PE20091819A1 - DERIVADOS POLISUSTITUIDOS DE 2-HETEROARIL-6-FENIL-IMIDAZO[1,2-a] PIRIDINAS, SU PREPARACION Y SU APLIACION EN TERAPEUTICA - Google Patents

DERIVADOS POLISUSTITUIDOS DE 2-HETEROARIL-6-FENIL-IMIDAZO[1,2-a] PIRIDINAS, SU PREPARACION Y SU APLIACION EN TERAPEUTICA

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Publication number
PE20091819A1
PE20091819A1 PE2009000417A PE2009000417A PE20091819A1 PE 20091819 A1 PE20091819 A1 PE 20091819A1 PE 2009000417 A PE2009000417 A PE 2009000417A PE 2009000417 A PE2009000417 A PE 2009000417A PE 20091819 A1 PE20091819 A1 PE 20091819A1
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PE
Peru
Prior art keywords
imidazo
pyridin
halo
phenyl
alkyl
Prior art date
Application number
PE2009000417A
Other languages
English (en)
Inventor
Peretti Danielle De
Yannick Evanno
Patrick Lardenois
Original Assignee
Sanofi Aventis
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Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39764968&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20091819(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sanofi Aventis filed Critical Sanofi Aventis
Publication of PE20091819A1 publication Critical patent/PE20091819A1/es

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    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
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    • 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
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    • 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
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P25/00Drugs for disorders of the nervous system
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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    • 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
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    • 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
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    • A61P25/00Drugs for disorders of the nervous system
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    • 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]
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    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
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    • A61P9/00Drugs for disorders of the cardiovascular system
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen 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
    • C07D213/72Nitrogen atoms
    • C07D213/73Unsubstituted amino or imino radicals
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    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/18Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804Compounds having Si-O-C linkages

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
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  • Addiction (AREA)
  • Urology & Nephrology (AREA)
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  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

SE REFIERE A COMPUESTOS DERIVADOS POLISUSTITUIDOS DE 2-HETEROARIL-6-FENIL-IMIDAZO[1,2-a]PIRIDINAS DE FORMULA I, DONDE R1 ES HETEROARILO, HETEROCICLILO SUSTITUIDO O NO CON HALO, ALQUILO C1-C10, ENTRE OTROS; X ES 1-4 SUSTITUYENTES IDENTICOS O DIFERENTES SELECCIONADOS DE H, HALO, ALQUILO C1-C10, ENTRE OTROS; R ES 1-4 SUSTIUYENTES IDENTICOS O DIFERENTES SELECCIONADOS DE H, HALOALQUILO C1-C10, ALCOXI C1-C10, ENTRE OTROS; R2 Y R3 SON CADA UNO H, ALQUILO C1-C10, ARILO OPCIONALMENTE SUSTITUIDO CON HALO, NO2, ALQUILO C1-C10, ENTRE OTROS; R4 ES H, ARILO, ALQUILO(C1-C10) OPCIONALMENTE SUSTITUIDO CON Rf; Rf ES HALO, OH, ALCOXI(C1-C10), ENTRE OTROS. SON COMPUESTOS SELECCIONADOS: {3-[2-(5-METILISOXAZOL-4-IL)IMIDAZO[1,2-a]PIRIDIN-6-IL]FENIL}METANOL; [3-[2-(PIRIDIN-4-IL)IMIDAZO[1,2-a]PIRIDIN-6-IL]FENIL]METANOL; [3-[2-(TIAZOL-4-IL)IMIDAZO[1,2-a]PIRIDIN-6-IL]FENIL]METANOL; ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO DE PREPARACION Y UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON AFINES A RECEPTORES NUCLEARES Nurr-1 SIENDO UTILES EN EL TRATAMIENTO DE ENFERMEDAD DE PARKINSON, ESCLEROSIS MULTIPLE, CANCERES, ENTRE OTROS
PE2009000417A 2008-03-21 2009-03-19 DERIVADOS POLISUSTITUIDOS DE 2-HETEROARIL-6-FENIL-IMIDAZO[1,2-a] PIRIDINAS, SU PREPARACION Y SU APLIACION EN TERAPEUTICA PE20091819A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0801584A FR2928923B1 (fr) 2008-03-21 2008-03-21 Derives polysubstitues de 2-heteroaryl-6-phenyl-imidazo °1,2-a!pyridines, leur preparation et leur application en therapeutiques

