A series of new pyrazoline carbothioamides bearing furan moiety were synthesized by simple one pot procedure. The method involves base catalyzed cyclocondensation reaction of chalcones 1a-e and thiosemicarbazide 2 in ethanol under optimum temperature. The reaction yielded the title compounds 5-aryl-3-(furan-2-yl)-4,5-dihydro-1Hpyrazole- 1-carbothioamides 3a-e in excellent yields. The synthesized new compounds were characterized by spectral studies and elemental analysis, and were evaluated in vitro for their antifungal susceptibility
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