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Synthesis of 2-{(5-phenyl-1,3,4-Oxadiazol-2-yl)sulfanyl}-N-substituted acetamides as potential antimicrobial and hemolytic agents. | LitMetric

AI Article Synopsis

  • - A new series of compounds called N-substituted derivatives of 2-{(5-phenyl-1,3,4-Oxadiazol-2-yl)sulfanyl}acetamides was created through a multi-step synthesis process starting with benzoic acid and ending with various derivatives.
  • - The synthesized compounds were characterized using techniques like mass spectrometry (EI-MS), infrared (IR) spectroscopy, and proton nuclear magnetic resonance ((1)H-NMR) to confirm their structure.
  • - The compounds were tested for antimicrobial and hemolytic activities, with most showing effectiveness against certain microbes; compound 6h was the most active, while 6m exhibited higher toxicity, suggesting the series may have potential

Article Abstract

A new series of N-substituted derivatives of 2-{(5-phenyl-1,3,4-Oxadiazol-2-yl)sulfanyl}acetamides was synthesized. The synthesis was carried out by converting benzoic acid (1) into ethyl benzoate (2), benzohydrazide (3) and then 5-pheny-1,3,4-Oxadiazol-2-thiol (4) step by st0ep. The target compounds 6a-p were synthesized by reaction of compound 4 with equimolar ratios of different N-alkyl/aryl substituted 2-bromoacetamide (5a-p) in the presence of DMF and sodium hydride (NaH). The spectral (EI-MS, IR, (1)H-NMR) characterization of all the synthesized compounds reveal their successful synthesis. The compounds were also screened for antimicrobial & hemolytic activity and most of them were found to be active against the selected microbial species at variable extent relative to reference standards. But 6h was the most active against the selected panel of microbes. This series showed less toxicity and may be considered for further biological screening and application trial except 6m, possessing higher cytotoxicity.

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