Chemical Research in Chinese Universities ›› 2005, Vol. 21 ›› Issue (6): 663-667.

• Articles • Previous Articles     Next Articles

Facile Syntheses of New Pyrazolo[1,5-a] pyrimidines Derivatives via Reactions of Enaminones with Aminopyrazole

LI Ming1, WANG Shu-wen1, WEN Li-rong1, KE Zi-qin2   

  1. 1. College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, P. R. China;
    2. Department of Chemistry, Xinjiang Normal University, Urumuqi 830054, P. R. China
  • Received:2005-02-22 Online:2005-11-23 Published:2011-08-06
  • Supported by:

    Supported by the National Natural Science Foundation of China(No.Y2003B01)

Abstract: Ethyl 7-aryl-2-benzylthiopyrazolo [1,5-a] pyrimidine-3-carboxylates (3a-3f) were conveniently synthesized through the reactions of enaminones with 5-amino-3-benzylthio-4-ethoxycarbonyl-1H-pyrazole in good yields and high regioselectivity.The structures of the new compounds were fully characterized by spectroscopic measurments, elemental analysis and X-ray diffraction analysis.A plausible reaction mechanism for the formation of the title compounds was also presented.

Key words: Pyrazolo[1,5-a]pyrimidine, Enaminone, Synthesis, Mechanism, Crystal structure