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ES2101824T3 - N-acil-n-heterociclil-onaftalenil-alquil-aminoacidos como antagonistas de angiotensina ii. - Google Patents

N-acil-n-heterociclil-onaftalenil-alquil-aminoacidos como antagonistas de angiotensina ii.

Info

Publication number
ES2101824T3
ES2101824T3 ES92810603T ES92810603T ES2101824T3 ES 2101824 T3 ES2101824 T3 ES 2101824T3 ES 92810603 T ES92810603 T ES 92810603T ES 92810603 T ES92810603 T ES 92810603T ES 2101824 T3 ES2101824 T3 ES 2101824T3
Authority
ES
Spain
Prior art keywords
instead
alkyl
variables
carbonyl
hydrogen
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
ES92810603T
Other languages
English (en)
Inventor
Tibur Dr Schmidlin
Paul Zbinden
Peter Dr Buhlmayer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
Original Assignee
Ciba Geigy AG
Novartis AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ciba Geigy AG, Novartis AG filed Critical Ciba Geigy AG
Application granted granted Critical
Publication of ES2101824T3 publication Critical patent/ES2101824T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D257/00Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
    • C07D257/02Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D257/04Five-membered rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/06Antiglaucoma agents or miotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • 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
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/12Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/12Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
    • C07D217/14Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/50Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D333/52Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
    • C07D333/54Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
    • C07D333/60Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/10Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/10Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/10Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Furan Compounds (AREA)
  • Indole Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Pyrrole Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

LA INVENCION SE REFIERE A AMINOACIDOS N-ACILO-NHETEROCICLILOALQUILO DE LA FORMULA EN LA QUE R1 SIGNIFICA ALQUILO C1-C7, EL CUAL ESTA INSUSTITUIDO O ESTA SUSTITUIDO POR HALOGENO O HIDROXIDO, O SIGNIFICA ALQUENILO C2-C7, CICLOALQUILOC3-C7, CICLOALQUILOXILO C3-C7, ALCOXILOC1-C7 O CICLOALQUILOC3-C7-ALCOXILOC1-C7; R2 ES 1H-TETRAZOL-5-YL, CARBOXILO, ALCOXILO-CARBONILO-C1-C7, SO3H, PO2H2, PO3H2 O HALOGENO-C1-C7-ALCANOSULFONILAMINO; R3 SIGNIFICA 1H-TETRAZOL-5-YL, HIDROXIMETILO, ALCOXI-METILO-C1-C7, FORMILO, CARBOXILO, ALCOXI-CARBONILO-C1-C7, C1-C7 ALCOXILOCARBONILO-C1-C7, C1-C7ALCOXILO-C1-C7-ALCOXILO-CARBONILO, FENIL-C1-C4ALCOXILO-CARBONILO O CARBAMOYLO, CUYO GRUPO AMINO ESTA INSUSTITUIDO O ESTA DISUSTITUIDO POR ALQUILO C1-C7, ALQUENILO-C1-C7 O FENILO-C1-C7-ALQUILO MONO O INDEPENDIENTE ENTRE SI O ESTA DISUSTITUIDO POR AQUILENO C2-C7 O C2-C4-ALQUILENOXILO-C2-C4; ALK METILEL, ES ETILEL O ETILIDEL HET, SIGNIFICA (I) EN LA QUE Y1 ESTA EN LUGAR DE O, S O N(R) Y R SIGNIFICA ALQUILOC1-C7; O SIGNIFICA (II)EN LA QUE UNA DE LAS VARIABLES Y2 E Y3 ESTA EN LUGAR DE C(R'') Y LA OTRA EN LUGAR DE N, O LAS DOS VARIABLES EN LUGAR DE C(R''); Y R'' SIGNIFICA HIDROGENO, HALOGENO, ALQUILO-C1-C7, ALCOXILO-C1-C7, ALQUENILOXILO-C2-C7, FELOXILO, BENCILOXILO, TRIFLUOROMETILO O S(O)M-R, EN DONDE M, ES 0, 1 O 2; Y R ES HIDROGENO O ALQUILOU EL INDICE M ESTA EN LUGAR DE 0, 1 O 2; UNA DE LAS VARIABLES X2 Y X4 ESTA EN LUGAR DE ALQUILOS-C1-C4 Y LAS OTRAS VARIABLES X2 Y X4 ESTAN EN LUGAR DE UN ENLACE; O LAS DOS VARIABLES X2 Y X4 ESTAN CADA VEZ EN LUGAR DE UN ENLACE; X3 SIGNIFICA C3-C7-CICLOALQUILIDOS O EL ELEMENTO DE ESTRUCTURA C(XA)(XB) IDROGENO O ALQUILO-C1-C7 Y XB ES ALQUILO C1-C7; Y LOS ANILLOS A, B, C Y D, HASTA LOS SUSTITUYENTES INDICADOS EN LA FORMULA, ASI COMO LOS SUSTITUYENTES AROMATICOS, ESTAN INSUSTITUIDOS INDEPENDIENTES ENTRE SI O SUSTITUIDOS UNA O VARIAS VECES POR SUSTITUYENTES ESCOGIDOS DEL GRUPO COMPUESTO DE HALOGENO, ALQUILO-C1-C7, ALCOXILO-C1-C7, ALQUENILOXILO-C2-C7, FENOXILO, BENCILOXILO, TRIFLUOROMETILO Y S(O)M-R, EN DONDE M, ES 0, 1 O 2; Y R ES HIDROGENO O ALQUILO-C1-C7; Y SUS SALES; METODO PARA LA FABRICACION, PREPARADOS FARMACEUTICOS QUE CONTIENEN UNA COMBINACION DE LA FORMULA I O UNA SAL DE ELLA DE EMPLEO FARMACEUTICO, ASI COMO EL EMPLEO.
ES92810603T 1991-08-15 1992-08-06 N-acil-n-heterociclil-onaftalenil-alquil-aminoacidos como antagonistas de angiotensina ii. Expired - Lifetime ES2101824T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CH240591 1991-08-15
CH37592 1992-02-07
CH114192 1992-04-08

