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公开(公告)号:HU226108B1
公开(公告)日:2008-04-28
申请号:HU9701984
申请日:1997-11-12
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN DR , GERLACH UWE DR , GOEGELEIN HEINZ DR , KLAUS ERIK DR , LINZ WOLFGANG DR , MANIA DIETER DR
IPC: C07D311/04 , C07D311/58 , A61K31/35 , A61K31/352 , A61K31/353 , A61K31/355 , A61K31/40 , A61K31/4025 , A61P9/00 , A61P9/06 , C07D207/26 , C07D209/34 , C07D211/76 , C07D217/24 , C07D227/02 , C07D311/16 , C07D311/18 , C07D311/42 , C07D311/70 , C07D405/12
Abstract: 3-Amido-chromanylsulphonyl-urea or -thiourea derivatives of formula (I), in all stereoisomer (or mixture) forms, and their salts are new. R1 = H, alkyl, alkoxy, alkoxyalkoxy, alkylthio, F, Cl, Br, I or CF3; R2 = H, Me or Et; R3 = H or alkyl; Z = O or S; A = phenyl (optionally substituted by 1-3 halo, Me, Et, OMe or OEt), lactam residue of formula (i), 1-oxo-1,2,3,4-tetrahydroisoquinolin-2-yl, 1-oxo-perhydroisoquinolin-2-yl, 1-oxo-2,3-isoindolin-2-yl or 1-oxo-perhydroisoindolin-2-yl; B = 3-6C alkylene or 3-6C alkenylene (both optionally substituted by 1-3 alkyl); all alkyl moieties have 1-4C.
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公开(公告)号:DE19546736A1
公开(公告)日:1997-06-19
申请号:DE19546736
申请日:1995-12-14
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN DR , GERLACH UWE DR , MANIA DIETER DR , LINZ WOLFGANG DR , GOEGELEIN HEINZ DR , KLAUS ERIK DR , CRAUSE PETER DR
IPC: C07D311/58 , A61K31/35 , A61K31/352 , A61K31/353 , A61K31/40 , A61K31/4015 , A61K31/4025 , A61K31/4412 , A61K31/443 , A61K31/445 , A61P9/00 , A61P9/06 , A61P9/10 , C07D311/64 , C07D311/70 , C07D405/12 , C07D311/60 , C07D227/087 , A61K31/44
Abstract: N-(4-Amidoalkyl-chroman-5-yl-sulphonyl)-urea or -thiourea derivatives of formula (I) and their salts are new. R1 = H, alkyl, alkoxy, F, Cl, Br, I, CF3, NH2, mono- or dialkylamino or alkylthio; R2a = H, Me or Et; R2b, R2d = H, Me or Et; or phenyl or benzyl (both optionally ring-substituted by 1-3 of halogen, Me, Et, OMe and OEt); R2c,R2e = H, Me or Et; R3 = H, alkyl, cycloalkyl, cycloalkylmethyl or CF3; n = 1 or 2; Z = O or S; A = phenyl (optionally substituted by 1-3 of halogen, Me, OMe, Et or OEt), a lactam residue of formula (a), 1-oxo-1,2,3,4-tetrahydroisoquinolin-2-yl, 1-oxo-per-hydro-isoquinolin-2-yl, 1-oxo-1,2-dihydro-iso-indol-2-yl or 1-oxo-per-hydro-iso-indol-2-yl; B = 3-6C alkylene or 3-6C alkenylene (both optionally substituted by 1-3 alkyl); unless specified otherwise alkyl moieties have 1-4C and cycloalkyl moieties 3-6C.
