S04 and concentrated in vacuo and further purified by column chromatography (heptane/ethyl acetate = 1/1 (v/v), siiicagei) to give 2-(4-chlorophenyl)-1-(2J4-dichlorophenyl)-5-methyl-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide (0.220 gram, 13 % yield) as a white foam. MS: 463.
Analogously were prepared:
11. N~(t-Butoxy)-2-(4-chiorophenyl)-1 -(2J4-dichlorophenyl)-5-methyl-1 H-imidazoIe-4-
carboxamide: MS: 452. 12.1-(4-Chiorophenyl)-2-(2l4-dichlorophenyl)-5-methyl-N-(piperidin-1-yl)-1H-
imidazole-4-carboxamide: MS: 463; Melting point: 165-167 °C.
13. N-(t-Butoxy)-2-(2,4~dichiorophenyl)-1 -(4-chlorophenyl)-5-methyl-1 H-imidazole-4-
carboxamide: MS: 452.
14. N-(t-Butoxy)-1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-5-ethyl-1H-irnidazole-4-
carboxamide: Amorphous. MS: 468. 15.1-(4-Chlorophenyi)-2"(2,4-dichlorophenyl)-5-ethyl-N-(piperidin-1-y()-1H-imidazole-
4-carboxamide: MS: 477.
15. 1 -(4-Bromophenyl)-N-(t-butoxy>2-(2l4-dichlorophenyl)-5-methyl-1 H-imidazoie-4-
carboxamide: Amorphous. 17. 1 -(4-Bromophenyl)-2-(2l4-dichlorophenyl)-5-methyl-N-(piperidin-1 -yl)-1 H-
imidazole-4-carboxamide: MP: > 204 °C. TLC (Silicagel, EtOAc) Rf = 0.3. 18.1 -(4-Bromophenyl)-N-(t-butoxy)-2-(2,4-dichlorophenyl)-5-ethyi-1 H-imidazo!e-4-
carboxamide: Amorphous. TLC (Silicagel, CH2CI2/acetone = 9/1 (v/v)) Rf = 0.45.

19. 1 -(4-Bromophenyl)-2-(2>4-dichIorophenyl)-5-ethyl-N-(pfperidin--1 -yl)-1 H-imidazoIe-
4-carboxamide: MP: > 140 °C. TLC (Silicagei, EtOAc) Rf = 0.4.
20. 1-(4-Bromophenyi)-N-cyciohexyl-2-(2/^ carboxamide; Melting point > 135-140 °C.
21. 1-(4-Bromophenyl)-2-(2,4 carboxamide; Syrup. TLC (Silicagei, CH2CI2/acetone = 19/1 (v/v)) Rf = 0.4.
Example 22
Part A: To a stirred solution of ethyl 1-(4-bromophenyl)-2-(2,4-dichiorophenyl)-1H-imidazole-4-carboxy)ate (6.10 gram, 0.0139 mol) in THF (70 mL) is added UOH (0.67 gram, 0.0278 mol) and water (70 mL). The resulting mixture is stirred for 16 hours at 50 °C to give a clear solution. After cooling to room temperature, HCI (1N solution, 28 mL) is added to give an oily precipitate which completely solidifies on continued stirring and addition of water (70 mL). The precipitate is collected by filtration, washed with water and dried in vacuo to give 1-(4-bromophenyi)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylic acid (4.92 gram, 86 % yield). Melting point: 138-142 °C.
Part B: To a stirred suspension of 1-(4-bromophenyI)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylic acid (1.23 gram, 2.99 mmol) in dry acetonitrile (40 mL) is successively added diisopropylethylamine (DIPEA) (1.15 mL, 6.6 mmol), O-benzotriazol-1-yl-N, N, 1ST, N'-tetramethyluronium hexafluorophos-phate (HBTU) (1.36 gram, 3.6 mmol) and 1-aminopiperidine (0.39 mL, 3.6 mmol). After stirring for 16 hours, the resulting mixture is concentrated in vacuo. The residue is dissolved in ethylacetate and an aqueous NaHC03 solution is added. The ethyiacetate layer is collected, washed with water and brine, dried over Na2SO^f filtered and concentrated in vacuo to give a crude solid. This solid is further purified by recrystallisation from acetonitrile to give 1-(4-bromophenyl)-2-(2,4-d/chlorophenyl)-N-(piperidin-'}7yI)-1H-imidazole-4-carboxamide (830 mg, 56 % yield). Melting point: 219-221 °C.
Analogously were prepared:
23. N-(t-Butoxy)-1-(4-bromophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxamide. Amorphous. TLC (Silicagei, Et20) Rf = 0.3.
24. 1-(4-Bromophenyl)-2-(2,4-dichIorophenyI)-N-(pyrrolidin-1-yl)-1H-irnidazoIe-4-carboxamide. Melting point: 238-240 °C.
25. N-(Azepan-1-yi)-1-(4-bromophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxamide. Melting point: 201-204 °C.
26. 1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-N-(hexahydrocyclopenta[c]pyrrol 2(1H)«yl)-lH-imidazole-4-carboxamide. MS: 475.
27. 1 -(4-Chlorophenyi)-2-(2,4-dichlorophenyl)-N-(4-fluorobenzyl)-1 H-imidazole-4-carboxamide. MS: 474.

