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公开(公告)号:US08975438B2
公开(公告)日:2015-03-10
申请号:US13541795
申请日:2012-07-05
申请人: Beat Birrer , Leo Clarke , Walter Deichtmann , John Hayes , Julius Jeisy , Christian Lautz , Rainer E. Martin , Michael Meade , Joaquim Pintao , Michelangelo Scalone , Juergen Schaefer , Dennis Smith , Andreas Staempfli , Joachim Veits , Christian Walch , Andrew Walsh , Andreas Zogg
发明人: Beat Birrer , Leo Clarke , Walter Deichtmann , John Hayes , Julius Jeisy , Christian Lautz , Rainer E. Martin , Michael Meade , Joaquim Pintao , Michelangelo Scalone , Juergen Schaefer , Dennis Smith , Andreas Staempfli , Joachim Veits , Christian Walch , Andrew Walsh , Andreas Zogg
IPC分类号: C07C259/04 , C07C319/20 , C07C51/06 , C07C51/08 , C07C319/06 , C07C327/30 , C07C51/02
CPC分类号: C07C319/20 , C07C51/02 , C07C51/06 , C07C51/08 , C07C319/06 , C07C327/30 , C07C2601/14 , C07C323/40 , C07C61/08
摘要: A process for the preparation of a compound of formula (I): which is useful as an intermediate in the preparation of pharmaceutically active compounds.
摘要翻译: 制备式(I)化合物的方法:其可用作药物活性化合物的制备中的中间体。
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公开(公告)号:US20130018201A1
公开(公告)日:2013-01-17
申请号:US13541795
申请日:2012-07-05
申请人: Beat Birrer , Leo Clarke , Walter Deichtmann , John Hayes , Julius Jeisy , Christian Lautz , Rainer E. Martin , Michael Meade , Joaquim Pintao , Michelangelo Scalone , Juergen Schaefer , Dennis Smith , Andreas Staempfli , Joachim Veits , Christian Walch , Andrew Walsh , Andreas Zogg
发明人: Beat Birrer , Leo Clarke , Walter Deichtmann , John Hayes , Julius Jeisy , Christian Lautz , Rainer E. Martin , Michael Meade , Joaquim Pintao , Michelangelo Scalone , Juergen Schaefer , Dennis Smith , Andreas Staempfli , Joachim Veits , Christian Walch , Andrew Walsh , Andreas Zogg
IPC分类号: C07C327/30 , C07C319/06 , C07C319/22 , C07C51/08 , C07C51/60
CPC分类号: C07C319/20 , C07C51/02 , C07C51/06 , C07C51/08 , C07C319/06 , C07C327/30 , C07C2601/14 , C07C323/40 , C07C61/08
摘要: A process for the preparation of a compound of formula (I): which is useful as an intermediate in the preparation of pharmaceutically active compounds.
摘要翻译: 制备式(I)化合物的方法:其可用作药物活性化合物的制备中的中间体。
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公开(公告)号:US08664403B2
公开(公告)日:2014-03-04
申请号:US13324199
申请日:2011-12-13
IPC分类号: A61K31/428 , C07D277/64
CPC分类号: A61K31/16 , A61K31/167 , C07C319/06 , C07C327/30 , C07C327/34 , C07C2601/14 , C07D277/64 , C07C323/40
摘要: The present invention relates to a process for the preparation of S-[2-[1-(2-ethylbutyl)cyclohexylcarbonylamino]-phenyl]2-methylthiopropionate which is useful as a pharmaceutically active compound.
摘要翻译: 本发明涉及可用作药物活性化合物的S- [2- [1-(2-乙基丁基)环己基羰基氨基] - 苯基] -2-甲硫基丙酸酯的制备方法。
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公开(公告)号:US20120157504A1
公开(公告)日:2012-06-21
申请号:US13324199
申请日:2011-12-13
IPC分类号: A61K31/428 , C07C319/06 , A61P3/06 , A61K31/22 , A61P9/10 , C07D277/64 , C07C327/30
CPC分类号: A61K31/16 , A61K31/167 , C07C319/06 , C07C327/30 , C07C327/34 , C07C2601/14 , C07D277/64 , C07C323/40
摘要: The present invention relates to a process for the preparation of S-[2-[1-(2-ethylbutyl)cyclohexylcarbonylamino]-phenyl]2-methylthiopropionate which is useful as a pharmaceutically active compound.
