JOURNAL


Organic Communications
VOLUME & ISSUE
Available Online: September 04,2018
PAGES
p.1 - 14
DOI ADDRESS
http://doi.org/10.25135/acg.oc.46.18.05.104
(DOI number will be activated after the manuscript has been available in an issue.)
STATISTICS
Viewed 62 times.
Downloaded 10 times
AUTHORS
    Mohd Fazli Mohammat, Muhammad Siddiq Maarop, Zurina Shaameri, Agustono Wibowo, Saiful Azmi Johari and Ahmad Sazali Hamzah
PDF OF ARTICLE

ABSTRACT


A practical and efficient synthesis of non-spiro and spiropyrano[2,3-c]pyrazole-3-carboxylate derivatives was developed. The synthesis was achieved via a domino one-pot, four-component reaction of diethyl oxaloacetate, hydrazine, aldehyde and malanonitrile in refluxing acidic ethanolic solution under non-catalytic system. This method is rapid, simple and provides products in good yields and can be accessed via different classes of carbonyls, malanonitriles and hydrazine derivatives. Mechanistic study envisaged that this domino four-component reaction proceeds via sequential reactions of pyrazolone formation, Michael reaction and Thorpe-Ziegler cyclization reaction. Strong electronic effects of Knoevenagel and pyrozolone product contribute significantly towards successful cyclization of the title compounds.

KEYWORDS
  • Pyrano[2
  • 3-c]pyrazole-3-carboxylate
  • diethyloxaloacetate
  • Michael reaction

SUPPORTING INFORMATION


Supporting Information
Download File 46-OC-1805-104-SI.pdf (2.13 MB)