Publications (1)

Publication Number Publication Date
ES2101824T3 true ES2101824T3 (es) 1997-07-16

Family

ID=27172057

Family Applications (1)

Application Number Title Priority Date Filing Date
ES92810603T Expired - Lifetime ES2101824T3 (es) 1991-08-15 1992-08-06 N-acil-n-heterociclil-onaftalenil-alquil-aminoacidos como antagonistas de angiotensina ii.

Country Status (16)

Country Link
US (3) US5955487A (es)
EP (1) EP0528762B1 (es)
JP (1) JPH05230022A (es)
KR (1) KR930004295A (es)
AT (1) ATE152718T1 (es)
AU (1) AU659469B2 (es)
CA (1) CA2076057A1 (es)
DE (1) DE59208448D1 (es)
DK (1) DK0528762T3 (es)
ES (1) ES2101824T3 (es)
FI (1) FI923612A7 (es)
GR (1) GR3023708T3 (es)
HU (1) HUT62880A (es)
IL (1) IL102802A0 (es)
MX (1) MX9204703A (es)
NO (1) NO923182L (es)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2683819B1 (fr) * 1991-10-28 1994-02-11 Synthelabo Derives de quinoleine, leur procede de preparation et leur application en therapeutique.
GB9208116D0 (en) 1992-04-13 1992-05-27 Ici Plc Therapeutic agents
ES2135472T3 (es) * 1992-04-13 1999-11-01 Zeneca Ltd Antagonistas de angiotensina ii contra trastornos asociados con la velocidad de conduccion neuronal deteriorada, especialmente la neuropatia diabetica.
US5478832A (en) * 1992-05-08 1995-12-26 The Green Cross Corporation Quinoline compounds
GB9218449D0 (en) 1992-08-29 1992-10-14 Boots Co Plc Therapeutic agents
FR2710914B1 (fr) * 1993-10-04 1995-11-24 Synthelabo Dérivés de 2-[2-(tétrazol-5-yl)phényl]-1,2-dihydroquinoléine, leur préparation et leur utilisation comme intermédiaires de synthèse.
JPH09202774A (ja) 1996-01-25 1997-08-05 Green Cross Corp:The 2−アリールキノリン類およびその製造方法
US5919792A (en) * 1996-10-30 1999-07-06 Merck & Co., Inc. Integrin antagonists
JP3892963B2 (ja) * 1998-03-17 2007-03-14 住友化学株式会社 L−バリンベンジルエステルp−トルエンスルホン酸塩の製造方法
SE9903028D0 (sv) 1999-08-27 1999-08-27 Astra Ab New use
TW200505442A (en) * 2003-05-19 2005-02-16 Genomics Inst Of The Novartis Res Foundation Immunosuppressant compounds and compositions
MY150088A (en) * 2003-05-19 2013-11-29 Irm Llc Immunosuppressant compounds and compositions
BRPI0412694A (pt) * 2003-07-15 2006-10-03 Smithkline Beecham Corp compostos
US7868037B2 (en) 2004-07-14 2011-01-11 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US7772271B2 (en) 2004-07-14 2010-08-10 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US7781478B2 (en) 2004-07-14 2010-08-24 Ptc Therapeutics, Inc. Methods for treating hepatitis C
JP2008507518A (ja) 2004-07-22 2008-03-13 ピーティーシー セラピューティクス,インコーポレーテッド C型肝炎を治療するためのチエノピリジン
CN103601792B (zh) 2007-06-04 2016-06-29 协同医药品公司 有效用于胃肠功能紊乱、炎症、癌症和其他疾病治疗的鸟苷酸环化酶激动剂
US8969514B2 (en) 2007-06-04 2015-03-03 Synergy Pharmaceuticals, Inc. Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases
AU2009256157B2 (en) 2008-06-04 2014-12-18 Bausch Health Ireland Limited Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders
ES2624828T3 (es) 2008-07-16 2017-07-17 Synergy Pharmaceuticals Inc. Agonistas de la guanilato ciclasa útiles para el tratamiento de trastornos gastrointestinales, inflamación, cáncer y otros
CA2775328A1 (en) * 2009-09-23 2011-03-31 Medivation Technologies, Inc. Pyrido[4,3-b]indoles and methods of use
US9616097B2 (en) 2010-09-15 2017-04-11 Synergy Pharmaceuticals, Inc. Formulations of guanylate cyclase C agonists and methods of use
WO2014151206A1 (en) 2013-03-15 2014-09-25 Synergy Pharmaceuticals Inc. Agonists of guanylate cyclase and their uses
US9486494B2 (en) 2013-03-15 2016-11-08 Synergy Pharmaceuticals, Inc. Compositions useful for the treatment of gastrointestinal disorders
EP4424697A3 (en) 2013-06-05 2024-12-25 Bausch Health Ireland Limited Ultra-pure agonists of guanylate cyclase c, method of making and using same

