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WO2007038571A3 - Prolyl hydroxylase antagonists - Google Patents

Prolyl hydroxylase antagonists Download PDF

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Publication number
WO2007038571A3
WO2007038571A3 PCT/US2006/037611 US2006037611W WO2007038571A3 WO 2007038571 A3 WO2007038571 A3 WO 2007038571A3 US 2006037611 W US2006037611 W US 2006037611W WO 2007038571 A3 WO2007038571 A3 WO 2007038571A3
Authority
WO
WIPO (PCT)
Prior art keywords
antagonists
prolyl hydroxylase
quinolin
carbonyl
useful
Prior art date
Application number
PCT/US2006/037611
Other languages
French (fr)
Other versions
WO2007038571A2 (en
Inventor
Deping Chai
Mariela Colon
Kevin J Duffy
Duke M Fitch
Rosanna Tedesco
Michael N Zimmerman
Original Assignee
Smithkline Beecham Corp
Deping Chai
Mariela Colon
Kevin J Duffy
Duke M Fitch
Rosanna Tedesco
Michael N Zimmerman
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 Smithkline Beecham Corp, Deping Chai, Mariela Colon, Kevin J Duffy, Duke M Fitch, Rosanna Tedesco, Michael N Zimmerman filed Critical Smithkline Beecham Corp
Publication of WO2007038571A2 publication Critical patent/WO2007038571A2/en
Publication of WO2007038571A3 publication Critical patent/WO2007038571A3/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
    • C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
    • C07D215/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3 with oxygen atoms in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/06—Heterocyclic 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 only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic 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
    • C07D491/02—Heterocyclic 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
    • C07D491/04—Ortho-condensed systems
    • C07D491/056—Ortho-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

This invention relates to certain 2-[(quinolin-3-yl)carbonyl]aminoacetic acid derivatives of formula (I), where the various groups are defined herein, and which are useful in treating anemia.
PCT/US2006/037611 2005-09-26 2006-09-26 Prolyl hydroxylase antagonists WO2007038571A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US72052005P 2005-09-26 2005-09-26
US60/720,520 2005-09-26

Publications (2)

Publication Number Publication Date
WO2007038571A2 WO2007038571A2 (en) 2007-04-05
WO2007038571A3 true WO2007038571A3 (en) 2007-10-11

Family

ID=37900404

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2006/037611 WO2007038571A2 (en) 2005-09-26 2006-09-26 Prolyl hydroxylase antagonists

Country Status (1)

Country Link
WO (1) WO2007038571A2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8927591B2 (en) 2008-11-14 2015-01-06 Fibrogen, Inc. Thiochromene derivatives as HIF hydroxylase inhibitors