28. 1-(4-ChIorophenyO-2-(2-methoxy-4-chlorophenyl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: 220 °C.
29. 1 -(4-Chlorophenyl)-N-cyclohexyl-2-(2-methoxy-4-chlorophenyl)-1 H-imidazole-4-carboxamide. Melting point: 177-179 °C.
30. 1 -(4-Chlorophenyl)-2-(2-fluoro-4-chlorophenyl)-N-(piperidin-1 -yl)-1 H-imidazole-4-carboxamide. Melting point: 217-218 °C.
31. 2-(2,4-Dichlorophenyl)-1-(4-fluorophenyl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: 175-176 °C.
32. N-Cyclohexyl-2-(2,4-dichiorophenyl)-1 -(4-fluoropheny])-1 H-imidazole-4-carboxamide. Melting point: 184-185 °C.
33. N-Cyclohexyl-2-(2-fluoro-4-chlorophenyl)-1-(4-chlorophenyl)-1H-imidazole-4-carboxamide. Melting point: 157-159 °C.
34. 1 -(4-Chlorophenyl)-2-(2-methoxy-4-chlorophenyl)-N-(n-pentyl)-1 H-imidazole-4-carboxamide. Melting point: 115 °C.
35. 2-(2,4-Dichlorophenyl)-1-(4-methoxyphenyf)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: 178-179 °C.
36. N-Cyclohexyl-2-(2,4-dichlorophenyl)-1 -(4-methoxyphenyl)-1 H-imidazoie-4-carboxamide. Melting point: 175-176 °C.
37. 1-(4-Chlorophenyl)-2-(2,4-dichloropheny[)-N,N-diethyl-1H-imidazole-4-
carboxamide. Melting point: 177-179 °C.
38. 1 -(4-Chlorophenyl)-N-cyclohexyl-2-(2-trifluoromethyl-4-chlorophenyl)-1 H-
imidazole-4-carboxamide. Melting point: 172 °C.
39. 1-(4-Chlorophenyl)-N-(piperidin-1-yl)-2-(24rifluoromethyl-4-chlorophenyl)-1H-
imidazoie-4-carboxamide. Melting point: 219°C.
40. N-(1-Adamantyl)-1-(4-chlorophenyl)-2-(2-trifluoromethyl-4-chloropheny!)-1H-
imidazole-4-carboxamide. Melting point: 288 °C.
41. 1-(4-Chloropheny!)-N-(2t2l2-trifluoroethyl)-2-(2-trifluoromethyl-4-chloroph^ 1H-imidazole-4-carboxamide. Melting point: 149 °C.
42. 2-(2,4-Dichlorophenyl)-1-(pyridin-3-yl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: 165-170 °C.
43. N-Cyciohexyl-2-(2l4-dichlorophenyl)-1-(pyridin-3-yl)-1H-imidazole-4-carboxamide.Melting point: 195 °C.
44. 2-(2,4-Dichlorophenyl)-1 -(pyridin-3-yl)-N-(n-pentyl)-1 H-imidazole-4-carboxamide. Melting point: 117°C.
Example 45
Part A: 2,4-Dichlorobenzoyl chloride (40.0 g, 0.19 mol) is dissolved in tetrahydrofuran (1 L). To the resulting stirred solution is successively added diisopropylethylamine (DIPEA) (73.4 mL, 2.2 molar equivalent) and 4-(trifluoromethyl)phenylamine (30.7 g, 0.19 mol). After one hour the mixture is concentrated in vacuo to give an oil. This oil is crystallised from ethanol to give pure 2,4-dichloro-N-(4-(trifluoromethyl)phenyl)benzamide (53.2 g, 83 % yield). 1H-NMR

(200 MHz, DMSO-d6): 5 10.90 ( br s, 1H), 7.91 (br d, J = 8 Hz, 2H), 7.63-7.77 (m, 4H), 7.57 (dt, J = 8 Hz, J= 2 Hz, 1H).
Part B: 2,4"Dich!oro-N-(4-(trifluoromethyl)phenyl)benzamide (19.0 g, 0.057 mol) is dissolved in benzene (150 mL) and PCI5 (13.0 g, 1.1 molar equivalent) is added. The resulting mixture is heated at reflux temperature for two hours, allowed to attain room temperature and concentrated in vacuo to give a residue. The residue is dissolved in anhydrous THF, cooled to 0 °C and transferred into an autoclave. Excess NH3 is quickly added from a lecture bottle and the mixture is stirred at room temperature for 50 hours. A mixture of ethylacetate and aqueous NaHC03 is added. The ethylacetate layer is collected, dried over Na2S04, filtered and concentrated in vacuo. The resulting oil is purified by column chromatography (diethyl ether/petroleum ether = 1/1 (v/v), silicagel) to give pure 2]4-dichIoro-N-(4-(trifIuoromethy[)phenyl)benzene-carboxamidine (16.9 g, 89 % yield). Melting point: 108-109 °C. Part C: 2I4-Dichloro-N-(4-(trifluoromethyl)phenyl)benzenecarboxamidine (15.0 g, 0.0450 mol) is dissolved in 2-propanol and ethyl 3-bromo-2-oxobutanoate (20.8 g, 2 molar equivalent) and NaHC03 are successively added. The resulting mixture is heated at reflux temperature for 40 hours and allowed to attain room temperature. The 2-propanoi is removed in vacuo, ethyl acetate is added to the residue and the resulting organic layer is washed with NaHC03 (5 % aqueous solution). The ethylacetate layer is collected, dried over Na2S04, filtered and concentrated in vacuo. The resulting oil is purified by column chromatography (diethyl ether/petroleum ether - 1/3 (v/v), silicagel) and further purified by crystallisation from cyclohexane to give ethyl 2-(2l4-dichlorophenyi)-5-methyl-1-(4-(trifluoromethyl)phenyl)-1H-imidazoie-4-carboxylate (10.45 g, 52 % yield) as a yellow solid. Melting point: 160-162 °C. Part D: The formed ethyl 2-(2,4-dichlorophenyI)-5-methyl-1-(4-(trifluoromethyl) phenyi)-1H-fmidazole-4-carboxy!ate is converted to 2-(2,4-dichlorophenyl)-5-methyl-1-(4-(trif[uoromethyl)phenyl)-1H-imidazole-4-carboxylic acid (melting point: -224-226 °C), which carboxylic acid is converted to 2-(2,4-dichlorophenyl)-5-methyl-N-(piperidin-1-yl)-1-(4-(trifiuoromethyl)phenyl)-1H*-imidazole-4-carboxamide (melting point: 173-174 °C) according to the procedure described in example 22 above. Analogously were prepared
46. 2-(2t4-dichlorophenyl)-N-(piperidin-1-yl)-1-(4-(trifluoromethyl)phenyl)-1H-imidazole-4-carboxamide. Melting point >200 °C (decomposition).
47. N-Cyclohexyl-2-(2)4-dlchlorophenyl)-5-methyl-1-(4-(trif!uoromethyI) phenyl)-1H-imidazole-4-carboxamide. Melting point: 178-179 °C.
48. N-Cyclohexyl-2-(2,4-dichlorophenyl)-1-(4-(tnfluoromethyl)phenyl)-1H-imidazo!e-4-carboxamide. Melting point: 199-200 °C.
Example 49
Part A: N-(4-methoxyphenyl)-2J4-dichlorobenzenecarboxamidine (15.0 gram, 50.8
mmol) is dissolved in 2-propanol and ethyl 3-bromo-2-oxobutanoate (23.5 g, 2 molar s

