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公开(公告)号:US20050222456A1
公开(公告)日:2005-10-06
申请号:US10522261
申请日:2003-07-30
申请人: Karel Brands , Antony Davies , Paul Oakley , Jeremy Scott , Duncan Shaw , Martin Teall
发明人: Karel Brands , Antony Davies , Paul Oakley , Jeremy Scott , Duncan Shaw , Martin Teall
IPC分类号: C07C315/04 , C07C317/24 , C07C317/44
CPC分类号: C07C315/04 , C07C2601/14 , C07C317/24 , C07C317/44
摘要: A novel process for preparing cyclohexanones (1) is described. The products are useful as gamma-secretase in-hibitors, or as intermediates in the synthesis of other gamma-secretase inhibitors.
摘要翻译: 描述了一种制备环己酮(1)的新方法。 该产品可用作γ-分泌酶抑制剂,或作为合成其它γ-分泌酶抑制剂的中间体。
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2.Stereoselective Synthesis of a 4,4-Disubstituted Cyclohexanepropanoic Acid 有权
标题翻译: 立体选择性合成4,4-二取代的环己丙酸公开(公告)号:US20070225520A1
公开(公告)日:2007-09-27
申请号:US10589098
申请日:2005-02-16
申请人: Karel Brands , Sarah Brewer , Antony Davies , Ulf Dolling , Deborah Hammond , David Lieberman , Jeremy Scott
发明人: Karel Brands , Sarah Brewer , Antony Davies , Ulf Dolling , Deborah Hammond , David Lieberman , Jeremy Scott
IPC分类号: C07C51/353 , C07C315/02 , C07C317/44 , C07C319/14 , C07C59/56 , C07C53/23 , C07C319/16 , C07C323/61
CPC分类号: C07C57/62 , C07B2200/09 , C07C51/60 , C07C59/56 , C07C315/02 , C07C319/14 , C07C319/16 , C07C2601/14 , C07C2601/16 , C07C63/68 , C07C317/44 , C07C323/61
摘要: There is provided stereoselective route to a compound of formula I: wherein R represents H or an alkali metal, Ar1 represents 4-chlorophenyl and Ar2 represents 2,5-difluorophenyl.
摘要翻译: 提供了式I化合物的立体选择性途径:其中R表示H或碱金属,Ar 1表示4-氯苯基,Ar 2表示2,5-二氟苯基 。
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公开(公告)号:USD668556S1
公开(公告)日:2012-10-09
申请号:US29406777
申请日:2011-11-18
申请人: Jeremy Scott
设计人: Jeremy Scott
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公开(公告)号:US20140206605A1
公开(公告)日:2014-07-24
申请号:US14239389
申请日:2012-08-16
申请人: Gregory L. Beutner , Robert M. Wenslow, JR. , Eric J. Choi , Clinton Scott Shultz , Jeremy Scott , Juan D. Arredondo , Laura Artino
发明人: Gregory L. Beutner , Robert M. Wenslow, JR. , Eric J. Choi , Clinton Scott Shultz , Jeremy Scott , Juan D. Arredondo , Laura Artino
IPC分类号: C07K5/12
CPC分类号: C07C35/04 , A61K38/00 , C07C67/14 , C07C69/013 , C07C69/12 , C07C269/04 , C07C271/34 , C07D403/12 , C07D498/16 , C07K5/0808 , C07K5/126
摘要: The present invention relates to different forms of a HCV inhibitory compound.
