Reduction Products of 2-Nitrophenyl Esters of Arylsulfonic Acids

LC Raiford, JR Shelton

Index: Raiford; Shelton Journal of the American Chemical Society, 1943 , vol. 65, p. 2048

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Abstract

Summary Six derivatives of p-(0-aminopheny1)-benzene sulfonamide, in which a hydrogen of the sulfonamide nitrogen was replaced by an aryl group were prepared from p-(0- aeetamidopheny1)-ben-zenesulfonyl chloride and from p-(0-nitropheny1)-benzenesulfonyl chloride. These and the parent compound were inactive when tested in vitro against E. Coli and in vivo against streptococcal infected mice.