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公开(公告)号:US06200971B1
公开(公告)日:2001-03-13
申请号:US09420304
申请日:1999-10-18
申请人: Richard Connell , Siegfried Goldmann , Ulrich Müller , Stefan Lohmer , Hilmar Bischoff , Dirk Denzer , Rudi Gr{umlaut over (u )}tzmann , Stefan Wohlfeil
发明人: Richard Connell , Siegfried Goldmann , Ulrich Müller , Stefan Lohmer , Hilmar Bischoff , Dirk Denzer , Rudi Gr{umlaut over (u )}tzmann , Stefan Wohlfeil
IPC分类号: A61K3154
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.
摘要翻译: 双环杂环化合物通过相应地取代的羧酸与胺,特别是苯基甘氨酚的反应来制备。 根据本发明的双环杂环化合物适合作为药物中的活性化合物,特别是具有抗动脉粥样硬化作用的药物。
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公开(公告)号:US06235770B1
公开(公告)日:2001-05-22
申请号:US09435544
申请日:1999-11-08
申请人: Richard Connell , Siegfried Goldmann , Ulrich Müller , Stefan Lohmer , Hilmar Bischoff , Dirk Denzer , Rudi Grützmann , Stefan Wohlfeil
发明人: Richard Connell , Siegfried Goldmann , Ulrich Müller , Stefan Lohmer , Hilmar Bischoff , Dirk Denzer , Rudi Grützmann , Stefan Wohlfeil
IPC分类号: A61K31405
CPC分类号: C07D471/04 , C07D209/08 , C07D209/42 , C07D235/16
摘要: The indolyl-substituted phenylacetic acid derivatives are prepared by reacting the corresponding phenylacetic acids with the required amines. The indolyl-substituted phenylacetic acid derivatives are suitable as active compounds in medicaments, in particular in antiarteriosclerotic medicaments.
摘要翻译: 吲哚基取代的苯乙酸衍生物通过使相应的苯乙酸与所需的胺反应来制备。 吲哚基取代的苯乙酸衍生物在药物,特别是抗动脉硬化药物中适合作为活性化合物。
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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:US6025378A
公开(公告)日:2000-02-15
申请号:US99557
申请日:1998-06-18
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 , A61K31/42 , A61K31/47 , C07D215/00 , C07D263/04 , C07D263/30 , C07D403/02 , 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.
摘要翻译: 双环杂环化合物通过相应地取代的羧酸与胺,特别是苯基甘氨酚的反应来制备。 根据本发明的双环杂环化合物适合作为药物中的活性化合物,特别是具有抗动脉粥样硬化作用的药物。
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公开(公告)号:US5714494A
公开(公告)日:1998-02-03
申请号:US710503
申请日:1996-09-18
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: A61K31/52 , A61K31/522 , A61P9/00 , A61P9/10 , C07D473/06 , C07D473/08 , C07D473/22
CPC分类号: C07D473/06 , C07D473/08
摘要: Substituted xanthines of formula ##STR1## in which A represents a radical of the formula ##STR2## in which R.sup.3, R.sup.4, R.sup.6 and R.sup.7 denote hydrogen, cycloalkyl, aryl having 6 to 10 carbon atoms, or denote straight-chain of branched alkyl or alkenyl, each of which is optionally substituted; T, V, X and Y are identical or different and denote an oxygen or sulphur atom; R.sup.5 and R.sup.8 are identical or different and denote hydrogen, halogen, cycloalkyl having 3 to 8 carbon atoms or straight-chain or branched alkyl or alkenyl in each case having up to 8 carbon atoms, optionally substituted or R.sup.5 and R.sup.8 denote aryl having 6 to 10 carbon atoms or a 5- to 7-membered aromatic, optionally benzo-fused heterocycle having up to 3 heteroatoms S, N and/or O, each of which is optionally substituted; L represents an oxygen or sulphur atom; R.sup.2 represents mercapto, hydroxyl, straight-chain or branched alkoxy having up to 8 carbon atoms or the group of the formula ##STR3## in which R.sup.13 denotes hydrogen or straight-chain or branched alkyl having up to 4 carbon atoms; R.sup.14 denotes hydrogen, phenyl or a 5- to 6-membered aromatic heterocycle having up to 3 heteroatoms S, N and/or O; and R.sup.15 denotes hydrogen or straight-chain or branched alkyl having up to 8 carbon atom, optionally substituted by hydroxyl, and their salts are prepared by reaction of the suitable unsubstituted xanthines with halogenomethylphenylacetic acids and subsequent reaction of the carboxylic esters or acids with phenylglycinolamine. The substituted xanthines are suitable as active compounds in medicaments, in particular in antiatherosclerotic medicaments.
