AR090293A1 - Inhibidores de quinasa a base de arileter - Google Patents

Inhibidores de quinasa a base de arileter

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Publication number
AR090293A1
AR090293A1 ARP130100766A ARP130100766A AR090293A1 AR 090293 A1 AR090293 A1 AR 090293A1 AR P130100766 A ARP130100766 A AR P130100766A AR P130100766 A ARP130100766 A AR P130100766A AR 090293 A1 AR090293 A1 AR 090293A1
Authority
AR
Argentina
Prior art keywords
alkyl
amino
halo
alkoxy
hydrogen
Prior art date
Application number
ARP130100766A
Other languages
English (en)
Inventor
M Vrudhula Vivekananda
Sivasamban Karatholuvhu Maheswaran
J Bronson Joanne
Diane Dzierba Carolyn
E Macor John
Rajamani Ramkumar
Jethanand Nara Susheel
Pan Senliang
Original Assignee
Bristol Myers Squibb Co
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 Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of AR090293A1 publication Critical patent/AR090293A1/es

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • 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
    • 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
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A61P29/02Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/052Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/12Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
    • C07D491/20Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/99Enzyme inactivation by chemical treatment

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

Abstract

Compuestos que pueden inhibir la AAK1 (quinasa asociada con el adaptador 1), composiciones que comprenden tales compuestos y métodos para inhibir la AAK1. Útil para tratar esquizofrenia, Parkinson, dolor neuropático, trastorno bipolar y Alzheimer. Reivindicación 1: Un compuesto caracterizado por la fórmula (1) o una de sus sales farmacéuticamente aceptables, en donde: R¹ y R² están seleccionados, de modo independiente, de hidrógeno, cicloalquilo C₃₋₆ y alquilo C₁₋₃, en donde el alquilo C₁₋₃ está opcionalmente sustituido con uno, dos o tres grupos seleccionados, de modo independiente, de alcoxi C₁₋₃, alquil C₁₋₃-amino, amino, ciano, dialquil C₁₋₃-amino, halo e hidroxi; o R¹ y R² juntos son oxo; o R¹ y R², junto con el átomo de carbono al que están unidos, forman un anillo oxetano; R³ es alquil C₁₋₃-Y o alquilo C₂₋₈, en donde el alquilo C₂₋₈ está opcionalmente sustituido con uno, dos, tres o cuatro grupos seleccionados, de modo independiente, de alcoxi C₁₋₃, alquil C₁₋₃-amino, alcoxi C₁₋₃-alquil C₂₋₃-amino, amino, arilo, halo, haloalquil C₁₋₃-amino, haloalquil C₁₋₃-carbonilamino, hidroxi, -NRˣRʸ y cicloalquilo C₃₋₈, en donde el cicloalquilo está también opcionalmente sustituido con uno, dos o tres grupos seleccionados, de modo independiente, de alcoxi C₁₋₃, alquilo C₁₋₃, alquil C₁₋₃-amino, alcoxi C₁₋₃-alquil C₂₋₃-amino, amino, arilo, arilalquilo C₁₋₃, halo, haloalquilo C₁₋₃, haloalquil C₁₋₃-amino e hidroxi; R⁴ está seleccionado de hidrógeno, alcoxi C₁₋₃, alcoxi C₁₋₃-carbonilamino, alquilo C₁₋₃, alquil C₁₋₃-amino, alquil C₁₋₃-carbonilamino, amino, arilamino, arilcarbonilamino, cicloalquil C₃₋₆-amino, cicloalquil C₃₋₆-carbonilamino, cicloalquil C₃₋₆-oxi, halo, haloalcoxi C₁₋₃, haloalquil C₂₋₃amino, haloalquil C₂₋₃carbonilamino e hidroxi; R⁵ está seleccionado de hidrógeno, alquilo C₁₋₃, ciano, cicloalquilo C₃ y halo; R⁶ está seleccionado de hidrógeno, alquilo C₁₋₃, alquil C₁₋₃-carbonilamino, amino; R⁷ está seleccionado de hidrógeno, alcoxi C₁₋₃, alquilo C₁₋₃, ciano, -CH₂OH, -CH₂OCH₃, CH(CH₃)OH, C(CH₃)₂OH, halo y haloalquilo C₁₋₃; R⁸ está seleccionado de hidrógeno, alcoxi C₁₋₃, ciano y halo; Rˣ y Rʸ, junto con el átomo de nitrógeno al que están unidos, forman un anillo de tres a seis miembros; e Y está seleccionado del grupo de fórmulas (2); en donde R⁹ está seleccionado de hidrógeno, alquilo C₁₋₆, cicloalquilo C₃₋₆ y alquil C₁₋₆-carbonilo; n es 0, 1, 2 ó 3; cada R¹⁰ está seleccionado, de modo independiente, de hidrógeno, alquilo C₁₋₆, arilo, arilalquilo C₁₋₃, cicloalquilo C₃₋₆, halo y haloalquilo C₁₋₃; y cada R¹¹ está seleccionado, de modo independiente, de hidrógeno, alcoxi C₁₋₃ e hidroxi.
ARP130100766A 2012-03-09 2013-03-11 Inhibidores de quinasa a base de arileter AR090293A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201261608737P 2012-03-09 2012-03-09

