Synthesis and Fungitoxicity of 2-Oxo/Thiopyrimidine Derivatives
Tirthankar Banerjee, H.K. Taneja, S. S. Tomar
Abstract
Tirthankar Banerjee, H.K. Taneja, S. S. Tomar
Abstract
Ten derivatives of pyrimidin-2-one, four derivatives of pyrimidin-2-thione and six phenyl hydrazone derivatives of pyrimidin-2-one were synthesised. These compounds exhibited fungitoxicity to the mycelial growth of Rhizoctonia bataticola ana Sclerotium rolfsii. 1 -H-5, 6-dihydro-6-(4-N,N-dimethylaminophenyl)-4-pheny 1-2-oxopyrimidine (EC50 = 98 mg/L) was found to be the most active compound against R. bataticola, while 1-H-5,6-dihydro-2-oxo-6-phenylpyrimidine (EC50 = 292 mg/L) exhibited promising activity against S. rolfsii. Structure activity relationships of these compounds are discussed.
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Ten derivatives of pyrimidin-2-one, four derivatives of pyrimidin-2-thione and six phenyl hydrazone derivatives of pyrimidin-2-one were synthesised. These compounds exhibited fungitoxicity to the mycelial growth of Rhizoctonia bataticola ana Sclerotium rolfsii. 1 -H-5, 6-dihydro-6-(4-N,N-dimethylaminophenyl)-4-pheny 1-2-oxopyrimidine (EC50 = 98 mg/L) was found to be the most active compound against R. bataticola, while 1-H-5,6-dihydro-2-oxo-6-phenylpyrimidine (EC50 = 292 mg/L) exhibited promising activity against S. rolfsii. Structure activity relationships of these compounds are discussed.
Key concepts: Sclerotium, Mycelium, EC50, Veterinary medicine, Mathematics, Biology, Medicine, Botany