Preparation of 2-Azido-1-Substituted-1H-Benzo[d]imidazoles Using a Copper-Promoted Three-Component Reaction and Their Further Conversion into 2-Amino and 2-Triazolyl Derivatives

被引:55
作者
Ramana, Tamminana [1 ]
Punniyamurthy, Tharmalingam [1 ]
机构
[1] Indian Inst Technol Guwahati, Dept Chem, Gauhati 781039, India
关键词
benzimidazoles; copper; cycloaddition; multicomponent reactions; heterocycles; ONE-POT SYNTHESIS; AROMATIC-SUBSTITUTION; BIOLOGICAL EVALUATION; COUPLING REACTIONS; ARYL; BENZIMIDAZOLES; CYCLOADDITION; PIPERIDINYL; REDUCTION; DISCOVERY;
D O I
10.1002/chem.201202215
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multicomponent reaction: 2-Azido-1-substituted-1H-benzo[d]imidazoles were prepared using a copper-catalyzed three-component reaction involving 2-bromoaniline derivatives, isothiocyanates, and sodium azide. The reaction conditions were mild and the scope was broad. The azido compounds were transformed into their 2-amino and 2-triazolyl derivatives using copper-mediated reduction and cycloaddition, respectively (see scheme). © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:13279 / 13283
页数:5
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