Authors Sakhno, YI; Murlykina, M; Zbruyev, OI; Kozyryev, AV; Shishkina, S; Sysoiev, D; Musatov, VI; Desenko, SM; Chebanov, VA in BEILSTEIN-INSTITUT published article about HETEROCYCLIZATION REACTIONS; CYCLOCONDENSATION REACTIONS; MULTICOMPONENT REACTION; BIGINELLI REACTION; PYRUVIC ACIDS; AMINOAZOLES; 3-AMINO-1,2,4-TRIAZOLE; TETRAHYDROPYRIMIDINES; 5-AMINOPYRAZOLES; ALDEHYDES in [Sakhno, Yana, I; Murlykina, Maryna; Zbruyev, Oleksandr, I; Kozyryev, Anton, V; Shishkina, Svetlana; Musatov, Vladimir, I; Desenko, Sergey M.; Chebanov, Valentyn A.] Natl Acad Sci Ukraine, Inst Single Crystals, State Sci Inst, Div Chem Funct Mat, Nauky Av 60, UA-61072 Kharkiv, Ukraine; [Murlykina, Maryna; Shishkina, Svetlana; Desenko, Sergey M.; Chebanov, Valentyn A.] Kharkov Natl Univ, Fac Chem, Svobody Sq 4, UA-61077 Kharkiv, Ukraine; [Sysoiev, Dmytro] Czech Acad Sci, Inst Organ Chem & Biochem, Flemingovo Namesti 542-2, Prague 16610 6, Czech Republic in 2020.0, Cited 37.0. Recommanded Product: 1H-1,2,4-Triazol-5-amine. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5
Four-component reactions of 3-amino-1,2,4-triazole or 5-amino-1H-pyrazole-4-carbonitrile with aromatic aldehydes and pyruvic acid or its esters under ultrasonication were studied. Unusual for such a reaction type, a cascade of elementary stages led to the formation of 7-azolylaminotetrahydroazolo[1,5-a]pyrimidines.
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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