NUCLEOPHILIC SUBSTITUTION IN 1,5-BENZODIAZEPIN-2-ONES

Authors

  • В. И. Божанов Dnepropetrovsk State University
  • С. П. Ивонин Dnepropetrovsk State University

DOI:

https://doi.org/10.1007/493

Keywords:

1, 5-benzodiazepin-2-ones, thiazolo[4, 5-b][1, 5]benzodiazepine, bromination, phase-transfer catalysis, nucleophilic substitution

Abstract

The reaction of 3-bromo-4-phenyl-2,3-dihydro-1H-1,5-benzodiazepin-2-one with cyclic amines gives 3 aminoalkyl-4-phenyl-2,3-dihydro-1H-1,5-benzodiazepin-2-one. Thiazolo[4,5-b][1,5]benzodiazepine was isolated along with the substitution product when thiourea was used.

Authors: V. I. Bozhanov and S. P. Ivonin.

English Translation in Chemistry of Heterocyclic Compounds, 2000, 36 (12), pp 1446-1448

http://link.springer.com/article/10.1023/A%3A1017578614850

Published

2013-04-15

Issue

Section

Original Papers