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【结 构 式】

【分子编号】22593

【品名】2,6-dichloro-1,4-benzenediamine; 4-amino-2,6-dichlorophenylamine

【CA登记号】609-20-1

【 分 子 式 】C6H6Cl2N2

【 分 子 量 】177.03252

【元素组成】C 40.71% H 3.42% Cl 40.05% N 15.82%

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:(II)

The cyclization of 2-amino-4'-bromobenzophenone (I) with ethyl 2-(methylthio)acetate (II) by means of tert-butyl hypochlorite in dichloromethane at 70 C gives 7-(4-bromobenzoyl)-3-(methylthio)-2,3-dihydro-1H-indol-2-one (III), which is desulfurized by a treatment with Raney Nickel in THF yielding 7-(4-bromobenzoyl)-2,3-dihydro-1H-indol-2-one (IV). Finally, this compound is hydrolyzed with refluxing 3N NaOH and acidified with concentrated HCl.

1 York, B.M. Jr. (Alcon Laboratories, Inc.); Method for lowering intraocular pressure using phenylimino-imidazoles. US 4517199 .
2 Cavero, I.; Langer, S.Z.; York, B.M. Jr.; Method of lowering intraocular pressure using phenylimino-imidazoles. US 4515800 .
3 Prous, J.; Castaner, J.; Aplonidine hydrochloride. Drugs Fut 1988, 13, 6, 507.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 22592 2,6-dichloro-4-nitrophenylamine; 2,6-dichloro-4-nitroaniline 99-30-9 C6H4Cl2N2O2 详情 详情
(II) 14754 ethylenediamine;1,2-Diaminoethane;ethane-1,2-diamine;1,2-Ethanediamine 107-15-3 C2H8N2 详情 详情
(II) 22593 2,6-dichloro-1,4-benzenediamine; 4-amino-2,6-dichlorophenylamine 609-20-1 C6H6Cl2N2 详情 详情
(III) 22594 N-(4-amino-3,5-dichlorophenyl)-2,2,2-trichloroacetamide C8H5Cl5N2O 详情 详情
(IV) 22595 2,2,2-trichloro-N-[3,5-dichloro-4-(formylamino)phenyl]acetamide C9H5Cl5N2O2 详情 详情
(V) 22596 1,3-dichloro-2-[(dichloromethylene)amino]-5-[(2,2,2-trichloroacetyl)amino]benzene C9H3Cl7N2O 详情 详情
(VII) 22597 2,2,2-trichloro-N-[3,5-dichloro-4-(2-imidazolidinylideneamino)phenyl]acetamide C11H9Cl5N4O 详情 详情
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