equivalents) and NaHC03 (8.5 gram, 2 molar equivalents) are successively added. The resulting mixture is heated at reflux temperature for 40 hours and allowed to attain room temperature. The 2-propanol is removed in vacuo, ethyl acetate is added to the residue and the resulting organic layer is washed with NaHC03 (5 % aqueous solution). The ethylacetate layer Is collected, dried over Na2S04, filtered and concentrated in vacuo. The resulting oil is purified by column chromatography (diethyl ether/petroleum ether = 1/3 (v/v), silicagel) to give ethyl 2-(2,4-dichiorophenyl)"5-methyl-1«(4-methoxy-phenyI)-1H-imidazole-4-carboxyIate (8.61 g, 42 % yield) as a solid. 1H-NMR (200 MHz, CDCI3): 5 7.33 (d, J = 8 Hz, 1H), 7.27 (d, J = 2 Hz, 1H), 7.18 (dd, J = 8 Hz, J = 2 Hz, 1H), 7.03 (dt, J = 8 Hz, J = 2 Hz, 2H), 6.85 (dt, J = 8 Hz, J = 2 Hz, 2H), 4.42 (q, J = 7 Hz, 2H), 3.80 (s, 3H), 2.43 (s, 3H), 1.43 (t, J =7 Hz, 3H).
Part B: To a stirred solution of ethyl 2-(2,4-dichlorophenyl)-5-methyl-1 -(4-methoxyphenyl)-1H-imidazole-4-carboxylate (8.00 gram, 0.0198 mol) in THF (80 mL) is added LiOH (0.59 gram, 2 molar equivalents) and water (80 mL). The resulting mixture is stirred for 16 hours at 80 °C. After cooling to room temperature, HCI (2N solution, 12.3 mL) is added to give an oily precipitate. After addition of water and extraction with ethylacetate, the ethylacetate layer is collected, dried over Na2S04, filtered and concentrated in vacuo. The residue is crystallised from diisopropyl ether and dried to give 2-(2,4-dichlorophenyl)-5-methyl-1-(4-methoxyphenyl)-1H-irnidazole-4-carboxyiic acid (4.04 gram, 87 % yield) as a pale grey solid. Melting point: 189-191 CC.
Part C: To 2-(2,4-dichlorophenyl)-5-methyl-1 -(4-methoxyphenyl)-1 H-imidazole-4-carboxyiic acid (1.00 gram, 2.65 mmol) in dry acetonitrile (25 mL) is successively added diisopropyiethylamine (DIPEA) (1.02 mL, 2.2 molar equivalents), O-benzotriazol-1-yl-N, N, N', N'-tetramethyluronium hexafluoro-phosphate (HBTU) (1.21 gram, 1.2 molar equivalents) and the resulting solution is stirred for 15 minutes. Cyclohexylamine (0.36 mL, 1.2 molar equivalents) is added. After stirring for 50 hours, the resulting mixture is concentrated in vacuo. The residue is dissolved in dichloromethane and an aqueous NaHC03 solution is added. The dichloromethane layer is collected, dried over Na2S04l filtered and concentrated in vacuo. The residue is further purified by column chromatography (gradient: dichloromethane => dichloromethane/methanol = 99/1 (v/v), silicagel) to give N-(1-cyclohexyI)-2-(2,4-dichlorophenyl)-5-methyl-1-(4-methoxyphenyl)-1H-imidazole-4-carboxamide (1.03 gram, 85 % yield). Melting point: 160-161 °C.
Analogously were prepared:
50. 1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-N,N,5-trimethyl-1H-imidazoie-4-carboxamide. Melting point: 101-104 °C.
51. 1-(4-Chioropyridin-2-yl)-2-(2)4-dichlorophenyl)-5-methyl-N-(piperidin-1--yl)-1H-imidazole-4-carboxamide. MS: 464 (MH+).

