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作 者:Ren-xin SHI Yun-kui LIU Zhen-yuan XU
出 处:《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》2010年第2期102-108,共7页浙江大学学报(英文版)B辑(生物医学与生物技术)
基 金:Project supported by the Natural Science Foundation of Zhejiang Province (No. Y407168);the Foundation of Education of Zhejiang Province (No. Z200803599);the Opening Foundation of Zhejiang Provincial Top Key Discipline (No. 56310101634), China
摘 要:Both 1,5-benzodiazepine and quinoxaline derivatives are important heterocycles in pharmaceuticals. We describe an efficient and clean method for the synthesis of 1,5-benzodiazepines from o-phenylenediamine and ketones catalyzed by sodium tetrachloroaurate(Ⅲ) dihydrate under mild conditions. The catalyst was shown to be equally effective for the synthesis of quinoxalines from o-phenylenediamine and α-bromo ketones under the similar reaction conditions. This method produced good yields.Both 1,5-benzodiazepine and quinoxaline derivatives are important heterocycles in pharmaceuticals. We describe an efficient and clean method for the synthesis of 1,5-benzodiazepines from o-phenylenediamine and ke-tones catalyzed by sodium tetrachloroaurate(III) dihydrate under mild conditions. The catalyst was shown to be equally effective for the synthesis of quinoxalines from o-phenylenediamine and α-bromo ketones under the similar reaction conditions. This method produced good yields.
关 键 词:1 5-benzodiaepines O-PHENYLENEDIAMINE KETONES QUINOXALINES Gold catalyst
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