NUCLEOPHILIC SUBSTITUTION IN 1,5-BENZODIAZEPIN-2-ONES
DOI:
https://doi.org/10.1007/493Keywords:
1, 5-benzodiazepin-2-ones, thiazolo[4, 5-b][1, 5]benzodiazepine, bromination, phase-transfer catalysis, nucleophilic substitutionAbstract
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