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Lactam acetals

X. Synthesis and some properties of 1H,1-methyl-6-oxo-2,3,4,5,6,11-hexahydroazepino[2,3-b]quinoline and its analogs

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Derivatives of pyrrolo-, pyrido-, and azepino[2,3-b]quinolones were synthesized by condensation of N-methylbutyro-, N-methylvalero-, and N-methylcaprolactam diethyl acetals with ethyl anthranilate. The corresponding ethoxy derivatives were obtained by reaction of these compounds with triethyloxonium tetrafluoroborate, and condensed 4-chloroquinolines were synthesized with POCl3.

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Literature cited

  1. V. G. Granik, A. M. Zhidkova, T. F. Vlasova, R. G. Glushkov, and Yu. N. Sheinker, Khim. Geterotsikl. Soedin., 533 (1974).

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Authors and Affiliations

  1. S. Ordzhonikidze All-Union Scientific-Research Pharmaceutical Chemistry Institute, Moscow

    A. M. Zhidkova, V. G. Granik, R. G. Glushkov, T. F. Vlasova, O. S. Anisimova, T. A. Gus'kova & G. N. Pershin

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  1. A. M. Zhidkova
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  2. V. G. Granik
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  3. R. G. Glushkov
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  4. T. F. Vlasova
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  5. O. S. Anisimova
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  6. T. A. Gus'kova
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  7. G. N. Pershin
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Additional information

See [1] for communication IX.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 670–674, May, 1974.

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Zhidkova, A.M., Granik, V.G., Glushkov, R.G. et al. Lactam acetals. Chem Heterocycl Compd 10, 579–582 (1974). https://doi.org/10.1007/BF00471332

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  • DOI: https://doi.org/10.1007/BF00471332

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