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公开(公告)号:EP2890686B1
公开(公告)日:2017-01-04
申请号:EP13779396.4
申请日:2013-08-29
发明人: OKADA, Minoru , KABUKI, Takashi , FUJIEDA, Shigeo , KOSEKI, Nao
IPC分类号: C07D263/32
CPC分类号: C07D263/32
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公开(公告)号:EP0651747A1
公开(公告)日:1995-05-10
申请号:EP94914603.0
申请日:1994-05-11
发明人: NISHI, Takao , UNO, Tetsuyuki , SHU, Yoshio , TAMURA, Katsumi , OKADA, Minoru
CPC分类号: C07D401/12
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公开(公告)号:EP4357335A1
公开(公告)日:2024-04-24
申请号:EP22825008.0
申请日:2022-06-14
发明人: OKADA, Minoru , ITO, Nobuaki , SHIBATA, Masakazu
IPC分类号: C07D209/52 , A61K31/403 , A61P25/00
CPC分类号: A61K31/403 , A61P25/00 , C07D209/52
摘要: The present invention provides a new azabicyclo[3.1.0]hexane compound that is represented by the following formula:
and that is for use in treating central nervous system (CNS) disorders. In the formula, X represents -C(=O)-O- or the like, and R represents H, an optionally substituted C1-C18 alkyl, or the like.-
公开(公告)号:EP3397619B1
公开(公告)日:2020-07-29
申请号:EP16828990.8
申请日:2016-12-27
发明人: MURAKAMI, Yoshihiro , MATSUSHITA, Hitoshi , MATSUMOTO, Kengo , OKADA, Minoru , YUKI, Yohei , KOYAMA, Noriyuki , KANAI, Naohiko
IPC分类号: C07D263/32 , A61K31/421 , A61P17/00
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公开(公告)号:EP1954684A2
公开(公告)日:2008-08-13
申请号:EP06823467.3
申请日:2006-11-14
发明人: OKADA, Minoru , KATO, Masaya , SATO, Norifumi , UNO, Tetsuyuki , KITAGAKI, Hideki , HARUTA, Junpei , HIYAMA, Hidetaka , SHIBATA, Tomonori
IPC分类号: C07D263/34 , C07D263/32 , C07D413/12 , A61K31/422 , A61P17/00
CPC分类号: A61K31/421 , A61K31/4439 , A61K31/4709 , A61K31/496 , A61K31/497 , A61K31/5377 , C07D263/32 , C07D263/34 , C07D413/06 , C07D413/12 , C12N9/16 , C12Y301/04012
摘要: The present invention provides a oxazole compound represented by Formula (1), or a salt thereof: wherein R1 is an aryl group which may have one or more substituents; R2 is an aryl group or a nitrogen atom-containing heterocyclic group each of which may have one or more substituents; and W is a divalent group represented by -Y1-A1- or -Y2-C(=O)- wherein Y1 is a group such as -C(=O)-, A1 is a group such as a lower alkylene group, and Y2 is a group such as a piperazinediyl group. The oxazole compound has a specific inhibitory action against phosphodiesterase 4.
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公开(公告)号:EP0651747B1
公开(公告)日:1996-03-27
申请号:EP94914603.9
申请日:1994-05-11
发明人: NISHI, Takao , UNO, Tetsuyuki , SHU, Yoshio , TAMURA, Katsumi , OKADA, Minoru
IPC分类号: C07D401/00 , A61K31/33
CPC分类号: C07D401/12
摘要: Carbostyril derivatives represented by general formula (1) [wherein, R1 is a hydrogen atom, a fluorine atom or a methyl group; R is a group of formula (a) (R2 is a methyl group, a trifluoromethyl group or a nitro group), or a group of formula (b) (R3 is a fluorine atom and p is an integer of 2 or 3); and n^_ is an integer of 2 or 3], or salts thereof. Said carbostyril derivatives or salts are useful as an agent for inhibiting the adhesion of platelets.
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公开(公告)号:EP4347597A1
公开(公告)日:2024-04-10
申请号:EP22732679.0
申请日:2022-06-01
发明人: UEMATSU, Yukitaka , OKADA, Minoru , SAITO, Akihiro , TAKAHASHI, Akira , NAKAMURA, Yuichi , HANARI, Taiki , MENJO, Yasuhiro , YAMAUCHI, Takahito , YAMAGUCHI, Atsushi , YUKI, Yohei , WATANABE, Kenji , MATSUDA, Satoshi
IPC分类号: C07D487/04 , A61P17/00 , A61P37/00 , A61K31/519
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8.
公开(公告)号:EP2890686A1
公开(公告)日:2015-07-08
申请号:EP13779396.4
申请日:2013-08-29
发明人: OKADA, Minoru , KABUKI, Takashi , FUJIEDA, Shigeo , KOSEKI, Nao
IPC分类号: C07D263/32
CPC分类号: C07D263/32
摘要: An object of the present invention is to provide a novel method for producing an oxazole compound. The invention relates to a method for producing a compound represented by formula (1): wherein R
1 is lower alkyl group or halogen substituted lower alkyl group, R
2 is lower alkyl group, R
5 is lower alkyl group, R
11 is lower alkyl group, halogen substituted lower alkyl group or a group represented by formula: -CY
2 COOR
12 , wherein Y is a halogen atom, R
12 is an alkali metal atom or lower alkyl group, Ar
1 is phenyl group substituted with lower alkyl group, etc., or pyridyl group substituted with lower alkyl group, etc., X
2 , X
3 and X
9 are the same or different and are halogen atoms, X
4 is a leaving group, and M is an alkali metal atom.摘要翻译: 本发明的目的是提供一种制备恶唑化合物的新方法。 本发明涉及一种由式(1)表示的化合物的制备方法:其中R1是低级烷基或卤素取代的低级烷基,R2是低级烷基,R5是低级烷基,R11是低级烷基,卤素取代 低级烷基或由式-CY2COOR12表示的基团,其中Y是卤素原子,R12是碱金属原子或低级烷基,Ar1是被低级烷基取代的苯基等,或被低级烷基取代的吡啶基 烷基等,X 2,X 3和X 9相同或不同,为卤素原子,X 4为离去基团,M为碱金属原子。
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公开(公告)号:EP1954684B1
公开(公告)日:2014-05-07
申请号:EP06823467.3
申请日:2006-11-14
发明人: OKADA, Minoru , KATO, Masaya , SATO, Norifumi , UNO, Tetsuyuki , KITAGAKI, Hideki , HARUTA, Junpei , HIYAMA, Hidetaka , SHIBATA, Tomonori
IPC分类号: C07D263/34 , C07D263/32 , C07D413/12 , A61K31/422 , A61P17/00
CPC分类号: A61K31/421 , A61K31/4439 , A61K31/4709 , A61K31/496 , A61K31/497 , A61K31/5377 , C07D263/32 , C07D263/34 , C07D413/06 , C07D413/12 , C12N9/16 , C12Y301/04012
摘要: The present invention provides a oxazole compound represented by Formula (1), or a salt thereof: wherein R1 is an aryl group which may have one or more substituents; R2 is an aryl group or a nitrogen atom-containing heterocyclic group each of which may have one or more substituents; and W is a divalent group represented by -Y1-A1- or -Y2-C(=O)- wherein Y1 is a group such as -C(=O)-, A1 is a group such as a lower alkylene group, and Y2 is a group such as a piperazinediyl group. The oxazole compound has a specific inhibitory action against phosphodiesterase 4.
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