Synthesis of hetarylsubstituted pyrazolo[3,4-c] isoquinolines under Pictet—Spengler reaction conditions

Authors

  • N.M. Bogdan Institute of Organic Chemistry of the NAS of Ukraine, Kiev
  • Ya.S. Borodkin Institute of Organic Chemistry of the NAS of Ukraine, Kiev
  • S.Yu. Sujkov Institute of Organic Chemistry of the NAS of Ukraine, Kiev
  • A.R. Khairulin Institute of Organic Chemistry of the NAS of Ukraine, Kiev
  • S.L. Bogza L.M. Litvinenko Institute of Physical Organic and Coal Chemistry of the NAS of Ukraine, Kiev

DOI:

https://doi.org/10.15407/dopovidi2018.04.081

Keywords:

5-aminopyrazoles, anticancer compounds, benzothiazole, Pictet—Spengler reaction, pyrazolo[3;4-c] isoquinolines, pyridine, pyrimidine

Abstract

The synthesis and reactions of 1 and 3-hetaryl-substituted 5-aminopyrazoles with aldehydes under the Pictet—Spengler reaction conditions have been studied. It has been shown that the possibility of formation and yields of pyrazolo [3,4-c] isoquinoline derivatives essentially depends on the structure and location of the heterocyclic substituent in the pyrazole core.

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References

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Published

12.05.2024

How to Cite

Bogdan, N., Borodkin, Y., Sujkov, S., Khairulin, A., & Bogza, S. (2024). Synthesis of hetarylsubstituted pyrazolo[3,4-c] isoquinolines under Pictet—Spengler reaction conditions . Reports of the National Academy of Sciences of Ukraine, (4), 81–87. https://doi.org/10.15407/dopovidi2018.04.081