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公开(公告)号:AT233747T
公开(公告)日:2003-03-15
申请号:AT99125083
申请日:1999-12-16
Applicant: BASF AG
Inventor: RIECHERS HARTMUT DR , SIMON JOACHIM DR , HENNE ANDREAS DR , HOEHN ARTHUR DR
IPC: C07D295/08 , B01J23/72 , C07D295/088
Abstract: 2,2'-Dimorpholinodiethyl ether is produced by reacting diethylene glycol with ammonia under pressure at elevated temperature in the presence of hydrogen. The active hydrogenation catalyst, before reduction with hydrogen, contains 20-85 wt.% alumina, zirconium dioxide, titanium dioxide and/or silica, 1-70 wt.% copper oxide (CuO), less than 20 wt.% nickel oxide with respect to CuO and 0-50 wt.% other metal oxide(s). In the production of 2,2'-dimorpholinodiethyl ether (DMDEE) by reacting diethylene glycol with ammonia under pressure at elevated temperature in the presence of hydrogen and a hydrogenation catalyst, the active catalyst, before reduction with hydrogen, contains 20-85 wt.% aluminum oxide (Al2O3), zirconium dioxide (ZrO2), titanium dioxide (TiO2) and/or silica (SiO2), 1-70 wt.% copper oxide (expressed as CuO), 0-50 wt.% magnesium, chromium, zinc, barium and/or calcium oxide (expressed as MgO, Cr2O3, ZnO, BaO and CaO) and less than 20 wt.% nickel oxide (expressed as NiO) with respect to CuO.
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公开(公告)号:DE19614542A1
公开(公告)日:1997-10-16
申请号:DE19614542
申请日:1996-04-12
Applicant: BASF AG
Inventor: AMBERG WILHELM DR , KLING ANDREAS DR , KLINGE DAGMAR DR , RIECHERS HARTMUT DR , BAUMANN ERNST DR , UNGER LILIANE DR , RASCHACK MANFRED DR , HERGENROEDER STEFAN , SCHULT SABINE DR
IPC: A61K31/00 , A61K31/47 , A61K31/505 , A61P9/00 , A61P9/12 , A61P13/00 , A61P13/12 , C07D215/22 , C07D215/227 , C07D239/34 , C07D239/60 , C07D401/12 , C07D403/12 , C07D239/32 , C07D213/60 , C07C215/16 , C07C217/22 , C07D227/08 , C07D247/02 , A61K31/44
Abstract: The present invention relates to carboxylic acid derivatives of formula (I) in which the radicals have the meaning given in the description, and the production of these substances and their use as medicaments.
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公开(公告)号:DE19614534A1
公开(公告)日:1997-10-16
申请号:DE19614534
申请日:1996-04-12
Applicant: BASF AG
Inventor: RIECHERS HARTMUT DR , KLINGE DAGMAR DR , AMBERG WILHELM DR , KLING ANDREAS DR , HILLEN HEINZ DR , UNGER LILIANE DR , ELGER BERND DR
IPC: C07D251/30 , A61K31/00 , A61K31/505 , A61K31/517 , A61K31/529 , A61K31/53 , A61P7/00 , A61P9/00 , A61P9/02 , A61P9/12 , A61P13/00 , A61P13/08 , A61P13/12 , C07D239/34 , C07D239/46 , C07D239/52 , C07D239/60 , C07D239/70 , C07D251/48 , C07D403/12 , C07D491/044 , C07D251/26
Abstract: Carboxylic acid derivatives having the formula (I) are disclosed, as well as the production of these compounds and their use as medicaments. In the formula, the radicals have the meanings defined in the description.
