Beijing Jincheng Taier Pharmaceutical Co., Ltd.

Yi Kang

Zhen Liu

Li Li

Qiang Li

Hongliang Liu

Dongye Xing

Yan Mi

Yangong Han

Zhongzheng Zhang

Jingang Tang

Yali Cui

Liru Wang

The present disclosure relates to the technical field of drug synthesis, in particular to a method for preparing lornoxicam. The method includes the following steps: using 6-chloro-4-hydroxy-2-methyl-2-H-thieno[2,3-e]-1,2-thiazine methyl carboxylate-1,1-dioxide and 2-aminopyridine as raw materials, and xylene as a solvent; mixing the raw material and solvent, and adding a stabilizer, to obtain a mixture; subjecting the mixture to an ammonolysis; cooling the resulting reactant; conducting a vacuum concentration to remove the solvent; adding an organic solvent and slurrying, and filtering, to obtain a crude lornoxicam; and refining the crude lornoxicam to obtain the lornoxicam. In the present disclosure, p-toluenesulfonic acid is used as a stabilizer to reduce the reaction temperature and promote the reaction to proceed forward, thereby improving the quality and yield of the product.

Method for preparing lornoxicam

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Beijing, China

Yi Kang