【结 构 式】 |
【分子编号】33852 【品名】2-bromo-N-(4-chlorophenyl)-N-(2,2,2-trifluoroethyl)acetamide 【CA登记号】 |
【 分 子 式 】C10H8BrClF3NO 【 分 子 量 】330.5315696 【元素组成】C 36.34% H 2.44% Br 24.17% Cl 10.73% F 17.24% N 4.24% O 4.84% |
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:(XVI)N-bromoacetyl compound (IV) can also be obtained by bromoacetylation of (XV) with bromoacetyl bromide (B) in refluxing benzene affording 4-chloro-N-bromoacetyl-N-(2,2,2-trifluoroethyl)aniline (XVI), followed by a Friedel-Crafts reaction with benzoyl chloride by means of AlCl3.
【1】 Topliss, J.G.; 2-Polyfluoroweralkyl benzophenones. US 3641147 . |
【2】 Topliss, J.G.; 1-Polyhalogenoalkyl-2-oxo-1,3-dihydro-2H-14-benzodiazepines. US 3429874 . |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(D) | 10463 | Benzoyl chloride | 98-88-4 | C7H5ClO | 详情 | 详情 |
(B) | 14005 | 2-Bromoacetyl bromide; Bromoacetyl bromide | 598-21-0 | C2H2Br2O | 详情 | 详情 |
(IV) | 33849 | N-(2-benzoyl-4-chlorophenyl)-2-bromo-N-(2,2,2-trifluoroethyl)acetamide | C17H12BrClF3NO2 | 详情 | 详情 | |
(XV) | 33475 | N-(4-chlorophenyl)-N-(2,2,2-trifluoroethyl)amine; 4-chloro-N-(2,2,2-trifluoroethyl)aniline | C8H7ClF3N | 详情 | 详情 | |
(XVI) | 33852 | 2-bromo-N-(4-chlorophenyl)-N-(2,2,2-trifluoroethyl)acetamide | C10H8BrClF3NO | 详情 | 详情 |
Extended Information