Department of Chemistry, Shibli National P.G.College , Azamgarh India
4-Arylthiosemicarbazides (Ia-e) were prepared by mixing appropriate aromatic amines (in NH3) with CS2, sodium chloroacetate followed by hydrazine hydrate. These 4-arylthiosemicarbazides was added in pyridine and thionyl chloride to prepare 5-aryl-4-mercapto-1- sulpho-2,3,5-triazoles (IIa-e). These 5-aryl-4-mercapto-1-sulpho-2,3,5- triazoles were converted to their potassium salts and further treated with appropriate aryl halide to get 5-aryl-4-thioaryl-1-sulpho-2,3,5-
triazoles (IIIa-y). Fungitoxicity of the prepared compounds have been compared with Dithane M-45 a commercial fungicide, for their fungitoxic action against Puccinia recondita and Ustilagonude var. 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 5-aryl-4-thioaryl-1- sulpho-2,3,5-triazole", Journal of Ultra Chemistry, Volume 8, Issue 3, Page Number 442-446, 2016Copy the following to cite this URL:
Ranjeeta Srivastava and Abdul Wahab, "Synthesis and fungitoxicity of 5-aryl-4-thioaryl-1- sulpho-2,3,5-triazole", Journal of Ultra Chemistry, Volume 8, Issue 3, Page Number 442-446, 2016Available from: http://journalofchemistry.org/paper/445/