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An array of heterocyclic amides was synthesized efficiently by combining corresponding amines and benzoyl chloride in one-pot under microwave irradiation. The reaction times were shorter, yields were higher. What is more, the regioselectivity was excellent, which made the protocol support us an entry to selective protection of diverse amino groups.

MICROWAVE-PROMOTED CONVERSION OF HETEROCYCLIC AMINES TO CORRESPONDING AMIDES UNDER SOLVENT-FREE CONDITIONS