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Synthesis of 2-ethyl-3,5-dimethylpyridine by heterocyclization of allylamine, cyclopropylamine, and diallylamine in the presence of palladium complexes

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Abstract

2-Ethyl-3,5-dimethylpyridine was synthesized by disproportionation and heterocyclization of allylamine, cyclopropylamine, and diallylamine in the presence of palladium catalysts.

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Authors and Affiliations

  1. Institute of Petroleum Chemistry and Catalysis, Russian Academy of Sciences, pr. Oktyabrya 141, Ufa, 450075, Bashkortostan, Russia

    A. M. Atnabaeva, Z. S. Muslimov, R. I. Khusnutdinov & U. M. Dzhemilev

Authors
  1. A. M. Atnabaeva
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  2. Z. S. Muslimov
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  3. R. I. Khusnutdinov
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  4. U. M. Dzhemilev
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Correspondence to A. M. Atnabaeva.

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Original Russian Text © A.M. Atnabaeva, Z.S. Muslimov, R.I. Khusnutdinov, U.M. Dzhemilev, 2008, published in Zhurnal Organicheskoi Khimii, 2008, Vol. 44, No. 12, pp. 1858–1861.

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Atnabaeva, A.M., Muslimov, Z.S., Khusnutdinov, R.I. et al. Synthesis of 2-ethyl-3,5-dimethylpyridine by heterocyclization of allylamine, cyclopropylamine, and diallylamine in the presence of palladium complexes. Russ J Org Chem 44, 1831–1835 (2008). https://doi.org/10.1134/S1070428008120208

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  • DOI: https://doi.org/10.1134/S1070428008120208

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