Issue 6, 2024

Electrochemical C3-methylthiolation of imidazopyridines with dimethyl sulfoxide

Abstract

An efficient electrochemical methylthiolation reaction of imidazo[1,2-a]pyridines was achieved. The method used DMSO as both the methylthiolating reagent and solvent and KI as both the hydrogen atom transfer reagent and supporting electrolyte. The reaction was performed under transition metal- and chemical oxidant-free conditions. For various substituted 2-arylimidazo[1,2-a]pyridines, C-3 methylthiolation products were obtained regioselectively with good yields.

Graphical abstract: Electrochemical C3-methylthiolation of imidazopyridines with dimethyl sulfoxide

Supplementary files

Article information

Article type
Paper
Submitted
19 Jan 2024
Accepted
12 Feb 2024
First published
13 Feb 2024

Green Chem., 2024,26, 3517-3521

Electrochemical C3-methylthiolation of imidazopyridines with dimethyl sulfoxide

Z. Feng, Y. Fan, C. Qiang, P. Liu and P. Sun, Green Chem., 2024, 26, 3517 DOI: 10.1039/D4GC00314D

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