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公开(公告)号:CZ9701547A3
公开(公告)日:1997-12-17
申请号:CZ154797
申请日:1997-05-20
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , HEITSCH HOLGER DR , NOLKEN GERHARD DR , WIRTH KLAUS DR , SCHOLKENS BERNWARD PROF DR
IPC: C07D277/60 , A61K31/38 , A61K31/395 , A61K31/41 , A61K31/425 , A61K31/428 , A61K31/53 , A61P43/00 , C07D253/10 , C07D277/64 , C07D277/66 , C07D277/68 , C07D277/70 , C07D277/74 , C07D277/82 , C07D417/12
CPC classification number: C07D417/12 , C07D277/64
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公开(公告)号:CZ81097A3
公开(公告)日:1997-10-15
申请号:CZ81097
申请日:1997-03-17
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , HEITSCH HOLGER DR , NOLKEN GERHARD DR , WIRTH KLAUS DR , SCHOLKENS BERNWARD PROF DR
IPC: C07D237/28 , A61K31/345 , A61K31/47 , A61K31/495 , A61K31/53 , A61P43/00 , C07D215/04 , C07D215/26 , C07D239/72 , C07D239/74 , C07D241/36 , C07D241/44 , C07D253/04 , C07D253/065 , C07D257/10
Abstract: Fluoroalkyl- and fluoroalkoxy-substituted benzyloxy-azaheterocyclic compounds of formula (I) and their salts are new: X1-X3 = N or CR ; R , R = H or halo; R , R = H, halo, 1-5C alkyl or 2-5C alkenyl; R = 2-5C alkenediyl, halo, OR , SR , NHR , -COOR or COOH; 1-6C alkyl, 6-12C aryl or 6-12C aryl-1-3C alkyl (all optionally substituted by e.g. OR , SR , NO2, CN, NHR or halo); R , R = H, 1-5C alkyl, 3-5C alkenyl or 6-12C aryl-1-3C alkyl; R = 1-5C alkyl or 1-5C alkoxy (both substituted by 1 or more F or Cl); B = amino acid; D = 2-5C alkanediyl, 1-5C alkanediyl or -(CH2)n-Yp-(CH2)m-; E = O or S; Y = O, S or NR ; n, m = 0-3; o = 1-3; and p = 0 or 1.
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公开(公告)号:ID16274A
公开(公告)日:1997-09-18
申请号:ID970863
申请日:1997-03-17
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , HEITSCH HOLGER DR , NOLKEN GERHARD DR , WIRTH KLAUS DR , SCHOLKENS BERNWARD PROF DR
IPC: C07D237/28 , A61K31/345 , A61K31/47 , A61K31/495 , A61K31/53 , A61P43/00 , C07D215/04 , C07D215/26 , C07D239/72 , C07D239/74 , C07D241/36 , C07D241/44 , C07D253/04 , C07D253/065 , C07D257/10 , C07D257/00
Abstract: Fluoroalkyl- and fluoroalkoxy-substituted benzyloxy-azaheterocyclic compounds of formula (I) and their salts are new: X1-X3 = N or CR ; R , R = H or halo; R , R = H, halo, 1-5C alkyl or 2-5C alkenyl; R = 2-5C alkenediyl, halo, OR , SR , NHR , -COOR or COOH; 1-6C alkyl, 6-12C aryl or 6-12C aryl-1-3C alkyl (all optionally substituted by e.g. OR , SR , NO2, CN, NHR or halo); R , R = H, 1-5C alkyl, 3-5C alkenyl or 6-12C aryl-1-3C alkyl; R = 1-5C alkyl or 1-5C alkoxy (both substituted by 1 or more F or Cl); B = amino acid; D = 2-5C alkanediyl, 1-5C alkanediyl or -(CH2)n-Yp-(CH2)m-; E = O or S; Y = O, S or NR ; n, m = 0-3; o = 1-3; and p = 0 or 1.
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公开(公告)号:CZ281983B6
公开(公告)日:1997-04-16
申请号:CS381192
申请日:1992-12-21
Applicant: HOECHST AG
Inventor: HEITSCH HOLGER DR , HENNING RAINER DR , WAGNER ADALBERT DR , GERHARDS HERMANN DR , BECKER REINHARD DR , SCHOLKENS BERNWARD PROF DR
IPC: A61K31/415 , A61K31/4164 , A61K31/64 , A61P9/10 , A61P9/12 , C07D233/84 , C07D233/86 , C07D233/90
Abstract: Compounds of the formula (I) in which R is, for example, ethyl, R is, for example, methyl, n is, for example, zero, R is, for example, COOH and R is, for example, SO2NHCONHCH3 are highly active antagonists of angiotensin II receptors.
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公开(公告)号:ES2092737T3
公开(公告)日:1996-12-01
申请号:ES93116788
申请日:1993-10-18
Applicant: HOECHST AG
IPC: C07B39/00 , C07C17/14 , C07C22/04 , C07C67/307 , C07C67/343 , C07C69/65 , C07C69/76 , C07C205/12 , C07C255/50 , C07C257/12 , C07C257/20 , C07C311/05 , C07C311/18 , C07C311/53 , C07D275/04 , C07D275/06 , C07D333/24 , C07D333/60 , C07D333/68 , C07D333/70 , C07D471/04 , C07D487/04 , C07D495/04
Abstract: Aromatic bromomethyl compounds play an important role in the synthesis of active substances. They can be obtained in particularly high purity by free-radical bromination of aromatic methyl compounds in the solvent chlorobenzene.
