Abstract:
The Ni(acac)2-catalyzed 1,2,4-triazole formation from cyanamides and carbohydrazides was extended onto N-(4,6-dimethylpyrimidin-2-yl)cyanamide and glycine hydrazides. The obtained N-(5-aminomethyl-4H-1,2,4-triazol-3-yl)-4,6-dimethylpyrimidin-2-amines may be attractive for the estimation of their biological activity.
Citation:
M. A. Prezent, S. V. Baranin, Yu. N. Bubnov, “A convenient synthesis of new (1,2,4-triazolylamino)pyrimidines from cyanamide precursor”, Mendeleev Commun., 30:4 (2020), 500–501
Linking options:
https://www.mathnet.ru/eng/mendc1237
https://www.mathnet.ru/eng/mendc/v30/i4/p500
This publication is cited in the following 2 articles:
Pavlo V. Zadorozhnii, Vadym V. Kiselev, Alona A. Fedorus, Aleksandr V. Kharchenko, Oxana V. Okhtina, “Synthesis, Spectral Characteristics, and Molecular Structure of N-((N-(p-tolyl)Cyanamido)Methyl)Benzamide”, Chemistry Africa, 6:1 (2023), 545
Pavlo V. Zadorozhnii, Vadym V. Kiselev, Alona A. Fedorus, Aleksandr V. Kharchenko, Oxana V. Okhtina, “Synthesis, Spectral Characteristics, and Molecular Structure of N-((N-(P-Tolyl)Cyanamido)Methyl)Benzamide”, SSRN Journal, 2022
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