Green Synthesis and Characterisation of New Hydroquinoline Derivatives by the Fusion Method, and Evaluation of Their Antibacterial Activity

Authors

  • Mohammed Khalaf Tikrit University, College of Basic Education, Al-Sharqat, Iraq

DOI:

https://doi.org/10.51699/cajmns.v7i4.3366

Keywords:

Heterocyclic, Hydroquinazoline, Bacterial Bioactivity

Abstract

In this study, A new solvent-free, and eco-friendly technique called the fusion method was used to create a number of compounds with a hydroquinazoline ring by reacting hydrazone with 2-aminobenzoic acid. Basic organic chemistry analyzes (FT-IR, ¹H, and ¹³C-NMR) demonstrated a clear disappearance of azomethine, suggesting full consumption of the reactants, confirming the correctness of the synthesis. Additionally, antimicrobial activity was assessed against two common bacterial species: Escherichia coli and Staphylococcus aureus. When compared to the antibiotic ampicillin, which served as a control for inhibition, the molecule (M3) had the strongest antimicrobial activity against the bacterial strains employed in the investigation, and the results demonstrated that inhibition improved with increasing concentration. All things considered, these substances have encouraging potential for upcoming medicinal uses.

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Published

2026-08-11

How to Cite

Khalaf, M. (2026). Green Synthesis and Characterisation of New Hydroquinoline Derivatives by the Fusion Method, and Evaluation of Their Antibacterial Activity. Central Asian Journal of Medical and Natural Science, 7(4), 209–215. https://doi.org/10.51699/cajmns.v7i4.3366

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