Issue 14, 2021

Metal-free electrochemical C3-sulfonylation of imidazo[1,2-a]pyridines

Abstract

Electrochemical oxidative cross-coupling represents one of the most atom-economical and green approaches to synthesize various useful compounds. In this work, an electrochemical C3-sulfonylation of imidazo[1,2-a]pyridines with sodium benzenesulfinates as sulfonylation reagents has been developed. This transformation provides an effective and straightforward metal-free protocol towards the synthesis of biologically and synthetically useful 3-(arylsulfonyl)imidazo[1,2-a]pyridine. Up to 94% yields were obtained. The scale-up experiment gave 1.56 g of the desired product in 90% yield.

Graphical abstract: Metal-free electrochemical C3-sulfonylation of imidazo[1,2-a]pyridines

Supplementary files

Article information

Article type
Research Article
Submitted
03 Mar 2021
Accepted
29 Apr 2021
First published
29 Apr 2021

Org. Chem. Front., 2021,8, 3815-3819

Metal-free electrochemical C3-sulfonylation of imidazo[1,2-a]pyridines

J. Zhu, Z. Chen, M. He, D. Wang, L. Li, J. Qi, R. Shi and A. Lei, Org. Chem. Front., 2021, 8, 3815 DOI: 10.1039/D1QO00348H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements