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Addition of hydrazine to 4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidines: Hydrazine derivatives of 4,5,6,7-tetrahydro[1,2,4]triazolo[1,5-a]pyrimidine
โ Scribed by Sergey A. Komykhov; Konstantin S. Ostras; Kyryl M. Kobzar; Vladimir I. Musatov; Sergey M. Desenko
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2009
- Tongue
- English
- Weight
- 63 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.218
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โฆ Synopsis
Abstract
magnified image The 7โarylโ4,7โdihydro[1,2,4]triazolo[1,5โa]pyrimidines 1a, 1b, 1c can undergo addition of hydrazine to the enamine double bond leading to hydrazine derivatives of tetrahydrotriazolopyrimidines 2a, 2b, 2c; the process is usually accompanied by partial opening of pyrimidine ring leading to 3a, 3b. J. Heterocyclic Chem., (2009).
๐ SIMILAR VOLUMES
## Abstract The cyclocondensation of 6โacetylโ4,7โdihydroโ5โmethylโ7โphenyl[1,2,4]triazolo[1,5โ__a__]pyrimidine (3) with hydroxylamine or hydrazine leads to 3a,4,9,9aโtetrahydroโ3,9aโdimethylโ4โphenylisoxazoloโ[5,4โ__d__][1,2,4]triazolo[1,5โ__a__]pyrimidine (4a) and 3a,4,9,9aโtetrahydroโ3,9aโdimeth