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1.Method for separating methyl 4-(2-chloro-4-fluorophenyl)-2-(3,5-difluoro-2-pyridinyl)-6-methyl-1,4-dihydro-5-pyrimidine-carboxylate-recemate 有权
标题翻译: 分离甲基4-(2-氯-4-氟苯基)-2-(3,5-二氟-2-吡啶基)-6-甲基-1,4-二氢-5-嘧啶羧酸甲酯的方法公开(公告)号:US06987185B2
公开(公告)日:2006-01-17
申请号:US10478602
申请日:2002-05-15
申请人: Siegfried Goldmann , Peter Fey
发明人: Siegfried Goldmann , Peter Fey
IPC分类号: C07D401/04
CPC分类号: C07D401/04 , C07B2200/07
摘要: The enantiomers of methyl 4-(2-chloro-4-fluorophenyl)-2-(3,5-difluoro-2-pyridinyl)-6-methyl)-1,4-dihydro-5-pyrimidinecarboxylate can be separated with the aid of (−)-camphanic acid.
摘要翻译: 4-(2-氯-4-氟苯基)-2-(3,5-二氟-2-吡啶基)-6-甲基)-1,4-二氢-5-嘧啶甲酸甲酯的对映异构体可以借助于 ( - ) - 樟脑酸。
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2.3-'Hydroxy-(-4-trifluoromethylphenyl)-methyl-7-spirocyclobutyl-5,6,7 8-tetrahydroquinolin-5-ol derivatives and the use of the same as cholesterol ester transfer protein (cetp) inhibitors 审中-公开
标题翻译: 3-羟基 - ( - 4-三氟甲基苯基) - 甲基-7-螺环丁基-5,6,7,8-四氢喹啉-5-醇衍生物及其与胆固醇酯转移蛋白(cetp)抑制剂的用途公开(公告)号:US20050043341A1
公开(公告)日:2005-02-24
申请号:US10491465
申请日:2002-09-18
申请人: Heike Gielen , Siegfried Goldmann , Jorg Keldenich , Holger Paulsen , Carsten Schmeck , Stephan Siegel , Hilmar Bischoff , Martin Raabe , Delf Schmidt , Christiane Faeste
发明人: Heike Gielen , Siegfried Goldmann , Jorg Keldenich , Holger Paulsen , Carsten Schmeck , Stephan Siegel , Hilmar Bischoff , Martin Raabe , Delf Schmidt , Christiane Faeste
IPC分类号: C07D215/20 , A61K31/47 , A61K31/4709 , A61P3/04 , A61P3/06 , A61P9/00 , A61P9/10 , A61P25/28 , A61P43/00 , C07D221/20 , C07D409/04 , A61K31/4747
CPC分类号: C07D221/20 , C07D409/04
摘要: The application relates to substituted tetrahydroquinoline derivatives, processes for their preparation and their use in medicaments.
摘要翻译: 本申请涉及取代的四氢喹啉衍生物,其制备方法及其在药物中的用途。
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公开(公告)号:US06858622B2
公开(公告)日:2005-02-22
申请号:US10198315
申请日:2002-07-18
申请人: Ulrich Müller , Richard Connell , Siegfried Goldmann , Rudi Grützmann , Martin Beuck , Hilmar Bischoff , Dirk Denzer , Anke Domdey-Bette , Stefan Wohlfeil
发明人: Ulrich Müller , Richard Connell , Siegfried Goldmann , Rudi Grützmann , Martin Beuck , Hilmar Bischoff , Dirk Denzer , Anke Domdey-Bette , Stefan Wohlfeil
IPC分类号: C07D209/86 , A61K31/40 , A61K31/403 , A61K31/4035 , A61K31/435 , A61K31/4353 , A61K31/44 , A61P1/00 , A61P3/04 , A61P3/06 , A61P9/08 , A61P9/10 , C07D20060101 , C07D209/00 , C07D209/82 , C07D209/94 , C07D219/02 , C07D221/00 , C07D471/04 , A61K31/437 , C07D471/06
CPC分类号: C07D471/04 , C07D219/02
摘要: Cycloalkano-indole and -azaindole derivatives are prepared by reaction of appropriately substituted carboxylic acids with amines. The cycloalkano-indole and -azaindole derivatives are suitable as active compounds for medicaments, preferably antiatherosclerotic medicaments.
