WO2005054232A1 - 1-acetic acid-indole, -indazole and-benzimidazole derivatives usful for the treatment of respiratory disorders - Google Patents

1-acetic acid-indole, -indazole and-benzimidazole derivatives usful for the treatment of respiratory disorders Download PDF

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Publication number
WO2005054232A1
WO2005054232A1 PCT/GB2004/004937 GB2004004937W WO2005054232A1 WO 2005054232 A1 WO2005054232 A1 WO 2005054232A1 GB 2004004937 W GB2004004937 W GB 2004004937W WO 2005054232 A1 WO2005054232 A1 WO 2005054232A1
Authority
WO
WIPO (PCT)
Prior art keywords
acetic acid
alkyl
pyrrolo
pyridine
optionally substituted
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.)
Ceased
Application number
PCT/GB2004/004937
Other languages
English (en)
French (fr)
Inventor
Roger Victor Bonnert
Rukhsana Tasneem Mohammed
Simon Teague
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.)
AstraZeneca UK Ltd
AstraZeneca AB
Original Assignee
AstraZeneca UK Ltd
AstraZeneca AB
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 AstraZeneca UK Ltd, AstraZeneca AB filed Critical AstraZeneca UK Ltd
Priority to JP2006540603A priority Critical patent/JP2007512299A/ja
Priority to US10/580,576 priority patent/US20080027092A1/en
Priority to EP04798644A priority patent/EP1699781A1/en
Publication of WO2005054232A1 publication Critical patent/WO2005054232A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • 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
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/02—Nasal agents, e.g. decongestants
    • 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
    • A61P11/06—Antiasthmatics
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
    • 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
    • C07D401/04—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 directly linked by a ring-member-to-ring-member bond

Definitions

  • Examples of 5- to 7-membered heterocyclic rings include pyridine, pyrimidine, thiazole, oxazole, isoxazole, pyrazole, imidazole, furan, thiophene, pyrrole, isothiazole and azulene.
  • R 3 is quinoline or phenyl, both optionally substituted as defined above.
  • Substituents can be present on any suitable position of an R 3 group, including nitrogen atoms where these are present.
  • Preferred substituents for R groups include halogen, S(O) x R , more preferably fluoro, chloro or SO 2 Me.
  • the compounds of formula (I) above may be converted to a pharmaceutically acceptable salt or solvate thereof, preferably a basic addition salt such as sodium, potassium, calcium, aluminium, lithium, magnesium, zinc, benzathine, chloroprocaine, choline, diethanolamine, ethanolamine, ethyldiamine, meglumine, tromethamine or procaine, or ano acid addition salt such as a hydrochloride, hydrobromide, phosphate, acetate, fumarate, maleate, tartrate, citrate, oxalate, methanesulphonate or -toluenesulphonate.
  • Preferred salts include sodium salts. It will be appreciated that certain functional groups may need to be protected using standard protecting groups.
  • a compound of the invention can be used in the treatment of: (1) ( respiratory tract) - obstructive diseases of the airways including: asthma, including bronchial, allergic, intrinsic, extrinsic, exercise-induced, drug-induced (including aspirin and NSAID-induced) and dust-induced asthma, both intermittent and persistent and of all severities, and other causes of airway hyper-responsiveness ; chronic obstructive pulmonary disease (COPD) ; bronchitis , including infectious and eosinophilic bronchitis; emphysema; bronchiectasis; cystic fibrosis; sarcoidosis; farmer's lung and related diseases; hypersensitivity pneumonitis; lung fibrosis, including cryptogenic fibrosing alveolitis, idiopathic interstitial pneumonias, fibrosis complicating anti- neoplastic therapy and chronic infection, including tuber
  • the present invention still further relates to the combination of a compound of the invention together with other modulators of chemokine receptor function such as CCR1, CCR2, CCR2A, CCR2B, CCR3, CCR4, CCR5, CCR6, CCR7, CCR8, CCR9, CCR10 and CCR11 (for the C-C family); CXCR1, CXCR3, CXCR4 and CXCR5 (for the C-X-C family)5 and CX 3 CR1 for the C-X3-C family.
  • the present invention still further relates to the combination of a compound of the invention together with antiviral agents such as Viracept, AZT, aciclovir and famciclovir, and antisepsis compounds such as Valant.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pulmonology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Otolaryngology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
PCT/GB2004/004937 2003-11-26 2004-11-24 1-acetic acid-indole, -indazole and-benzimidazole derivatives usful for the treatment of respiratory disorders Ceased WO2005054232A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP2006540603A JP2007512299A (ja) 2003-11-26 2004-11-24 呼吸器系疾患の処置に有用な１−酢酸−インドール、−インダゾールおよび−ベンズイミダゾール誘導体
US10/580,576 US20080027092A1 (en) 2003-11-26 2004-11-24 1-Acetic Acid-Indole, -Indazole and -Benzimidazole Derivatives Useful for the Treatment of Respiratory Disorders
EP04798644A EP1699781A1 (en) 2003-11-26 2004-11-24 1-acetic acid-indole, -indazole and -benzimidazole derivatives useful for the treatment of respiratory disorders

