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公开(公告)号:PL344043A1
公开(公告)日:2001-09-24
申请号:PL34404399
申请日:1999-05-10
Applicant: SOLVAY PHARM GMBH
Inventor: REGGELIN MICHAEL , HEINRICH TIMO , JUNKER BERND , ANTEL JOCHEN , PREUSCHOFF ULF
IPC: C07D219/06 , C07C381/10 , C07D207/12 , C07D209/52 , C07D221/16 , C07D221/22 , C07D291/04 , C07F7/10 , C07C7/10
Abstract: A method for stereochemically controlled production of azacyclic compounds of general formula (I) in which the substituents have the meanings given in the specification. The invention also relates to intermediate products of this method and to novel azacyclenes.
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公开(公告)号:NO20005666L
公开(公告)日:2000-11-10
申请号:NO20005666
申请日:2000-11-10
Applicant: SOLVAY PHARM GMBH
Inventor: REGGELIN MICHAEL , HEINRICH TIMO , JUNKER BERND , ANTEL JOCHEN , PREUSCHOFF ULF
IPC: C07D219/06 , C07C381/10 , C07D207/12 , C07D209/52 , C07D221/16 , C07D221/22 , C07D291/04 , C07F7/10
Abstract: A method for stereochemically controlled production of azacyclic compounds of general formula (I) in which the substituents have the meanings given in the specification. The invention also relates to intermediate products of this method and to novel azacyclenes.
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公开(公告)号:AU1643899A
公开(公告)日:1999-08-26
申请号:AU1643899
申请日:1999-02-12
Applicant: SOLVAY PHARM GMBH
Inventor: JASSERAND DANIEL , EECKHOUT CHRISTIAN , PREUSCHOFF ULF
IPC: A61K31/00 , A61K31/70 , A61K31/7042 , A61K31/7048 , A61P1/00 , A61P1/06 , A61P1/14 , A61P43/00 , C07H17/08
Abstract: (2R,3S,4S,5R,6R,10R,11R)-2,4,6,8,10-Pentamethyl-11-acetyl-12,13- dioxabicyclo(8.2.1)tridec-8-en-1-one compounds are new. (2R,3S,4S,5R,6R,10R,11R)-2,4,6,8,10-pentamethyl-11-acetyl-12,13- dioxabicyclo(8.2.1)tridec-8-en-1-one compounds of formula (I) and their acid addition salts are new R1 = H or Me; R2 = H or lower alkanoyl.
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公开(公告)号:NO990675L
公开(公告)日:1999-08-16
申请号:NO990675
申请日:1999-02-12
Applicant: SOLVAY PHARM GMBH
Inventor: JASSERAND DANIEL , PREUSCHOFF ULF , EECKHOUT CHRISTIAN
IPC: A61K31/00 , A61K31/70 , A61K31/7042 , A61K31/7048 , A61P1/00 , A61P1/06 , A61P1/14 , A61P43/00 , C07H17/08
Abstract: (2R,3S,4S,5R,6R,10R,11R)-2,4,6,8,10-Pentamethyl-11-acetyl-12,13- dioxabicyclo(8.2.1)tridec-8-en-1-one compounds are new. (2R,3S,4S,5R,6R,10R,11R)-2,4,6,8,10-pentamethyl-11-acetyl-12,13- dioxabicyclo(8.2.1)tridec-8-en-1-one compounds of formula (I) and their acid addition salts are new R1 = H or Me; R2 = H or lower alkanoyl.
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公开(公告)号:CZ310697A3
公开(公告)日:1998-06-17
申请号:CZ310697
申请日:1997-10-01
Applicant: SOLVAY PHARM GMBH
Inventor: HOLTJE DAGMAR , PREUSCHOFF ULF , EECKHOUT CHRISTIAN , FINNER EMIL
IPC: A61K31/70 , A61K31/7042 , A61K31/7048 , A61P1/00 , A61P1/06 , A61P43/00 , C07H17/08 , A61K31/365
Abstract: Ä(1'R),2R,3S,4S,5R,6R,9R,11R,12R,14RÜ-11-(1'-hydroxypropyl)-2,4,6,8,11 ,14-hexamethyl-10,13,15-trioxatricycloÄ9.2.1.1 Ü pentadecan-1-one derivatives of formula (I) and their salts are new: R = H or Me.
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公开(公告)号:CA2219311A1
公开(公告)日:1998-04-24
申请号:CA2219311
申请日:1997-10-24
Applicant: SOLVAY PHARM GMBH
Inventor: PREUSCHOFF ULF , EECKHOUT CHRISTIAN , FINNER EMIL , HOELTJE DAGMAR
IPC: A61K31/70 , A61K31/7042 , A61K31/7048 , A61P1/00 , A61P1/06 , A61P43/00 , C07H17/08
Abstract: Ring-contracted N-demethyl-N-isopropyl-erythromycin-A-spiroacetal compounds corresponding to formula I I having gastrointestinally effective motilin-agonistic properties and the preparation thereof.