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公开(公告)号:AT122659T
公开(公告)日:1995-06-15
申请号:AT93102220
申请日:1993-02-12
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH DR , MANIA DIETER DR , WETTLAUFER DAVID DR , KLAUS ERIK DR
IPC: A61K31/44 , A61K31/4402 , A61K31/4406 , A61K31/4409 , A61K31/4418 , A61K31/4425 , A61P9/00 , A61P21/00 , C07D213/64 , C07D213/79 , C07D213/80 , C07D213/81 , C07D213/89 , C07D401/12 , A61K31/455 , C07D213/82 , A61K31/495 , A61K31/47
Abstract: Arylcarbonylaminoalkyl-dihydro-oxo-pyridines of Formula I are disclosed wherein aryl is an aromatic or heteroaromatic system, n is zero through 5; R and R(1), are hydrogen, or loweralkyl; W is hydrogen, (hetero)-(aryl)-loweralkyl; Z is hydrogen, CH2OR(2), CHO, (CO)OR(2), (CO)NR(2)2. Processes for the preparation of compound I are also disclosed. Compounds I are suitable for the treatment of disorders of the cardiovascular system, for example of hypertension, of cardiac insufficiency or of disturbances of blood flow in the coronary systems such as, for example, angina. Disturbances of cerebral and peripheral blood flow are likewise influenced beneficially. Furthermore, compounds I are able to influence smooth-muscle organs such as uterus, bronchi, intestines and biliary system, the urinary tract (ureter, bladder and urethra) in the sense of spasmolysis. They are therefore also suitable for the treatment of diseases associated with spasms of these organs, for example for the treatment of premature labor in pregnancy, of ureteral or biliary colic, of obstructive airway diseases such as asthma, of disturbances of intestinal motility such as, for example, of irritable colon or of bladder incontinence. Additionally, compounds of formula I can serve as anti-convulsants in the treatment of epilepsy and as hair growth inducers in the treatment of baldness.
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公开(公告)号:DE3881714D1
公开(公告)日:1993-07-22
申请号:DE3881714
申请日:1988-01-30
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN DR , LANG HANS-JOCHEN DR , MANIA DIETER DR , SCHOELKENS BERNWARD DR , KLAUS ERIK DR
IPC: A61K31/40 , A61K31/41 , A61K31/535 , A61K31/54 , C07D405/04 , C07D413/04 , C07D417/04
Abstract: 4-Heterocyclyl-3-hydroxy-benzopyran derivs. of formula (I) in which the C3 and C4 substits. are trans to each other are new; where R1 = CN, NO2; 1-6C alkyl-5(O)n or Ar5(O)n; n = 1 or 2; Ar = aromatic or heterocyclic system opt. substd. by 1-3 of 1-2C alkyl or alkoxy, halo, CF3, CN, NO2, 1-2C alkylcarbonyl or 1-2C alkyl-S (O)p; p = 1 or 2; R2 = H, OH, 1-2C alkyl or alkoxy, halo or NR5R6; R5 and R6 = H, 1-2C alkyl or 102C alkylcarbonyl; R3 and R4 = 1 -4C alkyl; the meanings for R1 and R2 may also be interchanged; X = (CH2)m substs. by at least 1 and a max. of (2m-1) 1-2C alkyl, and opt. interrupted by O, NR, or 5; R7 = H or 1-4C alkyl; m = 2-4.
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公开(公告)号:MY115229A
公开(公告)日:2003-04-30
申请号:MYPI9605219
申请日:1996-12-12
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN DR , GERLACH UWE DR , MANIA DIETER DR , LINZ WOLFGANG DR , GOGELEIN HEINZ DR , KLAUS ERIK DR , CRAUSE PETER DR
IPC: C07D311/58 , A61K31/35 , A61K31/352 , A61K31/353 , A61K31/40 , A61K31/4015 , A61K31/4025 , A61K31/4412 , A61K31/443 , A61K31/445 , A61P9/00 , A61P9/06 , A61P9/10 , C07D311/64 , C07D311/70 , C07D405/12
Abstract: CHROMANYSULFONYL(THIO)UREAS OF THE FORMULA I ARE USEFUL PHARMACEUTICALS FOR THE TREATMENT OF CARDIAC ARRHYTHMIAS AND FOR THE PREVENTION OF SUDDEN HEART DEATH DUE TO ARRHYTHMIA. THEY CAN BE USED AS ANTIARRHYTHMICS AND ARE SUITABLE FOR THE PREVENTION OF SUDDEN HEART DEATH, FOR THE TREATMENT OF CARDIAC INSUFFICIENCY AND ALSO HEART FAILURE AS A RESULT OF THE EFFECTS OF SHOCK.
