Issue 14, 2022

Facile tin(ii)-catalyzed synthesis of N-heterocycles from dicarboxylic acids and arylamines

Abstract

A novel efficient transformation reaction of dicarboxylic acids into N-aryl-substituted azacycles is described. In this synthetic procedure, both catalytic SnCl2 and phenylsilane were used as crucial reagents for reaction of arylamines with dicarboxylic acids to produce the desired azacycles. Using this SnCl2-catalyzed synthetic method, various N-aryl-substituted azacycles were successfully prepared from arylamines with dicarboxylic acids in high yield. This practical synthetic method using catalytic SnCl2 can provide a useful approach for preparation of the desired azacycle products from many available dicarboxylic acid starting materials.

Graphical abstract: Facile tin(ii)-catalyzed synthesis of N-heterocycles from dicarboxylic acids and arylamines

Supplementary files

Article information

Article type
Paper
Submitted
17 Feb 2022
Accepted
17 Mar 2022
First published
17 Mar 2022

Org. Biomol. Chem., 2022,20, 2881-2888

Facile tin(II)-catalyzed synthesis of N-heterocycles from dicarboxylic acids and arylamines

V. H. Tran and H. Kim, Org. Biomol. Chem., 2022, 20, 2881 DOI: 10.1039/D2OB00330A

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