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PE20080671A1 - DERIVADOS DE 2-ARIL-6-FENIL-IMIDAZO[1,2-a]PIRIDINAS, SU PREPARACION Y SU APLICACION EN TERAPEUTICA - Google Patents

DERIVADOS DE 2-ARIL-6-FENIL-IMIDAZO[1,2-a]PIRIDINAS, SU PREPARACION Y SU APLICACION EN TERAPEUTICA

Info

Publication number
PE20080671A1
PE20080671A1 PE2007001266A PE2007001266A PE20080671A1 PE 20080671 A1 PE20080671 A1 PE 20080671A1 PE 2007001266 A PE2007001266 A PE 2007001266A PE 2007001266 A PE2007001266 A PE 2007001266A PE 20080671 A1 PE20080671 A1 PE 20080671A1
Authority
PE
Peru
Prior art keywords
phenyl
imidazo
cycloalkyl
alkyl
pyridines
Prior art date
Application number
PE2007001266A
Other languages
English (en)
Inventor
Antonio Almario-Garcia
Patrick Lardenois
Anne Olivier
Original Assignee
Sanofi Aventis
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 Sanofi Aventis filed Critical Sanofi Aventis
Publication of PE20080671A1 publication Critical patent/PE20080671A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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
    • A61K31/437Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection

Landscapes

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

Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE 2-ARIL-6-FENIL-IMIDAZO[1,2-a]PIRIDINAS DE FORMULA (I) DONDE R1 ES FENILO O NAFTILO OPCIONALMENTE SUSTITUIDO CON HALOGENO, ALQUILO(C1-C6), CICLOALQUILO(C3-C7), ALCOXI(C1-C6), ENTRE OTROS; R2 Y R3 SON CADA UNO H, ALQUILO(C1-C6), CICLOALQUILO(C3-C7), CICLOALQUIL(C3-C7)ALQUILENO(C1-C3) OPCIONALMENTE SUSTITUIDO CON Rf, ENTRE OTROS, DONDE Rf ES HALOGENO, ALCOXI(C1-C6), CN, HIDROXILO, ENTRE OTROS; R4 ES H, ALQUILO(C1-C6), ARILO OPCIONALMENTE SUSTITUIDO CON HALOGENO, ALQUILO(C1-C6), CN, NITRO, ENTRE OTROS SUSTITUYENTES, CICLOALQUILO(C3-C7), ENTRE OTROS. SON COMPUESTOS PREFERIDOS: [4-(2-FENILIMIDAZO[1,2-a]PIRIDIN-6-IL)FENIL]METANOL, {4-[2-(4-PIRROLIDIN-1-ILFENIL)-IMIDAZO[1,2-a]PIRIDIN-6-IL]FENIL}METANOL, [4-(2-BIFENIL-4-ILIMIDAZO[1,2-a]PIRIDIN-6-IL)FENIL]METANOL, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON MODULADORES DE LOS RECEPTORES NUCLEARES NURR1 SIENDO UTILES EN EL TRATAMIENTO DE EPILEPSIA, OSTEOPOROSIS, ENFERMEDAD DE PARKINSON, ENFERMEDAD DE ALZHEIMER
PE2007001266A 2006-09-22 2007-09-20 DERIVADOS DE 2-ARIL-6-FENIL-IMIDAZO[1,2-a]PIRIDINAS, SU PREPARACION Y SU APLICACION EN TERAPEUTICA PE20080671A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0608350A FR2906250B1 (fr) 2006-09-22 2006-09-22 Derives de 2-aryl-6phenyl-imidazo(1,2-a) pyridines, leur preparation et leur application en therapeutique

Publications (1)

Publication Number Publication Date
PE20080671A1 true PE20080671A1 (es) 2008-07-14

Family

ID=37841968

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2007001266A PE20080671A1 (es) 2006-09-22 2007-09-20 DERIVADOS DE 2-ARIL-6-FENIL-IMIDAZO[1,2-a]PIRIDINAS, SU PREPARACION Y SU APLICACION EN TERAPEUTICA

Country Status (43)

