A practical synthesis for the key intermediate of apixaban

被引:4
|
作者
Dong, Wenwen [1 ]
Gong, Tengfei [1 ]
Liu, Chaoyang [1 ]
Lin, Jia [1 ]
Jia, Qiang [2 ]
Chu, Changhu [1 ]
机构
[1] East China Univ Sci & Technol, Engn Res Ctr Pharmaceut Proc Chem, Sch Pharm, Shanghai Key Lab New Drug Design,Minist Educ, 130 Meilong Rd, Shanghai 200237, Peoples R China
[2] Seasons Biotechnol Taizhou Co Ltd, 21 Jiutiao Rd, Taizhou 318000, Zhejiang, Peoples R China
来源
MONATSHEFTE FUR CHEMIE | 2024年 / 155卷 / 01期
基金
中国国家自然科学基金;
关键词
Apixaban intermediate; Synthesis; Amine oxidation; Sodium chlorite; ORALLY BIOAVAILABLE INHIBITOR; FACTOR XA INHIBITOR; HIGHLY POTENT; BMS-562247; DISCOVERY; SAFETY;
D O I
10.1007/s00706-023-03143-7
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Apixaban is a highly potent, selective, and efficacious inhibitor of blood coagulation factor Xa. A practical and efficient process has been developed for the preparation of the key intermediate of apixaban. Starting from inexpensive 4-chloronitrobenzene and piperidine, an eight-step procedure for the intermediate has been developed. In this case, sodium chlorite is used twice to oxidize the piperidine cycle to the corresponding lactam under a CO2 atmosphere, resulting in the construction of two lactams. Furthermore, most of these reactions are highly efficient and practical as they occur under mild conditions. Most of the intermediates can be obtained through simple slurry or recrystallization, and column chromatography purification is not necessary.
引用
收藏
页码:99 / 104
页数:6
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