Issue 52, 2019

Concise synthesis of N-thiomethyl benzoimidazoles through base-promoted sequential multicomponent assembly

Abstract

An efficient method for the synthesis of N-thiomethyl benzimidazoles from o-phenylenediamines, thiophenols, and aldehydes via C–N/C–S bond formation under metal-free conditions is described. A broad range of functional groups attached to the substrates were well tolerated in this reaction system. Stable and low-toxicity paraformaldehyde was used as the carbon source.

Graphical abstract: Concise synthesis of N-thiomethyl benzoimidazoles through base-promoted sequential multicomponent assembly

Supplementary files

Article information

Article type
Paper
Submitted
07 Aug 2019
Accepted
21 Sep 2019
First published
26 Sep 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 30570-30574

Concise synthesis of N-thiomethyl benzoimidazoles through base-promoted sequential multicomponent assembly

J. Tian, S. Yuan, F. Xiao, H. Huang and G. Deng, RSC Adv., 2019, 9, 30570 DOI: 10.1039/C9RA06144D

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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