Highly selective C3–H iodination of pyrrolo[1,2-<i>a</i>]quinoxalines

Abstract

We report a C3-H direct iodination of pyrrolo[1,2-a]quinoxalines with TBAI or I2; a series of novel 3-iodopyrrolo[1,2-a]quinoxaline derivatives were obtained with excellent regioselectivity and broad substrate scope. Mechanism studies show that a catalytic amount of p-toluenesulfonic acid significantly promotes the selectivity and conversion of the reaction. Notably, the reaction can be performed on a gram scale, and the iodinated products can be further transformed into potentially biologically active pyrrolo[1,2-a]quinoxaline derivatives by palladium-catalyzed coupling reactions.

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