Reaction of benzylidene-2-naphthylamine with the ethyl ester of 3-pyridyl-β-oxopropionic acid

Authors

  • K. H. Гусак Institute of Organophysical Chemistry, Belorussian Academy of Sciences, Minsk 220072
  • H. Г. Козлов Institute of Organophysical Chemistry, Belorussian Academy of Sciences, Minsk 220072
  • P. Д. Саyц Institute of Organophysical Chemistry, Belorussian Academy of Sciences, Minsk 220072
  • В. А. Сержанина Institute of Organophysical Chemistry, Belorussian Academy of Sciences, Minsk 220072

Abstract

The reaction of benzylidene-2-naphthylamine with ethyl β-(3-ethyl)-β-oxopropionate under various conditions gave the ethyl ester of α-(2-naphthylamino)benzyl-β-(3-pyridyl)-β-oxopropionic acid, 1-(3-pyridyl)-3 phenylbenzo[f]quinoline, ethyl ester of 1-(3-pyridyl)-3-phenylbenzo[f]quinoline-2-carboxylic acid, and N-(2-naphthyl)amide of β-(3-pyridyl)-β-oxopropionic acid. The IR, UV, and mass spectra of the products were studied and the pathways for their formation were discussed.

How to Cite
Gusak, K. N.; Kozlov, N. G.; Sauts, R. D.; Serzhanina V. A. Chem. Heterocycl. Compd. 1996, 32, 696. [Khim. Geterotsikl. Soedin. 1996, 807.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01164869

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Published

1996-06-25

Issue

No. 6 (1996)

Section

Original Papers