摘要翻译: 本发明涉及不同形式的HCV抑制化合物。
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公开(公告)号:USD672254S1
公开(公告)日:2012-12-11
申请号:US29408132
申请日:2011-12-07
申请人: Jeremy Scott
设计人: Jeremy Scott
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公开(公告)号:US20140107346A1
公开(公告)日:2014-04-17
申请号:US14119063
申请日:2012-06-25
申请人: Michael J. Zacuto , Robert F. Dunn , Aaron J. Moment , Jacob M. Janey , David Lieberman , Faye Sheen , Nadine Bremeyer , Jeremy Scott , Jeffrey T. Kuethe
发明人: Michael J. Zacuto , Robert F. Dunn , Aaron J. Moment , Jacob M. Janey , David Lieberman , Faye Sheen , Nadine Bremeyer , Jeremy Scott , Jeffrey T. Kuethe
IPC分类号: C07D487/04
CPC分类号: C07D487/04 , A61K31/4162 , A61K31/4439 , A61K31/4985 , A61K31/513 , C07B2200/13 , Y02P20/55
摘要: A process for the preparation of pyrazolopyrolidines of structural formula I: and W is or P, wherein in P is an amine protecting group. These compounds are useful in the synthesis of dipeptidyl peptidase-IV inhibitors for the treatment of Type 2 diabetes. Also provided are useful intermediates obtained from the process.
摘要翻译: 制备结构式I的吡唑并吡咯烷的方法:W是或P,其中在P中是胺保护基团。 这些化合物可用于合成用于治疗2型糖尿病的二肽基肽酶-IV抑制剂。 还提供了从该方法获得的有用的中间体。
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公开(公告)号:US20120010262A1
公开(公告)日:2012-01-12
申请号:US13144031
申请日:2010-01-08
申请人: John Y.L. Chung , Yanfeng Zhang , Laura Artino , Jennifer Baxter , Aaron S. Cote , Donal Desmond , Jeremy Scott , Yekaterina Vaynshteyn
发明人: John Y.L. Chung , Yanfeng Zhang , Laura Artino , Jennifer Baxter , Aaron S. Cote , Donal Desmond , Jeremy Scott , Yekaterina Vaynshteyn
IPC分类号: A61K31/404 , A61P3/10 , C07D209/20
CPC分类号: C07D209/18 , C07B2200/13
摘要: The present invention relates to polymorphic forms of a compound of formula A: This compound is useful as a glucagon receptor antagonist and serves as a pharmaceutically active ingredient for the treatment of type 2 diabetes and related conditions, such as hyperglycemia, obesity, dyslipidemia, and the metabolic syndrome. Hydrates, hemihydrates, anhydrates and similar polymorphic forms are included.
摘要翻译: 本发明涉及式A化合物的多晶型物质:该化合物可用作胰高血糖素受体拮抗剂并用作用于治疗2型糖尿病和相关病症的药物活性成分,例如高血糖症,肥胖症,血脂异常和 代谢综合征。 包括水合物,半水合物,水合物和类似的多晶型物质。
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公开(公告)号:US09242917B2
公开(公告)日:2016-01-26
申请号:US14239389
申请日:2012-08-16
申请人: Gregory L Beutner , Robert M Wenslow, Jr. , Eric J Choi , Clinton Scott Shultz , Jeremy Scott , Juan D Arredondo , Laura Artino
发明人: Gregory L Beutner , Robert M Wenslow, Jr. , Eric J Choi , Clinton Scott Shultz , Jeremy Scott , Juan D Arredondo , Laura Artino
IPC分类号: C07K5/08 , C07C35/04 , C07K5/083 , C07D403/12 , C07D498/16 , C07K5/12 , C07C67/14 , C07C69/013 , C07C69/12 , C07C269/04 , C07C271/34 , A61K38/00
CPC分类号: C07C35/04 , A61K38/00 , C07C67/14 , C07C69/013 , C07C69/12 , C07C269/04 , C07C271/34 , C07D403/12 , C07D498/16 , C07K5/0808 , C07K5/126
摘要: The present invention relates to different forms of a HCV inhibitory compound.
摘要翻译: 本发明涉及不同形式的HCV抑制化合物。
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公开(公告)号:USD700071S1
公开(公告)日:2014-02-25
申请号:US29430590
申请日:2012-08-28
申请人: Jeremy Scott
设计人: Jeremy Scott
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公开(公告)号:USD651098S1
公开(公告)日:2011-12-27
申请号:US29391707
申请日:2011-05-12
申请人: Jeremy Scott
设计人: Jeremy Scott
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