摘要翻译: 本发明涉及可用作药物活性化合物的S- [2- [1-(2-乙基丁基)环己基羰基氨基] - 苯基] -2-甲硫基丙酸酯的制备方法。
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公开(公告)号:US20110313196A1
公开(公告)日:2011-12-22
申请号:US13153651
申请日:2011-06-06
申请人: Stephan Bachmann , Fritz Bliss , Ralph Diodone , Stefan Hildbrand , Michael Kammerer , Christophe Pfleger , Reinhard Reents , Michelangelo Scalone
发明人: Stephan Bachmann , Fritz Bliss , Ralph Diodone , Stefan Hildbrand , Michael Kammerer , Christophe Pfleger , Reinhard Reents , Michelangelo Scalone
IPC分类号: C07C231/12 , C07C209/60
CPC分类号: C07C231/12 , C07C51/60 , C07C209/52 , C07C209/56 , C07C231/02 , C07C249/02 , C07C233/11 , C07C211/29 , C07C211/27 , C07C251/24 , C07C233/66 , C07C63/70
摘要: The present invention relates to a process for the preparation of benzamide derivatives which are useful as intermediates in the preparation of pharmaceutically active compounds.
摘要翻译: 本发明涉及一种制备苯甲酰胺衍生物的方法,其可用作制备药物活性化合物的中间体。
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公开(公告)号:US07691876B2
公开(公告)日:2010-04-06
申请号:US11655377
申请日:2007-01-19
申请人: Holger Kuehne , Thomas Luebbers , Patrizio Mattei , Cyrille Maugeais , Philippe Pflieger , Michelangelo Scalone
发明人: Holger Kuehne , Thomas Luebbers , Patrizio Mattei , Cyrille Maugeais , Philippe Pflieger , Michelangelo Scalone
IPC分类号: A61K31/437 , C07D471/04
CPC分类号: C07D471/04
摘要: Compounds of formula I processes for their preparation and pharmaceutical compositions comprising them.
摘要翻译: 式I化合物的制备方法和包含它们的药物组合物。
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公开(公告)号:US20080021219A1
公开(公告)日:2008-01-24
申请号:US11820602
申请日:2007-06-19
IPC分类号: C07F15/00
CPC分类号: C07F15/0046 , B01J31/2265 , B01J31/2269 , B01J31/2273 , B01J2231/54 , B01J2531/821 , C07C253/30 , C07C255/23
摘要: Disclosed are novel metathesis catalysts of the formula wherein R1, R2, R3, R4, R5, R6, X1, X2, L and Y are as described herein, a process for making the same and their use in metathesis reactions such as ring closing or cross metathesis.
摘要翻译: 公开了下式的新的复分解催化剂:其中R 1,R 2,R 3,R 4,R 4,R 4, R 5,R 6,X 1,X 2,L和Y如本文所述,其方法为 使其在复分解反应如闭环或交叉复分解中起作用。
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公开(公告)号:US20070249842A1
公开(公告)日:2007-10-25
申请号:US11811071
申请日:2007-06-08
IPC分类号: C07D263/30
CPC分类号: C07D413/12
摘要: The present invention is concerned with a novel process for the preparation of compounds of formula I comprising catalytic asymmetric hydrogenation of a compound of formula (II) in the presence of a catalyst comprising ruthenium and a chiral diphosphine ligand or comprising rhodium and a chiral diphosphine ligand, wherein R1, R2, R3 and R4 are as defined in the specification and claims. The compounds of formula I and the corresponding salts and/or esters are pharmaceutically active substances.
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公开(公告)号:US07259176B2
公开(公告)日:2007-08-21
申请号:US10872871
申请日:2004-06-21
IPC分类号: A61K31/381 , A61K31/422 , C07D263/30 , C07D277/04
CPC分类号: C07D417/14
摘要: A novel process for the preparation of compounds of formula I and optionally converting a compound of formula I into a pharmaceutically acceptable salt is disclosed. The compounds of formula I and the corresponding salts, e.g. the sodium salts, are pharmaceutically active substances. Processes for the creation of intermediates are also disclosed.
摘要翻译: 公开了制备式I化合物和任选将式I化合物转化成药学上可接受的盐的新方法。 式I化合物和相应的盐,例如 钠盐是药物活性物质。 还公开了制备中间体的方法。
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公开(公告)号:US07169935B2
公开(公告)日:2007-01-30
申请号:US10763296
申请日:2004-01-22
IPC分类号: C07D209/88
CPC分类号: C07D405/12 , C07D209/12 , C07D209/88
摘要: A process for the preparation heterocyclic indene analogs, especially with the preparation of 4-hydroxycarbazole or N-protected 4-hydroxycarbazole, involves cyclocarbonylation followed by saponification. This process avoids high temperatures and high catalyst loadings.
摘要翻译: 制备杂环茚类似物的方法,特别是制备4-羟基咔唑或N-保护的4-羟基咔唑的方法涉及环化羰基化,随后皂化。 该过程避免了高温和高催化剂负载。
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