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公开(公告)号:CZ287396A3
公开(公告)日:1997-04-16
申请号:CZ287396
申请日:1995-03-23
Applicant: BASF AG
Inventor: BAUMANN ERNST DR , VOGELBACHER UWE JOSEF DR , RHEINHEIMER JOACHIM DR , KLINGE DAGMAR DR , RIECHERS HARTMUT DR , KROGER BURKHARD DR , BIALOJAN SIEGFRIED DR , BOLLSCHWEILER CLAUS DR , WERNER VOLFGANG DR , UNGER LILIANE DR , RASCHACK MANFRED DR
IPC: C07D251/26 , A61K31/00 , A61K31/505 , A61K31/506 , A61K31/53 , A61P9/00 , A61P9/08 , A61P9/10 , A61P9/12 , A61P11/08 , A61P13/02 , A61P15/00 , A61P25/04 , A61P39/02 , C07D239/26 , C07D239/34 , C07D239/38 , C07D401/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12
Abstract: PCT No. PCT/EP95/01099 Sec. 371 Date Sep. 30, 1996 Sec. 102(e) Date Sep. 30, 1996 PCT Filed Mar. 23, 1995 PCT Pub. No. WO95/26716 PCT Pub. Date Oct. 12, 1995A method of inhibiting endothelin receptors by administering to a patient a compound of the formula I I
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公开(公告)号:DE4411225A1
公开(公告)日:1995-10-05
申请号:DE4411225
申请日:1994-03-31
Applicant: BASF AG
Inventor: BAUMANN ERNST DR , VOGELBACHER UWE JOSEF DR , RHEINHEIMER JOACHM DR , KLINGE DAGMAR DR , RIECHERS HARTMUT DR , KROEGER BURKHARD DR , BIALOJAN SIEGFRIED DR , BOLLSCHWEILER CLAUS DR , WERNET WOLFGANG DR , UNGER LILIANE DR , RASCHACK MANFRED DR
IPC: C07D251/26 , A61K31/00 , A61K31/505 , A61K31/506 , A61K31/53 , A61P9/00 , A61P9/08 , A61P9/10 , A61P9/12 , A61P11/08 , A61P13/02 , A61P15/00 , A61P25/04 , A61P39/02 , C07D239/26 , C07D239/34 , C07D239/38 , C07D401/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12
Abstract: The invention concerns the use of carboxylic acid derivatives of formula I (I) in which R means a formyl group, a CO2H group or a residue which can be hydrolysed to form COOH; X means nitrogen or CR , wherein R means hydrogen or, together with R , forms a 3- to 4-member alkylene or alkenylene chain in each of which a methyl group can be replaced by oxygen; Y means sulphur or oxygen or a single bond; Z means sulphur or oxygen; and the other substituents have the meanings given in the description. These derivatives can be used for preparing medicaments.
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公开(公告)号:ES2173064T3
公开(公告)日:2002-10-16
申请号:ES00114475
申请日:2000-07-06
Applicant: BASF AG
Inventor: RIECHERS HARTMUT DR , HOHN ARTHUR DR , SIMON JOACHIM DR , LANG ORTMUND , SCHOENMAKERS HARTMUT DR , RAULS MATTHIAS DR
IPC: C07D487/08 , C07D471/08
Abstract: Preparation of a solution of pure triethylenediamine (TEDA) comprises vaporizing TEDA and passing the TEDA vapor into a liquid solvent. An Independent claim is also included for the preparation of pure TEDA by preparing the solution as above and crystallizing TEDA from this solution.
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公开(公告)号:DE19726146A1
公开(公告)日:1998-12-24
申请号:DE19726146
申请日:1997-06-19
Applicant: BASF AG
Inventor: AMBERG WILHELM DR , KLING ANDREAS DR , KLINGE DAGMAR DR , RIECHERS HARTMUT DR , HERGENROEDER STEFAN DR , RASCHACK MANFRED DR , UNGER LILIANE DR
IPC: C07D251/16 , A61K31/4965 , A61K31/50 , A61K31/505 , A61K31/517 , A61K31/519 , A61K31/53 , A61P7/02 , A61P9/02 , A61P9/04 , A61P9/10 , A61P9/12 , A61P11/06 , A61P13/08 , A61P13/12 , A61P25/06 , A61P35/00 , A61P35/04 , A61P43/00 , C07C247/12 , C07D213/68 , C07D237/14 , C07D237/16 , C07D239/34 , C07D239/52 , C07D239/56 , C07D239/60 , C07D239/70 , C07D239/80 , C07D239/95 , C07D241/18 , C07D251/22 , C07D251/34 , C07D251/52 , C07D253/06 , C07D403/12 , C07D491/048 , C07D239/28 , C07D237/10 , C07D251/12 , C07D257/08 , C07D213/60 , A61K31/44
Abstract: The invention relates to carboxylic acid derivatives of formula (I) wherein the constituents have the meaning given in the description. The invention also relates to the production of said derivatives, and to their use as endothelin receptor antagonists.
