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公开(公告)号:EP3919485A1
公开(公告)日:2021-12-08
申请号:EP20749295.0
申请日:2020-01-31
发明人: ZHANG, Xiquan , WANG, Shanchun , GENG, Wenjun , LIU, Yanlong , ZHANG, Huihui , LIU, Fei , ZHU, Shanliang , LI, Xinlu , ZHAO, Rui , GU, Hongmei
IPC分类号: C07D401/12 , A61P35/00 , A61K31/4709
摘要: The present application relates to the field of medicine, and relates to crystals of quinoline derivatives, and in particular, to crystals of a quinoline derivative anhydride and a solvate, as well as a method for preparing the crystals, pharmaceutical compositions containing the crystals, and a use thereof in the field of medicine. The present application further provides a preparation method therefor, which has a high yield, has mild crystallization conditions, is suitable for industrial production, and may better meet the needs of the pharmaceutical industry.
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公开(公告)号:EP3896063A1
公开(公告)日:2021-10-20
申请号:EP19897084.0
申请日:2019-12-13
发明人: QIAN, Wenyuan , WANG, Hongjian , ZHANG, Ming , LIU, Fei , XING, Lei , HU, Zhongyuan , GUO, Yahui , LIU, Yanlong , ZHANG, Huihui
IPC分类号: C07D401/14 , A61K31/498 , A61K31/4709 , A61P35/00 , A61P29/00
摘要: Provided is a salt of an Syk inhibitor and a crystalline form thereof, and more specifically, provided are 5-fluoro-1-methyl-3-((5-(4-(oxetan-3-yl)piperazine-1)-yl)pyridin-2-yl)amino)-6-(1H-pyrazol-3-yl)quinoline-2(1H )-ketamine hydrochloride, a crystalline form thereof, a preparation method therefor, a pharmaceutical composition thereof and a use thereof. The hydrochloride of the compound represented by formula I and the crystalline form thereof have good salt-forming properties, high stability and low hygroscopicity, have advantages in terms of physical properties, safety and metabolic stability, and have value in prepared medicines.
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公开(公告)号:EP4129998A1
公开(公告)日:2023-02-08
申请号:EP21796153.1
申请日:2021-04-29
发明人: FENG, Weiwei , LIU, Yanlong , ZHANG, Huihui , LIU, Fei , WANG, Bin , YAO, Yiyan , CHEN, Zhilin , ZHU, Jinlei , LU, Chenghui
IPC分类号: C07D471/04 , C07D211/96 , C07D215/20 , A61K31/404 , A61P35/00
摘要: A crystal of a trifluoromethyl/chloro disubstituted sulfonamide selective BCL-2 inhibitor, specifically related to a crystal of a compound of formula I, a preparation method therefor, and use thereof in preventing and treating diseases related to anti-apoptotic protein BCL-2, such as cancers.
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