Abstract

AbstractA simple and mild copper‐catalyzed sulfonylation of 8‐aminoquinolines with sodium and lithium sulfinates is reported. In the presence of manganese(III) acetate [Mn(OAc)3] as cooxidant a highly site‐selective C−H functionalization at the C‐5 position takes place. The reaction proceeds readily at room temperature in air and various sulfones were synthesized in moderate to high yields. Moreover, a straightforward procedure for the conversion of organolithium reagents and sulfur dioxide into C‐5 sulfonylated quinolines was developed.magnified image

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