Publications (1)

Publication Number Publication Date
AR090293A1 true AR090293A1 (es) 2014-11-05

Family

ID=47892007

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP130100766A AR090293A1 (es) 2012-03-09 2013-03-11 Inhibidores de quinasa a base de arileter

Country Status (11)

Country Link
US (2) US8703953B2 (es)
EP (1) EP2822952B1 (es)
JP (1) JP2015510881A (es)
CN (1) CN104144932A (es)
AR (1) AR090293A1 (es)
CA (1) CA2866671A1 (es)
EA (1) EA201491647A1 (es)
MX (1) MX2014010684A (es)
TW (1) TW201341387A (es)
UY (1) UY34666A (es)
WO (1) WO2013134036A1 (es)

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WO2015002926A1 (en) 2013-07-02 2015-01-08 Bristol-Myers Squibb Company Tricyclic pyrido-carboxamide derivatives as rock inhibitors
TW201506024A (zh) 2013-07-02 2015-02-16 必治妥美雅史谷比公司 作為有效rock抑制劑的三環甲醯胺衍生物
WO2015006100A1 (en) 2013-07-08 2015-01-15 Bristol-Myers Squibb Company Aryl amide kinase inhibitors
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CN105979950A (zh) 2013-10-11 2016-09-28 百时美施贵宝公司 吡咯并三嗪激酶抑制剂
US20160333006A1 (en) * 2014-01-29 2016-11-17 Bristol-Myers Squibb Company Aryl lacta kinase inhibitors
CN106132951B (zh) * 2014-01-31 2019-02-12 百时美施贵宝公司 基于喹啉的激酶抑制剂
SG11201608195QA (en) 2014-04-02 2016-10-28 Bristol Myers Squibb Co Biaryl kinase inhibitors
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TWI673271B (zh) 2016-12-15 2019-10-01 瑞士商赫孚孟拉羅股份公司 製備btk抑制劑之方法

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Also Published As

Publication number Publication date
CN104144932A (zh) 2014-11-12
US20140179725A1 (en) 2014-06-26
MX2014010684A (es) 2014-10-17
CA2866671A1 (en) 2013-09-12
US8969564B2 (en) 2015-03-03
JP2015510881A (ja) 2015-04-13
WO2013134036A1 (en) 2013-09-12
TW201341387A (zh) 2013-10-16
UY34666A (es) 2013-09-30
EP2822952B1 (en) 2016-04-06
EP2822952A1 (en) 2015-01-14
US8703953B2 (en) 2014-04-22
EA201491647A1 (ru) 2014-12-30
US20130237555A1 (en) 2013-09-12

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