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作 者:LI Ming WANG Shu-wen WEN Li-rong KE Zi-qin
机构地区:[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
出 处:《Chemical Research in Chinese Universities》2005年第6期663-667,共5页高等学校化学研究(英文版)
基 金:SupportedbytheNationalNaturalScienceFoundationofChina(No.Y2003B01).
摘 要:Ethyl 7-aryl-2-benzyhhiopyrazolo [ 1,5-a ] pyrimidine-3-carboxylates (3a-3f) were conveniently synthesized through the reactions of enaminones with 5-amino-3-benzyhhio4-ethoxycarbonyl-1 H-pyrazole in good yields and high regioselectivity. The structures of the new compounds were fully characterized by spectroscopic measurmehts, elemental analysis and X-ray diffraction analysis. A plausible reaction mechanism for the formation of the title compounds was also presented.Ethyl 7-aryl-2-benzyhhiopyrazolo [ 1,5-a ] pyrimidine-3-carboxylates (3a-3f) were conveniently synthesized through the reactions of enaminones with 5-amino-3-benzyhhio4-ethoxycarbonyl-1 H-pyrazole in good yields and high regioselectivity. The structures of the new compounds were fully characterized by spectroscopic measurmehts, elemental analysis and X-ray diffraction analysis. A plausible reaction mechanism for the formation of the title compounds was also presented.
关 键 词:Pyrazolo [ 1 5-a ] pyrimidine ENAMINONE Synthesis Mechanism Crystal structure
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