Synthesis and in vitro screening of benzo[h]coumarinyl heterocycles as promising antibacterial agents
Year: 2024
Type: article
Abstract: In this study, benzo[h]coumarin and the corresponding substituted chalcones were designed and synthesized. These compounds have been used as a precursor to prepare various heterocyclic compounds like pyrimidines, pyrazole, pyrazole-1-carbothioamide, diazepines, oxazepines, isoxazoles and epoxides. The structures of the synthesized compounds were confirmed by FT-IR, 1H and 13C-NMR spectroscopy. These target heterocyclic derivatives were biologically screened against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) pathogenic bacteria. The best obtained result was for compound (6b) against S. aureus, Gram-positive bacteria. KEY WORDS: Benzo[h]coumarin, heterocyclic compounds, antibacterial activity Bull. Chem. Soc. Ethiop. 2024, 38(6), 1815-1826. DOI: https://dx.doi.org/10.4314/bcse.v38i6.24
Institution: University of Mosul
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: diamond
Funder: University of Mosul
OpenAlex ID: W4402730171
