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AR058728A1 - Derivados de aril-isoxazol-4-il-imidazo[1,5-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[1,5-a]piridina, metodo de preparacion,medicamentos que los contienen y usos en el tratamiento de trastornos cognitivos.

Info

Publication number
AR058728A1
AR058728A1 ARP060105770A ARP060105770A AR058728A1 AR 058728 A1 AR058728 A1 AR 058728A1 AR P060105770 A ARP060105770 A AR P060105770A AR P060105770 A ARP060105770 A AR P060105770A AR 058728 A1 AR058728 A1 AR 058728A1
Authority
AR
Argentina
Prior art keywords
lower alkyl
isoxazol
imidazo
treatment
links
Prior art date
Application number
ARP060105770A
Other languages
English (en)
Inventor
A P Thomas
Bernd Buettelmann
Jiaqiang Dong
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
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of AR058728A1 publication Critical patent/AR058728A1/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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41881,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

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

Abstract

La presente se refiere a derivados de aril-isoxazol-4-il-imidazo[1,5-a]piridina de la formula (1) en la que R1 es H, halogeno, hidroxi, alquilo inferior, benciloxi o -O-(CH2)-(CO)-heteroarilo de 5 o 6 eslabones opcionalmente sustituido por arilo y alquilo inferior; R2 es H, alquilo inferior o -(CO)-Ra; R3 es H, halogeno, ciano, alquilo inferior, o -(CO)-Ra; Ra es hidroxi, alcoxi inferior, NR'Rö, en el que R' y Rö con independencia entre sí son H, cicloalquilo, heterocicloalquilo de 5 o 6 eslabones o alquilo inferior opcionalmente sustituido por cicloalquilo, ciano, heterocicloalquilo de 5 o 6 eslabones o heteroarilo de 5 o 6 eslabones; y a sales de adicion de ácido farmacéuticamente aceptables de los mismos. Se ha encontrado que este grupo de compuestos posee una gran afinidad y selectividad para los sitios de fijacion del receptor alfa5 del GABA y puede ser util como mejorador cognitivo o para el tratamiento de trastornos cognitivos, tales como la enfermedad de Alzheimer.
ARP060105770A 2005-12-27 2006-12-26 Derivados de aril-isoxazol-4-il-imidazo[1,5-a]piridina, metodo de preparacion,medicamentos que los contienen y usos en el tratamiento de trastornos cognitivos. AR058728A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP05112988 2005-12-27

Publications (1)

Publication Number Publication Date
AR058728A1 true AR058728A1 (es) 2008-02-20

Family

ID=37909303

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP060105770A AR058728A1 (es) 2005-12-27 2006-12-26 Derivados de aril-isoxazol-4-il-imidazo[1,5-a]piridina, metodo de preparacion,medicamentos que los contienen y usos en el tratamiento de trastornos cognitivos.

Country Status (17)

