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Condensation of quinolin-6-amine with 5-(p-methoxyphenyl)-cyclohexane-1,3-dione and substituted benzaldehydes

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Abstract

New 12-aryl-9-(p-methoxyphenyl)-8,9,10,12-tetrahydro-7H-benzo[b][4,7]phenanthrolin-11-ones having two asymmetric carbon atoms (C9 and C12) were synthesized by three-component condensation of quinolin-6-amine with 5-(p-methoxyphenyl)cyclohexane-1,3-dione and substituted benzaldehydes. According to the 1H NMR data, the products are mixtures of diastereoisomers.

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Authors and Affiliations

  1. Institute of Physical Organic Chemistry, National Academy of Sciences of Belarus, ul. Surganova 13, Minsk, 220072, Belarus

    N. G. Kozlov, K. N. Gusak & A. P. Kadutskii

  2. Institute of New Materials Chemistry, National Academy of Sciences of Belarus, Minsk, Belarus

    E. V. Koroleva & Zh. V. Ignatovich

Authors
  1. N. G. Kozlov
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  2. E. V. Koroleva
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  3. Zh. V. Ignatovich
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  4. K. N. Gusak
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  5. A. P. Kadutskii
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Additional information

Original Russian Text © N.G. Kozlov, E.V. Koroleva, Zh.V. Ignatovich, K.N. Gusak, A.P. Kadutskii, 2007, published in Zhurnal Organicheskoi Khimii, 2007, Vol. 43, No. 6, pp. 902–907.

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Kozlov, N.G., Koroleva, E.V., Ignatovich, Z.V. et al. Condensation of quinolin-6-amine with 5-(p-methoxyphenyl)-cyclohexane-1,3-dione and substituted benzaldehydes. Russ J Org Chem 43, 901–906 (2007). https://doi.org/10.1134/S1070428007060176

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  • DOI: https://doi.org/10.1134/S1070428007060176

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