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公开(公告)号:US20080119505A1
公开(公告)日:2008-05-22
申请号:US11795981
申请日:2006-01-31
申请人: Ulrich Kautz , Beate Schmidt , Dieter Flockerzi , Maria Vittoria Chiesa , Armin Hatzelmann , Christof Zitt , Johannes Barsig , Andrea Wohlsen , Degenhard Marx , Hans-Peter Kley
发明人: Ulrich Kautz , Beate Schmidt , Dieter Flockerzi , Maria Vittoria Chiesa , Armin Hatzelmann , Christof Zitt , Johannes Barsig , Andrea Wohlsen , Degenhard Marx , Hans-Peter Kley
IPC分类号: A61K31/4741 , A61K31/473 , C07D491/02 , C07D221/12
CPC分类号: C07D401/04
摘要: Compounds of a certain formula (I), in which R1, R2, R3, R31, R4, R5, R51 and Har have the meanings indicated in the description, are novel effective PDE4 inhibitors.
摘要翻译: 其中R1,R2,R3,R31,R4,R5,R51和Har具有说明书中所示含义的某种式(I)的化合物是新的有效的PDE4抑制剂。
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公开(公告)号:US20080214536A1
公开(公告)日:2008-09-04
申请号:US11885425
申请日:2006-03-09
申请人: Ulrich Kautz , Beate Schmidt , Dieter Flockerzi , Maria Vittoria Chiesa , Armin Hatzelmann , Christof Zitt , Johannes Barsig , Degenhard Marx , Hans-Peter Kley
发明人: Ulrich Kautz , Beate Schmidt , Dieter Flockerzi , Maria Vittoria Chiesa , Armin Hatzelmann , Christof Zitt , Johannes Barsig , Degenhard Marx , Hans-Peter Kley
IPC分类号: A61K31/473 , C07D221/12 , C07D401/02 , A61K31/5377 , A61P11/00 , A61K31/497 , C07D413/02
CPC分类号: C07D401/10 , C07D221/12
摘要: Compounds of a certain formula (I) in which R1, R2, R3, R31, R4, R5, R51, R6 and R7 have the meanings indicated in the description, are novel effective PDE4 inhibitors.
摘要翻译: 其中R 1,R 2,R 3,R 31,R 4,R 5,R 51,R 6和R 7具有说明书中所示含义的某种式(I)的化合物是新的有效的PDE4抑制剂。
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3.6-Heteroaryl-1,2,3,4,4A, 10B-Hexahydrophenanthridines as Pde4-Inhibitors for the Treatment of Inflammatory Disorders 审中-公开
标题翻译: 6-杂芳基-1,2,3,4,4A,10B-六氢吡啶作为治疗炎性疾病的Pde4抑制剂公开(公告)号:US20080167316A1
公开(公告)日:2008-07-10
申请号:US11884935
申请日:2006-03-01
申请人: Ulrich Kautz , Beate Schmidt , Dieter Flockerzi , Maria Vittoria Chiesa , Armin Hatzelmann , Christof Zitt , Adrea Wohlsen , Degenhard Marx , Hans-Peter Kley
发明人: Ulrich Kautz , Beate Schmidt , Dieter Flockerzi , Maria Vittoria Chiesa , Armin Hatzelmann , Christof Zitt , Adrea Wohlsen , Degenhard Marx , Hans-Peter Kley
IPC分类号: A61K31/473 , C07D221/12 , A61K31/501 , A61P43/00 , C07D401/02
CPC分类号: C07D401/04
摘要: Compounds of a certain formula I in which R1, R2, R3, R31, R4, R5, R51 and Har have the meanings indicated in the description, are novel effective PDE4 inhibitors.
摘要翻译: 其中R1,R2,R3,R31,R4,R5,R51和Har具有说明书中所示含义的某种式I的化合物是新的有效的PDE4抑制剂。
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公开(公告)号:US20090093473A1
公开(公告)日:2009-04-09
申请号:US11921508
申请日:2006-06-13
申请人: Peter Jan Zimmermann , Jorg Senn-Bilfinger , Christof Brehm , Wilm Buhr , Maria Vittoria Chiesa , Andreas Palmer , Wolfgang-Alexander Simon , Stefan Postius , Wolfgang Kromer
发明人: Peter Jan Zimmermann , Jorg Senn-Bilfinger , Christof Brehm , Wilm Buhr , Maria Vittoria Chiesa , Andreas Palmer , Wolfgang-Alexander Simon , Stefan Postius , Wolfgang Kromer
IPC分类号: A61K31/438 , C07D471/10 , A61P1/00 , A61K31/5377
CPC分类号: C07D471/10
摘要: The invention provides compounds of the formula (I) In which the substituents and symbols are as defined in the description. The compounds inhibit the secretion of gastric acid.
摘要翻译: 本发明提供式(I)化合物,其中取代基和符号如说明书中所定义。 这些化合物抑制胃酸的分泌。
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5.Process For the Production of Intermediates For the Preparation of Tricyclic Benzimidazoles 审中-公开
标题翻译: 制备三环苯并咪唑的中间体的制备方法公开(公告)号:US20080280855A1
公开(公告)日:2008-11-13
申请号:US11922213
申请日:2006-06-20
申请人: Maria Vittoria Chiesa , Andreas Palmer , Wilm Buhr , Peter Jan Zimmermann , Christof Brehm , Wolfgang-Alexander Simon , Stefan Postius , Wolfgang Kromer , Antonio Zanotti-Gerosa
发明人: Maria Vittoria Chiesa , Andreas Palmer , Wilm Buhr , Peter Jan Zimmermann , Christof Brehm , Wolfgang-Alexander Simon , Stefan Postius , Wolfgang Kromer , Antonio Zanotti-Gerosa
IPC分类号: A61K31/695 , C07F7/08 , C07D403/02 , A61K31/4184 , A61K31/4188 , C07D491/052
CPC分类号: C07D235/08 , C07D401/06 , C07D409/06 , C07D491/04
摘要: The invention relates to a process for the synthesis of compounds of the formula 1-a and compounds of the formula 1-b. The compounds of the formula 1-a and the compounds of the formula 1-b, in which the substituents R1, R2, R3, and Ar have the meanings indicated in the description, are valuable intermediates for the preparation of pharmaceutically active compounds.
摘要翻译: 本发明涉及一种合成式1-a化合物和式1-b化合物的方法。 式1-a的化合物和其中取代基R 1,R 2,R 3和Ar具有说明书中所示含义的式1-b的化合物是制备药学活性化合物的有价值的中间体。
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