摘要翻译: 通过适当取代的羧酸与胺的反应制备环烷基 - 吲哚和吖啶衍生物。 环烷基 - 吲哚和吖啶衍生物适合用作药物,优选抗动脉粥样硬化药物的活性化合物。
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公开(公告)号:US06265431B1
公开(公告)日:2001-07-24
申请号:US09313035
申请日:1999-05-17
申请人: Ulrich Müller , Richard Connell , Siegfried Goldmann , Rudi Grützmann , Martin Beuck , Hilmar Bischoff , Dirk Denzer , Anke Domdey-Bette , Stefan Wohlfeil
发明人: Ulrich Müller , Richard Connell , Siegfried Goldmann , Rudi Grützmann , Martin Beuck , Hilmar Bischoff , Dirk Denzer , Anke Domdey-Bette , Stefan Wohlfeil
IPC分类号: A61K31403
CPC分类号: C07D471/04 , C07D219/02
摘要: Cycloalkano-indole and -azaindole derivatives are prepared by reaction of appropriately substituted carboxylic acids with amines. The cycloalkano-indole and -azaindole derivatives are suitable as active compounds for medicaments, preferably antiatherosclerotic medicaments.
摘要翻译: 通过适当取代的羧酸与胺的反应制备环烷基 - 吲哚和吖啶衍生物。 环烷基 - 吲哚和吖啶衍生物适合用作药物,优选抗动脉粥样硬化药物的活性化合物。
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公开(公告)号:US5811429A
公开(公告)日:1998-09-22
申请号:US761921
申请日:1996-12-09
申请人: Richard Connell , Siegfried Goldmann , Ulrich Muller , Stefan Lohmer , Hilmar Bischoff , Dirk Denzer , Rudi Grutzmann , Stefan Wohlfeil
发明人: Richard Connell , Siegfried Goldmann , Ulrich Muller , Stefan Lohmer , Hilmar Bischoff , Dirk Denzer , Rudi Grutzmann , Stefan Wohlfeil
IPC分类号: C07D237/06 , A61K31/40 , A61K31/403 , A61K31/4035 , A61K31/415 , A61K31/4184 , A61K31/425 , A61K31/426 , A61K31/428 , A61K31/435 , A61K31/44 , A61K31/4427 , A61K31/4433 , A61K31/496 , A61K31/50 , A61K31/505 , A61K31/517 , A61K31/535 , A61K31/5355 , A61K31/54 , A61K31/541 , A61K31/5415 , A61P3/06 , A61P9/10 , C07D209/48 , C07D235/08 , C07D235/10 , C07D235/28 , C07D237/32 , C07D239/91 , C07D263/58 , C07D265/36 , C07D275/06 , C07D277/20 , C07D277/56 , C07D279/16 , C07D401/04 , C07D409/04 , C07D417/04 , C07D471/04 , C07D498/04 , C07D239/72 , C07D413/00
CPC分类号: C07D209/48 , C07D235/08 , C07D235/10 , C07D235/28 , C07D237/32 , C07D239/91 , C07D263/58 , C07D275/06 , C07D279/16 , C07D401/04 , C07D409/04 , C07D417/04
摘要: The bicyclic heterocyclic compounds are prepared by reaction of correspondingly substituted carboxylic acids with amines, in particular with phenylglycinolamine. The bicyclic heterocyclic compounds according to the invention are suitable as active compounds in medicaments, in particular in medicaments having an antiatherosclerotic action.