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AU2006326662B2 (en) 2005-12-09 2011-07-28 Amgen Inc. Quinolone based compounds exhibiting prolyl hydroxylase inhibitory activity, and compositions, and uses thereof
US7588924B2 (en) 2006-03-07 2009-09-15 Procter & Gamble Company Crystal of hypoxia inducible factor 1 alpha prolyl hydroxylase
ES2705587T3 (en) 2006-06-26 2019-03-26 Akebia Therapeutics Inc Prolyl hydroxylase inhibitors and methods of use
ES2380135T3 (en) 2006-11-22 2012-05-08 Ajinomoto Co., Inc. Method of preparation of phenylalanine derivatives having quinazolinadione skeleton and intermediates for their preparation
US8048892B2 (en) 2006-12-18 2011-11-01 Amgen Inc. Azaquinolone based compounds exhibiting prolyl hydroxylase inhibitory activity, compositions, and uses thereof
WO2008076427A2 (en) 2006-12-18 2008-06-26 Amgen Inc. Naphthalenone compounds exhibiting prolyl hydroxylase inhibitory activity, compositions, and uses thereof
CN101663037A (en) * 2007-04-18 2010-03-03 默克公司 Novel 1,8-naphthyridine compounds
ES2446418T3 (en) 2007-04-18 2014-03-07 Amgen, Inc Indanone derivatives that inhibit prolyl hydroxylase
JP2010524942A (en) 2007-04-18 2010-07-22 アムジエン・インコーポレーテツド Quinolone and azaquinolone that inhibit prolyl hydroxylase
AU2008248234B2 (en) 2007-05-04 2011-02-03 Amgen Inc. Thienopyridine and thiazolopyridine derivatives that inhibit prolyl hydroxylase activity
WO2008137084A2 (en) * 2007-05-04 2008-11-13 Amgen Inc. Diazaquinolones that inhibit prolyl hydroxylase activity
JP5466507B2 (en) 2007-09-27 2014-04-09 興和株式会社 A prophylactic and / or therapeutic agent for anemia comprising a tetrahydroquinoline compound as an active ingredient
US8269008B2 (en) 2007-12-03 2012-09-18 Fibrogen, Inc. Oxazolopyridine and isoxazolopyridine derivatives for use in the treatment of HIF-mediated conditions
JP2011507894A (en) * 2007-12-19 2011-03-10 グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー Prolyl hydroxylase inhibitor
WO2009089547A1 (en) 2008-01-11 2009-07-16 Fibrogen, Inc. Isothiazole-pyridine derivatives as modulators of hif (hypoxia inducible factor) activity
US8324405B2 (en) 2008-02-05 2012-12-04 Fibrogen, Inc. Chromene derivatives and use thereof as HIF hydroxylase activity inhibitors
JP2011513221A (en) * 2008-02-25 2011-04-28 メルク・シャープ・エンド・ドーム・コーポレイション Tetrahydroflopyridone
BRPI0911444B8 (en) 2008-04-28 2021-05-25 Janssen Pharmaceutica Nv benzoimidazoles as prolyl hydroxylase inhibitors and pharmaceutical composition comprising them
EP2334682B1 (en) 2008-08-20 2017-10-04 Fibrogen, Inc. Pyrrolo [ 1, 2 -b] pyridazine derivatives and their use as hif modulators
JP2012500802A (en) * 2008-08-21 2012-01-12 グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー Prolyl hydroxylase inhibitor
WO2010113498A1 (en) 2009-03-31 2010-10-07 興和株式会社 Prophylactic and/or therapeutic agent for anemia comprising tetrahydroquinoline compound as active ingredient
US8372857B2 (en) 2009-06-30 2013-02-12 Merck Sharp & Dohme Corp. Substituted 4-hydroxypyrimidine-5-carboxamides
CN102802629A (en) 2009-06-30 2012-11-28 默沙东公司 Substituted 4-hydroxypyrimidine-5-carboxamides
KR20120065311A (en) * 2009-07-15 2012-06-20 씬산 강 Compounds as hypoxia mimetics, and compositions, and uses thereof
NZ600017A (en) 2009-10-21 2014-03-28 Daiichi Sankyo Co Ltd 5-hydroxypyrimidine-4-carboxamide derivative
EP2496236B1 (en) 2009-11-06 2013-05-01 Aerpio Therapeutics Inc. Prolyl hydroxylase inhibitors
CA2813711A1 (en) 2010-10-14 2012-04-19 Immunahr Ab 1,2-dihydro-4-hydroxy-2-oxo-quinoline-3-carboxanilides as ahr activators.
WO2012106472A1 (en) 2011-02-02 2012-08-09 Fibrogen, Inc. Naphthyridine derivatives as inhibitors of hypoxia inducible factor (hif) hydroxylase
GB201102659D0 (en) 2011-02-15 2011-03-30 Isis Innovation Assay