52. 1-(4-Chloropyridin-2-y[)-2-(2,^ imidazole-4-carboxamide. MS: 466 (MH+).
53. N-(1-Azepanyl)-1-(4-Chloropyridin-2-yl)-2-(2,4-dichlorophenyl)-5-methyl-1H^ imidazole-4-carboxamide. MS: 478 (MH+).
54. 1-(4-Chioropyridin-2-yl)-N-cyclohexyl-2-(2,4-dichlorophenyI>5-methyl^ imidazole-4-carboxamide. MS: 463.
55. 1-(4-Chloropyridin-2-yl^ imidazole-4-carboxamide. MS: 451.
55. 1 -(4-Ch!oropyridin-2-yl)-2-(2,4-dichlorophenyi)-N-(4~fluorobenzyI)-5-methyl-1 H-imidazole-4-carboxamide. MS: 489. Melting point: 123-126 °C.
57. 1-(4-Chloropheny!)-N-cyclohexyl-5-methyl-2-(2-trffluoromethyl-4-chlorophenyl)-1H-imidazole-4-carboxamide. Melting point: 212 °C.
53. 1 -(4-Chlorophenyl)-5-methyI-N-(piperidin-1 -yl)-2-(2-trifiuoromethyl-4-chlorophenyl)-1H-imidazole-4-carboxamide. Melting point: 165 °C.
59. 1-(4-ChlorophenyO-2-(2-methoxy-4-chIorophenyi)-5-methyl-N-(n-pentyi)-1H-imidazole-4-carboxamide. Melting point 131 °C.
60. 1-(4-Chlorophenyl)-2-(2-methoxy-4-chloropheny^ imidazole-4-carboxamide. Melting point: > 256 °C.
61. N-Cyclohexyl-1-(4-chlorophenyl)-2-(2-methoxy-4-chlorophenyl)~5-methyl-1H-imidazole-4-carboxamide. Melting point: 201 °C.
62. 2-(2,4-Dfchlorophenyl)-1-(4-fliJorophenyl)-5-methyl-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: 223-224 °C.
63. 2-(2I4-Dichlorophenyl)-5-methyl-1-(4-methoxyphenyl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: > 90 °C (decomposition).
64. N-Cyclohexyl-1-(4-fiuorophenyl)-2-(2,4-dichlorophenyl)-5-methyl-1H-imidazole-4-carboxamide. Melting point: 229-230 °C.
65. 1-(4-Chloropheny!)-5-methyl-N-^ imidazole-4-carboxamide. Amorphous.
66. 1-(4-ChlorophenyO-2-(2-fluoro-4-chlorophenyl)-5-methyl-N-(piperidin-1-y[)-1H-imidazole-4-carboxamide. Melting point: 195 °C.
67. 1-(4-Chiorophenyl)-2-(2-fluoro-4-chlorophenyl)-5-methyl-N-(n-pentyl)--1H-imidazole-4-carboxamide. Melting point: 115°C.
68. 1 -(4-Chlorophenyl)-N-(cyciohexy[)-2-(2-fiuoro-4-chlorophenyl)-5-methyl-1 H-imidazole-4-carboxamide. Melting point: 188 °C.
69. 1-(4-Chlorophenyl)-N-(cyclohexyl)-2-(1,5-dimethyl-1H-pyrrol-2-yl)-5-methyl-1H-imidazole-4-carboxamide. Melting point: 183-189 °C.
70. 1-(4-ChIoropheny!)-2-(1,5-dime^ imidazole-4-carboxamide. Melting point: 208-210 °C.
71. 2-(2-Chlorophenyl)-1-(3-fluorophenyl)-5-methyl-N-(piperidin-1-yl)-1H-imidazo!e-4-carboxamide. Melting point: 236-238 °C.
72. 2-(2-Chlorophenyl)-1-(3-fluorophenyl)-5-methyl-N-(n-pentyl)-1H-imidazo!e-4-carboxamide. Melting point: 97-102 °C.

