Efficient preparative synthesis of isoflavones with the amide function

Authors

  • V. S. Moskvina
  • O. V. Shablykina
  • V. V. Ishchenko
  • V. P. Khilya

DOI:

https://doi.org/10.15407/dopovidi2015.09.079

Keywords:

2-(2-(morpholin-4-ylcarbonyl)phenyl)-1-(2-hydroxyphenyl)ethanones, 3-[2-(morpholin-4-ylcarbonyl)phenyl]-4H-chromen-4-ones, N; N-dimethylformamide dimethylacetal

Abstract

The reactivity of amides of 2-hydroxydezoxybenzoine-2′-carboxylic acids is investigated. A convenient method to obtain isoflavones with a carboxamide group is developed, using the interaction 2-[2-(morpholin-4-ylcarbonyl)phenyl]-1-(2-hydroxyphenyl)ethanones with DMFDMA. Acetylation of 2-[2-(morpholin-4-ylcarbonyl)phenyl]-1-(2-hydroxyphenyl)ethanones in basic solutions passes to the cyclization to form an isocoumarin system.

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References

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Published

06.02.2025

How to Cite

Moskvina, V. S., Shablykina, O. V., Ishchenko, V. V., & Khilya, V. P. (2025). Efficient preparative synthesis of isoflavones with the amide function . Reports of the National Academy of Sciences of Ukraine, (9), 79–83. https://doi.org/10.15407/dopovidi2015.09.079