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公开(公告)号:CH509274A
公开(公告)日:1971-06-30
申请号:CH1098069
申请日:1969-07-17
Applicant: HOECHST AG
Inventor: BEERMANN CLAUS DR , GEORGI VOLKMAR DR , WALDMANN KARL DR , WOLF ERHARD DR
IPC: D06M13/425 , C07C125/06
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公开(公告)号:SI0812844T1
公开(公告)日:2003-02-28
申请号:SI9730414
申请日:1997-06-03
Applicant: HOECHST AG
Inventor: GEBERT ULRICH DR , WOLF ERHARD DR , DEFOSSA ELISABETH DR , HEINELT UWE DR , ANAGNOSTOPULOS HIRISTO DB , RUDOLPHI KARL DR , GROME JOHN J DR
IPC: C07D473/04 , A61K31/505 , A61K31/52 , A61K31/522 , A61P7/08 , A61P9/00 , A61P9/10 , A61P31/04 , A61P31/12 , A61P43/00 , C07D473/06
Abstract: The use of at least one theophylline 1-ether analogue of formula (I) or its diastereoisomer or salt is claimed for the preparation of a medicament for the treatment and/or prophylaxis of shock states. R1 = 1-5C alkyl or (1-2C)alkoxy-(1-3C) alkyl; or phenyl or phenyl-(1-2C)alkyl (both optionally mono- or dihalo-substituted in the ring); A = 1-4C alkylene; R2 = 1-5C alkyl, 3-6C cycloalkyl, 4-8C cycloalkyl, phenyl or phenyl-(1-2C)alkyl. Compounds (I) and their stereoisomers and salts are new, with the exception of compounds in which (a) R2 = n-propyl, R1= Me or Et and A = CH2CH2 or (b) R2 = n-propyl, R1 = Me and A = (CH2)3. Certain intermediates in the preparation of (I) are also new.
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公开(公告)号:DK0812844T3
公开(公告)日:2003-02-17
申请号:DK97108870
申请日:1997-06-03
Applicant: HOECHST AG
Inventor: ANAGNOSTOPULOS HIRISTO DB , GEBERT ULRICH DR , DEFOSSA ELISABETH DR , HEINELT UWE DR , WOLF ERHARD DR , RUDOLPHI KARL DR , GROME JOHN J DR
IPC: C07D473/04 , A61K31/505 , A61K31/52 , A61K31/522 , A61P7/08 , A61P9/00 , A61P9/10 , A61P31/04 , A61P31/12 , A61P43/00 , C07D473/06
Abstract: The use of at least one theophylline 1-ether analogue of formula (I) or its diastereoisomer or salt is claimed for the preparation of a medicament for the treatment and/or prophylaxis of shock states. R1 = 1-5C alkyl or (1-2C)alkoxy-(1-3C) alkyl; or phenyl or phenyl-(1-2C)alkyl (both optionally mono- or dihalo-substituted in the ring); A = 1-4C alkylene; R2 = 1-5C alkyl, 3-6C cycloalkyl, 4-8C cycloalkyl, phenyl or phenyl-(1-2C)alkyl. Compounds (I) and their stereoisomers and salts are new, with the exception of compounds in which (a) R2 = n-propyl, R1= Me or Et and A = CH2CH2 or (b) R2 = n-propyl, R1 = Me and A = (CH2)3. Certain intermediates in the preparation of (I) are also new.
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公开(公告)号:ID19469A
公开(公告)日:1998-07-16
申请号:ID971930
申请日:1997-06-05
Applicant: HOECHST AG
Inventor: GEBERT ULRICH DR , WOLF ERHARD DR , DEFOSSA ELISABETH DR , HEINELT UWE DR , ANAGNOSTOPULOS DB HIRISTO , RUDOLPHI KARL DR , GROME JOHN J DR
IPC: C07D473/04 , A61K31/505 , A61K31/52 , A61K31/522 , A61P7/08 , A61P9/00 , A61P9/10 , A61P31/04 , A61P31/12 , A61P43/00 , C07D473/06
Abstract: The use of at least one theophylline 1-ether analogue of formula (I) or its diastereoisomer or salt is claimed for the preparation of a medicament for the treatment and/or prophylaxis of shock states. R1 = 1-5C alkyl or (1-2C)alkoxy-(1-3C) alkyl; or phenyl or phenyl-(1-2C)alkyl (both optionally mono- or dihalo-substituted in the ring); A = 1-4C alkylene; R2 = 1-5C alkyl, 3-6C cycloalkyl, 4-8C cycloalkyl, phenyl or phenyl-(1-2C)alkyl. Compounds (I) and their stereoisomers and salts are new, with the exception of compounds in which (a) R2 = n-propyl, R1= Me or Et and A = CH2CH2 or (b) R2 = n-propyl, R1 = Me and A = (CH2)3. Certain intermediates in the preparation of (I) are also new.
