Thi-Dan Thach, T. Tuong-Vi Le, H. Thien-An Nguyen, Chi-Hien Dang, Van-Su Dang, Nguyễn Thành Danh (2020). Synthesis of sulfonamides bearing 1,3,5-triarylpyrazoline and 4-thiazolidinone moieties as novel antimicrobial agents Journal of the Serbian Chemical Society, 85 (2), 158-162. (ISI, IF = 0.828)
Two series of sulfonamides were synthesized from 4-hydrazinylbenzenesulfonamide as the key starting material. 1,3,5-Triarylpyrazoline sulfonamides (2a–i) were obtained by cyclocondensation of various chalcones in 53–64 % yields, while 4-thiazolidinone derivatives (4a–e) were synthesized by cyclocondensation between mercaptoacetic acid and different phenylhydrazones in 43–62 % yields. The synthesized compounds were characterized based on FTIR, 1H-NMR, 13C-NMR and HRMS data. The sulfonamides were evaluated for their in vitro antimicrobial activities against four bacterial strains (E. coli, P. aeruginosa, B. subtillis and S aureus), two filamentous fungal strains (A. niger and F. oxysporum) and two yeast strains (C. albicans and S. cerevisiae). Seven pyrazolines, 2a–c and 2e–h, exhibited significant inhibition of different microbial strains. Among them, compound 2b displayed good antifungal activity against A. niger (MIC value at 12.5 mg mL-1) over the reference drug.
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