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Synthesis and chemical transformations of partially hydrogenated [1,2,4]triazolo[5,1-b]quinazolines
Authors:V V Lipson  S M Desenko  I V Ignatenko  O V Shishkin  S V Shishkina
Institution:(1) V. Ya. Danilevsky Institute of Endocrine Pathology Problems, Academy of Medical Sciences of Ukraine, 10 ul. Artema, 61002 Kharkov, Ukraine;(2) State Scientific Institution “Institute for Single Crystals,”, National Academy of Sciences of Ukraine, 60 prosp. Lenina, 61001 Kharkov, Ukraine
Abstract:The reaction of 5-methyl-7-phenyl-4,7-dihydro-1,2,4-triazolo1,5-a]pyrimidine with α,β-unsaturated carbonyl compounds in MeOH in the presence of MeONa affords partially hydrogenated aryl-substituted 1,2,4]triazolo5,1-b]quinazolines. Hydrolysis, oxidation, reduction, and alkylation of 5,6,8-triphenyl-5,6,7,10-tetrahydro1,2,4]triazolo5,1-b]quinazoline were studied. The structure of one oxidation product, viz., 7-hydroxy-5,6,8-triphenyl-6,7-dihydro1,2,4]triazolo5,1-b]quinazoline, was established by X-ray diffraction. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 335—340, February, 2006.
Keywords:partially hydrogenated [1  2  4]triazolo[5  1-b]quinazolines  synthesis  chemical properties  X-ray diffraction study
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