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE0303180A SE0303180D0 (sv) 2003-11-26 2003-11-26 Novel compounds
SE0303180-4 2003-11-26

Publications (1)

Publication Number Publication Date
WO2005054232A1 true WO2005054232A1 (en) 2005-06-16

Family

ID=29729190

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB2004/004937 Ceased WO2005054232A1 (en) 2003-11-26 2004-11-24 1-acetic acid-indole, -indazole and-benzimidazole derivatives usful for the treatment of respiratory disorders

Country Status (6)

Country Link
US (1) US20080027092A1 (https=)
EP (1) EP1699781A1 (https=)
JP (1) JP2007512299A (https=)
CN (1) CN1906189A (https=)
SE (1) SE0303180D0 (https=)
WO (1) WO2005054232A1 (https=)

Cited By (49)

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WO2005094816A1 (en) * 2004-03-11 2005-10-13 Actelion Pharmaceuticals Ltd Indol-1-yl-acetic acid derivatives
WO2005121141A1 (en) * 2004-06-10 2005-12-22 Oxagen Limited Pyrrolopyridine derivatives and use thereof for treating diseases mediated by prostaglandin d2 (pgd2)
WO2006081343A1 (en) * 2005-01-26 2006-08-03 Aventis Pharmaceuticals Inc. 2-phenyl-indoles as prostaglandin d2 receptor antagonists
GB2422830A (en) * 2005-02-04 2006-08-09 Oxagen Ltd Pyrrolopyridines and their use in the treatment of diseases mediated by PGD2 at the CRTH2 receptor
WO2006095183A1 (en) * 2005-03-11 2006-09-14 Oxagen Limited 1-acetic acid-indole derivatives with pgd2 antagonist activity
WO2007007778A1 (ja) * 2005-07-13 2007-01-18 Taiho Pharmaceutical Co., Ltd. プロスタグランジンｄ合成酵素を阻害するベンゾイミダゾール化合物
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WO2007010965A1 (ja) * 2005-07-22 2007-01-25 Shionogi & Co., Ltd. Ｐｇｄ２受容体アンタゴニスト活性を有するアザインドール酸誘導体
WO2009077728A1 (en) * 2007-12-14 2009-06-25 Argenta Discovery Limited Indoles and their therapeutic use
WO2009093026A1 (en) * 2008-01-22 2009-07-30 Oxagen Limited Compounds having crth2 antagonist activity
WO2010006944A1 (en) * 2008-07-15 2010-01-21 F. Hoffmann-La Roche Ag Aminotetrahydroindazoloacetic acids
US7687535B2 (en) 2003-05-27 2010-03-30 Astrazeneca Ab Substituted 3-sulfur indoles
US7709521B2 (en) 2003-08-18 2010-05-04 Astrazeneca Ab Substituted indole derivatives for pharmaceutical compositions for treating respiratory diseases
US7723373B2 (en) 2002-07-17 2010-05-25 Astrazeneca Ab Indole-3-sulphur derivatives
US7741360B2 (en) 2006-05-26 2010-06-22 Astrazeneca Ab Bi-aryl or aryl-heteroaryl substituted indoles
US7754735B2 (en) 2002-05-30 2010-07-13 Astrazeneca Ab Substituted indoles
US7781598B2 (en) 2005-01-13 2010-08-24 Astrazeneca Ab Process for the preparation of substituted indoles
US7781454B2 (en) 2006-12-13 2010-08-24 Merck Sharp & Dohme Corp. Non-nucleoside reverse transcriptase inhibitors
US8039474B2 (en) 2004-12-27 2011-10-18 Actelion Pharmaceutical Ltd. 2,3,4,9-tetrahydro-1H-carbazole derivatives as CRTH2 receptor antagonists
JP4870166B2 (ja) * 2005-12-09 2012-02-08 ノバルティス アーゲー 抗炎症剤としての二環式ヘテロ環式化合物
US8124629B2 (en) 2008-11-17 2012-02-28 Hoffmann-La Roche Inc. Naphthylacetic acids
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US8470884B2 (en) 2011-11-09 2013-06-25 Hoffmann-La Roche Inc. Alkenyl naphthylacetic acids
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WO2012104007A3 (de) * 2011-02-01 2013-10-17 Merck Patent Gmbh 7-azaindolderivate
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US9096595B2 (en) 2011-04-14 2015-08-04 Actelion Pharmaceuticals Ltd 7-(heteroaryl-amino)-6,7,8,9-tetrahydropyrido[1,2-a]indol acetic acid derivatives and their use as prostaglandin D2 receptor modulators
