CO4900070A1 - NUEVOS DERIVADOS DE ACIDO CARBONICO, SU PRODUCCION Y APLICA- CION COMO ANTAGONISTAS MIXTOS DE RECEPTORES ET(sub A)/ET- (sub B) - Google Patents

NUEVOS DERIVADOS DE ACIDO CARBONICO, SU PRODUCCION Y APLICA- CION COMO ANTAGONISTAS MIXTOS DE RECEPTORES ET(sub A)/ET- (sub B)

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Publication number
CO4900070A1
CO4900070A1 CO97051479A CO97051479A CO4900070A1 CO 4900070 A1 CO4900070 A1 CO 4900070A1 CO 97051479 A CO97051479 A CO 97051479A CO 97051479 A CO97051479 A CO 97051479A CO 4900070 A1 CO4900070 A1 CO 4900070A1
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CO
Colombia
Prior art keywords
alkyl
substituted
phenyl
alkenyl
cycloalkyl
Prior art date
Application number
CO97051479A
Other languages
English (en)
Inventor
Wilhelm Amberg
Rolf Jansen
Andreas Kling
Dagmar Klinge
Hartmut Riechers
Stefan Hergenroder
Manfred Raschack
Liliane Unger
Original Assignee
Basf Ag
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Filing date
Publication date
Application filed by Basf Ag filed Critical Basf Ag
Publication of CO4900070A1 publication Critical patent/CO4900070A1/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/58Unsaturated compounds containing ether groups, groups, groups, or groups
    • C07C59/64Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
    • C07C59/66Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/66Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
    • C07C69/73Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
    • C07C69/734Ethers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/34One oxygen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/60Three or more oxygen or sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Cardiology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Derivados de ácido carbónico de la fórmula I:CARACTERIZADOS porqueR1 significa tetrazol o a un grupo en el que R tiene el siguiente significado: a) un residuo OR7 , en donde R7 significa: hidrógeno, el catión de un metal alcalino, el catión de un metal alcalinotérreo, o un ión amonio fisiológicamente compatible;C3 -C8 cicloalquilo, C1 -C8 alquilo, CH2 -fenilo, que puede ser sustituido Un C3 -C6 -alquenilo o un grupo C3 -C6 -alquinilo, que puede ser sustituido o fenilo, en caso dado, sustituido. b) un heteroaromato de 5 eslabones ligado con un átomo de nitrógeno, c) un grupo en el que k toma los valores 0, 1 y 2, p los calores 1, 2, 3 y 4 y R8 representa C1 -C4 -alquilo, - 2 -C3 -C8 -cicloalquilo, C3 -C6 -alquenilo, C3 -C6-alquinilo o fenilo, que puede ser sustituido d) un residuo en el que R9 significa: C1 -C4 -alquilo, C3 -C6 -alquenilo, C3 -C6 -alquinilo, C3 -C8 -cicloalquilo, donde estos residuos pueden tener un residuo C1 -C4 -alcoxi, C1 -C4 -alquiltio y/o un residuo de fenilo fenilo en caso de ser necesario sustituido e) un residuo.en donde R13 y R14 pueden ser iguales o diferentes y tienen el siguiente significado: hidrógeno, C1 -C8 -alquilo, C3 -C8 -cicloalquilo, C3 -C8 -alquenilo, C3 -C8 -alquinilo, bencilo, fenilo que puede ser sustituido o R13 y R14 forman juntos una cadena C4 -C7 -alquileno cerrada la cual puede ser sustituida, que, puede contener un heteroátomo R2 hidrógeno, hidrozi, NH2 NH(C1 -C4 -alquilo), N(C1 -C4 -alquilo)2 , halógeno, C1 -C4 -alquilo, C2 -C4 -alquenilo, C2 -C4 -alquinilo, C1 -C4 -hidroxialquilo, C1 -C4 -alquilo halógeno, C1 -C4 -alcoxi, C1 -C4 -alcoxi halógeno o C1 -C4 -alquiltio, o CR2 está unido con CR10 como se indica abajo en un anillo de 5 a 6 eslabonesX nitrógeno o metilo. Y nitrógeno o metilo Z nitrógeno o CR10 , en donde CR10 significa hidrógeno o C1 -C4 -alquilo o CR10 junto con CR2 o CR3 forma un anillo de alquileno de 5 o 6 eslabones o de alquenilo, que puede ser sustituido y en donde uno o más grupos metilenos pueden ser sustituidos por oxígeno, azufre - NH o N(C1 -C4 -alquilo) R3 hidrógeno, hidroxi, NH2 , NH (C1 -C4 -alquilo), N(C1 -C4 -alquilo)2 , halógeno, C1 -C4 -alquilo, C2 -C4 -alquenilo, C2 -C4 -alquinilo, C1 -C4 -alquilo halógeno, C1 -C4 -alcoxi, C1 -C4 -alcoxi halógeno, C1 -C4 -alquiltio o CR3 está unido con CR10 tal como se indica arriba en un anillo de 5 o 6 eslabones. R4 y R5 (que pueden ser iguales o distintos): fenilo o naftilo, que pueden ser sustituidos, o fenilo o naftilo, que pueden estar unidos en posición orto por una unión directa a un grupo metileno, etileno o etenileno, a un átomo de oxígeno o azufre o a un grupo SO2 , NHAND#8209; o NAND#8209;alquilo; C3 AND#8209;C8 AND#8209;cicloalquilo, en caso necesario, sustituido R6 en caso necesario C3 AND#8209;C8 AND#8209;cicloalquilo sustituido fenilo o naftilo, que pueden ser sustituidos en heteroaromato de cinco a seis eslabones conteniendo de uno a tres átomos de nitrógeno y/o átomo de azufre u oxígeno, que puede ser sustituidoW azufre y oxígenoQ Un distanciador que en su largo corresponda a una cadena C2 AND#8209;C4 . así como las sales fisiológicamente compatibles y las formas enantiómeras y diastereómeras.
CO97051479A 1996-09-05 1997-09-04 NUEVOS DERIVADOS DE ACIDO CARBONICO, SU PRODUCCION Y APLICA- CION COMO ANTAGONISTAS MIXTOS DE RECEPTORES ET(sub A)/ET- (sub B) CO4900070A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19636046A DE19636046A1 (de) 1996-09-05 1996-09-05 Neue Carbonsäurederivate, ihre Herstellung und Verwendung als gemischte ET¶A¶/ET¶B¶-Rezeptorantagonisten

