Issue 40, 2014

Mechanosynthesis of pharmaceutically relevant sulfonyl-(thio)ureas

Abstract

We demonstrate the first application of mechanochemistry to conduct the synthesis of sulfonyl-(thio)ureas, including known anti-diabetic drugs tolbutamide, chlorpropamide and glibenclamide, in good to excellent isolated yields by either stoichiometric base-assisted or copper-catalysed coupling of sulfonamides and iso(thio)cyanates.

Graphical abstract: Mechanosynthesis of pharmaceutically relevant sulfonyl-(thio)ureas

Supplementary files

Article information

Article type
Communication
Submitted
09 ذو الحجة 1434
Accepted
24 ذو الحجة 1434
First published
26 ذو الحجة 1434

Chem. Commun., 2014,50, 5248-5250

Mechanosynthesis of pharmaceutically relevant sulfonyl-(thio)ureas

D. Tan, V. Štrukil, C. Mottillo and T. Friščić, Chem. Commun., 2014, 50, 5248 DOI: 10.1039/C3CC47905F

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