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作 者:M. Bakavoli O. Sabzevari M. Rahimizadeh
机构地区:[1]Department of Chemistry, School of Sciences, Ferdowsi University, Mashhad 91775-1436, Iran
出 处:《Chinese Chemical Letters》2007年第5期533-535,共3页中国化学快报(英文版)
摘 要:A highly efficient synthesis of 2-amino-N-substituted-benzamides was performed by the condensation ofisatoic anhydride with several amines in solvent-free conditions under microwave irradiation. H-Y-zeolites induced heterocyclization of these products with ortho-esters under similar conditions afforded the relevant substituted-quinazolin-4(3H)ones in high yields.A highly efficient synthesis of 2-amino-N-substituted-benzamides was performed by the condensation ofisatoic anhydride with several amines in solvent-free conditions under microwave irradiation. H-Y-zeolites induced heterocyclization of these products with ortho-esters under similar conditions afforded the relevant substituted-quinazolin-4(3H)ones in high yields.
关 键 词:Isatoic anhydride 2-Aminobenzamide H-Y-zeolite QUINAZOLINONES
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