Abstract:
Heating of 5-methyl-6-nitro-7-(p-N,N-dimethylaminophenyl)-1,2,4-triazolo[1,5-a]pyrimidines with benzylamine in ethanol or DMF leads to 1-hydroxy-2-phenyl-4-methyl-5-benzylimino(p-N,N-dimethylaminophenyl)methylidinoimidazole.
Document Type:
Article
Language: English
Citation:
V. L. Rusinov, M. N. Kushnir, O. N. Chupakhin, G. G. Alexandrov, “Reaction of 6-Nitro-1,2,4-triazolo[1,5-a]pyrimidines with Benzylamine: an Unusual Synthesis of 1-Hydroxyimidazoles”, Mendeleev Commun., 3:5 (1993), 213–214
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https://www.mathnet.ru/eng/mendc5342
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This publication is cited in the following 6 articles:
Polina A. Nikitina, Tatiana Yu. Koldaeva, Vitaly S. Mityanov, Vladimir S. Miroshnikov, Elizaveta I. Basanova, Valery P. Perevalov, “Prototropic Tautomerism and Some Features of the IR Spectra of 2-(3-Chromenyl)-1-hydroxyimidazoles”, Aust. J. Chem., 72:9 (2019), 699
Polina A. Nikitina, Valery P. Perevalov, “Methods of synthesis and physicochemical properties of 1-hydroxyimidazoles, imidazole 3-oxides, and their benzoannulated analogs”, Chem Heterocycl Comp, 53:2 (2017), 123
Polina A. Nikitina, Aleksandr S. Peregudov, Tatiana Yu. Koldaeva, Ludmila G. Kuz'mina, Evgeniy I. Adiulin, Iosif I. Tkach, Valery P. Perevalov, “Synthesis and study of prototropic tautomerism of 2-(2-hydroxyphenyl)-1-hydroxyimidazoles”, Tetrahedron, 71:33 (2015), 5217
Gunther Fischer, Advances in Heterocyclic Chemistry, 95, 2007, 143
E.S.H. Elashry, N. Rashed, Advances in Heterocyclic Chemistry, 72, Advances in Heterocyclic Chemistry Volume 72, 1998, 127
V. L. RUSINOV, M. N. KUSHNIR, O. N. CHUPAKHIN, G. G. ALEXANDROV, “ChemInform Abstract: Reaction of 6‐Nitro‐1,2,4‐triazolo(1,5‐a)pyrimidines with Benzylamine: An Unusual Synthesis of 1‐Hydroxyimidazoles.”, ChemInform, 25:15 (1994)
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