【结 构 式】 |
【分子编号】46025 【品名】4-[(3-bromopropyl)sulfanyl]-2,6-di(tert-butyl)phenyl acetate 【CA登记号】 |
【 分 子 式 】C19H29BrO2S 【 分 子 量 】401.40806 【元素组成】C 56.85% H 7.28% Br 19.91% O 7.97% S 7.99% |
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:(I)The condensation between bromide (I) and piperazine (II) in refluxing acetonitrile provided the disubstituted piperazine (III). The acetate ester was then hydrolyzed by means of NaOH to yield the title compound.
【1】 Regnier, G.; Vilaine, J.-P.; Villeneuve, N.; Bidouard, J.-P.; Iliou, J.-P.; Lenaers, A. (ADIR et Cie.); Trimetazidine derivs., process for their preparation and pharmaceutical compsns. containing them. EP 0533579; FR 2681324; JP 1993194451; US 5283246 . |
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) | 46025 | 4-[(3-bromopropyl)sulfanyl]-2,6-di(tert-butyl)phenyl acetate | C19H29BrO2S | 详情 | 详情 | |
(II) | 24354 | 2,3-dimethoxy-4-(1-piperazinylmethyl)phenyl methyl ether | C14H22N2O3 | 详情 | 详情 | |
(III) | 46026 | 2,6-di(tert-butyl)-4-([3-[4-(2,3,4-trimethoxybenzyl)-1-piperazinyl]propyl]sulfanyl)phenyl acetate | C33H50N2O5S | 详情 | 详情 |
Extended Information