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Merck
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  • CuI-catalyzed amination of arylhalides with guanidines or amidines: a facile synthesis of 1-H-2-substituted benzimidazoles.

CuI-catalyzed amination of arylhalides with guanidines or amidines: a facile synthesis of 1-H-2-substituted benzimidazoles.

The Journal of organic chemistry (2009-06-17)
Xiaohu Deng, Heather McAllister, Neelakandha S Mani
摘要

CuI/L5 (N,N'-dimethylethylenediamine) proves to be an efficient catalyst system for the amination of arylhalides with guanidines. The same catalyst system is then successfully applied to the one-step synthesis of 1-H-2-amino-benzimidazoles through tandem aminations of 1,2-dihaloarenes in modest yields. This methodology is also applicable for the preparation of 1-H or 1-substutituted 2-aryl- or 2-alkyl-benzimidazoles.

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Sigma-Aldrich
N,N′-二甲基乙二胺, 98%
Sigma-Aldrich
N,N′-二甲基乙二胺, 85%