Issue 20, 2022

Cobalt-catalyzed tandem one-pot synthesis of polysubstituted imidazo[1,5-a]pyridines and imidazo[1,5-a]isoquinolines

Abstract

An efficient cobalt-catalyzed tandem one-pot method has been developed for the synthesis of polysubstituted imidazo[1,5-a]-N-heteroaromatics. The method involves Knoevenagel condensation followed by cobalt-catalyzed direct alkenylation to give the desired polysubstituted imidazo[1,5-a]pyridines and imidazo[1,5-a]isoquinolines in a one-pot manner. This method exhibits a broad substrate scope, provides moderate to good (39–74%) yields and is amenable to scale-up to the gram scale.

Graphical abstract: Cobalt-catalyzed tandem one-pot synthesis of polysubstituted imidazo[1,5-a]pyridines and imidazo[1,5-a]isoquinolines

Supplementary files

Article information

Article type
Paper
Submitted
19 Mar 2022
Accepted
04 May 2022
First published
04 May 2022

Org. Biomol. Chem., 2022,20, 4215-4223

Cobalt-catalyzed tandem one-pot synthesis of polysubstituted imidazo[1,5-a]pyridines and imidazo[1,5-a]isoquinolines

N. Meena, S. Dhiman, K. Rangan and A. Kumar, Org. Biomol. Chem., 2022, 20, 4215 DOI: 10.1039/D2OB00526C

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