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Formation of furo- and difuro-1,4-dihydropyridines in the bromination 0f 2,6-dimethyl-3,5-dimethoxycarbonyl-4-(o-nitrophenyl)-1,4-dihydropyridine

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Furo- and difuro-1,4-dihydropyridines were obtained by bromination of 2,6-dimethyl-3,5-dimethoxycarbonyl-4-(o-nitrophenyl)-1,4-dihydropyridine with mild brominating agents (pyridinium bromide perbromide, N-bromosuccinimide, and dioxane dibromide).

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Authors and Affiliations

  1. Institute of Organic Synthesis, Academy of Sciences of the Latvian SSR, 226006, Riga

    I. P. Skrastin'sh, V. V. Kastron, G. Ya. Dubur, I. B. Mazheika & V. P. Kadysh

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  1. I. P. Skrastin'sh
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  2. V. V. Kastron
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  3. G. Ya. Dubur
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  4. I. B. Mazheika
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  5. V. P. Kadysh
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1227–1232, September, 1987.

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Skrastin'sh, I.P., Kastron, V.V., Dubur, G.Y. et al. Formation of furo- and difuro-1,4-dihydropyridines in the bromination 0f 2,6-dimethyl-3,5-dimethoxycarbonyl-4-(o-nitrophenyl)-1,4-dihydropyridine. Chem Heterocycl Compd 23, 981–985 (1987). https://doi.org/10.1007/BF00475365

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  • DOI: https://doi.org/10.1007/BF00475365

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