Country Link
US (1) US7915284B2 (es)
EP (1) EP2069342B1 (es)
JP (1) JP5336378B2 (es)
KR (1) KR101470039B1 (es)
CN (1) CN101516881B (es)
AR (1) AR062897A1 (es)
AT (1) ATE467633T1 (es)
AU (1) AU2007298856B2 (es)
BR (1) BRPI0718517A2 (es)
CA (1) CA2662848C (es)
CL (1) CL2007002733A1 (es)
CO (1) CO6160308A2 (es)
CR (1) CR10643A (es)
CY (1) CY1110232T1 (es)
DE (1) DE602007006525D1 (es)
DK (1) DK2069342T3 (es)
EA (1) EA017442B1 (es)
ES (1) ES2345016T3 (es)
FR (1) FR2906250B1 (es)
GT (1) GT200900049A (es)
HN (1) HN2009000502A (es)
HR (1) HRP20100408T1 (es)
IL (1) IL197352A (es)
JO (1) JO2643B1 (es)
MA (1) MA30792B1 (es)
ME (1) ME00615B (es)
MX (1) MX2009002802A (es)
MY (1) MY145603A (es)
NI (1) NI200900037A (es)
NO (1) NO20091562L (es)
NZ (1) NZ575337A (es)
PE (1) PE20080671A1 (es)
PL (1) PL2069342T3 (es)
PT (1) PT2069342E (es)
RS (1) RS51412B (es)
SI (1) SI2069342T1 (es)
SV (1) SV2009003193A (es)
TN (1) TN2009000081A1 (es)
TW (1) TWI381837B (es)
UA (1) UA95976C2 (es)
UY (1) UY30603A1 (es)
WO (1) WO2008034974A1 (es)
ZA (1) ZA200901551B (es)

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FR2928923B1 (fr) * 2008-03-21 2010-04-23 Sanofi Aventis Derives polysubstitues de 2-heteroaryl-6-phenyl-imidazo °1,2-a!pyridines, leur preparation et leur application en therapeutiques
FR2928922B1 (fr) * 2008-03-21 2010-04-23 Sanofi Aventis Derives de 2-aryl-6-phenyl-imidazo°1,2-a!pyridines polysubstitues, leur preparation et leur application en therapeutique
FR2928921B1 (fr) 2008-03-21 2010-04-23 Sanofi Aventis Derives polysubstitues de 2-aryl-6-phenyl-imidazo°1,2-a!pyridines, leur preparation et leur application en therapeutique
FR2933609B1 (fr) 2008-07-10 2010-08-27 Fournier Lab Sa Utilisation de derives d'indole comme activateurs de nurr-1, pour le traitement de la maladie de parkinson.
FR2950345B1 (fr) * 2009-09-18 2011-09-23 Sanofi Aventis Derives acetyleniques de 5-phenyl-pyrazolopyridine, leur preparation et leur application en therapeutique
FR2950344B1 (fr) * 2009-09-18 2011-11-25 Sanofi Aventis Derives de 5-phenyl-pyrazolopyridine, leur preparation et leur aplication en therapeutique.
FR2953520B1 (fr) * 2009-12-04 2011-11-25 Sanofi Aventis Derives de diphenyl-pyrazolopyridines, leur preparation et leur application en therapeutique
EP2925756B1 (en) * 2012-11-29 2017-02-01 F. Hoffmann-La Roche AG Imidazopyridine derivatives
TWI644899B (zh) 2013-02-04 2018-12-21 健生藥品公司 Flap調節劑
EP3070085B1 (en) * 2013-02-04 2019-01-09 Janssen Pharmaceutica NV Flap modulators
DK3027615T3 (da) * 2013-08-02 2021-10-25 Pasteur Institut Korea Antiinfektionsforbindelser
KR20170137165A (ko) 2015-04-10 2017-12-12 베이진 엘티디 인돌아민 및/또는 트립토판 2,3-디옥시게나아제로서 신규한 5 또는 8-치환된 이미다조[1,5-a]피리딘
US20170107216A1 (en) 2015-10-19 2017-04-20 Incyte Corporation Heterocyclic compounds as immunomodulators
SG11201804152RA (en) 2015-11-19 2018-06-28 Incyte Corp Heterocyclic compounds as immunomodulators
MA44075A (fr) 2015-12-17 2021-05-19 Incyte Corp Dérivés de n-phényl-pyridine-2-carboxamide et leur utilisation en tant que modulateurs des interactions protéine/protéine pd-1/pd-l1
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AR108396A1 (es) 2016-05-06 2018-08-15 Incyte Corp Compuestos heterocíclicos como inmunomoduladores
TW201808902A (zh) 2016-05-26 2018-03-16 美商英塞特公司 作為免疫調節劑之雜環化合物
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EP3515914A4 (en) * 2016-09-24 2020-04-15 BeiGene, Ltd. INNOVATIVE 5- OR 8-SUBSTITUTED IMIDAZO [1,5-A] PYRIDINE AS SELECTIVE INHIBITORS OF INDOLEAMINE AND / OR TRYPTOPHANE-2,3-DIOXYGENASES
WO2018119286A1 (en) 2016-12-22 2018-06-28 Incyte Corporation Bicyclic heteroaromatic compounds as immunomodulators
PE20200005A1 (es) 2016-12-22 2020-01-06 Incyte Corp Derivados de tetrahidro imidazo[4,5-c]piridina como inductores de internalizacion pd-l1
IL295660A (en) 2016-12-22 2022-10-01 Incyte Corp Benzooxazole derivatives as immunomodulators
EP3558989B1 (en) 2016-12-22 2021-04-14 Incyte Corporation Triazolo[1,5-a]pyridine derivatives as immunomodulators
US20180179179A1 (en) 2016-12-22 2018-06-28 Incyte Corporation Heterocyclic compounds as immunomodulators
WO2019101188A1 (en) 2017-11-25 2019-05-31 Beigene, Ltd. Novel benzoimidazoles as selective inhibitors of indoleamine 2, 3-dioxygenases
KR20250067967A (ko) 2018-03-30 2025-05-15 인사이트 코포레이션 면역조절제로서 복소환형 화합물
HUE061503T2 (hu) 2018-05-11 2023-07-28 Incyte Corp Tetrahidro-imidazo[4,5-C]piridin-származékok mint PD-L1 immunmodulátorok
EP4010342A1 (en) 2019-08-09 2022-06-15 Incyte Corporation Salts of a pd-1/pd-l1 inhibitor
TWI879811B (zh) 2019-09-30 2025-04-11 美商英塞特公司 作為免疫調節劑之吡啶并[3,2-d]嘧啶化合物
PH12022551136A1 (en) 2019-11-11 2023-10-09 Incyte Corp Salts and crystalline forms of a pd-1/pd-l1 inhibitor
TWI759962B (zh) * 2019-11-13 2022-04-01 香港商新旭生技股份有限公司 用於降解tau蛋白聚集體的化合物及其用途
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Also Published As

