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作 者:Bai Ling Xu Jin Ping Chen Rong Zhang Qiao De Cai Fu
机构地区:[1]lnstitute of Materia Medica, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100050, China [2]Hebei University of Science and Technology, Shijiazhuang 050018, China [3]Department of Life Science and Technology, Beijing University of Chemical Technology, Beijing 100029, China
出 处:《Chinese Chemical Letters》2008年第5期537-540,共4页中国化学快报(英文版)
基 金:We are grateful to the National Natural Science Foundation of China(No.30672540);the Natural Science Foundation of Beijing(No.7072048)for financial support.
摘 要:A facile, efficient and novel approach to access 2-substituted-N1-carbethoxy-2,3-dihydro-4(1H)-quinazolinones was developed by condensation of substituted N-carbethoxyanthranilamide with alkyl, aromatic or heteroaromatic aldehydes in the refluxing 2,2,2- trifluoroethanol or hexafluoroisopropanol using p-toluenesulfonic acid as catalyst.A facile, efficient and novel approach to access 2-substituted-N1-carbethoxy-2,3-dihydro-4(1H)-quinazolinones was developed by condensation of substituted N-carbethoxyanthranilamide with alkyl, aromatic or heteroaromatic aldehydes in the refluxing 2,2,2- trifluoroethanol or hexafluoroisopropanol using p-toluenesulfonic acid as catalyst.
关 键 词:QUINAZOLINONES TRIFLUOROETHANOL HEXAFLUOROISOPROPANOL Fluorous solvent Solvent effect
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