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Stream/Area:
-
Subject:
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Paper ID:
10.55041/IJSREM.ISTCESD010
Volume:
10 |
9 |
Sep 2026
Pages:
1-6
Publication Frequency:
Monthly (12 issues per year)
License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.
Department of Chemistry,
Sambhaji Kendre Mahavidyalaya, Jalkot, Latur, MS, India-413532
Heterocycles are cyclic compounds containing at least one heteroatom and are ubiquitous in medicinal chemistry. Pyridine, pyrimidine, imidazole, pyrazole, triazole, oxazole, thiazole, quinoline, benzimidazole, and related fused systems occur in numerous biologically active molecules because their heteroatoms and aromatic frameworks can establish favorable interactions with enzymes, receptors, nucleic acids, membranes, and metal-containing biological sites [1]–[3]. Their substitutional flexibility also permits systematic structure–activity relationship (SAR) optimization. The emergence of antimicrobial resistance has intensified the requirement for new antimicrobial chemotypes. The World Health Organization has identified priority bacterial pathogens for which new preventive and therapeutic strategies are urgently required [4]. At the same time, the chemical preparation of candidate heterocycles can impose environmental and economic burdens through long synthetic sequences, stoichiometric reagents, hazardous solvents, and energy-intensive work-up. The principles of green chemistry provide a systematic framework for reducing these impacts [5]. Recent advances in catalytic C–H activation, multicomponent reactions, photoredox catalysis, electrochemistry, mechanochemistry, and flow chemistry provide complementary routes toward more sustainable heterocycle synthesis [6]–[11]. These methods are particularly relevant to antimicrobial medicinal chemistry because rapid analogue generation is essential for identifying meaningful SAR. A further opportunity is the integration of artificial intelligence (AI) with green synthesis. Machine-learning models can prioritize compounds, predict biological activity, suggest synthetic routes, optimize reaction conditions, and balance antimicrobial potency against toxicity and environmental impact. Thus, the future of antimicrobial heterocycle research should combine biological activity with synthetic and environmental performance.
KEYWORDS
Green and sustainable synthesis of bioactive heterocycles has direct relevance to the discovery and manufacture of antimicrobial agents. C–H activation, multicomponent reactions, photoredox catalysis, electrochemical synthesis, mechanochemistry, and flow processing provide complementary approaches for reducing waste and improving process efficiency. Their sustainability should be evaluated through atom economy, E-factor, PMI, solvent impact, energy demand, and life-cycle considerations. The integration of AI with green heterocycle chemistry represents a particularly promising next step. Machine learning can prioritize biologically promising structures, generative models can explore chemical space, retrosynthesis tools can assess synthetic feasibility, and active learning can minimize unnecessary experiments. However, computational predictions must be experimentally validated through reproducible synthesis and standardized antimicrobial testing. The convergence of AI, sustainable synthesis, medicinal chemistry, and microbiology therefore offers a realistic route toward antimicrobial candidates that are not only potent but also synthetically efficient, scalable, and environmentally responsible.
[1] A. Rusu, I.-M. Moga, L. Uncu, and G. Hancu, “The role of five-membered heterocycles in the molecular structure of antibacterial drugs used in therapy,” Pharmaceutics, vol. 15, no. 11, p. 2554, 2023 [2] A. R. Katritzky, C. A. Ramsden, J. A. Joule, and V. V. Zhdankin, Handbook of Heterocyclic Chemistry, 3rd ed. Oxford, U.K.: Elsevier, 2010. [3] J. A. Joule and K. Mills, Heterocyclic Chemistry, 5th ed. Chichester, U.K.: Wiley, 2010. Wiley confirms the fifth edition, authorship, and 2010 publication. [4] World Health Organization, WHO Bacterial Priority Pathogens List, 2024: Bacterial Pathogens of Public Health Importance to Guide Research, Development and Strategies to Prevent and Control Antimicrobial Resistance. Geneva, Switzerland: World Health Organization, 2024. The official WHO record gives the publication date as May 17, 2024 and ISBN 978-92-4-009346-1. [5] P. T. Anastas and J. C. Warner, Green Chemistry: Theory and Practice. Oxford, U.K.: Oxford University Press, 1998. [6] J. Wencel-Delord and F. Glorius, “C–H activation enables the rapid construction and late-stage diversification of heterocycles,” Nature Chemistry, vol. 5, pp. 369–375, 2013. [7] L. Banfi and G. Riva, “Multicomponent reactions: A methodology to build molecular diversity and complexity in a simple and effective way,” Chemical Reviews, vol. 109, no. 9, pp. 4272–4300, 2009. [8] D. P. Hari and B. König, “Synthetic applications of eosin Y in photoredox catalysis,” Chemical Communications, vol. 50, no. 51, pp. 6688–6699, 2014 [9] S. R. Waldvogel and B. Janek, “Modern electrochemical synthesis of heterocycles,” Accounts of Chemical Research, vol. 53, no. 2, pp. 292–302, 2020. [10] T. Friščić, “Mechanochemistry and organic synthesis: From mysticism to mechanistic understanding,” Angewandte Chemie International Edition, vol. 59, pp. 1018–1029, 2020.
Publication Date
9/28/2026
Peer Review Type
Double-Blind Peer Review
Review Rounds: 2
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