Country Link
US (1) US7399769B2 (es)
EP (1) EP1968977B1 (es)
JP (1) JP4864982B2 (es)
KR (1) KR101033719B1 (es)
CN (1) CN101346377B (es)
AR (1) AR058728A1 (es)
AT (1) ATE537171T1 (es)
AU (1) AU2006331363B2 (es)
BR (1) BRPI0620760A2 (es)
CA (1) CA2633536A1 (es)
ES (1) ES2376357T3 (es)
IL (1) IL192236A0 (es)
NO (1) NO20082748L (es)
RU (1) RU2420527C2 (es)
TW (1) TWI324156B (es)
WO (1) WO2007074089A1 (es)
ZA (1) ZA200805354B (es)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101351461B (zh) * 2005-12-27 2011-09-07 弗·哈夫曼-拉罗切有限公司 芳基-异*唑-4-基-咪唑衍生物
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
AU2008333326B2 (en) 2007-12-04 2013-05-30 F. Hoffmann-La Roche Ag Isoxazolo-pyridine derivatives
US20150374705A1 (en) 2012-02-14 2015-12-31 Shanghai Institues for Biological Sciences Substances for treatment or relief of pain
WO2014001278A1 (en) 2012-06-26 2014-01-03 Aniona Aps A phenyl triazole derivative and its use for modulating the gabaa receptor complex
JP6223443B2 (ja) 2012-06-26 2017-11-01 サニオナ・エイピイエス フェニルトリアゾール誘導体及びgabaa受容体複合体を調節するための該フェニルトリアゾール誘導体の使用
WO2014001280A1 (en) 2012-06-26 2014-01-03 Aniona Aps A phenyl triazole derivative and its use for modulating the gabaa receptor complex
KR20150033678A (ko) 2012-06-26 2015-04-01 사니오나 에이피에스 페닐 트리아졸 유도체 및 이의 gabaa 수용체 복합체 조절용 용도
WO2014001279A1 (en) 2012-06-26 2014-01-03 Aniona Aps A phenyl triazole derivative and its use for modulating the gabaa receptor complex
CN106488915B (zh) 2014-02-13 2020-10-02 因赛特公司 作为lsd1抑制剂的环丙胺
US9527835B2 (en) 2014-02-13 2016-12-27 Incyte Corporation Cyclopropylamines as LSD1 inhibitors
SG10201806849WA (en) 2014-02-13 2018-09-27 Incyte Corp Cyclopropylamines as lsd1 inhibitors
US9695168B2 (en) 2014-07-10 2017-07-04 Incyte Corporation Substituted imidazo[1,5-α]pyridines and imidazo[1,5-α]pyrazines as LSD1 inhibitors
US9695167B2 (en) 2014-07-10 2017-07-04 Incyte Corporation Substituted triazolo[1,5-a]pyridines and triazolo[1,5-a]pyrazines as LSD1 inhibitors
TW201613925A (en) 2014-07-10 2016-04-16 Incyte Corp Imidazopyrazines as LSD1 inhibitors
US9944647B2 (en) 2015-04-03 2018-04-17 Incyte Corporation Heterocyclic compounds as LSD1 inhibitors
UA126277C2 (uk) 2015-08-12 2022-09-14 Інсайт Корпорейшн Солі інгібітору lsd1
BR102019014802A2 (pt) 2018-07-20 2020-02-04 Boehringer Ingelheim Int difluorometil-fenil triazóis
US10968200B2 (en) 2018-08-31 2021-04-06 Incyte Corporation Salts of an LSD1 inhibitor and processes for preparing the same

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE258554T1 (de) * 1999-10-08 2004-02-15 Gruenenthal Gmbh Bicyclische imidazo-3-yl-aminderivate
WO2001034603A2 (en) 1999-11-12 2001-05-17 Neurogen Corporation Bicyclic and tricyclic heteroaromatic compounds
EP1448561B1 (en) * 2001-11-20 2008-02-20 Eli Lilly And Company Beta 3 adrenergic agonists

Also Published As

Publication number Publication date
TWI324156B (en) 2010-05-01
US20070191421A1 (en) 2007-08-16
IL192236A0 (en) 2008-12-29
JP4864982B2 (ja) 2012-02-01
AU2006331363B2 (en) 2012-07-05
JP2009521517A (ja) 2009-06-04
US7399769B2 (en) 2008-07-15
CN101346377B (zh) 2011-05-11
EP1968977A1 (en) 2008-09-17
NO20082748L (no) 2008-09-24
EP1968977B1 (en) 2011-12-14
ATE537171T1 (de) 2011-12-15
WO2007074089A1 (en) 2007-07-05
ZA200805354B (en) 2009-10-28
BRPI0620760A2 (pt) 2011-11-22
ES2376357T3 (es) 2012-03-13
TW200734328A (en) 2007-09-16
AU2006331363A1 (en) 2007-07-05
KR20080072072A (ko) 2008-08-05
RU2008125040A (ru) 2010-02-10
RU2420527C2 (ru) 2011-06-10
CA2633536A1 (en) 2007-07-05
KR101033719B1 (ko) 2011-05-09
CN101346377A (zh) 2009-01-14

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