Issue 5, 2017

N-Heterocyclic carbene–palladium(ii)–1-methylimidazole complex catalyzed direct C–H bond arylation of imidazo[1,2-a]pyridines with aryl chlorides

Abstract

We herein reported the N-heterocyclic carbene–palladium(II)–1-methylimidazole complex catalyzed direct C–H bond arylation of imidazo[1,2-a]pyridines with aryl chlorides. Under suitable conditions, all reactions between various imidazo[1,2-a]pyridines and aryl chlorides worked well to give the desired C3–H arylated products in acceptable to high yields, giving a convenient and alternative method for the direct C–H bond arylation of imidazo[1,2-a]pyridines, using economic and easily available aryl chlorides as the arylating reagents.

Graphical abstract: N-Heterocyclic carbene–palladium(ii)–1-methylimidazole complex catalyzed direct C–H bond arylation of imidazo[1,2-a]pyridines with aryl chlorides

Supplementary files

Article information

Article type
Paper
Submitted
12 Dec 2016
Accepted
23 Dec 2016
First published
23 Dec 2016

Org. Biomol. Chem., 2017,15, 1151-1154

N-Heterocyclic carbene–palladium(II)–1-methylimidazole complex catalyzed direct C–H bond arylation of imidazo[1,2-a]pyridines with aryl chlorides

Q. Liu, B. He, P. Qian and L. Shao, Org. Biomol. Chem., 2017, 15, 1151 DOI: 10.1039/C6OB02704K

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