The substituted N-{[2-(aminocarbonyl)phenylamino]thioxomethyl}benzamides and 2-arylquinazolin-4(3H)-ones are synthesized by the reaction of ammonium thiocyanate and aroyl chlorides with 2-amino-benzamide under solvent-free conditions or under reflux in MeCN.

This method allows for the facile one-pot synthesis of substituted N-[2-(aminocarbonyl)phenylamino]thioxomethylbenzamides and 2-aryl-quinazolin-4(3H)-ones, with potential applications in organic synthesis and pharmaceutical

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A facile one-pot synthesis of substituted N-{[2-(aminocarbonyl)phenylamino]thioxomethyl}benzamides and 2-aryl-quinazolin-4(3H)-ones

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