WO2012170442A1 (en) 2011-06-06 2012-12-13 Akebia Therapeutics Inc. Compounds and compositions for stabilizing hypoxia inducible factor-2 alpha as a method for treating cancer
NO2686520T3 (en) 2011-06-06 2018-03-17
GB201113101D0 (en) 2011-07-28 2011-09-14 Isis Innovation Assay
WO2013043624A1 (en) 2011-09-23 2013-03-28 Merck Sharp & Dohme Corp. Substituted pyrimidines
WO2013043621A1 (en) 2011-09-23 2013-03-28 Merck Sharp & Dohme Corp. Substituted pyrimidines
EP3091009B1 (en) 2011-10-25 2018-08-29 Janssen Pharmaceutica NV Meglumine salt formulations of 1-(5,6-dichloro-1h-benzo[d]imidazol-2-yl)-1h-pyrazole-4-carboxylic acid
IN2015DN01035A (en) 2012-07-30 2015-06-26 Taisho Pharmaceutical Co Ltd
CN102964301A (en) * 2012-11-26 2013-03-13 盛世泰科生物医药技术(苏州)有限公司 Method for synthesizing IOX2
JP6026013B2 (en) 2012-12-24 2016-11-16 カディラ・ヘルスケア・リミテッド New quinolone derivatives
BR112015031027A2 (en) 2013-06-13 2017-08-29 Akebia Therapeutics Inc USE OF A COMPOUND, IN VITRO METHOD, PHARMACEUTICAL COMPOSITION AND SINGLE DOSAGE FORM
SG10202012791TA (en) 2013-11-15 2021-01-28 Akebia Therapeutics Inc Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino}acetic acid, compositions, and uses thereof
CA2959688C (en) * 2014-09-02 2024-02-27 Sunshine Lake Pharma Co., Ltd. Quinolone compounds and their use to treat diseases related to hypoxia inducible factor and/or erythropoietin
WO2016045127A1 (en) * 2014-09-28 2016-03-31 Merck Sharp & Dohme Corp. Inhibitors of hif prolyl hydroxylase
WO2016045125A1 (en) * 2014-09-28 2016-03-31 Merck Sharp & Dohme Corp. Inhibitors of hif prolyl hydroxylase
EP3240785B1 (en) 2014-12-29 2021-07-07 The United States of America, as represented by The Secretary, Department of Health and Human Services Small molecule inhibitors of lactate dehydrogenase and methods of use thereof
BR112017015852A2 (en) 2015-01-23 2018-03-27 Akebia Therapeutics Inc crystal form, hemichalic salt, hemicalic salt dihydrate, hydrous monosodium salt, monohydrate bisodium salt, anhydrous monosodium salt and method for preparing compound 1
HUE056958T2 (en) 2015-04-01 2022-04-28 Akebia Therapeutics Inc Compositions and methods for treating anemia
CN105294648B (en) * 2015-11-30 2017-11-28 山东罗欣药业集团股份有限公司 A kind of preparation method of sitafloxacin
CN108069952B (en) * 2016-11-08 2022-09-27 广东东阳光药业有限公司 Quinolinone compound and application thereof in medicines
MX2020011845A (en) 2018-05-09 2021-01-15 Akebia Therapeutics Inc Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2- carbonyl]amino]acetic acid.
US11524939B2 (en) 2019-11-13 2022-12-13 Akebia Therapeutics, Inc. Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino} acetic acid
AU2020390281A1 (en) * 2019-11-28 2022-05-19 Sunshine Lake Pharma Co., Ltd. Crystal form of quinolinone compound and use thereof
CN111269177B (en) * 2019-11-28 2023-05-09 广东东阳光药业有限公司 Crystal forms of quinolinone compounds
CN115010664A (en) * 2021-03-05 2022-09-06 广东东阳光药业有限公司 Crystal form of quinolinone compound and application thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4738971A (en) * 1981-03-03 1988-04-19 Aktiebolaset Leo N-aryl-1,2-dihydro-4-substituted-1-alkyl-2-oxo-quinoline-3-carboxamides
US20030153503A1 (en) * 2001-12-06 2003-08-14 Klaus Stephen J. Methods of increasing endogenous erythropoietin (EPO)

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4738971A (en) * 1981-03-03 1988-04-19 Aktiebolaset Leo N-aryl-1,2-dihydro-4-substituted-1-alkyl-2-oxo-quinoline-3-carboxamides
US20030153503A1 (en) * 2001-12-06 2003-08-14 Klaus Stephen J. Methods of increasing endogenous erythropoietin (EPO)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8927591B2 (en) 2008-11-14 2015-01-06 Fibrogen, Inc. Thiochromene derivatives as HIF hydroxylase inhibitors
US9149476B2 (en) 2008-11-14 2015-10-06 Fibrogen, Inc. Thiochromene derivatives as HIF hydroxylase inhibitors

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