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【结 构 式】

【药物名称】CFT, Win-35428

【化学名称】(-)-3beta-(4-Fluorophenyl)-8-methyl-8-azabicyclo[3.2.1]octane-2beta-carboxylic acid methyl ester

【CA登记号】50370-56-4

【 分 子 式 】C16H20FNO2

【 分 子 量 】277.3417

【开发单位】National Institute on Drug Abuse (Originator), Research Triangle Institute (Originator), Sanofi-synthélabo (Originator)

【药理作用】Antagonists to Narcotics, Specific Antidotes, TREATMENT OF POISONING, DRUG ABUSE & DEPENDENCY

合成路线1

By condensation of (-)-anhydroecgonine methyl ester (I) with 4-fluorophenylmagnesium bromide (II) by means of cuprous chloride in refluxing ether.

1 Clarke, R.L.; Daum, S.J.; US 3813404 .
2 Clarke, R.L.; et al.; Compounds affecting the central nervous system. 4. 3beta-Phenyltropane-2-carboxylic esters and analogs. J Med Chem 1973, 16, 1, 1260-67.
3 Castañer, J.; Hillier, K.; WIN-35,428. Drugs Fut 1980, 5, 9, 459.
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) 39208 methyl 8-methyl-8-azabicyclo[3.2.1]oct-2-ene-2-carboxylate C10H15NO2 详情 详情
(II) 13643 4-fluorophenyl magnesium bromide;Bromo(4-fluorophenyl)magnesium;bromo(p-fluorophenyl)Magnesium;p-Fluorophenylmagnesium bromide 352-13-6 C6H4BrFMg 详情 详情
Extended Information