118757-37-2Relevant academic research and scientific papers
Imine-Enamine Tautomerism Of Dihydroazolopyrimidines 5. Steric Effects And The Tautomeric Equilibrium For Dihydro-1,2,4-Triazolopyrimidines
Desenko, S. M.,Orlov, V. D.,Shishkin, O. V.,Barykin, K. E.,Lindeman, S. V.,Struchkov, Yu. T.
, p. 1163 - 1168 (1993)
The reaction of 3-amino-1,2,4-triazole with β-dimethylaminopropiophenones or unsaturated ketones gives 5,7-disubstituted 4,7(6,7)-dihydro-1,2,4-triazolopyrimidines.An increase in the bulk of the substituent at C(7) in the bicyclic system leads to relative stabilization of the enamine tautomer of these compounds.An x-ray diffraction structural analysis of 7-tert-butyl-5-(4-methoxyphenyl)-4,7-dihydro-1,2,4-triazolopyrimidine showed that the introduction of a tert-butyl group into the dihydropyrimidine ring leads to significant loss of planarity of this system.
Cyclocondensation of α,β-Unsaturated Ketones with 3-Amino-1,2,4-Triazole
Orlov, V. D.,Desenko, S. M.,Potekhin, K. A.,Struchkov, Yu. T.
, p. 192 - 196 (2007/10/02)
Dihydro-1,2,4-triazolopyrimidine derivatives were obtained by condensation of 3-amino-1,2,4-triazole with 1,3-diaryl-1-propen-3-ones.The structure of 5-phenyl-7-(4-methylphenyl)-4,7-dihydro-1,2,4-triazolopyrimidine was established by x-ray diffraction analysis.
