Journal
TETRAHEDRON
Volume 66, Issue 21, Pages 3866-3870Publisher
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
Categories
Funding
- Bu-Ali Sina University Council
Ask authors/readers for more resources
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.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available