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公开(公告)号:EP3498704A1
公开(公告)日:2019-06-19
申请号:EP17838796.5
申请日:2017-08-11
申请人: Chia Tai Tianqing Pharmaceutical Group Co., Ltd. , Lianyungang Runzhong Pharmaceutical Co., Ltd. , Centaurus BioPharma Co., Ltd.
发明人: SANG, Guangming , LIU, Lin , ZHANG, Aiming , QIAO, Jiabin , GUO, Xiaopeng , ZHANG, Xiquan , XIA, Chunguang
IPC分类号: C07D405/04 , A61K31/4035 , A61P5/50 , A61P3/00 , A61P35/00 , A61P25/00 , A61P3/12
摘要: The present application relates a crystal of a compound represented by Formula (I), a salt thereof, and a crystal of the salt thereof, a method for preparing the crystal of the compound represented by Formula (I), the salt thereof, and the crystal of the salt thereof, a crystal comprising the compound represented by Formula (I), a crystal composition comprising the crystal of the salt thereof, a pharmaceutical composition thereof, and medical uses thereof.
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公开(公告)号:EP3828192A1
公开(公告)日:2021-06-02
申请号:EP19841191.0
申请日:2019-07-24
发明人: LIU, Lin , ZHAO, Rui , SANG, Guangming , ZHOU, Xingjian , GUO, Xiaopeng , ZHANG, Aiming , WU, Gang , XIA, Chunguang , ZHANG, Xiquan
IPC分类号: C07H19/073 , C07H1/00
摘要: The present application relates to a method for preparing trifluridine, comprising reacting a compound of formula III with a compound of formula IV in a first solvent in the presence of an acid to obtain a compound of formula II, and performing further reaction to obtain trifluridine.
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公开(公告)号:EP3705487A1
公开(公告)日:2020-09-09
申请号:EP18873405.7
申请日:2018-11-01
发明人: ZHANG, Xiquan , CHENG, Xingdong , ZHANG, Aiming , XIA, Chunguang , CHEN, Lang , GAO, Ce
IPC分类号: C07J9/00
摘要: The present application belongs to the field of pharmaceutical chemistry, and relates to a method for preparing a cholic acid compound. Specifically, the present application provides a process for preparing a compound as shown in formula I, comprising subjecting a compound of formula 2 to an oxidization reaction to obtain a compound of formula 3; attaching a trimethylsilyl group to the compound of formula 3 to obtain a compound of formula 4; reacting the compound of formula 4 with acetaldehyde to obtain a compound of formula 5; subjecting the compound of formula 5 to a catalytic hydrogenation reaction to obtain a compound of formula 6; and converting a cyano group of the compound of formula 6 to a carboxyl group to give the compound of formula I. The preparation method has high yield, requires less purification operations, and is suitable for industrial application.
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