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公开(公告)号:US5750783A
公开(公告)日:1998-05-12
申请号:US833824
申请日:1997-04-10
申请人: Siegfried Goldmann , Ulrich Muller , Richard Connell , Hilmar Bischoff , Dirk Denzer , Rudi Grutzmann , Martin Beuck
发明人: Siegfried Goldmann , Ulrich Muller , Richard Connell , Hilmar Bischoff , Dirk Denzer , Rudi Grutzmann , Martin Beuck
IPC分类号: C07D295/16 , A61K31/165 , A61K31/415 , A61K31/4184 , A61K31/44 , A61K31/4402 , A61K31/445 , A61K31/454 , A61K31/47 , A61K31/535 , A61K31/5355 , A61K31/5375 , A61P9/00 , A61P9/10 , C07C235/34 , C07C235/54 , C07C235/56 , C07C323/50 , C07D213/30 , C07D213/74 , C07D215/26 , C07D233/84 , C07D235/28 , C07D295/185 , C07C233/16 , A61K31/16 , A61K31/24 , C07C233/25
CPC分类号: C07D213/30 , C07C235/34 , C07C235/54 , C07C235/56 , C07D295/185 , C07C2101/08 , C07C2101/14 , C07C2101/18
摘要: Benzyloxy-substituted phenylglycinolamides are prepared by reaction of benzyloxy-substituted phenylacetic acids with phenylglycinols. The benzyloxy-substituted phenylglycinolamides are suitable as active compounds in medicaments, in particular in medicaments for the treatment of atherosclerosis.
摘要翻译: 苄氧基取代的苯基甘氨酰胺通过苄氧基取代的苯乙酸与苯基甘氨醇的反应来制备。 苄氧基取代的苯基甘氨酰胺适合作为药物中的活性化合物,特别是用于治疗动脉粥样硬化的药物。
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公开(公告)号:US5684014A
公开(公告)日:1997-11-04
申请号:US535698
申请日:1995-09-28
申请人: Ulrich Muller , Richard Connell , Siegfried Goldmann , Rudi Grutzmann , Martin Beuck , Hilmar Bischoff , Dirk Denzer , Anke Domdey-Bette , Stefan Wohlfeil
发明人: Ulrich Muller , Richard Connell , Siegfried Goldmann , Rudi Grutzmann , Martin Beuck , Hilmar Bischoff , Dirk Denzer , Anke Domdey-Bette , Stefan Wohlfeil
IPC分类号: C07D209/86 , A61K31/40 , A61K31/403 , A61K31/4035 , A61K31/435 , A61K31/4353 , A61K31/44 , A61P1/00 , A61P3/04 , A61P3/06 , A61P9/08 , A61P9/10 , C07D20060101 , C07D209/00 , C07D209/82 , C07D209/94 , C07D219/02 , C07D221/00 , C07D471/04 , C07D471/02
CPC分类号: C07D471/04 , C07D219/02
摘要: Cycloalkano-indole and -azaindole derivatives are prepared by reaction of appropriately substituted carboxylic acids with amines. The cycloalkano-indole and -azaindole derivatives are suitable as active compounds for medicaments, preferably antiatherosclerotic medicaments.
摘要翻译: 通过适当取代的羧酸与胺的反应制备环烷基 - 吲哚和吖啶衍生物。 环烷基 - 吲哚和吖啶衍生物适合用作药物,优选抗动脉粥样硬化药物的活性化合物。
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8.Substituted 4-phenyl-6-amino-nicotinic acid compounds useful in the treatment of CNS disorders 失效
标题翻译: 可用于治疗CNS病症的取代的4-苯基-6-氨基 - 烟酸化合物公开(公告)号:US5670525A
公开(公告)日:1997-09-23
申请号:US517873
申请日:1995-08-22
申请人: Klaus Urbahns , Siegfried Goldmann , Hans-Georg Heine , Bodo Junge , Rudolf Schohe-Loop , Henning Sommermeyer , Thomas Glaser , Reilinde Wittka , Jean-Marie Viktor De Vry
发明人: Klaus Urbahns , Siegfried Goldmann , Hans-Georg Heine , Bodo Junge , Rudolf Schohe-Loop , Henning Sommermeyer , Thomas Glaser , Reilinde Wittka , Jean-Marie Viktor De Vry
IPC分类号: A61K31/4412 , A61K31/4418 , A61K31/455 , A61P9/00 , A61P25/00 , A61P25/28 , C07D213/80 , C07D213/803 , C07D213/84 , C07D213/85 , A61K31/435
CPC分类号: C07D213/80 , C07D213/85
摘要: The application relates to substituted 4-phenyl-6-amino-nicotinic acid derivatives for therapeutic use, to novel active compounds and to their use as cerebrally active agents. The active compounds are prepared by oxidizing appropriately substituted dihydropyridines according to customary methods.