73. 2-(2-Chlorophenyl)-N-cyclohexyl-1-(3-fluorophenyl)-5-methyN1H-imidazoIe-4-carboxamide. Melting point: 180-182.5 °C.
74. 2-(2-Chiorophenyl)-1 -(3-fluorophenyi)-N-(2-(4-fluorophenyl)ethyi)-5-methyl-1 H-imidazole-4-carboxamide. Melting point: 123.5-126 °C.
75. 1-(4-CNoropyridin-2-yl)-2-(2,4-d^ imidazofe-4-carboxamide. Melting point: 146 CC.
76.. 1 -(4-Chloropyridin-2-yl)-2-(2,^ H-
imidazole-4-carboxamide. Melting point: 223 °C.
77. N-(1-Azepanyl)-1-(4-Ch!oropyridin-2-yl)-2-(2I4-dichlorophenyl)-5-ethyi-1H-imidazole-4-carboxamide. Melting point: 177 °C.
78. 1-(4-Chloropyridin-2-yI)-N-cyc!ohexyl-2-(2f4-dichlorophenyl)-5-ethyl-1H-imidazole-4-carboxamide. Melting point: 149 °C.
79. 1 -(4-Chloropyridin-2-yi)-2-(2,4-dichlorophenyl)-5-ethyl-N-(n-penty i)-1 H-imidazo(e-4-carboxamide. Melting point: Oil.
80. 1-(4-Chioropyridin-2-yl)-2-(2)4-dichlorophenyl)-5-ethyl-N-(4-fiuorophenylmethyi)-1H-imidazoie-4-carboxamide. MP: amorphous.
81. 1 -(4-Chiorophenyl)-2-(2,4-dichlorophenyl)-N-(hexahydrocyclopenta"[c]pyrroi-2(1H)-yl)-5-methyl-1H-imidazoie-4-carboxamide. MP: 143-146 °C.
82. 1 -(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyi-N-phenyl-1 H-imidazole-4-carboxamide. Melting point: 91-95 °C.
83. 1-(4-Chiorophenyl)-2-(2,4^ichloro^ yioxy)-1H-imidazole-4-carboxam(de. Melting point: 128-133 °C.
84. N-(Exo-bicycio[2.2.1]hept-2-yl)-1-(4-chlorophenyl)-2-(2,4-dichlorophenyi)-5-methyi-lH-imidazole-4-carboxamide. Melting point: 194-195 °C.
85. 1 -(4-Chloropheny l)-2-(2,4-dich!orophenyl)-N-(2-fiuoroethy l)-5-methyl-1 H-imidazoIe-4-carboxamide. Melting point: 128-133 °C.
85. 1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-N-(trans-4-hydroxycyclohexyl)-5-methyl-1H-imidazole-4-carboxamide. Melting point: 160 °C (dec).
87. 1 -{[1 -(4-Chlorophenyl)-2-(2,4-dichlorophenyi)-5-methyi-1 H-imidazol-4-yl]carbonyl}-4-hydroxypiperidine. Melting point: Amorphous.
88. 1-{E1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyi-1H-imidazol-4-ylJcarbonylJ-I^.S^-tetrahydrofsoquinoline. Melting point: 143-146 °C.
89. N-(Endo-bicyclo[2.2.1]hept-2-yl)-1-(4-chlorophenyl)-2-(2l4-dichiorophenyl)-5-methyl-1H-imidazole-4-carboxamide. Melting point: 194-195 °C.
90. 1 -(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-N-(4-fluorobenzyl)-5-methyl-1 H-imidazole-4-carboxamide. Melting point: 165-166 °C.
91. 1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyi-N-(n-pentyl)-1H-imidazole-4-carboxamide. Oil.
92. N-(Azepan-1-yl)-1-(4-ch[oropheny!)-2-(2,4-dichlorophenyl)-5-methyl-1H-imidazole-4-carboxamide. Melting point: 147-149 °C.
93. 1 -(4-Chlorophenyi)-2-(2,4-dichloropheny l)-5-methyl-N-(py rrolidin-1 -yi)-1 H-imidazole-4-carboxamide. Melting point: 205-206 °C.

94. l^-ChlorophenyO^^^-dichlorophenyQ-S-methyl-N^morpholin^-yO-IH-imidazote-4-carboxamide. Melting point: 225 °C (dec).
95. 2-(2,5-Dichlorophenyl)-5-methyi-1-phenyl-N-(piperidin-1-yi)-1H-imidazo!e-4-carboxamide. Melting point: 227 °C.
96. N-Cyclohexy!-2-(2,5-dichlorophenyl)-5-methyl-1-phenyl-1H-imidazole-4-carboxamide. Melting point: 236 °C.
97. N-Cyclohexyl-2-(2(4-dichiorophenyl)-1-(2,5-difluorophenyl)-5-ethyl-1H-imidazole-4-carboxamide. Melting point: 144-146 CC.
98. N-Cyclohexyl-2-(2I4-dichlorophenyl)-1-(2,5-difluorophenyl)-5-methyl-1H-imidazole-4-carboxamide. Melting point: 206-208 °C.
99. N-Cyclohexyl-2-(1,5-dimethyM H-pyrrol-2-yl)-5-ethyl-1-phenyl-1 H-imidazole-4-carboxamide. Melting point: 195-196 °C.

100. N-Cyclohexyl-2-(2,5-dichlorophenyl)-5-ethyl-1-phenyl-1H-imidazole-4-carboxamide. Melting point: 198-199 °C.
101. 2-(2J5-Dichlorophenyl)-5-ethyl-1-phenyl-N-(piperidin-1-yl)-1H-innidazole-4-carboxamide. Melting point: 207-208 °C.
102.1-(4-Chlorophenyl)-5-methyl-2-(3-methylpyridin-2-yl)-N-(piperidin-1-yl)-1H-
imidazole-4-carboxamide. Melting point: 211-213 °C. 103.1 -(4-Chlorophenyl)-N-cyclohexyl-5-methyl-2-(3-methylpyridin-2-yl)-1 H-
imidazoIe-4-carboxamide. Melting point: 188-190 °C. 104.1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyl-N-(3-
(trifluoromethyl)phenyl)-1H-imidazole-4-carboxamide. Melting point: 177°C. 105.1-(4-Chlorophenyl)-2-(2l4-dichlorophenyl)-5-methyl-N-(3-
(trifluoromethyl)benzyI)-1H-imidazole-4-carboxamide. Melting point: 138-140 °C. 106.1-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyl-N-(4-
(trifluoromethyl)benzyl)-1H-imidazole-4-carboxamide. Melting point: 232 °C. 107.1-(4-Chlorophenyl)-N-cyclopentyl-2-(2,4-dichlorophenyl)-5-methyl-1H-imfdazole-
4-carboxamide. Melting point: 172 °C. 108.1-(4-Chlorophenyl)-N-cycloheptyl-2-(2I4-dichlorophenyl)-5-methyl-1H-imidazole-
4-carboxamide. Melting point: 154-156 °C.
Example 109
Part A: Ethyl 1 -(4-bromophenyl)-2-(2,4-dichlorophenyl)-1 H-imidazole-4-carboxylate
is converted to ethyl 1-(4-bromophenyl)-5-chloro-2-(2,4-dichlorophenyl)-1H-
imidazole-4-carboxylate analogously to a published procedure (N. Kudo et al.T Chern.
Pharm. Bull. 1999, 47, 857-868) using excess of S02CI2 in dichloroethane at reflux
temperature for 50 hours.
Part B: Ethyl 1-(4-bromophenyl)-5-chloro-2-(2,4-dichlorophenyl)-1H-imidazole-4-
carboxylate is converted to 1 -(4-bromophenyl)-5-chloro-2-(2,4-dichloro-phenyl)-N-
(piperidin-1-yl)-1H-imidazole-4-carboxamide (melting point: > 150 °C; Rf (Silicagel,
EtOAc) - 0.35) analogously to the procedure described in example 22 above. 1H-
NMR (400 MHz, CDCI3): 5 7.85 (br s, 1H)T 7.52 (dt, J = 8 Hz; J = 2 Hz, 2H), 7.26-7.36,

