【结 构 式】 |
【分子编号】59111 【品名】1-(4-bromobutyl)-2-pyrrolidinone 【CA登记号】 |
【 分 子 式 】C8H14BrNO 【 分 子 量 】220.1093 【元素组成】C 43.65% H 6.41% Br 36.3% N 6.36% O 7.27% |
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 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 . |
Extended Information