【结 构 式】 |
【分子编号】64558 【品名】[1-(4-fluorophenethyl)-4-piperidinyl](4-fluorophenyl)methanone 【CA登记号】 |
【 分 子 式 】C20H21F2NO 【 分 子 量 】329.3896864 【元素组成】C 72.93% H 6.43% F 11.54% N 4.25% O 4.86% |
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)Alkylation of 4-(p-fluorobenzoyl)piperidine (I) with p-fluorophenethyl bromide (II) in hot methyl isobutyl ketone provides the disubstituted piperidine (III). Subsequent keto group reduction in (III) by means of NaBH4 furnishes the title carbinol compound.
【1】 Fu, X.; Tan, P.-Z.; Kula, N.S.; Baldessarini, R.; Tamagnan, G.; Innis, R.B.; Baldwin, R.M.; Synthesis, receptor potency, and selectivity of halogenated diphenylpiperidines as serotonin 5-HT2A ligands for PET or SPECT brain imaging. J Med Chem 2002, 45, 11, 2319. |
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) | 21497 | (4-Fluorophenyl)(4-piperidinyl)methanone; 4-(4-Fluorobenzoyl)piperidine; 4-(p-Fluorobenzoyl)piperidine | 56346-57-7 | C12H14FNO | 详情 | 详情 |
(II) | 17394 | 1-(2-bromoethyl)-4-fluorobenzene | C8H8BrF | 详情 | 详情 | |
(III) | 64558 | [1-(4-fluorophenethyl)-4-piperidinyl](4-fluorophenyl)methanone | C20H21F2NO | 详情 | 详情 |
Extended Information