Synthesis, Characterization, Antimicrobial Assessments, Potential Antioxidant and Molecular Docking Studies of Polyfunctional Substituted Azoles, Azines, and their Analogs linked Sulfamethoxazole moiety
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A new series of substituted azoles, azines, and their analogs linked sulfamethoxazole moiety was designed and synthesized. The antioxidant activity study of our synthesized compounds and molecular docking enhancement were achieved. Moreover, the antimicrobial assay indicated that compound 1 is the most active compound against all the strains compared to the reference drugs. So, reactions of β-oxobutanamide derivative 1 with different reagents afforded compounds 2a,b, 5, 7, 8, 12 and 14. Coupling of 1 with diazonium salt yield aryl hydrazones 10a,b which reacts with ethyl chloroformate to yield the triazinediones 11a,b. Reactions of enaminone 12 with some electrophilic and nucleophilic reagents to yield compounds 16, 21, 22, 23, 24 and 25 respectively. The structures of newly synthesized compounds were characterized by spectral and elemental analyses.
