Recommanded Product: 1H-1,2,4-Triazol-5-amine. Authors Kovygin, YA; Vandyshev, DY; Ledenyova, IV; Kosheleva, EA; Polikarchuk, VA; Kozaderov, OA; Shikhaliev, KS in SPRINGER published article about in [Kovygin, Yu A.; Vandyshev, D. Yu; Ledenyova, I., V; Kosheleva, E. A.; Polikarchuk, V. A.; Kozaderov, O. A.; Shikhaliev, Kh S.] Voronezh State Univ, 1 Univ Skaya Pl, Voronezh 394018, Russia in 2021.0, Cited 36.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5
A convenient method for the synthesis of 2-(2-R-5-oxo-6,7-dihydro-4H-[1,2,4]triazolo-[1,5-a]pyrimidin-6-yl)acetanilides based on the regioselective domino reaction of N-arylitaconimides with substituted 3-aminotriazoles was proposed. Presumably, the reaction pathway includes the conjugated aza-addition of the endo-nucleophilic center of triazole to imide, followed by the recyclization of the intermediate to triazolo[1,5-a]pyrimidine.
Recommanded Product: 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Kovygin, YA; Vandyshev, DY; Ledenyova, IV; Kosheleva, EA; Polikarchuk, VA; Kozaderov, OA; Shikhaliev, KS or concate me.
Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics