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WO2008003858A3 - Utilisation de dérivés d'imidazo[1, 2-a]pyridine-2-carboxamides en thérapeutique - Google Patents

Utilisation de dérivés d'imidazo[1, 2-a]pyridine-2-carboxamides en thérapeutique Download PDF

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Publication number
WO2008003858A3
WO2008003858A3 PCT/FR2007/001127 FR2007001127W WO2008003858A3 WO 2008003858 A3 WO2008003858 A3 WO 2008003858A3 FR 2007001127 W FR2007001127 W FR 2007001127W WO 2008003858 A3 WO2008003858 A3 WO 2008003858A3
Authority
WO
WIPO (PCT)
Prior art keywords
alkyl
phenyl group
carboxamides
imidazo
therapeutics
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/FR2007/001127
Other languages
English (en)
Other versions
WO2008003858A2 (fr
Inventor
Jean-Francois Peyronel
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.)
Sanofi Aventis France
Original Assignee
Sanofi Aventis France
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 to AU2007271010A priority Critical patent/AU2007271010A1/en
Priority to MX2008016550A priority patent/MX2008016550A/es
Priority to CA002656363A priority patent/CA2656363A1/fr
Priority to EP07803835A priority patent/EP2043643A2/fr
Priority to BRPI0714317-6A2A priority patent/BRPI0714317A2/pt
Priority to JP2009517334A priority patent/JP2009541473A/ja
Application filed by Sanofi Aventis France filed Critical Sanofi Aventis France
Publication of WO2008003858A2 publication Critical patent/WO2008003858A2/fr
Publication of WO2008003858A3 publication Critical patent/WO2008003858A3/fr
Priority to IL195949A priority patent/IL195949A0/en
Priority to US12/337,018 priority patent/US20090149494A1/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
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/08—Antiepileptics; Anticonvulsants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • 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

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Epidemiology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Psychology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Addiction (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

L'utilisation de composés répondant à la formule (I), dans laquelle R1, R2, R3 et R4 sont hydrogène et X un groupe phényle éventuellement substitué par un ou plusieurs groupes choisis indépendamment les uns des autres parmi les atomes ou groupes suivants halogène, (C1-C6)alcoxy, (C1-C6)alkyle, cyclo(C1-C6)alkyle(C1-C6)alkyle, cyclo(C1-C6)alkyle(C1-C6)alcoxy, NRaRb; ou R2 est chlore et X est un para-fluoro-phényle; ou R3 est un méthyle et X est un groupe phényle non substitué; ou R1 est un méthyle et X est un groupe phényle non substitué, Ra et Rb sont indépendamment l'un de l'autre, hydrogène, (C1-C6)alkyle ou forment avec l'atome d'azote un cycle de 4 à 7 chaînons, à l'état de base ou de sel d'addition à un acide pour la préparation d'un médicament pour le traitement et la prévention des maladies dans lesquelles le récepteur NOT est impliqué.
PCT/FR2007/001127 2006-07-03 2007-07-03 Utilisation de dérivés d'imidazo[1, 2-a]pyridine-2-carboxamides en thérapeutique Ceased WO2008003858A2 (fr)

Priority Applications (8)

Application Number Priority Date Filing Date Title
MX2008016550A MX2008016550A (es) 2006-07-03 2007-07-03 Utilizacion terapeutica de derivados de imidazo [1,2-a] piridin-2-carboxamidas.
CA002656363A CA2656363A1 (fr) 2006-07-03 2007-07-03 Utilisation de derives d'imidazo[1, 2-a]pyridine-2-carboxamides en therapeutique
EP07803835A EP2043643A2 (fr) 2006-07-03 2007-07-03 Utilisation de dérivés d'imidazo[1, 2-a]pyridine-2-carboxamides en thérapeutique
BRPI0714317-6A2A BRPI0714317A2 (pt) 2006-07-03 2007-07-03 Utilização de derivados de imidazo [ 1,2-alfa] piridina -21- carboxamidas em terapêutica.
JP2009517334A JP2009541473A (ja) 2006-07-03 2007-07-03 治療剤におけるイミダゾ［１，２−ａ］ピリジン−２−カルボキサミド誘導体の使用
AU2007271010A AU2007271010A1 (en) 2006-07-03 2007-07-03 Use of derivatives of imidazo[1, 2-a]pyridine-2-carboxamides in therapeutics
IL195949A IL195949A0 (en) 2006-07-03 2008-12-15 Use of derivatives of imidazo[1,2-a]pyridine-2-carboxamides in therapeutics
US12/337,018 US20090149494A1 (en) 2006-07-03 2008-12-17 THERAPEUTIC USE OF IMIDAZO[1,2-a]PYRIDINE-2-CARBOXAMIDE DERIVATIVES

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0606013A FR2903108B1 (fr) 2006-07-03 2006-07-03 Utilisation de derives d'imidazo[1,2-a] pyridine-2-carboxamides en therapeutique.
FR0606013 2006-07-03

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US12/337,018 Continuation US20090149494A1 (en) 2006-07-03 2008-12-17 THERAPEUTIC USE OF IMIDAZO[1,2-a]PYRIDINE-2-CARBOXAMIDE DERIVATIVES

Publications (2)

