SG45503A1 - Substituted quinoline-2-carboxyamides their preparation and their use as pharmaceuticals and intermediates - Google Patents

Substituted quinoline-2-carboxyamides their preparation and their use as pharmaceuticals and intermediates

Info

Publication number
SG45503A1
SG45503A1 SG1996010735A SG1996010735A SG45503A1 SG 45503 A1 SG45503 A1 SG 45503A1 SG 1996010735 A SG1996010735 A SG 1996010735A SG 1996010735 A SG1996010735 A SG 1996010735A SG 45503 A1 SG45503 A1 SG 45503A1
Authority
SG
Singapore
Prior art keywords
alkyl
opt
alkoxy
substd
cycloalkyl
Prior art date
Application number
SG1996010735A
Other languages
English (en)
Inventor
Klaus Dr Weidmann
Karl-Heinz Dr Baringhaus
Georg Dr Tschank
Martin Dr Bickel
Original Assignee
Hoechst 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
Priority claimed from DE19536263A external-priority patent/DE19536263A1/de
Application filed by Hoechst Ag filed Critical Hoechst Ag
Publication of SG45503A1 publication Critical patent/SG45503A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02—Heterocyclic 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
    • C07D215/16—Heterocyclic 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06—Dipeptides
    • C07K5/06139—Dipeptides with the first amino acid being heterocyclic
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02—Heterocyclic 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
    • C07D215/16—Heterocyclic 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Electroluminescent Light Sources (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
SG1996010735A 1995-09-28 1996-09-27 Substituted quinoline-2-carboxyamides their preparation and their use as pharmaceuticals and intermediates SG45503A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19536263A DE19536263A1 (de) 1995-09-28 1995-09-28 Substituierte Chinolin-2-carbonsäureamide, ihre Herstellung und ihre Verwendung als Arzneimittel
DE19605170 1996-02-13

Publications (1)

Publication Number Publication Date
SG45503A1 true SG45503A1 (en) 1998-01-16

Family

ID=26019051

Family Applications (1)

Application Number Title Priority Date Filing Date
SG1996010735A SG45503A1 (en) 1995-09-28 1996-09-27 Substituted quinoline-2-carboxyamides their preparation and their use as pharmaceuticals and intermediates

Country Status (20)

Country Link
US (2) US5719164A (fr)
EP (1) EP0765871B1 (fr)
JP (1) JPH09124606A (fr)
KR (1) KR970061869A (fr)
CN (2) CN1120157C (fr)
AT (1) ATE263155T1 (fr)
AU (1) AU728208B2 (fr)
CA (1) CA2186717A1 (fr)
CZ (1) CZ283396A3 (fr)
DE (1) DE59610950D1 (fr)
ES (1) ES2215184T3 (fr)
HU (1) HUP9602685A3 (fr)
IL (2) IL135495A (fr)
MX (1) MX9604378A (fr)
MY (1) MY133647A (fr)
NO (1) NO308600B1 (fr)
NZ (1) NZ299455A (fr)
PL (1) PL316321A1 (fr)
SG (1) SG45503A1 (fr)
SI (1) SI9600287A (fr)

