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

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Chemistry of Heterocyclic Compounds Aims and scope

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.

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Authors
  1. K. N. Gusak
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  2. N. G. Kozlov
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  3. R. D. Sauts
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  4. V. A. Serzhanina
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Additional information

Institute of Physical Organic Chemistry, Belorussian Academy of Sciences, Minsk 220603. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 807–810, June, 1996. Original article submitted December 30, 1995.

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Gusak, K.N., Kozlov, N.G., Sauts, R.D. et al. Reaction of benzylidene-2-naphthylamine with the ethyl ester of 3-pyridyl-β-oxopropionic acid. Chem Heterocycl Compd 32, 696–698 (1996). https://doi.org/10.1007/BF01164869

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  • DOI: https://doi.org/10.1007/BF01164869

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