(m, 3H), 7.01 (dt, J = 8 Hz, J = 2 Hz, 2H), 2.85-2.92 (m, 4H), 1.72-1.80 (m, 4H), 1.40 -1.44(m, 2H).
Example 110
Part A: To a stirred solution of 1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylic acid (18.38 gram, 50 mmol) in toluene (200 mL) in a nitrogen atmosphere is added N,N-dimethylformamide di-tert-butyl acetal (50 mL) and the resulting mixture is heated at 80 °C for 4 hours. After cooling to room temperature the reaction mixture is concentrated and diethyl ether is added. The resulting solution is twice washed with water, dried over MgS04p filtered and concentrated in vacuo. The residue is crystallised from diisopropyl ether to give pure tert-butyl 1-(4-chlorophenyl)-2-(2,4-dichlorophenyI)-1H-imidazoie-4-carboxylate (10.35 gram, 49 % yield). Melting point: 179-181 °C. PartB:
Lithium diisopropyl amide (LDA) (5.25 mL of a 2 M solution in THF, 0.0105 mol) is added dropwise to a cooled solution (-70 °C) of tert-butyl 1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylate (4.24 gram, 0.010 mol) in anhydrous THF (80 mL) in a nitrogen atmosphere and the resulting mixture is stirred for one hour. A solution of p-toluenesulfonyl cyanide (1.88 gram, 0.011 mol) in anhydrous THF (20 mL) is added dropwise and the resulting red solution is stirred for one hour at - 70 °C and then allowed to attain room temperature. Diethyl ether is added and the resulting solution is quenched with water and filtered over hyflo. The organic layer is collected and washed with water, dried over MgS04, filtered and concentrated in vacuo to give an oil. This oil is purified by column chromatography (dichloromethane, silicagel) to give 3.4 gram of tert-butyl 1 -(4-chlorophenyl)-5~cyano-2-(2,4-dichlorophenyl)-1H-imidazole-4-carboxylate. Recrystallisation from diisopropyl ether gave crystalline tert-butyl 1-(4-chlorophenyl)-5-cyano-2-(2,4-dichlorophenyl)-1H-imidazoie-4-carboxyIate (2.57 gram, 57 % yield). Melting point: 210-212 °C.
Analogously was prepared:
- Tert-butyl 1 -(4-chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyl-1 H-imidazole-4-carboxylate. 1H-NMR (400 MHz, CDCI3): 5 7.38 (d, J = 8 Hz, 1H), 7.34 (dt, J = 8 Hz, J = 2 Hz, 2H), 7.27 (d, J = 2 Hz, 1H), 7.22 (dd, J = 8 Hz, J = 2 Hz, 1H), 7.03 (dt, J = 8 Hz, J = 2 Hz, 2H), 2.40 (s, 3H), 1.63 (s, 9H).
PartC:
To a solution of tert-butyl 1 -(4-chlorophenyl)-2-(2,4-dichlorophenyl)-5-cyano-1 H-imidazoie-4-carboxylate (2.57 gram, 5.73 mmol) in dichloromethane (40 mL) is added trifluoroacetic acid and the resulting solution is stirred at room temperature for 20 hours and concentrated in vacuo. The residue is crystallised from diisopropyl ether to give pure 1 -(4-chlorophenyl)-5-cyano-2-(2,4-dichlorophenyl)-1 H-imidazole-4-carboxylic acid (1.95 gram, 87 % yield). Melting point: 200-202 °C (dec).

PartD:
1-(4-Chlorophenyl)-5-cyano-2-(2,4-dichloropheny!)-1 H-imidazole-4-carboxylic acid is converted to 1-(4-chlorophenyl)-5-cyano-2-(2,4-dichlorophenyl)-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide in 60 % yield, analogously to the procedure described in example 22, part B herein above. Melting point: 231-233.5 °C. Analogously were prepared:
111. 1-(4-Chlorophenyl)-2-(2,4-dichIorophenyl)-5-iodo-N-(piperidin-1-yl)-1H-imidazole-4-carboxamide. Melting point: 1S6-201 °C.
112.1-(4-Chlorophenyl)-N-cyclohexyl-2-(2,4-dichlorophenyl)-5-iodo-1 H-imidazole-4-
carboxamide. Melting point: 226-230 °C. 113.1 -(4-Chlorophenyl)-5-cyano-N-cyclohexyl-2-(2,4-dichlorophenyl)-1 H-imidazole-
4-carboxamide. Melting point: 157-158 °C.

