Synthesis and biological screening of N-Substituted derivatives of N-benzyl-4-chlorobenzenesulfonamide
DOI:
https://doi.org/10.5530/3bmkyt06Keywords:
Benzylamine, sulfonamide, antimicrobial activity, 1H-NMR, EI-MSAbstract
In the present study, a series of N-substituted derivatives of N-benzyl-4-chlorobenzenesulfonamide has been synthesized. The
reaction of benzylamine (1) with 4-chlorobenzenesulfonyl chloride (2) yielded the parent compound N-benzyl-4-chlorobenzenesulfonamide (3), which further on treatment with different electrophiles (4a-i) in the presence of sodium hydride
furnished into N-substituted sulfonamides (5a-i). The structure 1 of synthesized compounds has been established by IR, 1H-NMR
and EI-MS. All the compounds have been screened for their antimicrobial activity.
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2012-09-30
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Synthesis and biological screening of N-Substituted derivatives of N-benzyl-4-chlorobenzenesulfonamide. (2012). Asian Journal of Pharmaceutical and Health Sciences, 2(3), 384-389. https://doi.org/10.5530/3bmkyt06
