Issue 100, 2025

Diversity-oriented transformation of methyl triazine via sulfur-mediated pathways: access to 2,4-disubstituted triazines functionalized with thioamides and amides

Abstract

Herein, we report a sulfur-mediated strategy involving C-demethylation and C(sp3)–H bond activation for synthesizing triazine derivatives functionalized with thioamide or amide groups. This work provides a novel method for the functional group transformation of methyltriazines in the presence of sulfur and demonstrates good substrate compatibility.

Graphical abstract: Diversity-oriented transformation of methyl triazine via sulfur-mediated pathways: access to 2,4-disubstituted triazines functionalized with thioamides and amides

Supplementary files

Article information

Article type
Communication
Submitted
02 Oct 2025
Accepted
10 Nov 2025
First published
13 Nov 2025

Chem. Commun., 2025,61, 19878-19881

Diversity-oriented transformation of methyl triazine via sulfur-mediated pathways: access to 2,4-disubstituted triazines functionalized with thioamides and amides

D. Jiang, R. Niu, B. Yan, R. Liu, Y. Liang, H. Wu, F. Shang and M. Zeng, Chem. Commun., 2025, 61, 19878 DOI: 10.1039/D5CC05624A

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