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公开(公告)号:CZ9801045A3
公开(公告)日:1998-09-16
申请号:CZ104598
申请日:1996-09-26
Applicant: BASF AG
Inventor: KLINGE DAGMAR DR , AMBERG WILHELM DR , KLING ANDREAS DR , RIECHERS HARTMUT DR , UNGER LILIANE DR , RASCHACK MANFRED DR
IPC: A61K31/00 , A61K31/44 , A61K31/4427 , A61K31/443 , A61K31/444 , A61K31/505 , A61K31/53 , A61P5/24 , A61P5/36 , A61P5/42 , A61P9/12 , C07D213/74 , C07D239/10 , C07D239/42 , C07D239/46 , C07D239/48 , C07D239/50 , C07D239/52 , C07D239/58 , C07D251/46 , C07D401/04 , C07D405/12 , C07D405/14 , C07D471/04 , C07D487/04 , C07D491/052 , C07D491/056 , C07D239/70 , C07D251/42 , C07D487/02
CPC classification number: C07D213/74 , C07D239/42 , C07D239/47 , C07D239/52 , C07D239/58 , C07D251/46
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公开(公告)号:DE19652763A1
公开(公告)日:1998-06-25
申请号:DE19652763
申请日:1996-12-18
Applicant: BASF AG
Inventor: AMBERG WILHELM DR , JANSEN ROLF DR , KLING ANDREAS DR , KLINGE DAGMAR DR , RIECHERS HARTMUT DR , HERGENROEDER STEFAN DR , RASCHACK MANFRED DR , UNGER LILIANE DR
IPC: C07D237/14 , C07D237/16 , C07D241/18 , C07D253/07 , C07D253/075 , C07D253/10 , C07D491/04 , A61K31/195 , A61K31/53 , C07D241/14 , C07D241/36 , C07D255/00 , C07D487/06 , C07D493/04 , C07D495/04
Abstract: Heterocyclic compounds of formula (I) and their salts are new. R1 = tetrazolyl, or COR; R = OR6, O(CH2)pS(O)kR7, NHS(O)2R8 or a 5-membered azaheteroaryl; R2 = 1-4C alkyl, 2-4C alkenyl, 2-4C alkynyl (all optionally substituted), H, halo, 1-4C alkoxy, 1-4C haloalkoxy, 3-6C alkenyloxy, 3-6C alkynyloxy, 1-4C alkylthio, 1-4C alkylcarbonyl, 1-4C alkoxycarbonyl, NH(1-4C alkyl), N(1-4C alkyl)2, OH, carboxy or amino; R3, R4 = phenyl, naphthyl or 3-8C cycloalkyl (all optionally substituted); or R3+R4 = two of phenyl, naphthyl linked at the o-position by a bond, methylene, ethylene, ethenyl, S, SO2, NH or N-alkyl; R5 = H, 1-8C alkyl, 3-8C alkenyl, 3-8C alkynyl, Ph, naphthyl, 5-6 membered heteroaromatic (containing 1-3 N, S and/or O), or 3-8C cycloalkyl (all optionally substituted); R6 = H, alkali metal or earth-alkali metal, organic ammonium, 3-8C cycloalkyl, 1-8C alkyl, or (all optionally substituted) benzyl, 3-8C alkenyl, 3-8C alkynyl or phenyl; R7 = 1-4C alkyl, 3-8C cycloalkyl, 3-8C alkenyl, 3-8C alkynyl or optionally substituted phenyl; R8 = 1-4C alkyl, 3-8C alkenyl, 3-8C alkynyl, 3-8C cycloalkyl (all optionally substituted by 1-4C alkoxy, 1-4C alkylthio and/or phenyl), 1-4C haloalkyl or optionally substituted phenyl; X = N, Y = N or CR9 and Z = N; or X = CH, Y = N or CR9 and Z = N or CR10 provided that Y or Z = N; R9, R10 = 1-4C alkyl, 2-4C alkenyl or 2-4C alkynyl (all optionally substituted), H, OH, NH2, NH(1-4C alkyl), N(1-4C alkyl)2, halo, 1-4C alkoxy, 1-4C haloalkoxy or 1-4C alkylthio; or CR2+CR9 or CR2+CR10 completes a 5-6 membered alkylene or alkenyl ring (optionally substituted) with one or more CH2 optionally replaced by O, S, NH or N(1-4C alkyl); Q = N and W = bond; or Q = O and W = S, O or a bond; k = 0-2; and p = l-4.