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公开(公告)号:DE58908228D1
公开(公告)日:1994-09-29
申请号:DE58908228
申请日:1989-07-14
Applicant: HOECHST AG
IPC: C07D311/22 , A61K31/40 , A61K31/415 , A61K31/42 , A61K31/425 , A61K31/44 , A61K31/443 , A61K31/4433 , A61K31/445 , A61K31/495 , A61K31/50 , A61K31/505 , A61K31/535 , A61K31/54 , A61P11/00 , A61P11/08 , A61P13/02 , A61P15/00 , C07D405/04 , C07D409/12 , C07D413/04 , C07D417/04
Abstract: The use of 3,4-dihydro-2H-benzo[b]pyrans of the formula I in which R is H, OH, (C1-C2)-alkoxy, (C1-C2)-alkyl or NR R , where R and R are identical or different and are H, (C1-C2)-alkyl or (C1-C3)-alkylcarbonyl, R and R are identical or different and are alkyl with 1-4 C atoms, Ar is an aromatic or heteroaromatic system which is unsubstituted or substituted by 1 to 3 identical or different radicals (C1-C2)-alkyl, (C1-C2)-alkoxy, halogen, trifluoromethyl, CN, NO2, CO-(C1-C2)-alkyl or SOm-(C1-C2)-alkyl with m = 1 or 2, n is 1 or 2, X is a chain (CH2)r which can be interrupted by a heteroatom O, S or NR where R is H or (C1-C4)-alkyl and r is the numbers 2, 3, 4 or 5, for the production of a medicament for urinary tract disorders.
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公开(公告)号:GR3033300T3
公开(公告)日:2000-09-29
申请号:GR20000400982
申请日:2000-04-21
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN DR , GERLACH UWE DR , MANIA DIETER DR , LINZ WOLFGANG DR , GOEGELEIN HEINZ DR , KLAUS ERIK DR , CRAUSE PETER DR
IPC: C07D311/58 , A61K31/35 , A61K31/352 , A61K31/353 , A61K31/40 , A61K31/4015 , A61K31/4025 , A61K31/4412 , A61K31/443 , A61K31/445 , A61P9/00 , A61P9/06 , A61P9/10 , C07D311/64 , C07D311/70 , C07D405/12
Abstract: N-(4-Amidoalkyl-chroman-5-yl-sulphonyl)-urea or -thiourea derivatives of formula (I) and their salts are new. R1 = H, alkyl, alkoxy, F, Cl, Br, I, CF3, NH2, mono- or dialkylamino or alkylthio; R2a = H, Me or Et; R2b, R2d = H, Me or Et; or phenyl or benzyl (both optionally ring-substituted by 1-3 of halogen, Me, Et, OMe and OEt); R2c,R2e = H, Me or Et; R3 = H, alkyl, cycloalkyl, cycloalkylmethyl or CF3; n = 1 or 2; Z = O or S; A = phenyl (optionally substituted by 1-3 of halogen, Me, OMe, Et or OEt), a lactam residue of formula (a), 1-oxo-1,2,3,4-tetrahydroisoquinolin-2-yl, 1-oxo-per-hydro-isoquinolin-2-yl, 1-oxo-1,2-dihydro-iso-indol-2-yl or 1-oxo-per-hydro-iso-indol-2-yl; B = 3-6C alkylene or 3-6C alkenylene (both optionally substituted by 1-3 alkyl); unless specified otherwise alkyl moieties have 1-4C and cycloalkyl moieties 3-6C.