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2417763A1 (de) * 1974-04-11 1975-10-30 Bayer Ag Carbonsaeureamide, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel
ATE113281T1 (de) * 1989-08-02 1994-11-15 Takeda Chemical Industries Ltd Pyrazol-derivate, verfahren zu deren herstellung und anwendung.
GB8924392D0 (en) * 1989-10-30 1989-12-20 Bayer Ag Substituted cycloalkano/b/dihydroindole-and-indolesulphonamides
GB8924755D0 (en) * 1989-11-02 1989-12-20 Bayer Ag Iso-and heterocyclic phenylsulphonylamides
PT95899A (pt) * 1989-11-17 1991-09-13 Glaxo Group Ltd Processo para a preparacao de derivados indole
GB8927277D0 (en) * 1989-12-01 1990-01-31 Glaxo Group Ltd Chemical compounds
CA2032259A1 (en) * 1989-12-18 1991-06-19 Wayne J. Thompson Hiv protease inhibitors useful for the treatment of aids
DE59107440D1 (de) * 1990-02-19 1996-04-04 Ciba Geigy Ag Acylverbindungen
AU657498B2 (en) * 1990-12-14 1995-03-16 Novartis Ag Biphenylyl compounds
FR2689124A1 (fr) * 1992-03-27 1993-10-01 Adir Nouvelles naphtylalkylamines, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent.

Also Published As

Publication number Publication date
AU2098392A (en) 1993-02-25
DK0528762T3 (da) 1997-08-25
HUT62880A (en) 1993-06-28
FI923612A0 (fi) 1992-08-12
MX9204703A (es) 1993-12-01
DE59208448D1 (de) 1997-06-12
AU659469B2 (en) 1995-05-18
US5506240A (en) 1996-04-09
JPH05230022A (ja) 1993-09-07
EP0528762B1 (de) 1997-05-07
US5620998A (en) 1997-04-15
HU9202654D0 (en) 1992-10-28
NO923182D0 (no) 1992-08-14
EP0528762A1 (de) 1993-02-24
CA2076057A1 (en) 1993-02-16
US5955487A (en) 1999-09-21
FI923612A7 (fi) 1993-02-16
NO923182L (no) 1993-02-16
KR930004295A (ko) 1993-03-22
IL102802A0 (en) 1993-01-31
ATE152718T1 (de) 1997-05-15
GR3023708T3 (en) 1997-09-30

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