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Microwave Assisted Synthesis and Antifungal Studies of 5-Amino Thiadiazole Substituted Pyrimidine Compounds


Affiliations
1 PG & Research Department of Chemistry, Islamiah College, Vaniyambadi-635751, India
2 Department of Chemistry, Priyadarshini Engineering College, Vaniyambadi, India
     

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Simple synthetic methods of 5-(5-amino-1,3,4-thiadiazol-2yl)-3,4-dihydro-6-methyl-4-phenylpyrimidin-2(1H)-thione (3f-j) are described. Compound 1 is converted to carbothiamide 2 by reacting compound 1 with thiosemicarbazide in catalytic amount of acetone is irradiated with help of domestic microwave oven (200W) for 2 minutes. Compound 2 is act as a key intermediate for the final compounds. The compound 2 is converted to corresponding thiadiazole 3 by treatment with conc.H2SO4 and NH3. Structural elucidation is accomplished by IR, 1H and 13CNMR, Elemental analysis and GC-Mass spectral data of the synthesized compounds. Few of these Pyrimidine derivatives have been evaluated for their possible antifungal activity. Most of the tested compounds show significant antifungal activity.

Keywords

Pyrimidine, Thiadiazole, Carbothiamide, Thiosemicarbazide, Antifungal Activity.
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  • Microwave Assisted Synthesis and Antifungal Studies of 5-Amino Thiadiazole Substituted Pyrimidine Compounds

Abstract Views: 199  |  PDF Views: 3

Authors

R. Karthic
PG & Research Department of Chemistry, Islamiah College, Vaniyambadi-635751, India
B. Andrews
Department of Chemistry, Priyadarshini Engineering College, Vaniyambadi, India
K. Subramani
PG & Research Department of Chemistry, Islamiah College, Vaniyambadi-635751, India

Abstract


Simple synthetic methods of 5-(5-amino-1,3,4-thiadiazol-2yl)-3,4-dihydro-6-methyl-4-phenylpyrimidin-2(1H)-thione (3f-j) are described. Compound 1 is converted to carbothiamide 2 by reacting compound 1 with thiosemicarbazide in catalytic amount of acetone is irradiated with help of domestic microwave oven (200W) for 2 minutes. Compound 2 is act as a key intermediate for the final compounds. The compound 2 is converted to corresponding thiadiazole 3 by treatment with conc.H2SO4 and NH3. Structural elucidation is accomplished by IR, 1H and 13CNMR, Elemental analysis and GC-Mass spectral data of the synthesized compounds. Few of these Pyrimidine derivatives have been evaluated for their possible antifungal activity. Most of the tested compounds show significant antifungal activity.

Keywords


Pyrimidine, Thiadiazole, Carbothiamide, Thiosemicarbazide, Antifungal Activity.