Synthesis, Characterization and Antimicrobial Activity of N-Pyridin-3-yl-benzenesulfonamide

A.O. Ijuomah, D. C. Ike, M. Obi
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Abstract

This study describes a simple one-pot synthesis of N-pyridin-3-yl-benzenesulfonamide and its antimicrobial activity. The reaction of benzene sulfonyl chloride with 3-aminopyridine in the presence of aqueous Na2CO3 and HCl as a scavenger furnished the sulfonamide in 93.3% yield. The structure of the synthesized compound was established using the spectral data obtained from FTIR, 1HNMR and 13CNMR). All spectrometric spectrum bands and peaks obtained were sulfonamide-related. The antibacterial test carried out against Gram-positive bacterium (Staphylococcus aureus) and Gram-negative bacteria (Salmonella typhi and Eschericha coli) tested upon at concentrations 150, 100, 50 and 25 mg/ml revealed that the synthesized N-pyridin-3yl-benzenesulfonamide possesses great antimicrobial activity.
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n-吡啶-3-基苯磺酰胺的合成、表征及抗菌活性研究
研究了一锅法简单合成n-吡啶-3-基苯磺酰胺的方法及其抑菌活性。苯磺酰氯与3-氨基吡啶在Na2CO3水溶液和HCl作为清除剂存在下反应,得到磺胺的收率为93.3%。利用FTIR、1HNMR和13CNMR的光谱数据确定了合成化合物的结构。获得的所有光谱带和峰均与磺胺相关。对革兰氏阳性菌(金黄色葡萄球菌)和革兰氏阴性菌(伤寒沙门菌和大肠杆菌)在150、100、50和25 mg/ml浓度下的抑菌试验表明,合成的n-吡啶-3基苯磺酰胺具有良好的抑菌活性。
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