4.4 Article

Efficient synthesis of arylaminotetrazoles in water

Journal

TETRAHEDRON
Volume 66, Issue 21, Pages 3866-3870

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2010.03.003

Keywords

ZnCl2; 5-Arylamino-1H-tetrazole; 1-Aryl-5-amino-1H-tetrazole; Arylcyanamide; Sodium azide

Funding

  1. Bu-Ali Sina University Council

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Arylaminotetrazole derivatives are synthesized efficiently by the reaction of arylcyanamides and sodium azide in the presence of ZnCl2 under aqueous conditions at reflux. Generally, isomer of 5-arylamino-1H-tetrazole can be obtained from arylcyanamides carrying electron-withdrawing substituent on aryl ring and as the electropositivity of substituent is increased, the product is shifted toward the isomer of 1-aryl-5-amino-H-tetrazole. (C) 2010 Published by Elsevier Ltd.

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