Publications (1)

Publication Number Publication Date
CO4900070A1 true CO4900070A1 (es) 2000-03-27

Family

ID=7804712

Family Applications (1)

Application Number Title Priority Date Filing Date
CO97051479A CO4900070A1 (es) 1996-09-05 1997-09-04 NUEVOS DERIVADOS DE ACIDO CARBONICO, SU PRODUCCION Y APLICA- CION COMO ANTAGONISTAS MIXTOS DE RECEPTORES ET(sub A)/ET- (sub B)

Country Status (22)

Country Link
US (1) US6670367B1 (es)
EP (1) EP0929529A2 (es)
JP (1) JP2000517329A (es)
KR (1) KR20000068446A (es)
CN (1) CN1236362A (es)
AR (1) AR009543A1 (es)
AU (1) AU736414B2 (es)
BG (1) BG103258A (es)
BR (1) BR9711693A (es)
CA (1) CA2265504A1 (es)
CO (1) CO4900070A1 (es)
DE (1) DE19636046A1 (es)
HU (1) HUP0000664A3 (es)
ID (1) ID19417A (es)
IL (1) IL128743A0 (es)
NO (1) NO312674B1 (es)
NZ (1) NZ334548A (es)
PL (1) PL331998A1 (es)
SK (1) SK25999A3 (es)
TR (1) TR199900486T2 (es)
WO (1) WO1998009953A2 (es)
ZA (1) ZA977946B (es)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6030975A (en) * 1997-03-14 2000-02-29 Basf Aktiengesellschaft Carboxylic acid derivatives, their preparation and use in treating cancer
KR20010023615A (ko) * 1997-09-04 2001-03-26 스타르크, 카르크 신규 카르복실산 유도체, 그 제조 및 혼합 eta/etb엔도텔린 수용체 길항제로서의 용도
CA2304712C (en) * 1997-09-26 2008-04-29 Knoll Aktiengesellschaft Endothelin antagonist and a renin-angiotensin system inhibitor as a combined preparation
DE19743143A1 (de) 1997-09-30 1999-04-01 Knoll Ag Pharmazeutische Kombinationspräparate
JP5187991B2 (ja) * 1997-10-17 2013-04-24 アーク・セラピューティックス・リミテッド レニン−アンジオテンシン系の阻害剤の使用
DE19809144A1 (de) * 1998-03-04 1999-09-09 Basf Ag Neue unsymmetrisch substituierte Carbonsäurederivate, ihre Herstellung und Verwendung als gemischte ET¶LAMBDA¶/ET¶B¶-Rezeptorantagonisten
DE19836044A1 (de) * 1998-08-10 2000-02-17 Basf Ag Neue Carbonsäurederivate, die Ketoseitenketten tragen, ihre Herstellung und Verwendung als Endothelin-Rezeptorantagonisten
US7566452B1 (en) 1999-05-04 2009-07-28 New York University Cancer treatment with endothelin receptor antagonists
DE19933164A1 (de) * 1999-07-20 2001-01-25 Basf Ag Neue Carbonsäurederivate mit 5,6 substituiertem Pyrimidinring, ihre Herstellung und Verwendung als Endothelin Rezeptorantagonisten
DE19951671A1 (de) * 1999-10-27 2001-05-03 Basf Ag 2-(4,6-Dimethyl-pyrimidin-2-yloxy)-3-(2-(3,4-dimethoxyphenyl)ethoxy)-3,3-diphenylpropionssäure-Natriumsalz und seine Verwendung als Endothelinantagonist
DE10064797A1 (de) * 2000-12-22 2002-06-27 Knoll Ag Orale und parenterale pharmazeutische Formulierung, umfassend eine niedermolekulare Thrombininhibitor-Pro-Pharmakon
US20030152956A1 (en) * 2000-12-26 2003-08-14 Noriko Ohtani Method of examining allergic disease
EP1243262B1 (en) 2001-03-20 2006-05-31 Schwarz Pharma Ag Novel use of a peptide class of compound for treating non-neuropathic inflammatory pain
