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【结 构 式】

【分子编号】44715

【品名】1-[5-chloro-6-(4-methyl-1-piperazinyl)-2,3-dihydro-1H-indol-1-yl]-1-ethanone

【CA登记号】

【 分 子 式 】C15H20ClN3O

【 分 子 量 】293.79612

【元素组成】C 61.32% H 6.86% Cl 12.07% N 14.3% O 5.45%

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:(XI)

Catalytic hydrogenation of 1-acetyl-6-nitroindoline (V) afforded amine (VI). Condensation of (VI) with mechlorethamine hydrochloride (VIII) in the presence of K2CO3 in refluxing n-butanol produced piperazinylindoline (X). Alternatively, intermediate (X) was obtained by Sandmeyer reaction of amine (VI) in the presence of CuBr, followed by condensation of the resulting bromide (VII) with N-methylpiperazine (IX). Chlorination of (X) with N-chlorosuccinimide provided (XI). The acetamide function of (XI) was then hydrolyzed in refluxing 2M HCl to give amine (XII). Finally, coupling of (XII) with isocyanate (IV) gave rise to the corresponding urea.

1 Evans, M.; Gaster, L.M.; Gordon, l.; et al.; Mixed 5-HT1A/1B/1D receptor antagonists as novel antidepressants. 16th Int Symp Med Chem (Sept 18 2000, Bologna) 2000, Abst PB-77.
2 Gaster, L.M.; Rami, H.K.; Wyman, P.A. (SmithKline Beecham plc); Indole derivs. having combined 5HT1A, 5HT1B and 5HT1D receptor antagonist activity. EP 0975593; WO 9850358 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IV) 44709 4-(4-pyridinyl)-1-naphthyl isocyanate; 4-(4-isocyanato-1-naphthyl)pyridine C16H10N2O 详情 详情
(V) 44710 1-(6-nitro-2,3-dihydro-1H-indol-1-yl)-1-ethanone C10H10N2O3 详情 详情
(VI) 44711 1-(6-amino-2,3-dihydro-1H-indol-1-yl)-1-ethanone C10H12N2O 详情 详情
(VII) 44712 1-(6-bromo-2,3-dihydro-1H-indol-1-yl)-1-ethanone C10H10BrNO 详情 详情
(VIII) 44713 2-chloro-N-(2-chloroethyl)-N-methyl-1-ethanamine; N,N-bis(2-chloroethyl)-N-methylamine C5H11Cl2N 详情 详情
(IX) 10061 1-Methylpiperazine; 1-Methyl piperazine; N-Methylpiperazine 109-01-3 C5H12N2 详情 详情
(X) 44714 1-[6-(4-methyl-1-piperazinyl)-2,3-dihydro-1H-indol-1-yl]-1-ethanone C15H21N3O 详情 详情
(XI) 44715 1-[5-chloro-6-(4-methyl-1-piperazinyl)-2,3-dihydro-1H-indol-1-yl]-1-ethanone C15H20ClN3O 详情 详情
(XII) 44716 5-chloro-6-(4-methyl-1-piperazinyl)indoline C13H18ClN3 详情 详情
Extended Information