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Novel Synthesis of Some Imidazolyl‐, Benzoxazinyl‐, and Quinazolinyl‐2,4‐dioxothiazolidine Derivatives
36
Citations
20
References
2014
Year
Organic ChemistryAntimicrobial ChemotherapyNovel SynthesisHeterocycle ChemistrySynthesized CompoundsAntimicrobial TherapyAntimicrobial ResistanceAntimicrobial Drug DiscoveryDerivativesBiochemistryAntifungal AgentsAntibacterial AgentAcetic Acid 1Antimicrobial CompoundPharmacologyFood PreservativesAntifungal AgentAntibioticsMicrobiologyAntimicrobial AgentsAntimicrobial PharmacodynamicsMedicineDerivative (Chemistry)Chloride Derivative 2
2‐(2,4‐Dioxothiazolidin‐5‐yl)acetic acid 1 and its chloride derivative 2 were allowed to react with different aromatic amines such as o ‐phenylenediamine, o ‐aminothiophenol, p ‐aminoacetophenone, and anthranilic acid to give the biologically active nuclei such as imidazoles, thiazoles, benzoxazines, and quinazolines incorporated with the thiazolidindione nucleus. The antimicrobial activity of five of the synthesized compounds was examined against one gram positive bacteria ( Staphylococcus aureus ), one gram negative bacteria ( Escherichia coli ), and two fungi ( Aspergillus flavus and Candida albicans ). Four compounds showed moderate antibacterial and antifungal activities.
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