Copyright (c) 2025 Nawaj Ali beg chemistry, Dr. Maqdoom Farooqui
This work is licensed under a Creative Commons Attribution 4.0 International License.
Facile Synthesis of New Substituted 4-Thiazolidinones Conjugates containing Quinoline-Sulfamethoxazole Motifs and their Bioevaluation
Corresponding Author(s) : Nawaj Ali Beg
Asian Journal of Chemistry,
Vol. 37 No. 2 (2025): Vol 37 Issue 2, 2025
Abstract
Difunctional Brönsted acidic ionic liquid [DBN][HSO4] mediated synthesis of quinoline-sulfamethoxazole blended 4-thiazolidinones derivatives (7a-l) by reacting 4-amino-N-(5-methylisoxazol-3-yl) benzenesulfonamide (4), 2-chloro-3-formyl quinoline (5a-l) and mercapto acetic acid (6) in promising yields at 80 ºC. All the newly synthesized quinoline-sulfamethaoxazole incorporated 4-thiazolidinones derivatives were explored for their in vitro antifungal and antioxidant activity. The novel compounds, 4-thiazolidinones hybrids were evaluated against various fungal strains and compounds 7g, 7h, 7i, 7j and 7k displays promising antifungal activity. Furthermore, all the synthesized 4-thiazolidinones conjugates were evaluated for antioxidant activity and almost all derivatives (7b-l) exhibit excellent radical activity. Using [DBN][HSO4] protocol providing economical as well as environmental advantages and its applicable for divergent functional groups.
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