Publications (1)

Publication Number Publication Date
PE20091819A1 true PE20091819A1 (es) 2009-12-12

Family

ID=39764968

Family Applications (1)

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PE2009000417A PE20091819A1 (es) 2008-03-21 2009-03-19 DERIVADOS POLISUSTITUIDOS DE 2-HETEROARIL-6-FENIL-IMIDAZO[1,2-a] PIRIDINAS, SU PREPARACION Y SU APLIACION EN TERAPEUTICA

Country Status (22)

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US (2) US8338451B2 (es)
EP (1) EP2262805B1 (es)
JP (1) JP5508386B2 (es)
KR (1) KR20100125432A (es)
CN (2) CN102036987B (es)
AR (1) AR070994A1 (es)
AU (1) AU2009253235B8 (es)
BR (1) BRPI0908907A2 (es)
CA (1) CA2719127C (es)
CL (1) CL2009000697A1 (es)
CO (1) CO6300867A2 (es)
EA (1) EA201071113A1 (es)
FR (1) FR2928923B1 (es)
IL (1) IL208245A0 (es)
MA (1) MA32249B1 (es)
MX (1) MX2010010261A (es)
NZ (1) NZ588084A (es)
PE (1) PE20091819A1 (es)
TW (1) TW200944525A (es)
UY (1) UY31729A (es)
WO (1) WO2009144395A1 (es)
ZA (1) ZA201006726B (es)

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FR2928924B1 (fr) * 2008-03-21 2010-04-23 Sanofi Aventis Derives polysubstitues de 6-heteroaryle-imidazo°1,2-a! pyridines, 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
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
FR2953520B1 (fr) * 2009-12-04 2011-11-25 Sanofi Aventis Derives de diphenyl-pyrazolopyridines, leur preparation et leur application en therapeutique
US8975276B2 (en) 2011-06-29 2015-03-10 Bristol-Myers Squibb Company Inhibitors of PDE10
WO2013029338A1 (en) * 2011-09-01 2013-03-07 Glaxo Group Limited Novel compounds
CN103214481B (zh) * 2012-01-21 2016-08-03 中国科学院上海药物研究所 新型咪唑并[1,2-a]吡啶类化合物、其制备方法、包含此类化合物的药物组合物及其用途
WO2015013635A2 (en) * 2013-07-25 2015-01-29 Dana-Farber Cancer Institute, Inc. Inhibitors of transcription factors and uses thereof
WO2016033440A1 (en) * 2014-08-29 2016-03-03 Chdi Foundation, Inc. Probes for imaging huntingtin protein
AU2016276963C1 (en) 2015-06-12 2021-08-05 Dana-Farber Cancer Institute, Inc. Combination therapy of transcription inhibitors and kinase inhibitors
SG10202007099TA (en) 2015-09-11 2020-08-28 Dana Farber Cancer Inst Inc Acetamide thienotriazoldiazepines and uses thereof
US11306105B2 (en) 2015-09-11 2022-04-19 Dana-Farber Cancer Institute, Inc. Cyano thienotriazolodiazepines and uses thereof
CN114957291A (zh) 2015-11-25 2022-08-30 达纳-法伯癌症研究所股份有限公司 二价溴结构域抑制剂及其用途
MX2019002444A (es) * 2016-08-29 2019-09-02 Univ Texas Inhibidores de cinasa de cremallera de leucina dual (dlk) para el tratamiento de enfermedades.
CN106906486B (zh) * 2017-02-22 2018-12-11 华南理工大学 3-溴-2-苯基-咪唑并[1,2-α]吡啶类衍生物的电化学合成方法
CN111978318A (zh) * 2019-05-22 2020-11-24 上海道熵生物科技有限公司 咪唑并吡啶类mnk1/mnk2激酶抑制剂及其制备方法和应用
CN111978325B (zh) * 2019-05-22 2023-11-17 中国药科大学 咪唑并哒嗪类mnk1/mnk2激酶抑制剂及其制备方法和应用
US11560366B2 (en) 2019-10-21 2023-01-24 Board Of Regents, The University Of Texas System Bicyclo[1.1.1]pentane inhibitors of dual leucine zipper (DLK) kinase for the treatment of disease
CN115916338A (zh) * 2020-04-24 2023-04-04 加利福尼亚大学董事会 Nurr1受体调节剂及其用途
AR125239A1 (es) 2021-04-02 2023-06-28 Kumiai Chemical Industry Co Compuesto heterocíclico y uso del mismo
CN117916240A (zh) * 2021-07-16 2024-04-19 赛诺菲 用于疗法的咪唑并[1,2-b][1,2,4]***衍生物
WO2023285465A1 (en) * 2021-07-16 2023-01-19 Sanofi 6h-imidazo[1,2-a]pyrrolo[2,3-e]pyridine derivatives for use in therapy
CN115490687B (zh) * 2022-09-19 2023-10-27 国家烟草质量监督检验中心 3-苯并呋喃基硫咪唑并吡啶衍生物及其制备方法和应用

