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【结 构 式】

【分子编号】16795

【品名】1-(4-chlorophenyl)-2-[4-(4-fluorobenzyl)piperidino]-1-ethanone

【CA登记号】

【 分 子 式 】C20H21ClFNO

【 分 子 量 】345.8439832

【元素组成】C 69.46% H 6.12% Cl 10.25% F 5.49% N 4.05% O 4.63%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(III)

A new synthesis of eliprodil and the asymmetric synthesis of its two enantiomers have been reported: 1) Racemic eliprodil is obtained by condensation of 4-chlorophenacyl bromide (I) with 4-(4-fluorobenzyl)piperidine (II) by means of K2CO3 in refluxing ethanol to give 1-(4-chlorophenyl)-2-[4-(4-fluorobenzyl)piperidin-1-yl]ethanone (III), which is then reduced with KBH4 in methanol.

1 Di Fabio, R.; Thomas, R.J.; Pietra, C.; Ziviani, L.; The asymmetric synthesis of both enantiomers of eliprodil. Bioorg Med Chem Lett 1995, 5, 6, 551.
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) 16720 2-bromo-1-(4-chlorophenyl)-1-ethanone; 2-Bromo-4'-chloroacetophenone 536-38-9 C8H6BrClO 详情 详情
(II) 16794 4-(4-fluorobenzyl)piperidine 92822-02-1 C12H16FN 详情 详情
(III) 16795 1-(4-chlorophenyl)-2-[4-(4-fluorobenzyl)piperidino]-1-ethanone C20H21ClFNO 详情 详情
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