Abstract
Phenyl(methyl)-substituted 2- and 4-nitroso- and azoxypyrimidines were synthesized for the first time by the oxidation of phenyl(methyl)-substituted 2- and 4-hydroxy-aminopyrimidines by activated MnO2, Ag2CO3 on zeolite, or BaMnO4. Certain chemical properties of the synthesized nitrosopyrimidines were studied, such as reduction, nucleophilic substitution of the nitroso group, the condensation reaction with aniline and hydroxyaminopyrimidines.
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For Preliminary communication, see [1].
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 962–968, July, 1989.
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Moskalenko, G.G., Sedova, V.F. & Mamaev, V.P. Synthesis and properties of phenyl(methyl)-substituted 2- and 4-nitrosopyrimidines. Chem Heterocycl Compd 25, 805–811 (1989). https://doi.org/10.1007/BF00472754
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DOI: https://doi.org/10.1007/BF00472754