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Journal of the Korean Chemical Society (JKCS)

ISSN 1017-2548(Print)
ISSN 2234-8530(Online)
Volume 57, Number 2
JKCSEZ 57(2)
April 20, 2013 

Synthesis and Anti Bacterial and Anti-ulcer Evaluation of New S-mannich Bases of 4,6-diaryl-3,4-dihydropyrimidin-2(1H)-thiones
Venkateshwarlu Kodhati, Malla Reddy Vanga, Narsimha Reddy Yellu*
4, 6-diaryl-3,4-dihydropyramidin-2(1H)-thiones, Anti-ulcer activity, Antibacterial activity
The synthesis of title compounds were accomplished by synthetic sequence shown in Scheme 1. Chalcones on cyclocondensation with thiourea in ethanol and potassium hydroxide under reflux yielded the respective dihydropyramidin- 2(1H)-thiones. Each of the dihydropyrimidin thiones was, then subjected to the Mannich condensation in alkaline medium using three different secondary amines, viz., dimethylamine, diethylamine and morpholine to obtain a new series of S-Mannich bases. All the synthesised compounds (C1-C15) were evaluated for their antiulcer and antibacterial activities. Compounds C4, C5, C6, C14 and C15 exhibited relatively more potent antiulcer activity but not comparable to the standard; Omeprazole, while C1, C2, C3 and C13 were moderate in activity at 100 mg/kg p.o. All the compounds (C1-C15) showed mild to moderate activity against both Gram-positive (S.aureus, L.delbrueckii) and Gram-negative (P.vulgaris, E.coli) bacteria. Amongst the compounds tested, only C6, C9, C12 and C15 were found to be potent.
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