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AR059016A4 - Derivados de aril-isoxazol-4-il-imidazo[1,2-a]piridina, metodo de preparacion, medicamentos que los contienen y usos en el tratamiento de trastornos cognitivos. - Google Patents

Derivados de aril-isoxazol-4-il-imidazo[1,2-a]piridina, metodo de preparacion, medicamentos que los contienen y usos en el tratamiento de trastornos cognitivos.

Info

Publication number
AR059016A4
AR059016A4 ARM070100173A ARM070100173A AR059016A4 AR 059016 A4 AR059016 A4 AR 059016A4 AR M070100173 A ARM070100173 A AR M070100173A AR M070100173 A ARM070100173 A AR M070100173A AR 059016 A4 AR059016 A4 AR 059016A4
Authority
AR
Argentina
Prior art keywords
lower alkyl
links
heteroaryl
isoxazol
imidazo
Prior art date
Application number
ARM070100173A
Other languages
English (en)
Inventor
Andrew Thomas
Bernd Buettelmann
Bo Han
Henner Knust
Original Assignee
Hoffmann La Roche
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=37965110&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR059016(A4) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of AR059016A4 publication Critical patent/AR059016A4/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
    • 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

Landscapes

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

Abstract

Derivados de aril-isoxazol-4-il-imidazo[1,2-a]piridina de la formula (1) en la que R1 es hidrogeno, halogeno, hidroxi, alquilo inferior, benciloxi u -O-(CH2)-(CO)-heteroarilo de 5 o 6 eslabones opcionalmente sustituido por arilo o por alquilo inferior; R2 es H, halogeno, alquilo inferior, alquinilo inferior, amino,-NHC(O)-R' o -(CO)-R'; R' es H, halogeno, ciano, alquilo inferior, alquinilo inferior, amino, -NHC(O)-Ra, -(CO)-Ra, -heterocicloalquilo de 5 o 6 eslabones en la posicion 1, opcionalmente sustituido por =O o es un heteroarilo de 5 o 6 eslabones en la posicion 1; R4 es hidrogeno o -heteroarilo de 5 o 6 eslabones; R5 es alquilo inferior o cicloalquilo; Ra es alcoxi inferior o NR'Rö, en el que R' y Rö con independencia entre sí son hidrogeno, alquilo inferior opcionalmente sustituido por hidroxi, alquinilo inferior, -(CH2)n-cicloalquilo, -(CH2)n-heterocicloalquilo de 5 o 6 eslabones o -(CH2)n-heteroarilo de 5 o 6 eslabones; n es un numero de 0 a 3; así como a las sales de adicion de ácido farmacéuticamente aceptables de los mismos. Se ha encontrado que este grupo de compuestos presentan una gran afinidad y selectividad para los sitios de fijacion del receptor GABA A alfa5 y pueden ser utiles como mejoradores cognitivos o para el tratamiento de trastornos cognitivos, por ejemplo la enfermedad de Alzheimer.
ARM070100173A 2006-01-17 2007-01-16 Derivados de aril-isoxazol-4-il-imidazo[1,2-a]piridina, metodo de preparacion, medicamentos que los contienen y usos en el tratamiento de trastornos cognitivos. AR059016A4 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP06100426 2006-01-17

Publications (1)

Publication Number Publication Date
AR059016A4 true AR059016A4 (es) 2008-03-05

Family

ID=37965110

Family Applications (1)

Application Number Title Priority Date Filing Date
ARM070100173A AR059016A4 (es) 2006-01-17 2007-01-16 Derivados de aril-isoxazol-4-il-imidazo[1,2-a]piridina, metodo de preparacion, medicamentos que los contienen y usos en el tratamiento de trastornos cognitivos.

Country Status (15)

Country Link
US (1) US7585874B2 (es)
EP (1) EP1979350A1 (es)
JP (1) JP4913157B2 (es)
KR (1) KR101062583B1 (es)
CN (1) CN101370807B (es)
AR (1) AR059016A4 (es)
AU (1) AU2007207053B2 (es)
BR (1) BRPI0706560A2 (es)
CA (1) CA2636112A1 (es)
IL (1) IL192636A0 (es)
NO (1) NO20082956L (es)
RU (1) RU2426732C2 (es)
TW (1) TWI338691B (es)
WO (1) WO2007082806A1 (es)
ZA (1) ZA200805839B (es)

