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【结 构 式】

【分子编号】45061

【品名】4-chloro-1-(4-fluorophenyl)-1-butanol

【CA登记号】

【 分 子 式 】C10H12ClFO

【 分 子 量 】202.6557832

【元素组成】C 59.27% H 5.97% Cl 17.49% F 9.37% O 7.89%

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:(VI)

A new synthesis for [18F]-labeled BMY-14802 has been reported: The compound can be prepared by two related ways: 1) The fluorination of 4-(cyclopropylcarbonyl)nitrobenzene (I) with [18F]-FK and Kryptofix 2.2.2 gives 4-fluorophenyl cyclopropyl methanone (II), which is treated with HCl in methanol yielding 4-chloro-1-(4-fluorophenyl)-1-butanone (III). The condensation of (III) with 5-fluoro-2-piperazinopyrimidine (IV) affords 1-(4-fluorophenyl)-4-[4-(5-fluoropyrimidin-2-yl)piperazin-1-yl]-1-butan one (V), which is finally reduced with NaBH4 in methanol. 2) The reduction of butanone (III) with NaBH4 in methanol gives 4-chloro-1-(4-fluorophenyl)-1-butanol (VI), which is then condensed with pyrimidine (IV) as before.

1 Yevich, J.P.; Frick, M.P.; Shiue, G.G.; Huang, H.; Pleus, R.C.; Shiue, C.-Y.; Bai, L.-Q.; Catt, J.D.; Rysavy, J.A.; Fluorine-18 labeled BMY 14802: Synthesis and anatomical distribution in rodents. J Label Compd Radiopharm 1993, 32, 501.
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) 11423 Cyclopropyl(4-nitrophenyl)methanone C10H9NO3 详情 详情
(II) 11424 Cyclopropyl(4-fluorophenyl)methanone C10H9FO 详情 详情
(II) 27427 cyclopropyl(4-fluorophenyl)methanone 772-31-6 C10H9FO 详情 详情
(III) 11425 4-Chloro-1-(4-fluorophenyl)-1-butanone C10H10ClFO 详情 详情
(III) 35864 4-chloro-1-(4-fluorophenyl)-1-butanone 3874-54-2 C10H10ClFO 详情 详情
(IV) 11426 5-Fluoro-2-piperazinopyrimidine C8H11FN4 详情 详情
(V) 11427 1-(4-Fluorophenyl)-4-[4-(5-fluoro-2-pyrimidinyl)piperazino]-1-butanone C18H20F2N4O 详情 详情
(V) 28204 1-(4-fluorophenyl)-4-[4-(5-fluoro-2-pyrimidinyl)-1-piperazinyl]-1-butanone C18H20F2N4O 详情 详情
(VI) 11428 4-Chloro-1-(4-fluorophenyl)-1-butanol C10H12ClFO 详情 详情
(VI) 45061 4-chloro-1-(4-fluorophenyl)-1-butanol C10H12ClFO 详情 详情
Extended Information