Issue 46, 2023

Lewis base-catalyzed cascade [4 + 2]-annulation reaction of N-alkoxy acrylamides and acyl isothiocyanates: facile access to 2-imino-1,3-thiazinone derivatives

Abstract

A formal [4 + 2]-cycloaddition reaction of N-alkoxy acrylamides and acyl isothiocyanates was developed via a Lewis base-catalyzed cascade aza-nucleophilic addition/thio-Michael addition process under mild conditions. This study provides a facile approach for preparing 2-imino-1,3-thiazinone derivatives in moderate to excellent yields and enriches the field of heterocyclic acrylamide chemistry. The reported method features metal-free reaction conditions, high atom economy, and easy operation. Moreover, the reaction was successfully scaled up and derivatization reactions were successfully performed.

Graphical abstract: Lewis base-catalyzed cascade [4 + 2]-annulation reaction of N-alkoxy acrylamides and acyl isothiocyanates: facile access to 2-imino-1,3-thiazinone derivatives

Supplementary files

Article information

Article type
Paper
Submitted
07 Sep 2023
Accepted
31 Oct 2023
First published
01 Nov 2023

Org. Biomol. Chem., 2023,21, 9200-9209

Lewis base-catalyzed cascade [4 + 2]-annulation reaction of N-alkoxy acrylamides and acyl isothiocyanates: facile access to 2-imino-1,3-thiazinone derivatives

Z. Wang, G. Tian, Y. Shi, W. Liu, X. Xu, X. Li, L. Wu and L. Xie, Org. Biomol. Chem., 2023, 21, 9200 DOI: 10.1039/D3OB01440A

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