Some azoles were converted into corresponding 1H-carboxylic acids (2a-d) and acid chlorides in two steps, subsequently these acid chlorides were trapped with substituted amines (3a-e), to yield azole monoacetanilides ( 4c, 6c, 8a,b,c,e, 10a ) and diacetanilides (5a, 5b, 5e, 7a, d ).