四氢喹喔啉-6-羧酸甲酯的合成方法  

Synthesis of Methyl 1,2,3,4-Tetrahydroquinoxaline-6-carboxylate

作　　者：张永霞[1] 郑银平 靳三霖 毛文政 靳清贤 张洪培 Zhang Yongxia;Zheng Yinping;Jin Sanlin;Mao Wenzheng;Jin Qingxian;Zhang Hongpei(Public Basic Teaching Department Henan Vocational and Technical College of Communications,Zhengzhou,Henan 450005,China;School of Material and Chemical Engineering,Zhengzhou University of Light Industry,Zhengzhou,Henan 450001,China;Zhengzhou Weiyi Chemical Products Company Limited,Zhengzhou,Henan 450001,China)

机构地区：[1]河南交通职业技术学院公共基础教学部,河南郑州450005 [2]郑州轻工业大学材料与化学工程学院,河南郑州450001 [3]郑州为易化工产品有限公司,河南郑州450001

出　　处：《化学世界》2021年第7期410-413,共4页Chemical World

基　　金：国家自然科学基金(No.21401169)资助项目。

摘　　要：以3,4-二氨基苯甲酸为原料,经硫酸酯化、成环、硼氢化钠还原,三步反应制得目标分子,并通过质谱、核磁等方法进行了表征。所设计的合成路线简短,该制备路线和方法所用试剂廉价、反应条件温和、中间步骤及产物易于纯化处理,提供了一种制备1,2,3,4-四氢喹喔啉-6-羧酸甲酯的方法。Methyl 1,2,3,4-tetrahydroquinoxaline-6-carboxylate is an important drug intermediate. The target compound was synthesized by three steps with 3,4-diaminobenzoic acid as raw material: esterification by sulfuric acid, cyclization and reduction by sodium borohydride. The structure of compound was determined by mass spectrometry and nuclear magnetic resonance, which was consistent with the target molecular structure. We provided a method for preparing 1,2,3,4-tetrahydroquinoxaline-6-carboxylic acid methyl ester with following advantages: this route was short designed, the reagents were cheap, the reaction conditions were mild and the intermediate products were purified easily.

关 键 词：喹喔啉 杂环 还原 

分 类 号：O625.61[理学—有机化学] O625.7[理学—化学]