首页> 外国专利> Prepn. of 1,4-benzodiazepine cpds. - by reacting e.g. a 2-haloethyl-amino-benzophenone with hexa: methylene tetr:amine in presence of an ammonium salt and water alcohol solvent

Prepn. of 1,4-benzodiazepine cpds. - by reacting e.g. a 2-haloethyl-amino-benzophenone with hexa: methylene tetr:amine in presence of an ammonium salt and water alcohol solvent

机译:准备1,4-苯二氮卓cpds。 -通过反应在铵盐和水醇溶剂存在下,将2-卤乙基-氨基-二苯甲酮与六:亚甲基四胺:胺

摘要

Prepn. of 1,4-benzodiazepines (I) comprises reacting a 2-(2-haloacylamino)- or 2-(2-haloethylamino)-benzophenone (IIe with hexamethylene tetraamine (HMTA) in a solvent mixt. contg. 5-50 (pref. 15-35) vol. % water and a water-miscible alcohol, in the presence of an ammonium salt of an acid of pKa 3.2 or less. (I) is obtd. in higher yields (more than 85%) cf. previous processes (50%) in a shorter reaction time (1/5-1/2 the time previously). Prodn. of by-prods. is lower and isolation of (I) is easier. The process is esp. suitable for the prodn. of e.g. 7-chloro-1-(2,2,2-trifluoroethyl)-5-phenyl-1,3-dihydro-2H-1,4-ben- zodiazepin-2-one and 7-chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepin-2-one- . Pref. ammonium salts are NH4Br, NHEI and NH4NO3.
机译:准备1,4-苯并二氮杂((I)的方法包括在溶剂混合物中(浓度为5-50)使2-(2-卤代酰基氨基)-或2-(2-卤代乙基氨基)-二苯甲酮(IIe)与六亚甲基四胺(HMTA)反应(p。15-35)体积%的水和与水混溶的醇,在pKa 3.2或更低的酸的铵盐存在下(I)的产率较高(超过85%),参见先前可以在较短的反应时间(之前的1 / 5-1 / 2)中进行反应(50%),副产物的生成量较低,(I)的分离更容易,该方法尤其适用于该产物例如7-氯-1-(2,2,2-三氟乙基)-5-苯基-1,3-二氢-2H-1,4-苯并二氮杂-2--2-和7-氯1.3 -二氢-1-甲基-5-苯基-2H-1,4-苯并二氮杂-2--2-酮-优选的铵盐为NH 4 Br,NHEI和NH 4 NO 3。

著录项

  • 公开/公告号FR2364207B1

    专利类型

  • 公开/公告日1979-07-27

    原文格式PDF

  • 申请/专利权人 SCHERICO LTD;

    申请/专利号FR19760027149

  • 发明设计人

    申请日1976-09-09

  • 分类号C07D243/14;A61K31/55;

  • 国家 FR

  • 入库时间 2022-08-22 19:36:14

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