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公开(公告)号:CZ9701743A3
公开(公告)日:1997-12-17
申请号:CZ174397
申请日:1997-06-05
Applicant: HOECHST AG
Inventor: GEBERT ULRICH DR , WOLF ERHARD DR , DEFOSSA ELISABETH DR , HEINELT UWE DR , ANAGNOSTOPULOS HIRISTO DB , RUDOLPHI KARL DR , GROME JOHN J DR
IPC: C07D473/04 , A61K31/505 , A61K31/522 , A61P7/08 , A61P9/00 , A61P9/10 , A61P31/04 , A61P31/12 , A61P43/00 , C07D473/06 , C07D487/04 , A61K31/41 , A61K31/52
CPC classification number: C07D473/06
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公开(公告)号:CH511807A
公开(公告)日:1971-08-31
申请号:CH1193169
申请日:1969-08-06
Applicant: HOECHST AG
Inventor: BARTMANN WILHELM DR , DUEWEL DIETER DR , GEORGI VOLKMAR DR , WOLF ERHARD DR , BEERMANN CLAUS DR , LANDAUER FRANZ DR
IPC: A61K31/14 , C07C233/00 , C07C103/44 , C07C125/06
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公开(公告)号:MY117910A
公开(公告)日:2004-08-30
申请号:MYPI9702540
申请日:1997-06-06
Applicant: HOECHST AG
Inventor: GEBERT ULRICH DR , WOLF ERHARD DR , XDFA ELISABETH DEFO DR , HEINELT UWE DR , ANAGNOSTOPULOS DB HIRISTO , RUDOLPHI KARL DR , GROME JOHN J DR
IPC: C07D473/04 , A61K31/505 , A61K31/52 , A61K31/522 , A61P7/08 , A61P9/00 , A61P9/10 , A61P31/04 , A61P31/12 , A61P43/00 , C07D473/06
Abstract: THEOPHYLLINE DERIVATIVES HAVING AT LEAST ONE ETHER FUNCTION IN THE STRUCTURALLY MODIFIED METHYL RADICAL IN THE I-POSITION THAT ARE USEFUL IN THE TREATMENT AND PROPHYLAXIS OF STATES OF SHOCK, NEW XANTHINE COMPOUNDS HAVING THIS SUBSTITUTION PATTERN, AND PROCESSES FOR THEIR PREPARATION
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公开(公告)号:ES2185837T3
公开(公告)日:2003-05-01
申请号:ES97108870
申请日:1997-06-03
Applicant: HOECHST AG
Inventor: GEBERT ULRICH DR , WOLF ERHARD DR , DEFOSSA ELISABETH DR , HEINELT UWE DR , ANAGNOSTOPULOS HIRISTO DB , RUDOLPHI KARL DR
IPC: C07D473/04 , A61K31/505 , A61K31/52 , A61K31/522 , A61P7/08 , A61P9/00 , A61P9/10 , A61P31/04 , A61P31/12 , A61P43/00 , C07D473/06
Abstract: The use of at least one theophylline 1-ether analogue of formula (I) or its diastereoisomer or salt is claimed for the preparation of a medicament for the treatment and/or prophylaxis of shock states. R1 = 1-5C alkyl or (1-2C)alkoxy-(1-3C) alkyl; or phenyl or phenyl-(1-2C)alkyl (both optionally mono- or dihalo-substituted in the ring); A = 1-4C alkylene; R2 = 1-5C alkyl, 3-6C cycloalkyl, 4-8C cycloalkyl, phenyl or phenyl-(1-2C)alkyl. Compounds (I) and their stereoisomers and salts are new, with the exception of compounds in which (a) R2 = n-propyl, R1= Me or Et and A = CH2CH2 or (b) R2 = n-propyl, R1 = Me and A = (CH2)3. Certain intermediates in the preparation of (I) are also new.
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公开(公告)号:AT226583T
公开(公告)日:2002-11-15
申请号:AT97108870
申请日:1997-06-03
Applicant: HOECHST AG
Inventor: GEBERT ULRICH DR , WOLF ERHARD DR , DEFOSSA ELISABETH DR , HEINELT UWE DR , ANAGNOSTOPULOS HIRISTO DB , RUDOLPHI KARL DR , GROME JOHN J DR
IPC: C07D473/04 , A61K31/505 , A61K31/52 , A61K31/522 , A61P7/08 , A61P9/00 , A61P9/10 , A61P31/04 , A61P31/12 , A61P43/00 , C07D473/06
Abstract: The use of at least one theophylline 1-ether analogue of formula (I) or its diastereoisomer or salt is claimed for the preparation of a medicament for the treatment and/or prophylaxis of shock states. R1 = 1-5C alkyl or (1-2C)alkoxy-(1-3C) alkyl; or phenyl or phenyl-(1-2C)alkyl (both optionally mono- or dihalo-substituted in the ring); A = 1-4C alkylene; R2 = 1-5C alkyl, 3-6C cycloalkyl, 4-8C cycloalkyl, phenyl or phenyl-(1-2C)alkyl. Compounds (I) and their stereoisomers and salts are new, with the exception of compounds in which (a) R2 = n-propyl, R1= Me or Et and A = CH2CH2 or (b) R2 = n-propyl, R1 = Me and A = (CH2)3. Certain intermediates in the preparation of (I) are also new.
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公开(公告)号:DE19622737A1
公开(公告)日:1997-12-11
申请号:DE19622737
申请日:1996-06-07
Applicant: HOECHST AG
Inventor: GEBERT ULRICH DR , WOLF ERHARD DR , DEFOSA ELISABETH DR , HEINELT UWE DR , ANAGNOSTOPULOS HIRISTO , RUDOLPHI KARL DR , GROME JOHN J DR
IPC: C07D473/06 , A61K31/52 , C07D473/08
Abstract: Use of at least one compound of formula (I), or their salts or stereoisomeric forms for preparation of a medicament for treatment and/or prophylaxis of shock disorders is claimed: R1 = 1-5C alkyl, 1-2C alkoxy(1-3C)alkyl, or phenyl or phenyl(1-2C)alkyl (both optionally ring substituted by 1-2 halo); A = a 1-4C alkylene bridge; R2 = 1-5C alkyl, 3-6C cycloalkyl, 4-8C cycloalkyl-alkyl, phenyl or phenyl(1-2C)alkyl. Compounds (I), and their salts and stereoisomeric forms are new with the exception of those compounds in which (a) R2 = n-propyl, R1 = ethyl and A = a (m)ethylene bridge and (b) R2 = n-propyl, R1 = propyl and A = a methylene bridge.
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