Practical gram-scale synthesis of bicyclol metabolites M2 and M3

被引:1
|
作者
Ma, Bo [1 ]
Wang, Zhen-Wei [1 ]
Liu, Xiao-Yu [1 ]
Wang, Mi-Juan [2 ]
Zhang, Yong-Wang [2 ]
Zhang, Meng [2 ]
Jiao, Xiao-Zhen [1 ]
Xie, Ping [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, State Key Lab Bioact Subst & Funct Nat Med, Beijing Key Lab Act Subst Discovery & Druggabil Ev, Beijing 100050, Peoples R China
[2] Beijing Union Pharmaceut Factory Ltd, Beijing 102600, Peoples R China
关键词
Bicyclol; metabolites; gram-scale synthesis; Suzuki-Miyaura coupling; DEMETHYLATION; MECHANISM;
D O I
10.1080/10286020.2023.2270440
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Bicyclol, an innovative hepatoprotective drug, was approved by the Chinese National Medical Products Administration (NMPA) in 2001 to treat Hepatitis B and drug-induced liver injury. Two active metabolites of bicyclol have been identified as M2 and M3. To evaluate the impact on drug safety and efficacy of possible drug-drug interactions (DDIs) associated with these metabolites, a sufficient quantity of these metabolites is required. Herein, we report a concise novel route for the synthesis of M2 and M3 using the Suzuki-Miyaura coupling as the key step. Furthermore, we complete the gram-scale syntheses of M2 and M3.
引用
收藏
页码:342 / 352
页数:11
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