Abstract
The reaction of N-(2-naphthyl)-2-formimidoylpyridine with substituted acetophenones leads to the formation of 1,3-disubstituted benzo[f]quinolines with a pyridine ring in the 3 position. 1-Phenyl-3-(2-pyridyl)-3-(2-naphthylamino)-propan-1-one was isolated in the case of acetophenone. The IR, UV, and mass spectra of the synthesized compounds are discussed.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 516–518, April, 1983.
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Kozlov, N.S., Mikhalevskaya, S.V., Serzhanina, V.A. et al. Reaction of N-(2-naphthyl)-2-formimidoylpyridine with substituted acetophenones. Chem Heterocycl Compd 19, 422–424 (1983). https://doi.org/10.1007/BF00516214
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DOI: https://doi.org/10.1007/BF00516214