Expedited Synthesis and Comprehensive Characterization of Oxomorpholine-Imidazole Derivatives: Unraveling their Remarkable Antimicrobial Activity

Authors

  • S. M. Sitapara Department of Chemistry, Government Science College, Veraval-362266, Gujarat, India https://orcid.org/0000-0002-7770-8387
  • J. H. Pandya Department of Chemistry, D.K.V. Arts & Science college, Jamnagar-361310, Gujarat, India
  • S. K. Kangad Department of Chemistry, Kamani Science College, Amreli-365601, Gujarat, India

Abstract

This research focuses on synthesizing aromatic or heteroaromatic compounds with potential pharmaceutical and medicinal applications. Imidazole derivatives have garnered significant attention due to their versatile therapeutic potential, encompassing a broad spectrum of diseases, including cancer, bacterial infections, fungal infections, and malaria. To accomplish this, we have developed an efficient synthetic route to explore a diverse array of 2-((1,4-diphenyl-1H-imidazol-2-yl)thio)-N-(4-(3-oxomorpholino)phenyl) acetamide  derivatives. The structural elucidation of the synthesized compounds was carried out using advanced techniques, including 1H and 13C NMR, FT-IR spectroscopy, mass spectroscopy, and elemental analysis. Furthermore, the oxo morpholino-imidazole derivatives synthesized in this study were further employed to produce diverse chemotherapeutic agents with significant potential for clinical applications.

            

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Published

2024-01-01

How to Cite

Expedited Synthesis and Comprehensive Characterization of Oxomorpholine-Imidazole Derivatives: Unraveling their Remarkable Antimicrobial Activity. (2024). Journal of Scientific Research, 16(1), 321-330. https://doi.org/10.3329/jsr.v16i1.67728

Issue

Section

Section B: Chemical and Biological Sciences

How to Cite

Expedited Synthesis and Comprehensive Characterization of Oxomorpholine-Imidazole Derivatives: Unraveling their Remarkable Antimicrobial Activity. (2024). Journal of Scientific Research, 16(1), 321-330. https://doi.org/10.3329/jsr.v16i1.67728