Abstract
The esters having a substituted triazole ring (3-4a-c) were treated with dry ammonia in dry ethanol to yield substituted acetamides (5-6a-c) which on reaction with 4-toluenesulfonyl chloride yielded 4-toluenesulfonamides (7-8a-c). The acetamides (5-6a-c) furnished the sulfamic acids (9-10a-c) when treated with chlorosulfonic acid.