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Synthesis of substituted anilides of the alkaloid cytisine and molecular structure of N-(2′,6′-dichloro-4′-nitrophenyl)-2-N-cytisinoacetamide

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Chemistry of Natural Compounds Aims and scope

Anilides of cytisinylacetic acid were synthesized by reaction of the alkaloid cytisine with 2-bromo-N-(2,6-dihalo-4-nitrophenyl)acetamides. The compositions and structures of the products were confirmed by IR and PMR spectroscopy, mass spectrometry, and x-ray structure analysis.

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Authors and Affiliations

  1. Institute of Organic Synthesis and Carbon Chemistry of the Republic of Kazakhstan, Kazakhstan, 100008, Karaganda, ul. Alikhanova, 1

    I. V. Kulakov, Z. M. Zhambekov & O. A. Nurkenov

  2. Scientific-Production Center Fitokhimiya, Kazakhstan, 100009, Karaganda, ul. Gazalieva, 4

    D. M. Turdybekov & K. M. Turdybekov

  3. Institute of Bioorganic Chemistry, Uzbekistan, 100125, Tashkent, ul. Mirzo-Ulugbeka, 83

    B. T. Ibragimov & S. A. Talipov

Authors
  1. I. V. Kulakov
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  2. D. M. Turdybekov
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  3. Z. M. Zhambekov
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  4. O. A. Nurkenov
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  5. B. T. Ibragimov
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  6. S. A. Talipov
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  7. K. M. Turdybekov
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Corresponding author

Correspondence to I. V. Kulakov.

Additional information

Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 572–574, September–October, 2009.

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Kulakov, I.V., Turdybekov, D.M., Zhambekov, Z.M. et al. Synthesis of substituted anilides of the alkaloid cytisine and molecular structure of N-(2′,6′-dichloro-4′-nitrophenyl)-2-N-cytisinoacetamide. Chem Nat Compd 45, 681–684 (2009). https://doi.org/10.1007/s10600-009-9434-7

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  • DOI: https://doi.org/10.1007/s10600-009-9434-7

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