Synthesis of new 4-acetonylidene-1,5-benzodiazepinones. Condensation of monosubstituted o-phenylenediamines with triacetic acid lactone

被引:0
|
作者
ElAbbassi, M [1 ]
Essassi, EM [1 ]
Fifani, J [1 ]
机构
[1] FAC SCI RABAT,LAB CHIM ORGAN HETEROCYCLINE,CNCPRST,RABAT,MOROCCO
来源
BULLETIN DES SOCIETES CHIMIQUES BELGES | 1997年 / 106卷 / 04期
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中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Condensation of unsymmetrical aromatic diamines (4-methyl-,4-chloro-, and 4-nitrophenylenediamines) 2-4 with 2-hydroxy-6-methyl-4-pyrone 1 have been examined, The structure of isomerie 4-acetonylidene-1,5-benzodiazepin-2-ones 5-10 and benzimidazoles 11-16 obtained from competitive reactions have been established by the spectrale data (H-1 NMR, IR and mass spectrum). The position of the substituents in 6/9 and 7/10 was proved by comparison with samples with authentic structures.
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页码:205 / 210
页数:6
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