Synthesis of novel 1,2,4-triazoles and triazolo-thiadiazines as anticancer agents

Authors : THORAYA ABD ELREHEEM FARGHALY, MAGDA AHMAD ABDALLAH, HUDA KAMEL MMAHMOUD

Pages : 955-969

View : 13 | Download : 8

Publication Date : 0000-00-00

Article Type : Research Paper

Abstract :A new series of 7-arylazo-5$H$-3-insert ignore into journalissuearticles values(trifluoromethyl);-6-methyl-1,2,4-triazolo-[3,4-$b$]-1,3,4-thiadiazines was prepared by reaction of 4-amino-3-trifluoromethyl-5-mercapto-1,2,4-triazoles with $N$-aryl-2-oxo-propane hydrazonoyl chloride in dioxane under reflux in the presence of triethylamine. Furthermore, Schiff bases of 4-amino-5-mercapto-1,2,4-triazole derivatives were reacted with a variety of hydrazonoyl chlorides and gave the respective hydrazonothioates. In addition, the novel \textit{bis}-insert ignore into journalissuearticles values(1,2,4-triazole-3-thione); was reacted with the appropriate hydrazonoyl chloride in dioxane under reflux in the presence of triethylamine to give the corresponding \textit{bis}-insert ignore into journalissuearticles values(1,2,4-triazolethiohydrazonoate);. The structures of the new compounds were established based on elemental and spectral data. The mechanism of the studied reaction was also discussed. Moreover, some of the new products were screened for their anticancer activity and the results obtained are promising and indicate that compounds \textbf{4a }and \textbf{4i} are the most active inhibitors against HEPG-2 and compounds \textbf{4a} and \textbf{13b} are active against HCT cell lines.
Keywords : 4 Amino 3 trifluoromethyl 5 mercapto 1, 2, 4 triazole, hydrazonoyl halides, anticancer activity, triazolo 3, 4 b 1, 3, 4 thiadiazines