摘要翻译: 本申请涉及用于治疗用途的取代的4-苯基-6-氨基 - 烟酸衍生物,新型活性化合物及其作为脑活性剂的用途。 通过根据常规方法氧化适当取代的二氢吡啶来制备活性化合物。
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9.6-amino-1,4-dihydropyridine compounds as medicaments for treatment of the central nervous system, and processes for their preparation 失效
标题翻译: 6-氨基-1,4-二氢吡啶化合物作为治疗中枢神经系统的药物及其制备方法公开(公告)号:US5652251A
公开(公告)日:1997-07-29
申请号:US516597
申请日:1995-08-18
申请人: Klaus Urbahns , Siegfried Goldmann , Hans-Georg Heine , Bodo Junge , Rudolf Schohe-Loop , Henning Sommermeyer , Thomas Glaser , Reilinde Wittka , Jean-Marie-Viktor De Vry
发明人: Klaus Urbahns , Siegfried Goldmann , Hans-Georg Heine , Bodo Junge , Rudolf Schohe-Loop , Henning Sommermeyer , Thomas Glaser , Reilinde Wittka , Jean-Marie-Viktor De Vry
IPC分类号: A61K31/435 , A61K31/44 , A61K31/4427 , A61P9/10 , A61P25/00 , A61P43/00 , C07D211/90 , C07D401/04 , C07D471/04 , C07D471/02 , C07D211/92
CPC分类号: C07D211/90
摘要: The present invention relates to the new use of 6-amino-5-nitro- and -5-cyano-1,4-dihydropyridines of the general formula (I) ##STR1## in which A, D and R.sup.1 -R.sup.4 have the meaning given in the description, new 6-acylamino-dihydropyridines, processes for their preparation and their use as medicaments as selective potassium channel modulators, in particular for treatment of the central nervous system.
摘要翻译: 本发明涉及通式(I)的化合物(I)的6-氨基-5-硝基 - 和5-氰基-1,4-二氢吡啶的新用途,其中A,D和R 1 -R 4 具有描述中给出的含义,新的6-酰基氨基 - 二氢吡啶类,其制备方法及其作为药物用作选择性钾通道调节剂,特别是用于治疗中枢神经系统。
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10.3-quinolyl-substituted dihydropyridines, and their use in medicaments 失效
标题翻译: 3-喹啉基取代的二氢吡啶,以及它们在药物中的用途公开(公告)号:US5629320A
公开(公告)日:1997-05-13
申请号:US448930
申请日:1995-05-25
申请人: J urgen Stoltefuss , Siegfried Goldmann , Alexander Straub , Martin Bechem , Rainer Gross , Siegbert Hebisch , Joachim H utter , Howard-Paul Rounding
发明人: J urgen Stoltefuss , Siegfried Goldmann , Alexander Straub , Martin Bechem , Rainer Gross , Siegbert Hebisch , Joachim H utter , Howard-Paul Rounding
IPC分类号: A61K31/47 , C07C47/06 , C07D215/20 , C07D215/36 , C07D215/48 , C07D401/04 , C07D401/14 , C07D491/04 , C07D491/048 , A61K31/395
CPC分类号: C07D401/04 , C07D401/14 , C07D491/04
摘要: This invention relates to 3-quinolyl-substituted dihydropyridine derivatives, such as ##STR1## or a pharmaceutically acceptable salt thereof. These compounds are used in treating cardiovascular disease.
摘要翻译: 本发明涉及3-喹啉基取代的二氢吡啶衍生物,例如“IMAGE”或其药学上可接受的盐。 这些化合物用于治疗心血管疾病。
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