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DE19650215A1 (de) * 1996-12-04 1998-06-10 Hoechst Ag 3-Hydroxypyridin-2-carbonsäureamidester, ihre Herstellung und ihre Verwendung als Arzneimittel
DE19746287A1 (de) * 1997-10-20 1999-04-22 Hoechst Marion Roussel De Gmbh Substituierte Isochinolin-2-Carbonsäureamide, ihre Herstellung und ihre Verwendung als Arzneimittel
US20020198145A1 (en) * 1999-06-10 2002-12-26 Cognetix, Inc. MuO-conopeptides and their use as local anesthetics
US6706724B2 (en) 2000-12-21 2004-03-16 Nitromed, Inc. Substituted aryl compounds as novel cyclooxygenase-2 selective inhibitors, compositions and methods of use
AU2002241154A1 (en) * 2001-03-21 2002-10-03 Isis Innovation Ltd. Assays, methods and means relating to hypoxia inducible factor (hif) hydroxylase
EP2295060B1 (fr) 2001-12-06 2018-10-31 Fibrogen, Inc. Traitement de conditions ischémiques ou hypoxiques
CN102526044A (zh) * 2001-12-06 2012-07-04 法布罗根股份有限公司 提高内源性红细胞生成素(epo)的方法
US8124582B2 (en) 2002-12-06 2012-02-28 Fibrogen, Inc. Treatment of diabetes
US7618940B2 (en) * 2002-12-06 2009-11-17 Fibrogen, Inc. Fat regulation
US8614204B2 (en) 2003-06-06 2013-12-24 Fibrogen, Inc. Enhanced erythropoiesis and iron metabolism
EP1644336B1 (fr) * 2003-06-06 2011-01-19 Fibrogen, Inc. Composes heteroaryliques contenant de l'azote et leur utilisation dans l'augmentation de l'erythropoietine endogene
WO2005034929A2 (fr) * 2003-10-10 2005-04-21 Fibrogen, Inc. Remodelage et vascularisation de tissus
AU2006254897A1 (en) * 2005-06-06 2006-12-14 Fibrogen, Inc. Improved treatment for anemia using a HIF-alpha stabilising agent
MX2007016160A (es) 2005-06-15 2008-03-07 Fibrogen Inc Uso de moduladoers de hif-1 alfa para el tratamiento contra el cancer.
EP1910296B1 (fr) 2005-07-27 2010-04-21 F.Hoffmann-La Roche Ag 4-ARYLOXY QUINOLINES ET LEUR UTILISATION EN TANT QUE modulateurs de 5-HT6
ES2446416T3 (es) * 2005-12-09 2014-03-07 Amgen, Inc. Compuestos basados en quinolona que presentan actividad inhibidora de prolil hidroxilasa, composiciones y usos de los mismos
ZA200806752B (en) * 2006-01-27 2009-10-28 Fibrogen Inc Cyanoisoquinoline compounds that stabilize hypoxia inducible factor (HIF)
WO2007101204A1 (fr) * 2006-02-27 2007-09-07 Alcon Research, Ltd. Méthode de traitement du glaucome
US7745461B1 (en) 2006-02-27 2010-06-29 Alcon Research, Ltd. Method of treating dry eye disorders
AU2007232607B2 (en) * 2006-03-30 2010-09-16 Lg Electronics Inc. A method and apparatus for decoding/encoding a video signal
AU2007234408B2 (en) * 2006-04-04 2011-05-19 Fibrogen, Inc. Pyrrolo- and thiazolo-pyridine compounds as HIF modulators
EP2044005B8 (fr) 2006-06-26 2012-12-05 Warner Chilcott Company, LLC Inhibiteurs de la prolyl hydroxylase et procédés d'utilisation
CA2672656C (fr) * 2006-12-18 2012-03-20 Amgen Inc. Composes de naphtalenone presentant une activite inhibititrice de prolyle hydroxylase, compositions et utilisations de ceux-ci
US8048892B2 (en) * 2006-12-18 2011-11-01 Amgen Inc. Azaquinolone based compounds exhibiting prolyl hydroxylase inhibitory activity, compositions, and uses thereof
US7569726B2 (en) * 2007-04-18 2009-08-04 Amgen Inc. Indanone derivatives that inhibit prolyl hydroxylase
CA2683956C (fr) * 2007-04-18 2012-12-18 Amgen Inc. Quinolones et azaquinolones inhibant la prolyl hydroxylase
CA2685216C (fr) * 2007-05-04 2014-07-08 Amgen Inc. Derives de la thienopyridine et de la thiazolopyridine qui inhibent l'activite prolyle hydroxylase
CA2685219C (fr) * 2007-05-04 2012-06-19 Amgen Inc. Diazaquinolones inhibant l'activite de la prolyl hydroxylase
WO2009002533A1 (fr) * 2007-06-27 2008-12-31 The Brigham And Women's Hospital, Inc. Thérapies d'affection abdominale inflammatoire
US8927591B2 (en) 2008-11-14 2015-01-06 Fibrogen, Inc. Thiochromene derivatives as HIF hydroxylase inhibitors
UA107360C2 (en) 2009-08-05 2014-12-25 Biogen Idec Inc Bicyclic aryl sphingosine 1-phosphate analogs
MX336774B (es) * 2009-12-17 2016-01-28 Merck Sharp & Dohme Moduladores alostericos positivos de receptores m1 de la quinolina amida.
CN106278999B (zh) 2011-02-07 2019-10-25 比奥根Ma公司 S1p调节剂
NO2686520T3 (fr) 2011-06-06 2018-03-17
NZ700760A (en) 2012-03-09 2016-08-26 Fibrogen Inc 4 -hydroxy- isoquinoline compounds as hif hydroxylase inhibitors
US8883823B2 (en) 2012-07-16 2014-11-11 Fibrogen, Inc. Crystalline forms of a prolyl hydroxylase inhibitor
EP2872487B1 (fr) 2012-07-16 2017-04-26 Fibrogen, Inc. Procédé de fabrication de composés isoquinoléine
PT3470397T (pt) 2012-07-16 2022-02-18 Fibrogen Inc Formas cristalinas de um inibidor da prolil-hidroxilase
ES2668694T3 (es) * 2012-07-27 2018-05-21 Biogen Ma Inc. Derivados de ácido 1-[7-(cis-4-metil-ciclohexiloxi)-8-trifluorometil-naftalen-2-ilmetil]-piperidin-4-carboxílico como moduladores de autotaxina (ATX) para tratar inflamaciones y trastornos autoinmunitarios
ES2694297T3 (es) 2013-01-24 2018-12-19 Fibrogen, Inc. Formas cristalinas de ácido {[1-ciano-5-(4-clorofenoxi)-4-hidroxi-isoquinolina-3-carbonilo]-amino}-acético
EP3007695B1 (fr) 2013-06-13 2024-02-07 Akebia Therapeutics, Inc. Compositions et méthodes de traitement de l'anémie
MA39033A1 (fr) 2013-11-15 2017-11-30 Akebia Therapeutics Inc Formes solides d'acide {[5-(3-chlorophényl)-3-hydroxypyridine-2-carbonyl] amino}acétique, compositions et leurs utilisations
BR112017015852A2 (pt) 2015-01-23 2018-03-27 Akebia Therapeutics Inc forma de cristal, sal hemicálcico, sal hemicálcico di-hidratado, sal monossódico hidratado, sal bissódico monoidratado, sal monossódico anidro e método para preparar o composto 1
DK3277270T3 (da) 2015-04-01 2021-12-06 Akebia Therapeutics Inc Sammensætninger og fremgangsmåder til behandling af anæmi
US11713298B2 (en) 2018-05-09 2023-08-01 Akebia Therapeutics, Inc. Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino]acetic acid
WO2020097389A1 (fr) 2018-11-09 2020-05-14 Vivace Therapeutics, Inc. Composés bicycliques
AU2020257207A1 (en) 2019-04-16 2021-11-25 Vivace Therapeutics, Inc. Bicyclic compounds
US11524939B2 (en) 2019-11-13 2022-12-13 Akebia Therapeutics, Inc. Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino} acetic acid

