An Improved and Practical Synthesis of Tranexamic Acid

被引:15
|
作者
Li, Zhenhua [1 ]
Fang, Li [1 ]
Wang, Jian [2 ]
Dong, Liuhong [2 ]
Guo, Yanna [2 ]
Xie, Yuanyuan [1 ]
机构
[1] Zhejiang Univ Technol, Coll Pharmaceut Sci, Collaborat Innovat Ctr Yangtze River Delta Reg Gr, Hangzhou 310014, Zhejiang, Peoples R China
[2] Engn Res Ctr Middle High Pressure Catalyt Hydroge, Taizhou 317300, Peoples R China
基金
中国国家自然科学基金;
关键词
PRIMARY AMINES; CATALYZED HYDROGENATION; ANTIPLASMIN DRUGS; AROMATIC NITRILES; REDUCTION; CONVERSION; DISCOVERY; AMIDES;
D O I
10.1021/op500395b
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Tranexamic acid 1, a synthetic antifibrinolytic drug with the treatment being considered highly cost-effective in many countries, has been included in the WHO list of essential medicines. In this paper, we designed the synthesis of 1 via a novel seven-step route from the readily available starting material dimethyl terephthalate, performing with 99.6% purity in 59.2% overall yield. During the process, we successfully developed a direct and efficient method for the preparation of key intermediate methyl 4-(acetamidomethyl)benzoate by one-pot hydrogenation and acylation in acetic anhydride using Ni/Al2O3 as a catalyst. More importantly, it should be a straightforward and practical way to circumvent the usage of toxic reagents (CrO3, Cl-2), solvent (CCl4), and expensive catalyst (PtO2), etc., that plagued the previous methodologies.
引用
收藏
页码:444 / 448
页数:5
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