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EP1268478B1 (en) * 2000-03-31 2007-05-02 Ortho-McNeil Pharmaceutical, Inc. Phenyl-substituted imidazopyridines
OA13151A (en) 2003-02-26 2006-12-13 Sugen Inc Aminoheteroaryl compounds as protein kinase inhibitors.
FR2903105A1 (fr) * 2006-07-03 2008-01-04 Sanofi Aventis Sa Derives de 2-benzoyl-imidazopyridines, leur preparation et leur application en therapeutique
FR2903107B1 (fr) * 2006-07-03 2008-08-22 Sanofi Aventis Sa Derives d'imidazopyridine-2-carboxamides, leur preparation et leur application en therapeutique
FR2903106B1 (fr) * 2006-07-03 2010-07-30 Sanofi Aventis Utilisations de 2-benzoyl-imidazopyridines en therapeutique
FR2906250B1 (fr) * 2006-09-22 2008-10-31 Sanofi Aventis Sa Derives de 2-aryl-6phenyl-imidazo(1,2-a) pyridines, leur preparation et leur application en therapeutique
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
FR2928924B1 (fr) * 2008-03-21 2010-04-23 Sanofi Aventis Derives polysubstitues de 6-heteroaryle-imidazo°1,2-a! pyridines, leur preparation et leur application en therapeutique

Also Published As

Publication number Publication date
FR2928923A1 (fr) 2009-09-25
EA201071113A1 (ru) 2011-04-29
CA2719127C (fr) 2016-08-16
NZ588084A (en) 2012-07-27
MX2010010261A (es) 2010-12-06
WO2009144395A1 (fr) 2009-12-03
AU2009253235A1 (en) 2009-12-03
WO2009144395A8 (fr) 2010-10-14
MA32249B1 (fr) 2011-04-01
JP2011515383A (ja) 2011-05-19
FR2928923B1 (fr) 2010-04-23
CA2719127A1 (fr) 2009-12-03
EP2262805A1 (fr) 2010-12-22
CL2009000697A1 (es) 2010-04-09
AU2009253235B8 (en) 2013-07-25
JP5508386B2 (ja) 2014-05-28
CN103254221A (zh) 2013-08-21
US20130123288A1 (en) 2013-05-16
CN103254221B (zh) 2014-11-19
EP2262805B1 (fr) 2014-10-22
US20110065727A1 (en) 2011-03-17
CN102036987A (zh) 2011-04-27
US8338451B2 (en) 2012-12-25
CN102036987B (zh) 2014-01-01
UY31729A (es) 2009-11-10
AU2009253235B2 (en) 2013-07-04
ZA201006726B (en) 2011-11-30
AU2009253235A8 (en) 2013-07-25
KR20100125432A (ko) 2010-11-30
CO6300867A2 (es) 2011-07-21
AR070994A1 (es) 2010-05-19
IL208245A0 (en) 2010-12-30
TW200944525A (en) 2009-11-01
BRPI0908907A2 (pt) 2019-09-10

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