wherein
R represents phenyl, thienyl, 2-pyridinyI, 3-pyridinyl, 4-pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl or triazinyl, which groups may be substituted with 1, 2, 3 or 4 substituents Y, which can be the same or different, from the group d-3-alkyl or aikoxy, hydroxy, halogen, trifluoromethyl, trifluoromethylthio, trifluoromethoxy, nitro, amino, mono- or dialkyJ (d^-amino, mono- or dialkyi (C^-amido, (d-3)-aikoxycarbonyl, carboxyl, cyano, carbamoyl and acetyl, or R represents naphtyl, with the proviso that when R is 4-pyridinyl, R4 represents a halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyf, fluoroacetyl, propionyl, sulfamoyl, methanesulfonyl, methylsulfanyl or branched or unbranched d-4 alkyl group, which d-4 alkyl group may be substituted with 1-3 fluoro atoms or with a bromo, chloro, iodo, cyano or hydroxy group,
R! represents phenyl or pyridinyl, which groups may be substituted with 1-4 substituents Y, which can be the same or different, wherein Y has the above mentioned meaning, or R1 represents pyrimidinyl, pyrazinyl, pyridazinyl or triazinyl, which groups may be substituted with 1-2 substituents Y, which can be the same or different or R1 represents a five-membered aromatic heterocyclic ring having one or two heteroatoms from the group (N, O, S), which heteroatoms can be the same or different, which five-membered aromatic heterocyclic ring may be substituted with 1-2 substituents Y, which can be the same or different or Rt represents naphtyl,
R2 represents H, branched or unbranched d-s alkyl, d-3 cycloalkyl, C3-3 alkenyl, C5-8 cycloalkenyl which groups may contain a sulfur, oxygen or nitrogen atom, R3 represents branched or unbranched C2-e alkyl, d-s aikoxy, C5.s cycloalkyloxy, C3-3 cycloalkyl, C5.10 bicycloalkyl, Cs_10 tricycloalkyl, C3.5 alkenyl, d-s cycloalkenyl, which groups may optionally contain one or more heteroatoms from the group (O, N, S) and which groups may be substituted with a hydroxy group or 1-2 d-3 alkyl groups or 1-3 fiuoro atoms, or R3 represents a benzyl or phenethyl group which aromatic rings may be substituted with 1-5 substituents Z; which can be the same or different, from the group C1-3-alkyl or aikoxy, hydroxy, halogen, trifluoromethyl, trifluoromethylthio, trifluoromethoxy, nitro, amino, mono- or dialkyi (C1-2)-amino, mono- or dialkyi (C1-2)-amido, (C1-3-alkylsulfonyl, dimethyl-sulfamido, C1-3-

alkoxycarbonyl, carboxyl, trifluoromethylsulfonyl, cyano, carbamoyl, sulfamoyl and acetyl, or R3 represents a phenyl or pyridinyl group, which groups are substituted with 1-4 substituents Z, wherein Z has the meaning as indicated above,
or R3 represents a pyridinyl group, or R3 represents a phenyl group, with the proviso that R4 represents a halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyi, fluoroacetyl, propionyl, sulfamoyl methanesulfonyl, methylsulfanyl or d.4 alkyl group, which C1-4alkyl group may be substituted with 1-3 fluoro atoms or with a bromo, chloro, iodo, cyano or hydroxy group, or R3 represents a group NR5R5 with the proviso that R2 represents a hydrogen atom or a methyl group, wherein
R5 and R6 are the same or different and represent branched or unbranched C^ alkyl, or R5 and R6 - together with the nitrogen atom to which they are bonded -form a saturated or unsaturated, monocyclic or bicyclic heterocyclic group having 4 to 10 ring atoms which heterocyclic group contains one or two heteroatoms from the group (N, O, S), which heteroatoms can be the same or different, which heterocyclic group may be substituted with a Ci_3 alkyl group or a hydroxy group, or R2 and R3 - together with the nitrogen atom to which they are bonded - form a saturated or unsaturated heterocyclic group having 4 to 10 ring atoms which heterocyclic group contains one or two heteroatoms from the group (N, O, S), which heteroatoms can be the same or different, which heterocyclic group may be substituted with a C-i_3 alkyl group or a hydroxy group,
R4 represents a hydrogen or halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyi, fluoroacetyl, propionyl, sulfamoyl, methanesulfonyl, methylsulfanyl or branched or unbranched C1-4 alkyl group, which C-M alkyl group may be substituted with 1-3 fluoro atoms or with a bromo, chloro, iodo, cyano or a hydroxy group,
and prodrugs, stereoisomers and salts thereof.
Pharmaceutical compositions containing a pharmacologically active amount of at least one compound as claimed in 1 as an active component.
Method of preparing pharmaceutical compositions as claimed in claim 2 characterised in that a compound as claimed in claim 1 is brought in a form suitable for administration.
Process for the preparation of compounds having formula (I), characterised in that a compound is prepared wherein R, RrR3 have the meanings given in claim 1 and R4 represents a hydrogen or halogen atom or a cyano, carbamoyl, formyl, acetyl, trifluoroacetyi, propionyl, sulfamoyl, methanesulfonyl, methylsulfanyl or C1-4 alkyl group, which C1-4 alkyl group may be substituted with 1-3 fluoro atoms, ,t

