Abstract
Amidoalkylation of 5-aryl(hetaryl)tetrazoles with N-hydroxymethylamides of aliphatic and aromatic carboxylic acids occurs regioselectively and yields mainly 5-aryl(hetaryl)-2-acylaminomethyltetrazoles. These compounds arefairly stable in neutral media but are smoothly deprotected by the action of aqueous sodium hydroxide or hydrochloric acid.
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