【结 构 式】 |
【分子编号】40185 【品名】2,2-dichloro-N-[2-(3-chlorobenzoyl)phenyl]acetamide 【CA登记号】 |
【 分 子 式 】C15H10Cl3NO2 【 分 子 量 】342.60804 【元素组成】C 52.59% H 2.94% Cl 31.04% N 4.09% O 9.34% |
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)The reaction of 2-amino-3'-chlorobenzophenone (I) with dichloroacetyl chloride (II) in acetone gives o-(m'-chlorobenzoyl)-2,2-dichloroacetanilide (III), which is cyclized with potassium cyanide in water yielding 2-amino-3-(m-chlorophenyl-3H-indol-3-ol (IV). Finally, this compound is condensed with 1,3-dibromopropane (A) in refluxing ethanol.
【1】 White, A.C.; Bell, S.C. (John Wyeth & Brother Ltd.); Process for the preparation of diazepino[1,2-a]indoles. CH 590286; DE 2417917; FR 2247227; GB 1427066; US 3931226 . |
【2】 Weetman, D.F.; Castaner, J.; Ciclazindol. Drugs Fut 1977, 2, 8, 508. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(A) | 12581 | 1,3-Dibromopropane | 109-64-8 | C3H6Br2 | 详情 | 详情 |
(I) | 40184 | (2-aminophenyl)(3-chlorophenyl)methanone | C13H10ClNO | 详情 | 详情 | |
(II) | 17829 | 2,2-dichloroacetyl chloride; dichloroacetyl chloride | 79-36-7 | C2HCl3O | 详情 | 详情 |
(III) | 40185 | 2,2-dichloro-N-[2-(3-chlorobenzoyl)phenyl]acetamide | C15H10Cl3NO2 | 详情 | 详情 | |
(IV) | 40186 | 2-amino-3-(3-chlorophenyl)-3H-indol-3-ol | C14H11ClN2O | 详情 | 详情 |
Extended Information