Copper-Catalyzed Intramolecular C−N Bond Formation: A Straightforward Synthesis of Benzimidazole Derivatives in Water

A straightforward, efficient, and more sustainable copper-catalyzed method has been developed for intramolecular N-arylation providing the benzimidazole ring system. With Cu2O (5 mol %) as the catalyst, DMEDA (10 mol %) as the ligand, and K2CO3 as the base, this protocol was applied to synthesize a...

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Veröffentlicht in:Journal of organic chemistry 2011-01, Vol.76 (2), p.716-719
Hauptverfasser: Peng, Jinsong, Ye, Min, Zong, Cuijuan, Hu, Fangyun, Feng, Lingtong, Wang, Xiaoyan, Wang, Yufeng, Chen, Chunxia
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Sprache:eng
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Zusammenfassung:A straightforward, efficient, and more sustainable copper-catalyzed method has been developed for intramolecular N-arylation providing the benzimidazole ring system. With Cu2O (5 mol %) as the catalyst, DMEDA (10 mol %) as the ligand, and K2CO3 as the base, this protocol was applied to synthesize a small library of benzimidazoles in high yields. Remarkably, the reaction was exclusively carried out in water, rendering the methodology highly valuable from both environmental and economical points of view.
ISSN:0022-3263
1520-6904
DOI:10.1021/jo1021426