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Acetals of lactams and acid amides

XIX. Synthesis of 3-cyano-6-dimethylamino-2-pyridone and pyrrolo-, pyrido-, and azepino[2,3-b]pyridine derivatives

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The reaction of α-cyano-β-dimethylaminocrotonic acid amide with acetals of dimethyl acetamide and N-methylbutyro-, -valero-, and -caprolactams gave enaminoacrylamidines, cyclization of which gave 3-cyano-6-dimethylamino-2-pyridone and the corresponding pyrrolo-,pyrido-, and azepino[2,3-b]pyridine derivatives.

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Literature cited

  1. V. G. Granik, N. B. Marchenko, T, F. Vlasova, and R. G. Glushkov, Khim. Geterotsikl. Soedin., No. 11, 1509 (1976).

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  2. W. Leimgrüber and M. Weigele, U.S. Patent (Cl. 260/307 H, CO7d) (1970); Chem. Abstr., 77, 140130g (1972).

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See [1] for communication XVIII.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1106–1109, August, 1977.

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Granik, V.G., Belyaeva, O.Y., Glushkov, R.G. et al. Acetals of lactams and acid amides. Chem Heterocycl Compd 13, 891–894 (1977). https://doi.org/10.1007/BF00488918

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  • DOI: https://doi.org/10.1007/BF00488918

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