Publication number Publication date
MEP10709A (en) 2011-12-20
CN101516881B (zh) 2012-07-18
TW200833329A (en) 2008-08-16
JP5336378B2 (ja) 2013-11-06
CA2662848C (fr) 2014-12-23
DK2069342T3 (da) 2010-08-23
HRP20100408T1 (hr) 2010-09-30
RS51412B (sr) 2011-02-28
KR101470039B1 (ko) 2014-12-05
FR2906250B1 (fr) 2008-10-31
NO20091562L (no) 2009-04-20
CY1110232T1 (el) 2015-01-14
AR062897A1 (es) 2008-12-10
UA95976C2 (en) 2011-09-26
EA017442B1 (ru) 2012-12-28
MY145603A (en) 2012-03-15
CL2007002733A1 (es) 2008-04-11
JO2643B1 (en) 2012-06-17
US20090253735A1 (en) 2009-10-08
GT200900049A (es) 2010-03-04
EA200970311A1 (ru) 2009-08-28
PL2069342T3 (pl) 2010-10-29
ZA200901551B (en) 2010-06-30
NI200900037A (es) 2014-02-20
ATE467633T1 (de) 2010-05-15
KR20090054449A (ko) 2009-05-29
IL197352A0 (en) 2009-12-24
US7915284B2 (en) 2011-03-29
HN2009000502A (es) 2011-07-11
HK1135388A1 (en) 2010-06-04
CA2662848A1 (fr) 2008-03-27
FR2906250A1 (fr) 2008-03-28
TN2009000081A1 (en) 2010-08-19
NZ575337A (en) 2011-12-22
TWI381837B (zh) 2013-01-11
DE602007006525D1 (de) 2010-06-24
SV2009003193A (es) 2010-02-01
PT2069342E (pt) 2010-07-19
JP2010504309A (ja) 2010-02-12
CO6160308A2 (es) 2010-05-20
EP2069342A1 (fr) 2009-06-17
IL197352A (en) 2014-11-30
MA30792B1 (fr) 2009-10-01
MX2009002802A (es) 2009-04-01
ME00615B (me) 2011-12-20
SI2069342T1 (sl) 2010-09-30
WO2008034974A1 (fr) 2008-03-27
CN101516881A (zh) 2009-08-26
BRPI0718517A2 (pt) 2013-11-19
AU2007298856A1 (en) 2008-03-27
AU2007298856B2 (en) 2012-08-09
UY30603A1 (es) 2008-05-02
EP2069342B1 (fr) 2010-05-12
ES2345016T3 (es) 2010-09-13
CR10643A (es) 2009-04-29

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