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Lability of the β-diethylaminoethyl group under the conditions of the formation of a pyrrole ring via the Knorr synthesis

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The corresponding 3-acetyl- and 3-H-pyrroles are formed along with 2,4-dimethyl-3-(β-diethylaminoethyl)-5-carbethoxypyrrole in the condensation of 3-(β-diethylaminoethyl)pentane-2,4-dione with isonitrosoacetoacetic (I) and isonitrosomalonic (II) esters.

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Authors and Affiliations

  1. M. V. Lomonosov Moscow Institute of Precision Chemical Engineering, USSR

    A. F. Mironov, Kh. Kh. Alarkon & R. P. Evstigneeva

Authors
  1. A. F. Mironov
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  2. Kh. Kh. Alarkon
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  3. R. P. Evstigneeva
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1643–1645, December, 1973.

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Mironov, A.F., Alarkon, K.K. & Evstigneeva, R.P. Lability of the β-diethylaminoethyl group under the conditions of the formation of a pyrrole ring via the Knorr synthesis. Chem Heterocycl Compd 9, 1487–1489 (1973). https://doi.org/10.1007/BF00477563

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  • DOI: https://doi.org/10.1007/BF00477563

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