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【结 构 式】

【药物名称】SLV-319

【化学名称】4-Chloro-N-[1-[3-(4-chlorophenyl)-4(S)-phenyl-4,5-dihydro-1H-pyrazol-1-yl]-1-(methylamino)methylidene]benzenesulfonamide
      3-(4-Chlorophenyl)-N2-(4-chlorophenylsulfonyl)-N1-methyl-4(S)-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine

【CA登记号】362519-49-1 (racemate)

【 分 子 式 】C23H20Cl2N4O2S

【 分 子 量 】487.41145

【开发单位】Solvay (Originator)

【药理作用】Antiobesity Drugs, Antipsychotic Drugs, METABOLIC DRUGS, PSYCHOPHARMACOLOGIC DRUGS, Treatment of Nutritional Disorders, Cannabinoid CB1 Antagonists

合成路线1

Condensation of dihydropyrazole (I) with the sulfonyl carbamate (II) in the presence of pyridine gives rise to the 1-acyl dihydropyrazole (III). Subsequent chlorination of (III) using PCl5 in refluxing chlorobenzene affords the imidoyl chloride (IV). This is finally condensed with methylamine in CH2Cl2 to furnish the title compound.

1 Kruse, C.G.; Tulp, M.T.M.; Lange, J.H.M.; Tipker, J.; Van Vliet, B.J. (Solvay Pharmaceuticals BV); 4,5-Dihydro-1H-pyrazole derivs. having CB 1-antagonistic activity. EP 1268435; US 2001053788; US 6476060; WO 0170700 .
2 Kruse, C.G.; Lange, J.H.M.; Tipker, J.; Hoogendoorn, J. (Solvay Pharmaceuticals BV); 4,5-Dihydro-1H-pyrazole derivs. having CB1-antagonistic activity. WO 0276949 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 58393 3-(4-chlorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazole C15H13ClN2 详情 详情
(II) 15813 methyl N-[(4-chlorophenyl)sulfonyl]carbamate C8H8ClNO4S 详情 详情
(III) 58394 4-chloro-N-{[3-(4-chlorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazol-1-yl]carbonyl}benzenesulfonamide C22H17Cl2N3O3S 详情 详情
(IV) 58395 3-(4-chlorophenyl)-N-[(4-chlorophenyl)sulfonyl]-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidoyl chloride C22H16Cl3N3O2S 详情 详情
Extended Information