Synthesis of derivatives of N-(5-(methylsulfanyl)-4H-1,2,4-triazol-3-yl)pyridine-2-amines and their 1,2,4-triazine precursors

Authors

  • Ya. K. Shtaitz Ural Federal University, Ekaterinburg
  • Е. D. Ladin Ural Federal University, Ekaterinburg
  • V. V. Sharutin South Ural State University, Chelyabinsk
  • D. S. Kopchuk Ural Federal University, Ekaterinburg; I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of Russian Academy of Sciences
  • А. V. Rybakova South Ural State University, Chelyabinsk
  • E. R. Sharafieva Ural Federal University, Ekaterinburg; Ural State Medical University, Ekaterinburg
  • А. P. Krinochkin Ural Federal University, Ekaterinburg; I.Ya. Postovsky Institute of Organic Synthesis
  • G. V. Zyryanov Ural Federal University, Ekaterinburg; I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of Russian Academy of Sciences
  • Т. А. Pospelova Ural Federal University, Ekaterinburg
  • А. I. Matern Ural Federal University, Ekaterinburg

Keywords:

4Н-1, 2, 4-triazol-3-amines, 5-cyano-1, 4-triazines, nucleophilic ipso-substitution, aza-Diels-Alder reaction, X-ray crystallography

Abstract

A solvent-free interaction between 5-cyano-1.2.4-triazines and 5-methylsulfanyl-4H-1,2,4-triazol-3-amines has been studied. The structure of the product of ipso-substitution of cyano-group with the corresponding heterocyclic amine residue has been proven by 1Н NMR and ESI-MS data. Thus, in the 1Н NMR spectra a three-proton singlet at 2.61 ppm is present, which can be interpreted as the signal of the methylsulfanyl group protons. Subsequent transformation of 1,2,4-triazine scaffold of the resulting product into a pyridine one has been successfully per-formed under autoclave conditions. It has been found that methylsulfanyl group undergoes no transformations in both stages of synthesis. This fact is also proven by X-Ray crystallography data of the obtained functionalised bypyridines. According to the X-Ray crystallography data, compound 4 crystallizes as two crystallographically independent molecules in non-centrosymmetric space group P-1 with triclinic system. The crystal structure is formed by numerous intermolecular N∙∙∙H contacts between two crystallographically independent molecules of triazolylpyridine-2-amine. The 1Н NMR spectra of compound 4 contain two doublets of the new pyridine cycle at 7.37 and 7.61 ppm. Thus, properties of 5-methysulfanyl-4H-1,2,4-triazol-3-amine are different from these of its analogue with mercaptogroup at C5 position. Namely, in accordance to our previous results ipso-substitution of C5-cyanogroup of 1,2,4-triazine with moiety of the latter amine is accompanied by desulfurization reaction.

Author Biographies

Ya. K. Shtaitz, Ural Federal University, Ekaterinburg

младший научный сотрудник Лаборатории перспективных материалов, зеленых методов и биотехнологий; аспирант кафедры органической и биомолекулярной химии ХТИ

Е. D. Ladin, Ural Federal University, Ekaterinburg

лаборант-исследователь Лаборатории перспективных материалов, зеленых методов и биотехнологий; магистрант кафедры аналитической химии ХТИ

V. V. Sharutin, South Ural State University, Chelyabinsk

доктор химических наук, главный научный сотрудник управления научной и инновационной деятельности

D. S. Kopchuk, Ural Federal University, Ekaterinburg; I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of Russian Academy of Sciences

доктор химических наук, старший научный сотрудник Лаборатории координационных соединений; ведущий научный сотрудник Лаборатории перспективных материалов, зеленых методов и биотехнологий

А. V. Rybakova, South Ural State University, Chelyabinsk

кандидат химических наук, доцент кафедры теоретической и прикладной химии

E. R. Sharafieva, Ural Federal University, Ekaterinburg; Ural State Medical University, Ekaterinburg

лаборант-исследователь Лаборатории перспективных материалов, зеленых методов и биотехнологий; студент фармацевтического факультета

А. P. Krinochkin, Ural Federal University, Ekaterinburg; I.Ya. Postovsky Institute of Organic Synthesis

кандидат химических наук, научный сотрудник Лаборатории перспективных материалов, зеленых методов и биотехнологий; младший научный сотрудник Лаборатории органических материалов

G. V. Zyryanov, Ural Federal University, Ekaterinburg; I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of Russian Academy of Sciences

доктор химических наук, профессор РАН, ведущий научный сотрудник Лаборатории координационных соединений; профессор кафедры органической и биомолекулярной химии ХТИ

Т. А. Pospelova, Ural Federal University, Ekaterinburg

кандидат химических наук, ведущий специалист кафедры технологии органического синтеза ХТИ

А. I. Matern, Ural Federal University, Ekaterinburg

доктор химических наук, профессор кафедры аналитической химии ХТИ

Published

2023-05-01