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公开(公告)号:DE59004292D1
公开(公告)日:1994-03-03
申请号:DE59004292
申请日:1990-07-18
Applicant: HOECHST AG
Inventor: KLEEMANN HEINZ-WERNER DR , URBACH HANSJOERG DR , WAGNER ADALBERT DR , RUPPERT DIETER DR , LINZ WOLFGANG DR , KRAMER WERNER DR DR
IPC: C12N9/99 , A61K31/38 , A61K31/381 , A61K31/415 , A61K31/445 , A61K31/535 , A61K38/55 , A61P9/12 , C07C237/08 , C07C237/22 , C07D211/26 , C07D211/58 , C07D233/54 , C07D233/64 , C07D295/20 , C07D333/24 , C07D401/12 , C07D403/12 , C07D409/12 , C07D521/00 , C07K1/113 , C07K5/06 , C07K5/065 , C07K5/078 , C07K14/81 , A61K37/64
Abstract: The present invention relates to compounds of the formula I in which A, R , R , R and n are defined as indicated in the description, to processes for the preparation thereof, to the use thereof as medicines and to pharmaceutical compositions containing these.
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公开(公告)号:CS354591A3
公开(公告)日:1992-06-17
申请号:CS354591
申请日:1991-11-22
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , HENNING RAINER DR , NICKEL WOLF-ULRICH DR
IPC: A61K31/41 , A61K31/425 , A61P9/12 , A61P43/00 , C07D263/06 , C07D417/04 , C07D417/06 , C12N9/99 , C07D263/04 , A61K31/42
Abstract: The invention relates to compounds of the formula in which W represents -CO-, -O-CO-, -SO2- or -NH-CO-, R , R , R , R , R and R represent hydrogen or an organic radical and R denotes alkyl, cycloalkyl or cycloalkylalkyl, processes for their preparation, intermediates and their use in the preparation of inhibitors of renin and HIV protease.
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公开(公告)号:DE4037437A1
公开(公告)日:1992-05-27
申请号:DE4037437
申请日:1990-11-24
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , HENNING RAINER DR , NICKEL WOLF-ULRICH DR
IPC: A61K31/41 , A61K31/425 , A61P9/12 , A61P43/00 , C07D263/06 , C07D417/04 , C07D417/06 , C12N9/99
Abstract: The invention relates to compounds of the formula in which W represents -CO-, -O-CO-, -SO2- or -NH-CO-, R , R , R , R , R and R represent hydrogen or an organic radical and R denotes alkyl, cycloalkyl or cycloalkylalkyl, processes for their preparation, intermediates and their use in the preparation of inhibitors of renin and HIV protease.
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公开(公告)号:CS198090A2
公开(公告)日:1991-08-13
申请号:CS198090
申请日:1990-04-20
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , URBACH HANSJORG DR , RUPPERT DIETER DR , LINZ WOLFGANG DR , SCHOLKENS BERNWARD PROF DR
IPC: A61K38/55 , A61K38/00 , A61P9/00 , A61P9/12 , C07K1/06 , C07K1/113 , C07K5/02 , C07K5/06 , C07K5/065 , C07K14/81 , C07K5/08
Abstract: The present invention relates to compounds of the formula I in which A and B are, independently of one another, an amino acid, and R , R , R and R are as defined in the description, to processes for the preparation thereof, to their use as medicines and to pharmaceutical agents containing them.
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公开(公告)号:SI0796848T1
公开(公告)日:2003-12-31
申请号:SI9730572
申请日:1997-03-05
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , HEITSCH HOLGER DR , NOELKNE GERHARD DR , WIRTH KLAUS DR , BERNARD PROF-DR
IPC: C07D237/28 , A61K31/345 , A61K31/47 , A61K31/495 , A61K31/53 , A61P43/00 , C07D215/04 , C07D215/26 , C07D239/72 , C07D239/74 , C07D241/36 , C07D241/44 , C07D253/04 , C07D253/065 , C07D257/10
Abstract: Fluoroalkyl- and fluoroalkoxy-substituted benzyloxy-azaheterocyclic compounds of formula (I) and their salts are new: X1-X3 = N or CR ; R , R = H or halo; R , R = H, halo, 1-5C alkyl or 2-5C alkenyl; R = 2-5C alkenediyl, halo, OR , SR , NHR , -COOR or COOH; 1-6C alkyl, 6-12C aryl or 6-12C aryl-1-3C alkyl (all optionally substituted by e.g. OR , SR , NO2, CN, NHR or halo); R , R = H, 1-5C alkyl, 3-5C alkenyl or 6-12C aryl-1-3C alkyl; R = 1-5C alkyl or 1-5C alkoxy (both substituted by 1 or more F or Cl); B = amino acid; D = 2-5C alkanediyl, 1-5C alkanediyl or -(CH2)n-Yp-(CH2)m-; E = O or S; Y = O, S or NR ; n, m = 0-3; o = 1-3; and p = 0 or 1.
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