摘要翻译: 式(I)的取代黄嘌呤其中A表示式为“IMAGE”的基团,其中R 3,R 4,R 6和R 7表示氢,环烷基,具有6至10个碳原子的芳基,或表示直链 支链烷基或烯基,其各自任选被取代; T,V,X和Y相同或不同,表示氧或硫原子; R5和R8相同或不同,表示氢,卤素,具有3-8个碳原子的环烷基或具有至多8个碳原子的直链或支链烷基或链烯基,任选取代或R 5和R 8表示具有6至 10个碳原子或5至7元芳族,任选苯并稠合的杂环,其具有至多3个杂原子S,N和/或O,每个杂原子任选被取代; L表示氧或硫原子; R 2表示具有至多8个碳原子的巯基,羟基,直链或支链烷氧基或式“IMAGE”的基团,其中R13表示氢或具有至多4个碳原子的直链或支链烷基; R14表示氢,苯基或具有至多3个S,N和/或O的杂原子的5至6元芳族杂环; 并且R 15表示氢或具有至多8个碳原子的直链或支链烷基,任选被羟基取代,并且它们的盐通过合适的未取代黄嘌呤与卤代甲基苯基乙酸的反应制备,随后羧酸酯或酸与苯基甘氨酚的反应来制备。 取代黄嘌呤在药物,特别是抗动脉粥样硬化药物中适合作为活性化合物。
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公开(公告)号:US6034115A
公开(公告)日:2000-03-07
申请号:US761922
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: A61K31/40 , A61K31/403 , A61K31/404 , A61K31/415 , A61K31/4184 , A61K31/435 , A61P3/06 , A61P9/00 , A61P9/10 , C07D209/08 , C07D209/42 , C07D235/16 , C07D471/04 , C07D235/08 , C07D235/10 , C07D235/18
CPC分类号: C07D471/04 , C07D209/08 , C07D209/42 , C07D235/16
摘要: The indolyl-substituted phenylacetic acid derivatives are prepared by reacting the corresponding phenylacetic acids with the required amines. The indolyl-substituted phenylacetic acid derivatives are suitable as active compounds in medicaments, in particular in antiarteriosclerotic medicaments.
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公开(公告)号:US06479503B2
公开(公告)日:2002-11-12
申请号:US09814263
申请日:2001-03-21
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: A61K31437
CPC分类号: C07D471/04 , C07D219/02
摘要: Cycloalcanoindole and -azaindole derivatives are prepared by reaction of appropriately substituted carboxylic acids with anmines. The cycloahloanindole and -azaindole derivatives are suitable as active compounds for medicaments, preferably antiatherosclerotic medicaments.
摘要翻译: 环烷基吲哚和卤素衍生物通过适当取代的羧酸与烟矿的反应来制备。 环亚氨基吲哚和卤素衍生物适合作为药物的活性化合物,优选抗动脉粥样硬化药物。
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公开(公告)号:US06245775B1
公开(公告)日:2001-06-12
申请号:US08887781
申请日:1997-07-03
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: A61K31437
CPC分类号: C07D471/04 , C07D219/02
摘要: Cycloakano-indole and -azaindole derivatives are prepared by reaction of appropriately substituted carbonylic acids with amines. The cycloalkano-indole and -azaindole derivatives are suitable as active compounds for medicaments, preferably antiatherosclerotic medicaments.
摘要翻译: 通过适当取代的羰基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: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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