by reacting a compound having formula (II), (III) or (IV) with a compound of formula R2R3NH.
5. Process for the preparation of compounds having formula (II)

wherein R4 represents a C1-4alkyl group, which C-|.4 alkyl group may be substituted with 1-3 fluoro substituents, or wherein R4 represents a halogen atom or a cyano, formyl, acetyl, trifluoroacetyl, fluoroacetyl, methylsulfanyl or propionyl group, characterized in that a compound is prepared wherein R and R1 have the meanings given in claim 1 and R7 represents a branched or unbranched alkyl group (C1-4) or benzyl group, by reacting a compound having formula (II) wherein R4 is a hydrogen atom with a compound having formula R4'-X, wherein X represents a leaving group and R4' represents a C1-4 alkyl group, which CV4 alkyl group may be substituted with 1-3 fluoro substituents, or wherein R4' represents a halogen atom or a cyano, formyl, acetyl, trifluoroacetyl, fluoroacetyl, methylsulfanyl or propionyl group, in the presence of a strong non-nucleophilic base.
6. Process for the preparation of a compound having formula (II)

wherein R4 represents a branched or unbranched C-1-4 alkyl group, which C1-4 alkyi group may be substituted with 1-3 fluoro substituents, characterized in that a' compound is prepared wherein R, R1 have the meanings given in claim 1 and R7 represents a branched or unbranched alkyl group (C1-4) or benzyl group, by reacting a compound having formula (V) or its tautomer

wherein R and R-, have the meanings given in claim 1, with a compound having formula (V!)
wherein R4 represents a branched or unbranched C1-4 alkyl group, which C1-4 alkyl group may be substituted with 1-3 fluoro atoms and R8 represents a so-called leaving group and R7 represents a branched or unbranched alkyl group (C1-4) or benzyl group.
7. Compounds of formula (IX)

wherein R and R4 have the meanings given in claim 1 and wherein R1 represents a phenyl or pyridinyl group, which groups are substituted with 1-4 substituents Y, which can be the same or different, or R^ represents a pyrimidinyl, pyrazinyl, pyridazinyl or triazinyi group, which groups are substituted with 1-2 substituents Y, which can be the same or different or RT represents a five-membered aromatic heterocyclic moiety having one or two heteroatoms from the group (N, 0, S), which heteroatoms can be the same or different, which five-membered "aromatic heterocyclic moiety may be substituted with 1-2 substituents Y, which can be the same or different or R^ represents naphtyi and R9 represents a hydroxy group, a branched or unbranched alkoxy (C1-4) group, a benzyloxy group or a chloro substituent.
8. Compounds of formula (X) and tautomers thereof

wherein R represents a 4-chlorophenyl group, a 4-bromophenyl group or a 4-(trifluoromethyl)phenyl group.

9. Use of a compound as claimed in claim 1 for the preparation of a
pharmaceutical composition for the treatment of disorders involving
cannabinoid neurotransmission.
10. Use as claimed in claim 9 characterised in that said disorders are
psychiatric disorders such as psychosis, anxiety, depression, attention deficits,
memory disorders, cognitive disorders, appetite disorders, obesity, addiction, appetence, drug dependence and neurological disorders such as neurodegenerative disorders, dementia, dystonia, muscle spasticity, tremor, epilepsy, multiple sclerosis, traumatic brain injury, stroke, Parkinson's disease, Alzheimer's disease, epilepsy, Huntington's disease, Tourette's syndrome, cerebral' ischaemia, cerebral apoplexy, craniocerebral trauma, stroke, spinal cord injury, neuroinfiammatory disorders, plaque sclerosis, viral encephalitis, demyelinisation related disorders, as well as for the treatment of pain disorders, including neuropathic pain disorders, and other diseases involving cannabinoid neurotransmission, including the treatment of septic shock, glaucoma, cancer, diabetes, emesis, nausea, asthma, respiratory diseases, gastrointestinal disorders, gastric ulcers, diarrhoea and cardiovascular disorders.

11. Pharmaceutical compositions substantially as hereinabove
described and exemplified.
12. Method of preparing pharmaceutical compositions substantially as
hereinabove described and exemplified.

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Patent Number

223198

Indian Patent Application Number

574/CHENP/2004

PG Journal Number

47/2008

Publication Date

21-Nov-2008

Grant Date

05-Sep-2008

Date of Filing

17-Mar-2004

Name of Patentee

SOLVAY PHARMACEUTICALS B.V

Applicant Address

C.J VAN HOUTENLAAN 36, NL-1381 CP WEESP

Inventors:

#	Inventor's Name	Inventor's Address
1	KRUSE, CORNEILS G	C/O. SOLVAY PHARMACEUTICALS B.V., C.J VAN HOUTENLAAN 36, NL-1381 CP WEESP
2	LANGE, JOSEPHUS, H.M	C/O. SOLVAY PHARMACEUTICALS B.V., C.J VAN HOUTENLAAN 36, NL-1381 CP WEESP,
3	HERREMANS, ARNOLDUS H.J	C/O. SOLVAY PHARMACEUTICALS B.V., C.J VAN HOUTENLAAN 36, NL-1381 CP WEESP,
4	VAN STUIVENBERG, HERMAN H	C/O. SOLVAY PHARMACEUTICALS B.V., C.J VAN HOUTENLAAN 36, NL-1381 CP WEESP,

PCT International Classification Number

A61K31/4164

PCT International Application Number

PCT/EP02/10434

PCT International Filing date

2002-09-17

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	01203851.9	2001-09-21	EUROPEAN UNION