Publication Number Publication Date
WO2008003858A2 WO2008003858A2 (fr) 2008-01-10
WO2008003858A3 true WO2008003858A3 (fr) 2008-04-17

Family

ID=37846294

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/FR2007/001127 Ceased WO2008003858A2 (fr) 2006-07-03 2007-07-03 Utilisation de dérivés d'imidazo[1, 2-a]pyridine-2-carboxamides en thérapeutique

Country Status (13)

Country Link
US (1) US20090149494A1 (fr)
EP (1) EP2043643A2 (fr)
JP (1) JP2009541473A (fr)
KR (1) KR20090034861A (fr)
CN (1) CN101484168A (fr)
AU (1) AU2007271010A1 (fr)
BR (1) BRPI0714317A2 (fr)
CA (1) CA2656363A1 (fr)
FR (1) FR2903108B1 (fr)
IL (1) IL195949A0 (fr)
MX (1) MX2008016550A (fr)
RU (1) RU2009103302A (fr)
WO (1) WO2008003858A2 (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2903107B1 (fr) * 2006-07-03 2008-08-22 Sanofi Aventis Sa Derives d'imidazopyridine-2-carboxamides, leur preparation et leur application en therapeutique
FR2925903B1 (fr) * 2008-01-02 2011-01-21 Sanofi Aventis DERIVES 6-HETEROCYCLIQUE-IMIDAZO°1,2-a!PYRIDINE-2- CARBOXAMIDES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE
FR2925900B1 (fr) * 2008-01-02 2011-03-04 Sanofi Aventis DERIVES DE N-PHENYL-IMIDAZO°1,2-a!PYRIDINE-2-CARBOXAMIDES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE
FR2925906B1 (fr) * 2008-01-02 2010-08-20 Sanofi Aventis COMPOSES DE N-PHENYL-IMIDAZO°1,2-a!PYRIDINE-2-CARBOXAMIDES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE
US20150329540A1 (en) * 2012-12-28 2015-11-19 Shin Nippon Biomedical Laboratories, Ltd. Oct3 activity inhibitor containing imidazopyridine derivative as active component, and oct3 detection agent
CN111377917B (zh) * 2018-12-29 2022-12-06 武汉朗来科技发展有限公司 杂环类化合物、中间体、其制备方法及应用

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002080911A2 (fr) * 2001-04-05 2002-10-17 Grünenthal GmbH Utilisation de composes imidazo[1,2-a]-pyridine-3-yl-amide- et imidazo[1,2-a]-pyridine-3-yl-amine substitues comme medicaments
WO2004072050A1 (fr) * 2003-02-14 2004-08-26 Novartis Ag Composes heterocycliques utiles en tant qu'activateurs de nurr-1

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6379666B1 (en) * 1999-02-24 2002-04-30 Edward L. Tobinick TNF inhibitors for the treatment of neurological, retinal and muscular disorders
FR2903107B1 (fr) * 2006-07-03 2008-08-22 Sanofi Aventis Sa Derives d'imidazopyridine-2-carboxamides, leur preparation et leur application en therapeutique
FR2925900B1 (fr) * 2008-01-02 2011-03-04 Sanofi Aventis DERIVES DE N-PHENYL-IMIDAZO°1,2-a!PYRIDINE-2-CARBOXAMIDES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE
FR2925901B1 (fr) * 2008-01-02 2011-03-04 Sanofi Aventis DERIVES DE N-HETEROCYCLIQUE-IMIDAZO°1,2-a!PYRIDINE-2- CARBOXAMIDES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002080911A2 (fr) * 2001-04-05 2002-10-17 Grünenthal GmbH Utilisation de composes imidazo[1,2-a]-pyridine-3-yl-amide- et imidazo[1,2-a]-pyridine-3-yl-amine substitues comme medicaments
WO2004072050A1 (fr) * 2003-02-14 2004-08-26 Novartis Ag Composes heterocycliques utiles en tant qu'activateurs de nurr-1

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
SCHMITT M ET AL: "IMIDAZO(1,2-B)PYRIDAZINES. XXIII SOME 5-DEAZA ANALOGUES. SYNTHESES OF SOME 2-ARYL-6-(CHLORO, METHOXY OR UNSUBSTITUTED)-3- (VARIOUSLY SUBSTITUTED)IMIDAZO(1,2-A)PYRIDINES AND THEIR AFFINITY FOR CENTRAL AND MITOCHONDRIAL BENZODIAZEPINE RECEPTORS", AUSTRALIAN JOURNAL OF CHEMISTRY, vol. 50, no. 7, 1997, pages 719 - 725, XP001010372, ISSN: 0004-9425 *

Also Published As

Publication number Publication date
KR20090034861A (ko) 2009-04-08
IL195949A0 (en) 2009-09-01
BRPI0714317A2 (pt) 2014-06-24
WO2008003858A2 (fr) 2008-01-10
RU2009103302A (ru) 2010-08-10
FR2903108B1 (fr) 2008-08-29
FR2903108A1 (fr) 2008-01-04
JP2009541473A (ja) 2009-11-26
CA2656363A1 (fr) 2008-01-10
AU2007271010A1 (en) 2008-01-10
MX2008016550A (es) 2009-02-12
US20090149494A1 (en) 2009-06-11
CN101484168A (zh) 2009-07-15
EP2043643A2 (fr) 2009-04-08

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