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Reaction of 6-methyl-2-(2-oxo-2-phenyl-ethylidene)-2,3-dihydropyrimidin-4(1 H)-one with hydrazine and hydroxylamine.

Authors :
Yavolovskii, A.
Grishchuk, L.
Rakipov, I.
Stepanov, D.
Ivanov, Yu.
Kamalov, G.
Source :
Chemistry of Heterocyclic Compounds. Jan2013, Vol. 48 Issue 10, p1487-1491. 5p.
Publication Year :
2013

Abstract

The reaction of 6-methyl-2-(2-oxo-2-phenylethylidene)-2,3-dihydropyrimidin-4(1 H)-one and of its nitrosation product with hydroxylamine stops at the stage of forming the corresponding oximes. The reaction of 6-methyl-2-(2-oxo-2-phenylethylidene)-2,3-dihydropyrimidin-4(1 H)-one with hydrazine yields a mixture of 3-amino-5-phenylpyrazole and 3-methyl-2-pyrazolin-5-one in 71 and 62% yields, respectively. The ketoxime is used in the synthesis of a series of imidazole N(3)-oxides substituted at the 1, 4, and 5 positions of the imidazole ring. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00093122
Volume :
48
Issue :
10
Database :
Academic Search Index
Journal :
Chemistry of Heterocyclic Compounds
Publication Type :
Academic Journal
Accession number :
85596745
Full Text :
https://doi.org/10.1007/s10593-013-1162-z