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公开(公告)号:DE19636046A1
公开(公告)日:1998-03-12
申请号:DE19636046
申请日:1996-09-05
Applicant: BASF AG
Inventor: AMBERG WILHELM DR , JANSEN ROLF DR , KLING ANDREAS DR , KLINGE DAGMAR DR , RIECHERS HARTMUT DR , HERGENROEDER STEFAN DR , RASCHACK MANFRED DR , UNGER LILIANE DR
IPC: A61K31/505 , A61K31/506 , A61K31/519 , A61P9/04 , A61P9/08 , A61P9/12 , A61P43/00 , C07C59/66 , C07C69/734 , C07D239/34 , C07D239/52 , C07D239/60 , C07D239/70 , C07D491/04 , C07D491/048 , C07D405/10 , C07D403/12 , C07D251/12 , C07C59/64 , A61K31/41
Abstract: Carboxylic acid derivatives have the formula (I), in which R stands for tetrazole or a group (a); R stands for hydrogen, hydroxy, NH2, NH(C1-c4-alkyl), N(C1-C4-alkyl)2, halogen, C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkinyl, C1-C4-alkyl halide, C1-C4-alkoxy, C1-C4-alkoxy halide or C1-C4-alkylthio, or CR is linked with CR , as indicated below, into a 5- or 6-membered ring; X stands for nitrogen or methine; Y stands for nitrogen or methine; Z stands for nitrogen or CR , wherein R is hydrogen or C1-C4-alkyl or CR forms together with CR or CR an optionally substituted 5- or 6-membered alkylene or alkenylene ring, and wherein one or more methylene groups can be substituted by hydrogen, sulphur, -NH or -N(C1-C4-alkyl); R stands for hydrogen, hydroxy, NH2, NH(C1-C4-alkyl), N(C1-C4-alkyl)2, halogen, C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkinyl, C1-C4-hydroxyalkyl, C1-C4-alkyl halide, C1-C4-alkoxy, C1-C4-alkoxy halide, C1-C4-alkylthio; or CR is linked to CR as indicated above into a 5- or 6-membered ring, R and R (which may be identical or different) stand for optionally substituted phenyl or naphthyl, or for phenyl or naphthyl which are linked to each other at the ortho-position by a direct bond, a methylene, ethylene or ethenylene group, an oxygen or sulphur atom or an SO2, NH or N-alkyl group; optionally substituted C3-C8-cycloalkyl; R stands for optionally substituted C3-C8-cycloalkyl; optionally substituted phenyl or naphthyl, a 5- or 6-membered, optionally substituted heteroaromatic compound containing one to three nitrogen atoms and/or one sulphur or oxygen atom; W stands for sulphur or oxygen; Q is a spacer with a length that corresponds to a C2-C4 chain. Also disclosed are the physiologically tolerable salts of these compounds, as well as their pure enantiomer and diastereoisomer forms, their preparation and use as mixed ETA/ETB-receptor antagonists.
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