Синтез та алкілування 5-арил-1,2-дигідро-3H-1,2,4-триазол-3-тіонів

• Дата: 2021
• Автори: Dovbnya, Dmytro V., Kaplaushenko, Andrii G., Korzhova, Alla S.
• Формат: Стаття
• Мова: Ukrainian
• Опубліковано: National University of Pharmacy 2021
• Теми: 1,2,4-триазоли; 5-(2,4- та 3,4-диметоксифеніл)-3H-1,2,4-триазол-3-тіони; реакції алкілування; 547.79’286.2.057
• Онлайн доступ: https://ophcj.nuph.edu.ua/article/view/188135
• Назва журналу: Journal of Organic and Pharmaceutical Chemistry

5-R-1,2,4-triazole-3-thiones and their derivatives are easy to obtain; they have low toxicity and a broad spectrum of the biological activity. It makes this class of heterocyclic compounds promising for creating potential drugs. Aim. To develop the preparative methods for the synthesis of 5-aryl-1,2-dihydro-3H-1,2,4-triazole-3-thiones and study their reactivity in the alkylation reaction. Results and discussion. New 5-aryl-1,2-dihydro-3H-1,2,4-triazole-3-thiones were synthesized. The latter were used for the synthesis of 3-aryl-5-(alkylthio)-4H-1,2,4-triazoles. Experimental part. Using a series of four successive reactions based on the substituted benzoic acids new 5-aryl-1,2-dihydro-3H-1,2,4-triazole-3-thiones were synthesized. Alkylation of the thiones allowed obtaining a series of S-alkyl derivatives. The structure of the compounds synthesized was confirmed by elemental analysis, IR and 1H NMR spectroscopy, and their individuality was determined by high-performance liquid chromatography. Conclusions. The preparative methods have been developed, and new 5-aryl-1,2-dihydro-3H-1,2,4-triazole-3-thiones have been synthesized. Alkylation of the latter made it possible to obtain a series of 3-aryl-5-(alkylthio)-4H-1,2,4-triazoles with an alkylthio fragment of different length.