Department of Chemistry, Shibli National P.G. College, Azamgarh, UP (INDIA)
3-Methyl-1-phenylpyrazol-5-one (I) were prepared by mixing ethyl acetoacetate and phenyl hydrazine. These methyl phenyl pyrazolone was treated with bromine in glacial acetic acid to get 4-bromo-3-methyl-1-phenyl pyrazole-5-one (II). These were treated with ammonium N-(phenyldithiocarbamate) and sodium acetate in absolute ethanol to give 3-Methyl-1-phenylpyrazole-5-one-4-yl-N-(phenyl)-dithiocarbamates (IIIa-c). These carbamates when treated with concentrate H2SO4 give 4-methyl-6-phenyl-2-phenylimino-1,3,-dithiolo-[4,5-a]-pyrazole (IVa-c) and on treatment with methyl iodide in methanol gave 4-methyl-6-phenyl- 2-phenylimino-1,3-oxathialo [4,5-d] pyrazole (Va-c). Fungitoxicity of the prepared compounds have been compared with Dithane M-45 a commercial fungicide for their fungitoxic action against Puccinia recondita and Ustilago nuda maydis and the screening results have been correlated with the structural features of the prepared compounds
Copy the following to cite this article:
RANJEETA SRIVASTAVA and ABDUL WAHAB, "Synthesis and fungitoxicity of 4-methyl-6-phenyl -2-phenylimino-1,3-oxathiolo [4,5-d]-pyrazole", Journal of Ultra Chemistry, Volume 8, Issue 2, Page Number , 2016Copy the following to cite this URL:
RANJEETA SRIVASTAVA and ABDUL WAHAB, "Synthesis and fungitoxicity of 4-methyl-6-phenyl -2-phenylimino-1,3-oxathiolo [4,5-d]-pyrazole", Journal of Ultra Chemistry, Volume 8, Issue 2, Page Number , 2016Available from: http://journalofchemistry.org/paper/407/