WO2017019858A1 (en) 2015-07-30 2017-02-02 The Trustees Of The University Of Pennsylvania Single nucleotide polymorphic alleles of human dp-2 gene for detection of susceptibility to hair growth inhibition by pgd2
US9850241B2 (en) 2014-03-18 2017-12-26 Idorsia Pharmaceuticals Ltd Azaindole acetic acid derivatives and their use as prostaglandin D2 receptor modulators
US9879006B2 (en) 2014-03-17 2018-01-30 Idorsia Pharmaceuticals Ltd Azaindole acetic acid derivatives and their use as prostaglandin D2 receptor modulators
US9889082B2 (en) 2006-06-16 2018-02-13 The Trustees Of The University Of Pennsylvania Methods and compositions for inhibiting or reducing hair loss, acne, rosacea, prostate cancer, and BPH
WO2018042377A1 (en) * 2016-09-03 2018-03-08 Torrent Pharmaceuticals Limited Novel indazole compounds
CN108586311A (zh) * 2018-03-23 2018-09-28 温州医科大学 一种3-硫醚吲哚或3-硒醚吲哚的制备方法
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US10227350B2 (en) 2016-09-23 2019-03-12 Gilead Sciences, Inc. Phosphatidylinositol 3-kinase inhibitors
US10351560B2 (en) 2015-09-15 2019-07-16 Idorsia Pharmaceuticals Ltd Crystalline forms
US10479770B2 (en) 2016-09-23 2019-11-19 Gilead Sciences, Inc. Phosphatidylinositol 3-kinase inhibitors
US11046658B2 (en) 2018-07-02 2021-06-29 Incyte Corporation Aminopyrazine derivatives as PI3K-γ inhibitors
US11926616B2 (en) 2018-03-08 2024-03-12 Incyte Corporation Aminopyrazine diol compounds as PI3K-γ inhibitors
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JPWO2010087425A1 (ja) * 2009-01-30 2012-08-02 国立大学法人京都大学 前立腺癌の進行抑制剤および進行抑制方法
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US7754735B2 (en) 2002-05-30 2010-07-13 Astrazeneca Ab Substituted indoles
US7166607B2 (en) 2002-05-30 2007-01-23 Astrazeneca Ab Substituted indoles
US7723373B2 (en) 2002-07-17 2010-05-25 Astrazeneca Ab Indole-3-sulphur derivatives
US7687535B2 (en) 2003-05-27 2010-03-30 Astrazeneca Ab Substituted 3-sulfur indoles
US7709521B2 (en) 2003-08-18 2010-05-04 Astrazeneca Ab Substituted indole derivatives for pharmaceutical compositions for treating respiratory diseases
WO2005094816A1 (en) * 2004-03-11 2005-10-13 Actelion Pharmaceuticals Ltd Indol-1-yl-acetic acid derivatives
US7897788B2 (en) 2004-03-11 2011-03-01 Actelion Pharmaceutical Ltd. Indol-1-yl-acetic acid derivatives
WO2005121141A1 (en) * 2004-06-10 2005-12-22 Oxagen Limited Pyrrolopyridine derivatives and use thereof for treating diseases mediated by prostaglandin d2 (pgd2)
US8039474B2 (en) 2004-12-27 2011-10-18 Actelion Pharmaceutical Ltd. 2,3,4,9-tetrahydro-1H-carbazole derivatives as CRTH2 receptor antagonists
US7781598B2 (en) 2005-01-13 2010-08-24 Astrazeneca Ab Process for the preparation of substituted indoles
WO2006081343A1 (en) * 2005-01-26 2006-08-03 Aventis Pharmaceuticals Inc. 2-phenyl-indoles as prostaglandin d2 receptor antagonists
GB2422830A (en) * 2005-02-04 2006-08-09 Oxagen Ltd Pyrrolopyridines and their use in the treatment of diseases mediated by PGD2 at the CRTH2 receptor
WO2006095183A1 (en) * 2005-03-11 2006-09-14 Oxagen Limited 1-acetic acid-indole derivatives with pgd2 antagonist activity
US8044088B2 (en) 2005-03-11 2011-10-25 Oxagen Limited 1-acetic acid-indole derivatives with PGD2 antagonist activity
US7951956B2 (en) 2005-07-13 2011-05-31 Taiho Pharmaceuticals Co., Ltd. Benzoimidazole compound capable of inhibiting prostaglandin D synthetase
WO2007007778A1 (ja) * 2005-07-13 2007-01-18 Taiho Pharmaceutical Co., Ltd. プロスタグランジンｄ合成酵素を阻害するベンゾイミダゾール化合物
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WO2007010965A1 (ja) * 2005-07-22 2007-01-25 Shionogi & Co., Ltd. Ｐｇｄ２受容体アンタゴニスト活性を有するアザインドール酸誘導体
JP5064219B2 (ja) * 2005-07-22 2012-10-31 塩野義製薬株式会社 Ｐｇｄ２受容体アンタゴニスト活性を有するアザインドール酸誘導体
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