A New Synthetic Approach to Indazoles Synthesis
Publication Type
Original research
Authors
  • A. N. Zaid
  • Pier Giovanni Baraldi
  • Barbara Cacciari
  • Giampiero Spalluto
  • Romeo Romagnoli
  • Giovanni Braccioli
  • Maria J. Pineda de las Infantas

Stobbe condensation of 3-alkyl- or aryl-4-formylpyrazoles 3a-f with diethyl succinate in the presence of potassium t-butoxide, followed by intramolecular ring closure (Ac2O-NaOAc), afforded the corresponding indazole derivatives 5a-f in 65-85% overall yield. These compounds are good starting materials for transformation to biologically active molecules, such as new pyrazole analogs of the left-hand segment of the potent natural antineoplastic agent CC-1065.

Journal
Title
Synthesis ; 1997(10): 1140-1142
Publisher
--
Publisher Country
Palestine
Publication Type
Both (Printed and Online)
Volume
--
Year
1997
Pages
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