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International Journal of
Chemical Science
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VOL. 9, ISSUE 2 (2025)
Synthesis and antibacterial activity of 2,9-(disubstituted)-6,13-dimethoxy-5,12-dihydroquinoxalino [2,3-b] phenazine Derivatives
Authors
CH Sudhakar
Abstract
A novel series of 2,9-(disubstituted)-6,13-dimethoxy-5,12-dihydroquinoxalino [2,3-b] phenazine derivatives 3(a–d) was successfully synthesized with moderate yields (52–61%). The structures of these newly developed nitrogen-fused heterocyclic frameworks were confirmed via FT-IR, 1H-NMR, 13C-NMR, ESI-MS and elemental analysis. All synthesized target molecules were evaluated in vitro for their antibacterial efficacy against Gram-positive Staphylococcus aureus, Micrococcus luteus, Bacillus subtilis and Gram-negative Escherichia coli, Salmonella paratyphi, Klebsiella pneumoniae bacterial strains using the disk diffusion technique. Among the series, compounds 3b (chloro-substituted) and 3c (bromo-substituted) demonstrated moderate antibacterial activity, producing zones of inhibition (15–19 mm) compared to the commercial standard drug, Streptomycin. This study highlights the therapeutic potential of modified phenazine-quinoxaline hybrids as next-generation antibacterial scaffolds.
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Pages:101-104
How to cite this article:
CH Sudhakar "Synthesis and antibacterial activity of 2,9-(disubstituted)-6,13-dimethoxy-5,12-dihydroquinoxalino [2,3-<i>b</i>] phenazine Derivatives". International Journal of Chemical Science, Vol 9, Issue 2, 2025, Pages 101-104
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