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公开(公告)号:ES2146348T3
公开(公告)日:2000-08-01
申请号:ES96119262
申请日:1996-12-02
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN DR , GERLACH UWE DR , MANIA DIETER DR , LINZ WOLFGANG DR , GOGELEIN HEINZ DR , KLAUS ERIK DR
IPC: C07D311/58 , A61K31/35 , A61K31/352 , A61K31/353 , A61K31/40 , A61K31/4015 , A61K31/4025 , A61K31/4412 , A61K31/443 , A61K31/445 , A61P9/00 , A61P9/06 , A61P9/10 , C07D311/64 , C07D311/70 , C07D405/12
Abstract: N-(4-Amidoalkyl-chroman-5-yl-sulphonyl)-urea or -thiourea derivatives of formula (I) and their salts are new. R1 = H, alkyl, alkoxy, F, Cl, Br, I, CF3, NH2, mono- or dialkylamino or alkylthio; R2a = H, Me or Et; R2b, R2d = H, Me or Et; or phenyl or benzyl (both optionally ring-substituted by 1-3 of halogen, Me, Et, OMe and OEt); R2c,R2e = H, Me or Et; R3 = H, alkyl, cycloalkyl, cycloalkylmethyl or CF3; n = 1 or 2; Z = O or S; A = phenyl (optionally substituted by 1-3 of halogen, Me, OMe, Et or OEt), a lactam residue of formula (a), 1-oxo-1,2,3,4-tetrahydroisoquinolin-2-yl, 1-oxo-per-hydro-isoquinolin-2-yl, 1-oxo-1,2-dihydro-iso-indol-2-yl or 1-oxo-per-hydro-iso-indol-2-yl; B = 3-6C alkylene or 3-6C alkenylene (both optionally substituted by 1-3 alkyl); unless specified otherwise alkyl moieties have 1-4C and cycloalkyl moieties 3-6C.
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公开(公告)号:DK0779288T3
公开(公告)日:2000-07-31
申请号:DK96119262
申请日:1996-12-02
Applicant: HOECHST AG
Inventor: CRAUSE PETER DR , ENGLERT HEINRICH CHRISTIAN DR , GERLACH UWE DR , MANIA DIETER DR , LINZ WOLFGANG DR , GOEGELEIN HEINZ DR , KLAUS ERIK DR
IPC: C07D311/58 , A61K31/35 , A61K31/352 , A61K31/353 , A61K31/40 , A61K31/4015 , A61K31/4025 , A61K31/4412 , A61K31/443 , A61K31/445 , A61P9/00 , A61P9/06 , A61P9/10 , C07D311/64 , C07D311/70 , C07D405/12
Abstract: N-(4-Amidoalkyl-chroman-5-yl-sulphonyl)-urea or -thiourea derivatives of formula (I) and their salts are new. R1 = H, alkyl, alkoxy, F, Cl, Br, I, CF3, NH2, mono- or dialkylamino or alkylthio; R2a = H, Me or Et; R2b, R2d = H, Me or Et; or phenyl or benzyl (both optionally ring-substituted by 1-3 of halogen, Me, Et, OMe and OEt); R2c,R2e = H, Me or Et; R3 = H, alkyl, cycloalkyl, cycloalkylmethyl or CF3; n = 1 or 2; Z = O or S; A = phenyl (optionally substituted by 1-3 of halogen, Me, OMe, Et or OEt), a lactam residue of formula (a), 1-oxo-1,2,3,4-tetrahydroisoquinolin-2-yl, 1-oxo-per-hydro-isoquinolin-2-yl, 1-oxo-1,2-dihydro-iso-indol-2-yl or 1-oxo-per-hydro-iso-indol-2-yl; B = 3-6C alkylene or 3-6C alkenylene (both optionally substituted by 1-3 alkyl); unless specified otherwise alkyl moieties have 1-4C and cycloalkyl moieties 3-6C.
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公开(公告)号:CZ9703588A3
公开(公告)日:1998-06-17
申请号:CZ358897
申请日:1997-11-12
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN DR , GERLACH UWE DR , MANIA DIETER DR , LINZ WOLFGANG DR , GOEGELEIN HEINZ PROF DR , KLAUS ERIK DR
IPC: C07D311/04 , A61K31/35 , A61K31/352 , A61K31/353 , A61K31/355 , A61K31/40 , A61K31/4025 , A61P9/00 , A61P9/06 , C07D207/26 , C07D209/34 , C07D211/76 , C07D217/24 , C07D227/02 , C07D311/16 , C07D311/18 , C07D311/42 , C07D311/58 , C07D311/70 , C07D405/12 , C07D311/74 , A61K31/47 , C07D203/08 , C07D209/32 , C07D217/16
CPC classification number: C07D405/12 , C07D311/58 , C07D311/70
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