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DE4015255A1 (de) * 1990-05-12 1991-11-14 Hoechst Ag Oxalyl-aminosaeurederivate, verfahren zu ihrer herstellung und ihrer verwendung als arzneimittel zur inhibierung der prolyl-hydroxylase
US5192773A (en) * 1990-07-02 1993-03-09 Vertex Pharmaceuticals, Inc. Immunosuppressive compounds
EP0541042A1 (fr) * 1991-11-05 1993-05-12 Hoechst Aktiengesellschaft Dérivés d'acide pyridine 2,4- et 2,5-dicarboxyliques, leur procédé de préparation et leur utilisation comme médicaments
TW352384B (en) * 1992-03-24 1999-02-11 Hoechst Ag Sulfonamido- or sulfonamidocarbonylpyridine-2-carboxamides, process for their preparation and their use as pharmaceuticals
DE4233124A1 (de) * 1992-10-02 1994-04-07 Hoechst Ag Acylsulfonamido- und Sulfonamidopyridin-2-carbonsäureester sowie ihre Pyridin-N-oxide, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
DK122693D0 (da) * 1993-10-29 1993-10-29 Hempels Skibsfarve Fab J C Marin struktur
DE59401923D1 (de) * 1993-11-02 1997-04-10 Hoechst Ag Substituierte heterocyclische Carbonsäureamidester, ihre Herstellung und ihre Verwendung als Arzneimittel
EP0650961B1 (fr) * 1993-11-02 1997-03-05 Hoechst Aktiengesellschaft Amides d'acide carboxylique hétérocycliques substitués, leur preparation et leur utilisation comme médicaments
CA2138929A1 (fr) * 1993-12-30 1995-07-01 Klaus Weidmann Carboxamides heterocycliques substitues, leur preparation et leur utilisation comme composes pharmaceutiques

Also Published As

Publication number Publication date
SI9600287A (en) 1997-04-30
CN1154365A (zh) 1997-07-16
JPH09124606A (ja) 1997-05-13
DE59610950D1 (de) 2004-05-06
CZ283396A3 (en) 1997-04-16
HUP9602685A2 (hu) 1998-09-28
HU9602685D0 (en) 1996-11-28
NO308600B1 (no) 2000-10-02
IL135495A (en) 2002-12-01
PL316321A1 (en) 1997-04-01
US5719164A (en) 1998-02-17
HUP9602685A3 (en) 2001-04-28
CN1120157C (zh) 2003-09-03
US5726305A (en) 1998-03-10
IL119302A0 (en) 1996-12-05
CN1282737A (zh) 2001-02-07
EP0765871B1 (fr) 2004-03-31
NO964093D0 (no) 1996-09-27
AU728208B2 (en) 2001-01-04
ATE263155T1 (de) 2004-04-15
CA2186717A1 (fr) 1997-03-29
EP0765871A1 (fr) 1997-04-02
NZ299455A (en) 1997-06-24
MX9604378A (es) 1997-03-29
AU6583896A (en) 1997-04-10
NO964093L (no) 1997-04-01
KR970061869A (ko) 1997-09-12
ES2215184T3 (es) 2004-10-01
MY133647A (en) 2007-11-30

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