Introduction/Objectiv: The objective of this review is to explore the role of Micro-wave-Assisted Synthesis (MAS) for the efficient and eco-friendly synthesis of heterocyclic compounds, which are critical scaffolds in drug discovery. The review highlights how MAS aligns with green chemistry principles by reducing reaction time, enhancing yields, and mini-mizing solvent use. It particularly focuses on the synthesis of bioactive heterocycles, including pyrimidines, quinolines, imidazoles, and indoles. Methods: A comprehensive literature review was conducted to analyze studies involving MAS in the synthesis of heterocyclic compounds. The methodology involved comparing microwave-based synthetic protocols with conventional methods based on parameters such as reaction time, yield, solvent usage, selectivity, and scalability. Recent technological advances, including con-tinuous-flow microwave reactors and AI-assisted optimization techniques, were also evaluated for their role in overcoming existing limitations. Results: The studies reviewed consistently demonstrated that MAS significantly reduces reac-tion times (from hours to minutes), increases product yields, and improves selectivity compared to traditional thermal methods. For example, several heterocyclic compounds showed yield im-provements of over 20–30% when synthesized under microwave conditions. Additionally, MAS contributed to reduced solvent consumption, supporting environmentally sustainable practices. However, challenges related to industrial scalability and high equipment costs were noted. Conclusion: Microwave-assisted synthesis represents a powerful, sustainable, and time-effi-cient technique for the synthesis of pharmacologically important heterocycles. Despite limita-tions in scale-up and equipment accessibility, ongoing innovations—such as continuous-flow systems and AI-guided optimization—are addressing these barriers. MAS is expected to become increasingly vital in the future of drug discovery, offering a green alternative to conventional synthesis.
Tanwar et al. (Fri,) studied this question.