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【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