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公开(公告)号:AT155478T
公开(公告)日:1997-08-15
申请号:AT92122011
申请日:1992-12-24
Applicant: SOLVAY PHARM GMBH
Inventor: HOELTJE DAGMAR , PREUSCHOFF ULF , EECKHOUT CHRISTIAN
IPC: A61K31/70 , A61K31/7042 , A61K31/7048 , A61P1/14 , A61P43/00 , C07H17/08
Abstract: Ring-contracted N-demethyl-N-isopropylerythromycin A derivatives with gastrointestinally effective motilin-agonistic properties and the preparation thereof are described.
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公开(公告)号:UA84896C2
公开(公告)日:2008-12-10
申请号:UAA200607374
申请日:2004-12-09
Applicant: SOLVAY PHARM GMBH
Inventor: MENTZEL MATTHIAS , REICHE DANIA B , BRUCKNER REINHARD , DAVID SAMUEL , VAN STEEN BARTHOLOMEUS J , SCHON UWE , JASSERAND DANIEL , PREUSCHOFF ULF
IPC: C07D471/00 , A61K31/438 , A61K31/4747 , A61P9/06 , A61P9/12 , A61P29/00 , C07D221/00 , C07D233/00 , C07D471/10 , C07D487/08
Abstract: Изобретениекасаетсягруппыпроизводныхгидронопола, которыеявляютсяагонистамичеловеческихрецепторов ORL1 (ноцицептина).Изобретениетакжекасаетсяспособовполученияэтихсоединений, фармацевтическихкомпозиций, которыесодержатфармакологическиактивноеколичество, покрайнеймере, одногоизэтихновыхпроизводныхгидронополакакдействующеговещества, атакжепримененияэтихфармацевтическихкомпозицийдлялечениярасстройств, связанныхс рецепторами ORL1.Изобретениекасаетсясоединенийобщейформулы (1),гдерадикалыимеютзначения, которыеприведеныв описании.
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公开(公告)号:NO324867B1
公开(公告)日:2007-12-17
申请号:NO20024351
申请日:2002-09-12
Applicant: SOLVAY PHARM GMBH
Inventor: DAVID SAMUEL , BRUECKNER REINHARD , ANTEL JOCHEN , JASSERAND DANIEL , PREUSCHOFF ULF , SANN HOLGER , REICHE DANIA , EECKHOUT CHRISTIAN
IPC: C07D295/12 , A61K31/341 , A61K31/381 , A61K31/496 , A61P1/00 , A61P29/00 , A61P43/00 , C07D209/08 , C07D295/08 , C07D295/084 , C07D295/092 , C07D307/52 , C07D333/20 , C07D407/04 , C07D407/06 , C07D409/06
Abstract: 1-(1-(Hetero)aryl)-1-(polyhydroxyalkyl)-methyl)-4-(4-(N-methylbenzamid o)-3-phenylbutyl)-piperazine derivatives (I) are new. Also new are 1-unsubstituted analog intermediates (II). 1-(1-(Hetero)aryl)-1-(polyhydroxyalkyl)-methyl)-4-(4-(N-methylbenzamid o)-3-phenylbutyl)-piperazine derivatives of formula (I) and their acid addition salts are new. A = naphthyl, phenyl (optionally substituted by OH), mono- or bi-cyclic heteroaryl or 3-6C alkenyl (optionally substituted by phenyl); Q = (CHOR1)k-(CHOR2)l-(CHOR3)m-(CHOR4)n-CH2OR5 ; R1-R5 = H or lower alkanoyl, or two of R1-R5 = CO, CS or CH2 (optionally substituted by lower alkyl or 4-5C alkylene), completing a 5- or 6-membered ring; k, l, m, n = 0 or 1, and R6, R7 = H or halo. Independent claims are also included for: (1) the preparation of (I), and (2) new piperazine derivative intermediates of formula (II).
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公开(公告)号:CA2219311C
公开(公告)日:2007-09-04
申请号:CA2219311
申请日:1997-10-24
Applicant: SOLVAY PHARM GMBH
Inventor: EECKHOUT CHRISTIAN , FINNER EMIL , HOELTJE DAGMAR , PREUSCHOFF ULF
IPC: C07H17/08 , A61K31/70 , A61K31/7042 , A61K31/7048 , A61P1/00 , A61P1/06 , A61P43/00
Abstract: Ring-contracted N-demethyl-N-isopropyl-erythromycin-A- spiroacetal compounds corresponding to formula I having gastrointestinally effective motilin-agonistic properties and the preparation thereof.
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