【结 构 式】 |
【分子编号】60732 【品名】N-(tert-butyl)-N-[3-(2-cyanophenoxy)-2-hydroxypropyl]acetamide 【CA登记号】 |
【 分 子 式 】C16H22N2O3 【 分 子 量 】290.36236 【元素组成】C 66.18% H 7.64% N 9.65% O 16.53% |
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:(V)It can be prepared in several different ways: 3) By hydrolysis of 1-(2-cyanophenoxy)-2-hydroxy-3-(N-acetyl-N-tert-butylamino)propane (V) with KOH in refluxing ethanol. 4) By heating N,N'-di-tert-butyl-N-[(2-hydroxy-3-O-cyanophenoxy)propyl]urea (VI) at 200 C in tetralin. 5) By condensation of the 1-(2-cyanophenoxy)-2,3-epoxypropane (II) with tert-butylamine (C) in ethanol.
【1】 Koeppe, H.; et al. (Boehringer Ingelheim GmbH.); ZA 6803783 . |
【2】 Castaner, J.; Chatterjee, S.S.; Bunitrolol. Drugs Fut 1976, 1, 5, 210. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(II) | 37567 | 2-(2-oxiranylmethoxy)benzonitrile | C10H9NO2 | 详情 | 详情 | |
(V) | 60732 | N-(tert-butyl)-N-[3-(2-cyanophenoxy)-2-hydroxypropyl]acetamide | C16H22N2O3 | 详情 | 详情 | |
(VI) | 60733 | N,N'-di(tert-butyl)-N-[3-(2-cyanophenoxy)-2-hydroxypropyl]urea | C19H29N3O3 | 详情 | 详情 | |
(C) | 17895 | 2-Amino-2-methylpropane; tert-butylamine; 2-methyl-2-propanamine | 75-64-9 | C4H11N | 详情 | 详情 |
Extended Information