【结 构 式】 |
【分子编号】41310 【品名】4-isopropylbenzoyl chloride 【CA登记号】 |
【 分 子 式 】C10H11ClO 【 分 子 量 】182.64944 【元素组成】C 65.76% H 6.07% Cl 19.41% O 8.76% |
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:The condensation of aziridine (I) with methyl 4-hydroxybenzoate (II) in refluxing chloroform gives methyl 4-(2-aminoethoxy)benzoate (III), which is acylated with 4-isopropylbenzoyl chloride by means of K2CO3 in chloroform yielding methyl 4-[2-(4-isopropylbenzamido)ethoxy]benzoate (IV). Finally, this compound is hydrolyzed with NaOH in refluxing water.
【1】 Yoshikuni, Y.; Choaki, S.; Ozaki, T.; Yoshida, H. (Nippon Shinyaku Co., Ltd.); Benzoic acid derivs. CH 674204; DE 3718765; FR 2600059; GB 2191487; JP 1987292754; JP 1988159359; US 4831055 . |
【2】 Prous, J.; Castaner, J.; NS-1. Drugs Fut 1990, 15, 7, 682. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
41310 | 4-isopropylbenzoyl chloride | C10H11ClO | 详情 | 详情 | ||
(I) | 10151 | Ethyleneimine; Aziridine; Azirane | 151-56-4 | C2H5N | 详情 | 详情 |
(II) | 10251 | methyl 4-hydroxybenzoate; Methyl p-hydroxybenzoate | 99-76-3 | C8H8O3 | 详情 | 详情 |
(III) | 12457 | methyl 4-(2-aminoethoxy)benzoate | C10H13NO3 | 详情 | 详情 | |
(IV) | 12458 | methyl 4-[2-[(4-isopropylbenzoyl)amino]ethoxy]benzoate | C20H23NO4 | 详情 | 详情 |
Extended Information