Structurally diversified products from the reactions of 2-aminobenzamides with 1,3-cyclohexanediones catalyzed by iodine

Abstract Controlling the reaction temperature at 50 °C, 80 °C, and 110 °C, respectively, the iodine-catalyzed reaction of 2-aminobenzamides with 1,3-cyclohexanediones gave structurally diversified products. In the latter, it gave bis-quinazolin-4(3 H )-ones unexpectedly, with 1,3-cyclohexanediones ring-opening.