SYNTHESIS, ANTIMICROBIAL AND ANTIOXIDANT EVALUATION OF 3-(2-(4-FLUOROBENZYLTHIO) PYRIMIDIN-4-YL-AMINO)-2-(3- SUBSTITUTED PHENYL) THIAZOLIDIN-4-ONES
Naganna M Goudgaon* and Rohini Y Reddy
ABSTRACT
A series of novel 3-(2-(4-fluorobenzylthio)pyrimidin-4-ylamino)-2-(3-
substituted phenyl)thiazolidin-4-one analogues (6a-i) were synthesized
starting from 2-thiouracil (1). Reaction of compound 1 with 4-
fluorobenzylchloride gave 2-(4-fluorobenzylthio) pyrimidin-4(3H)-one
(2) which on chlorination with POCl3 yielded 2-(4-fluorobenzylthio)-
4-chloropyrimidine (3). Further reaction of compound 3 with
hydrazine hydrate generated the key intermediate 1-(2-(4-
fluorobenzylthio)pyrimidin-4-yl)hydrazine (4). Reaction of compound
4 with appropriate substituted aromatic aldehydes furnished 2-
(substituted benzylidene)-1-(2-(4-fluorobenzylthio)pyrimidin-4-yl)
hydrazine (5a-i), which on further cyclisation with thioglycolic acid in dry benzene furnished
3-(2-(4-fluorobenzylthio)pyrimidin-4-ylamino)-2-(3-substituted phenyl)thiazolidin-4-one
analogues (6a-i). Structural assignments of the synthesized compounds were based on their
IR, 1H NMR, Mass and analytical data. All the synthesized compounds 5a-i and 6a-i were
screened for their preliminary antimicrobial and antioxidant properties. Some of the
compounds exhibited promising antimicrobial and antioxidant activities.
Keywords: Pyrimidines, thiazolidinones, antibacterial, antifungal, antioxidant activity.
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