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公开(公告)号:AT53992T
公开(公告)日:1990-07-15
申请号:AT84111056
申请日:1982-11-02
Applicant: HOECHST AG
Inventor: TEETZ VOLKER DR , GEIGER ROLF PROF DR , URBACH HANSJOERG DR , BECKER REINHARD DR , SCHOELKENS BERNWARD DR
IPC: A61K31/40 , C07C229/28 , C07C229/36 , C07D209/52
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公开(公告)号:AT47838T
公开(公告)日:1989-11-15
申请号:AT85103730
申请日:1982-12-24
Applicant: HOECHST AG
Inventor: URBACH HANSJOERG DR , HENNING RAINER DR , TEETZ VOLKER DR , GEIGER ROLF PROF DR , BECKER REINHARD DR , GAUL HOLGER
IPC: A61K31/40 , C07D209/42 , C07D209/52
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公开(公告)号:DE3803225A1
公开(公告)日:1989-08-17
申请号:DE3803225
申请日:1988-02-04
Applicant: HOECHST AG
Inventor: RUEGER WOLFGANG DR , URBACH HANSJOERG DR , BECKER REINHARD DR , HOCK FRANZ DR
IPC: C07D209/02 , A61K31/55 , A61K38/00 , A61K38/55 , A61P9/12 , A61P25/28 , C07C237/02 , C07D207/08 , C07D207/16 , C07D209/42 , C07D209/54 , C07D209/56 , C07D487/04 , C07K5/02
Abstract: The invention relates to amides of the formula in which R is NR R and the other radicals have the meaning stated in the description, to processes for the preparation thereof, to intermediates in the preparation thereof, to agents containing them and the use thereof as pharmaceuticals with a psychotropic action. The invention furthermore relates to the use of known amides as pharmaceuticals with a psychotropic action.
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公开(公告)号:AT30151T
公开(公告)日:1987-10-15
申请号:AT83112506
申请日:1983-12-13
Applicant: HOECHST AG
Inventor: URBACH HANSJOERG DR , HENNING RAINER DR , TEETZ VOLKER DR , BECKER REINHARD DR
IPC: A61K31/40 , A61K31/403 , A61K38/00 , A61P9/12 , A61P43/00 , C07D209/52 , C07K1/113 , C07K5/02 , C07K5/06 , C07K14/81
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公开(公告)号:DE3532036A1
公开(公告)日:1987-03-26
申请号:DE3532036
申请日:1985-09-09
Applicant: HOECHST AG
Inventor: BECKER REINHARD DR , GEIGER ROLF PROF DR , HENNING RAINER DR , TEETZ VOLKER DR , URBACH HANSJOERG DR
IPC: A61K45/06 , A61K31/40 , A61K31/635 , A61K38/00 , A61K38/55 , A61P7/10 , A61P9/12 , A61P43/00 , A61K31/19 , A61K31/34
Abstract: The preparation contains an angiotensin converting enzyme inhibitor and a loop diuretic.
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公开(公告)号:DE3532035A1
公开(公告)日:1987-03-26
申请号:DE3532035
申请日:1985-09-09
Applicant: HOECHST AG
Inventor: URBACH HANSJOERG DR , HENNING RAINER DR , BECKER REINHARD DR
IPC: C07K5/08 , A61K38/00 , A61K38/55 , A61P9/12 , A61P43/00 , C07K1/113 , C07K5/02 , C07K14/81 , A61K37/02
Abstract: The N-alkylated tripeptides have the formula I in which A is the residue of an amino acid, R together with R and the atoms carrying them form a heterocyclic ring system, n is 1 or 2, and R, R , R and R are hydrogen or a defined radical.
