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【结 构 式】

【分子编号】59112

【品名】1-[4-(trifluoromethyl)-2-pyridinyl]piperazine

【CA登记号】

【 分 子 式 】C10H12F3N3

【 分 子 量 】231.2207096

【元素组成】C 51.95% H 5.23% F 24.65% N 18.17%

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:(IV)

Alkylation of 2-pyrrolidinone (I) with 1,4-dibromobutane (II) in the presence of KOH and tetraethylammonium bromide gave the N-(4-bromobutyl)pyrrolidinone (III). This was condensed with 1-[4-(trifluoromethyl)-2-pyridinyl]piperazine (IV) in the presence of Na2CO3 to produce the target disubstituted piperazine, which was then converted to the corresponding fumarate salt.

1 Carlier, P.; Combourieu, M.; Poisson, C.; Monteil, A.J.-C. (Akzo Nobel N.V.); 4-[4- or 6-(Trifluoromethyl-2-pyridinyl)]-1-piperazinyl-alkyl substd. lactams. EP 0482696; JP 1992282379; US 5180726 .
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) 27397 2-Pyrrolidinone 616-45-5 C4H7NO 详情 详情
(II) 11883 1,4-Dibromobutane; 1,4-Butylene bromide 110-52-1 C4H8Br2 详情 详情
(III) 59111 1-(4-bromobutyl)-2-pyrrolidinone C8H14BrNO 详情 详情
(IV) 59112 1-[4-(trifluoromethyl)-2-pyridinyl]piperazine C10H12F3N3 详情 详情
Extended Information