EP1243263B1 (en) 2001-03-21 2002-11-27 Schwarz Pharma Ag Novel use of a peptide class of compound for treating allodynia or other different types of chronic or phantom pain
MXPA06011937A (es) 2004-04-16 2007-01-26 Sanol Arznei Schwarz Gmbh Uso de compuestos peptidicos para la profilaxis y el tratamiento de dolor de cabeza cronico.
EP1604656A1 (en) 2004-06-09 2005-12-14 Schwarz Pharma Ag Novel use of peptide compounds for treating amyotrophic lateral sclerosis (ALS)
BRPI0514721A (pt) 2004-08-27 2008-06-24 Sanol Arznei Schwarz Gmbh uso de compostos de peptìdeos para tratar dor de cáncer ósseo, dor induzida por quimioterapia e nucleosìdeo
JP2009530284A (ja) * 2006-03-13 2009-08-27 エンサイシブ・ファーマシューティカルズ・インコーポレイテッド 拡張期心不全を治療するための方法と組成物
JP2009530280A (ja) * 2006-03-13 2009-08-27 エンサイシブ・ファーマシューティカルズ・インコーポレイテッド シタクスセンタンナトリウムの配合物
SI2462990T1 (sl) 2006-06-15 2014-04-30 Ucb Pharma Gmbh Farmacevtski sestavek, ki obsega lakozamid in levetiracetam, s sinergističnim antikonvulzivnim učinkom
US20080026061A1 (en) * 2006-06-22 2008-01-31 Reichwein John F Crystalline N-(4-chloro-3-methyl-5-isoxazolyl)-2-[2-methyl-4.5-(methylenedioxy)phenylacetyl]-thiophene-3-sulfonamide
CN103709106A (zh) * 2013-12-06 2014-04-09 石家庄博策生物科技有限公司 一种立体选择性制备安立生坦的方法
CN103739557B (zh) * 2013-12-30 2015-10-21 黄河三角洲京博化工研究院有限公司 一种4,6-二甲基-2-甲磺酰基嘧啶的合成方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4313412A1 (de) * 1993-04-23 1994-10-27 Basf Ag 3-(Het)aryl-Carbonsäurederivate, Verfahren und Zwischenprodukte zu ihrer Herstellung
DE4313413A1 (de) * 1993-04-23 1994-10-27 Basf Ag 3-(Het)aryloxy(thio)-Carbonsäurederivate, Verfahren und Zwischenprodukte zu ihrer Herstellung
DE4335950A1 (de) 1993-10-21 1995-04-27 Basf Ag Derivate von 3-Hydroxycarbonsäuren, deren Herstellung und Verwendung
DE4411225A1 (de) 1994-03-31 1995-10-05 Basf Ag Verwendung von Carbonsäurederivaten als Arzneimittel
DE19533023B4 (de) * 1994-10-14 2007-05-16 Basf Ag Neue Carbonsäurederivate, ihre Herstellung und Verwendung
DE19536891A1 (de) 1995-10-04 1997-04-10 Basf Ag Neue Aminosäurederivate, ihre Herstellung und Verwendung

Also Published As

Publication number Publication date
US6670367B1 (en) 2003-12-30
AR009543A1 (es) 2000-04-26
NO991079D0 (no) 1999-03-04
ZA977946B (en) 1999-03-04
KR20000068446A (ko) 2000-11-25
NZ334548A (en) 2000-09-29
NO312674B1 (no) 2002-06-17
BR9711693A (pt) 1999-08-24
CN1236362A (zh) 1999-11-24
WO1998009953A3 (de) 1998-10-29
HUP0000664A3 (en) 2001-07-30
ID19417A (id) 1998-07-09
IL128743A0 (en) 2000-01-31
BG103258A (en) 2000-12-29
SK25999A3 (en) 1999-09-10
NO991079L (no) 1999-05-04
AU4552497A (en) 1998-03-26
EP0929529A2 (de) 1999-07-21
CA2265504A1 (en) 1998-03-12
AU736414B2 (en) 2001-07-26
DE19636046A1 (de) 1998-03-12
HUP0000664A2 (hu) 2001-04-28
JP2000517329A (ja) 2000-12-26
PL331998A1 (en) 1999-08-16
WO1998009953A2 (de) 1998-03-12
TR199900486T2 (xx) 1999-06-21

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