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ZA200904477B (en) 2006-11-27 2010-09-29 Lundbeck & Co As H Heteroaryl amide derivatives
FR2913886B1 (fr) 2007-03-22 2012-03-02 Guerbet Sa Utilisation de nanoparticules metalliques dans le diagnostique de la maladie d'alzheimer
JP5416103B2 (ja) 2007-06-22 2014-02-12 エフ.ホフマン−ラ ロシュ アーゲー イソオキサゾール−イミダゾール誘導体
CA2707648C (en) 2007-12-04 2014-08-12 F. Hoffmann-La Roche Ag Isoxazolo-pyridine derivatives
PH12012500355A1 (en) * 2009-09-24 2019-11-29 Hoffmann La Roche Imidazopyridine or imidazopyrimidine derivatives as phosphodiesterase 10a inhibitors
US8410117B2 (en) * 2010-03-26 2013-04-02 Hoffmann-La Roche Inc. Imidazopyrimidine derivatives
WO2011143657A1 (en) 2010-05-14 2011-11-17 Dana-Farber Cancer Institute, Inc. Male contraceptive compositions and methods of use
WO2011143669A2 (en) 2010-05-14 2011-11-17 Dana-Farber Cancer Institute, Inc Compositions and methods for treating neoplasia, inflammatory disease and other disorders
MX354217B (es) 2010-05-14 2018-02-19 Dana Farber Cancer Inst Inc Composiciones y metodos para el tratamiento de leucemia.
US20150374705A1 (en) 2012-02-14 2015-12-31 Shanghai Institues for Biological Sciences Substances for treatment or relief of pain
CN104822679B (zh) * 2012-11-29 2016-10-19 霍夫曼-拉罗奇有限公司 咪唑并吡啶衍生物
US9714946B2 (en) 2013-03-14 2017-07-25 Dana-Farber Cancer Institute, Inc. Bromodomain binding reagents and uses thereof
MX2015014353A (es) * 2013-04-29 2016-04-07 Hoffmann La Roche Derivados de 2-fenil- o 2-hetaril-imidazol[1,2-a]piridina.
CA2918910A1 (en) 2013-07-25 2015-01-29 Dana-Farber Cancer Institute, Inc. Inhibitors of transcription factors and uses thereof
MX379463B (es) 2013-11-08 2025-03-10 Dana Farber Cancer Inst Inc Terapia de combinación para el cáncer usando inhibidores de la proteína bromodominio y extra-terminal.
EP3099677A4 (en) 2014-01-31 2017-07-26 Dana-Farber Cancer Institute, Inc. Diaminopyrimidine benzenesulfone derivatives and uses thereof
WO2015117087A1 (en) 2014-01-31 2015-08-06 Dana-Farber Cancer Institute, Inc. Uses of diazepane derivatives
CN105940005A (zh) 2014-01-31 2016-09-14 达纳-法伯癌症研究所股份有限公司 二氮杂环庚烷衍生物及其用途
JP2017506666A (ja) 2014-02-28 2017-03-09 テンシャ セラピューティクス,インコーポレイテッド 高インスリン血症に関連した症状の処置
EP3177147A4 (en) 2014-08-08 2018-01-24 Dana-Farber Cancer Institute, Inc. Dihydropteridinone derivatives and uses thereof
JP2017526741A (ja) 2014-08-08 2017-09-14 ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド ジアゼパン誘導体およびその使用
EP3212654B1 (en) 2014-10-27 2020-04-08 Tensha Therapeutics, Inc. Bromodomain inhibitors
US10702527B2 (en) 2015-06-12 2020-07-07 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
EP3347021A4 (en) 2015-09-11 2019-07-24 Dana-Farber Cancer Institute, Inc. CYANO-THIENOTRIAZOLOAZEPINES AND THEIR USES
SG11201803210YA (en) 2015-11-25 2018-05-30 Dana Farber Cancer Inst Inc Bivalent bromodomain inhibitors and uses thereof
MX2020003341A (es) * 2017-10-18 2020-09-17 Jubilant Epipad LLC Compuestos de imidazo-piridina como inhibidores de pad.

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1314191B1 (it) 1999-10-18 2002-12-06 Recordati Chem Pharm Derivati isossazolcarbossamidici
AU2001270297A1 (en) * 2000-06-30 2002-01-14 Neurogen Corporation 2-phenylimidazo(1,2-a)pyridine derivatives: a new class of gaba brain receptor ligands
PA8535601A1 (es) 2000-12-21 2002-11-28 Pfizer Derivados benzimidazol y piridilimidazol como ligandos para gabaa
US6596731B2 (en) * 2001-03-27 2003-07-22 Hoffmann-La Roche Inc. Substituted imidazo[1,2-A] pyridine derivatives
GB0108475D0 (en) * 2001-04-04 2001-05-23 Merck Sharp & Dohme New compounds
IL159697A0 (en) 2001-07-05 2004-06-20 Synaptic Pharma Corp Substituted anilinic piperidines as mch selective antagonists
GB0212048D0 (en) * 2002-05-24 2002-07-03 Merck Sharp & Dohme Therapeutic agents
JPWO2004035522A1 (ja) * 2002-08-30 2006-02-16 株式会社 ビーエフ研究所 プリオン蛋白蓄積性疾患の診断プローブおよび治療薬ならびにプリオン蛋白の染色剤
WO2004076452A1 (en) * 2003-02-26 2004-09-10 Merck Sharp & Dohme Limited 5,8-DIFLUOROIMIDAZO[1,2-a]PYRIDINES AS GABA-A α2/α3 LIGANDS FOR TREATING ANXIETY AND/OR DEPRESSION
JP2008502687A (ja) 2004-06-14 2008-01-31 タケダ サン ディエゴ インコーポレイテッド キナーゼ阻害剤

Also Published As

Publication number Publication date
TW200736257A (en) 2007-10-01
NO20082956L (no) 2008-08-06
RU2008126807A (ru) 2010-02-27
CN101370807B (zh) 2011-08-31
AU2007207053B2 (en) 2012-05-24
IL192636A0 (en) 2009-02-11
BRPI0706560A2 (pt) 2011-03-29
JP4913157B2 (ja) 2012-04-11
RU2426732C2 (ru) 2011-08-20
WO2007082806A1 (en) 2007-07-26
KR20080075924A (ko) 2008-08-19
TWI338691B (en) 2011-03-11
US7585874B2 (en) 2009-09-08
ZA200805839B (en) 2009-09-30
CN101370807A (zh) 2009-02-18
CA2636112A1 (en) 2007-07-26
US20070179178A1 (en) 2007-08-02
JP2009523752A (ja) 2009-06-25
EP1979350A1 (en) 2008-10-15
AU2007207053A1 (en) 2007-07-26
KR101062583B1 (ko) 2011-09-06

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