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Rimonabant hydrochloride, SR-141716A, Acomplia

盐酸利莫那班 利莫纳班 Chemical Name: 5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-N-(piperidin-1-yl)pyrazole-3-carboxamide hydrochloride
CAS No. 158681-13-1, 168273-06-1 (free base)
项目整合开发状态: Phase III
项目研究机构: Sanofi-Aventis (Originator), NIAAA (Not Determined)
合成路线:Claisen condensation of 4-chloropropiophenone (I) with diethyl oxalate in the presence of lithium hexamethyldisilazide afforded the corresponding diketo ester lithium salt (II).This was condensed with 2,4-dichlorophenylhydrazine (III) to afford hydrazone (IV),which was further cyclized to pyrazole (V) in refluxing HOAc.In an improved procedure,4-chloropropiophenone (I) was initially converted to the silyl enol ether (VI) using chlorotrimethylsilane and triethylamine.Acylation of (VI) with ethyl chloroglyoxylate in the presence of ZnCl2 produced diketo ester (VII).Condensation of (VII) with hydrazine (III),followed by acid cyclization of the intermediate hydrazone (IV),also produced pyrazole (V).Hydrolysis of ethyl ester (V) gave carboxylic acid (VIII),which was then activated as the acid chloride (IX).Finally,coupling of acid chloride (IX) with N-aminopiperidine (X) furnished the title hydrazide.
📌 参考资料/链接:
参考文献标题:Substd.N-piperidino 3-pyrazolecarboxamide
文献作者:Rinaldi,M.; Anne-Archard,G.; Barth,F.; Casellas,P.; Congy,C.; Martinez,S.(Sanofi-Synthabo)
参考来源:CA 2136893; EP 0576357; EP 0656354; FR 2692575; FR 2713224; FR 2713225; JP 1994073014; JP 1995309841; JP 2001026541; US 5624941

📄 详细内容


合成路线:The reaction of Rimonabant (I) with BuLi and 1-chloro-2-iodoethane gives a mixture of the iodo derivatives (II) and (III),which are separated by chromatography.The desired isomer (II) is then hydrogenated with tritium over Pd/C in ethanol.
参考文献标题:Tritiation of SR141716 by metallation-iodination-reduction: Tritium-proton nOe study
文献作者:Seltzman,H.H.; et al.
参考来源:J Label Compd Radiopharm 2002,45(1),59


产品链接: CAS No. 158681-13-1››

产品链接: CAS No.168273-06-1››