Published January 25, 2013 | Version v1
Journal article Open

Synthesis and Antibacterial Activity of N,NDiethylamide Bearing Benzenesulfonamide Derivatives

  • 1. Department of Chemistry, School of Natural and Applied Sciences, Covenant University, P.M.B. 1023, Ota, Ogun State 1100001, Nigeria.
  • 2. Department of Chemistry, University of Lagos, Akoka, Lagos State 10001, Nigeria.
  • 3. New Functional Polymeric Material Group, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences (CAS), Beijing 100190, P.R. China.
  • 4. Test Center of Antimicrobial Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences (CAS), Beijing 100190, P.R. China.

Description

Sulfonamides are known to represent a class of medicinally important compounds which are extensively used as antibacterial agents. Hence, a series of new N,N-diethyl amide bearing sulfonamides (2a-k) were synthesized via amidation of easily prepared benzenesulfonamide precursors (1a-k). The chemical structures of all synthesized compounds were substantiated using spectroscopic means such as IR, Mass spectra and 1H-NMR as well as analytical data. The antimicrobial activity of these compounds along with streptomycin, was investigated on Escherichia coli and Staphylococcus aureus. The results showed that this skeletal framework exhibited marked potency as antibacterial agents. The most active antibacterial agent against both targeted organisms was N,Ndiethyl- 1-(phenylsulfonyl) piperidine-2-carboxamide (2b).

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