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公开(公告)号:DE3275293D1
公开(公告)日:1987-03-05
申请号:DE3275293
申请日:1982-12-24
Applicant: HOECHST AG
Inventor: URBACH HANSJORG DR , HENNING RAINER DR , TEETZ VOLKER DR , GEIGER ROLF PROF DR , BECKER REINHARD DR , GAUL HOLGER
IPC: A61K38/55 , A61K31/40 , A61K31/403 , A61K31/404 , A61K38/00 , A61P7/10 , A61P9/08 , A61P9/12 , C07D209/02 , C07D209/08 , C07D209/32 , C07D209/34 , C07D209/42 , C07D209/52 , C07D215/22 , C07D215/227 , C07K1/02 , C07K1/113 , C07K5/02 , C07K5/06
Abstract: 1. Claims for the Contracting states ; BE, CH, DE, FR, GB, IT, Li, Lu, NL, SE A compound of the formula I see diagramm : EP0084164,P21,F7 in which the hydrogen atoms on the bridgehead C atoms 3a and (6+n)a have the trans configuration relative to one another and wherein n denotes 0, 1 or 2, R1 denotes methyl, R2 denotes hydrogen, (C1 -C4 )-alkyl or benzyl, Y denotes hydrogen or hydroxyl, Z denotes hydrogen or Y and Z together denote oxygen and X denotes phenyl, and its physiologically acceptable salts. 1. Claims for the Contracting state : Austria A process for the preparation of the compounds of the formula I see diagramm : EP0084164,P24,F4 in which the hydrogen atoms on the bridgehead C atoms 3a and (6+n)a have the trans configuration relative to one another and wherein n denotes 0, 1 or 2, R1 denotes methyl, R2 denotes hydrogen, (C1 -C4 )-alkyl or benzyl, Y denotes hydrogen or hydroxyl, Z denotes hydrogen or Y and Z together denote oxygen and X denotes phenyl, and its physiologically acceptable salts, which a) comprises reacting a compound of the formula II see diagramm : EP0084164,P24,F6 wherein R1 , R2 , X, Y and Z have the meanings as in formula I, with a compound of the formula III see diagramm : EP0084164,P25,F1 in which the H atoms on the C atoms 3a and (6+n)a have the trans configuration relative to one another and wherein n denotes 0, 1 or 2 and W denotes a radical which can be cleaved off by hydrogenolysis or by acid, and subsequently splitting off the radical W and, if appropriate, the radical R2 to form the free carboxyl groups, or b) for the preparation of compounds of the formula I, in which Y and Z together denote oxygen, comprises b1 ) reacting a compound of the formula IV see diagramm : EP0084164,P25,F3 in which the H atoms on the C atoms 3a and (6+n)a have the trans configuration relative to one another and wherein n and R1 have the meanings as in formula I and W has the meaning as in formula III, with a compound of the formula V, R2 O2 C-CH = CH-CO-X wherein R2 and X have the meanings as in formula I, and subsequently splitting off the radical W and, if appropriate, also the radical R2 to form the free carboxyl groups, or, b2 ) reacting a compound of the formula IV mentioned under b1 ) with a compound of the general formula VI, wherein R2 has the meaning as in formula I, and with a compound of the general formula VII OHC-CO2 R2 X-CO-CH3 wherein X has the meaning as in formula I, subsequently splitting off the radical W and, if appropriate, the radical R2 to form the free carboxyl group, or c) for the preparation of compounds of the formula I, in which Y and Z each denote hydrogen, comprises c1 ) reacting a compound of the formula IV mentioned under b1 ) with a compound of the formula VIII see diagramm : EP0084164,P25,F2 wherein R2 and X have the meanings as in formula I, reducing the Schiff's bases obtained and subsequently splitting off the radical W and, if appropriate, the radical R2 to form the free carboxyl groups, or c2 ) catalytically reducing a compound of the formula I in which Y and Z together denote oxygen, with hydrogen, or d) for the preparation of compounds of the formula I, in which Y denotes hydroxyl and Z denotes hydrogen, comprises reducing a compound of the formula I, in which Y and Z together denote oxygen, catalytically with hydrogen or with a reducing agent, such as sodium borohydride, and, if appropriate, converting the compounds obtained according to (a)-(d) into their physiologically acceptable salts.
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公开(公告)号:AT25244T
公开(公告)日:1987-02-15
申请号:AT82112007
申请日:1982-12-24
Applicant: HOECHST AG
Inventor: URBACH HANSJOERG DR , HENNING RAINER DR , TEETZ VOLKER DR , GEIGER ROLF PROF DR , BECKER REINHARD DR , GAUL HOLGER
IPC: A61K38/00 , C07D209/08 , C07D209/34 , C07D209/42 , C07D209/52 , C07D215/22 , C07D215/227 , C07K5/02 , A61K31/40
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公开(公告)号:DE3426720A1
公开(公告)日:1986-01-23
申请号:DE3426720
申请日:1984-07-20
Applicant: HOECHST AG
Inventor: URBACH HANSJOERG DR , HENNING RAINER DR , BECKER REINHARD DR
IPC: A61K38/00 , C07D201/18 , C07D233/54 , C07D281/10 , C07K5/02 , A61K31/395 , A61K31/55 , C07D209/04 , C07D417/06
Abstract: The invention relates to compounds of the formula I in which m = 1 or 2 and n = 0, 1 or 2, R and R denote identical or different hydrogen, alkyl, alkoxy, halogen, hydroxyl, nitro, amino, alkylamino or acylamino radicals or R and R together represent methylenedioxy, R and R denote identical or different radicals of hydrogen, alkyl which can optionally be substituted, alkenyl, cycloalkyl, cycloalkenyl, cycloalkylalkyl, aryl, partially hydrogenated aryl or aralkyl which can be substituted, R and R denote identical or different radicals of hydrogen, alkyl or aralkyl which can be substituted, Y denotes hydrogen or hydroxyl, Z denotes hydrogen or Y and Z together denote oxygen and X represents alkyl, alkenyl, cycloalkyl, aryl which can be substituted or indolyl, a process for their preparation, compositions containing them and their use, and also intermediates in their preparation.
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公开(公告)号:DE3408923A1
公开(公告)日:1985-09-26
申请号:DE3408923
申请日:1984-03-12
Applicant: HOECHST AG
Inventor: HENNING RAINER DR , URBACH HANSJOERG DR , BECKER REINHARD DR , TEETZ VOLKER DR
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