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AR041134A1 - Pirazolopirimidinas como inhibidores de la quinasa dependiente de ciclina - Google Patents

Pirazolopirimidinas como inhibidores de la quinasa dependiente de ciclina

Info

Publication number
AR041134A1
AR041134A1 ARP030103189A ARP030103189A AR041134A1 AR 041134 A1 AR041134 A1 AR 041134A1 AR P030103189 A ARP030103189 A AR P030103189A AR P030103189 A ARP030103189 A AR P030103189A AR 041134 A1 AR041134 A1 AR 041134A1
Authority
AR
Argentina
Prior art keywords
nr5r6
cycloalkyl
alkyl
aryl
group
Prior art date
Application number
ARP030103189A
Other languages
English (en)
Original Assignee
Schering Corp
Pharmacopeia Drug Discovery
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 Schering Corp, Pharmacopeia Drug Discovery filed Critical Schering Corp
Publication of AR041134A1 publication Critical patent/AR041134A1/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • 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
    • A61P25/28Drugs 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
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10Antimycotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Oncology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Communicable Diseases (AREA)
  • Rheumatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Immunology (AREA)
  • Hematology (AREA)
  • Cardiology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Virology (AREA)
  • Hospice & Palliative Care (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Compuestos de pirazolo[1,5-a]pirimidina, inhibidores de quinasas dependientes de ciclina, métodos de preparación de dichos compuestos, composiciones farmacéuticas que contienen uno o más de dichos compuestos, métodos de preparación de formulaciones farmacéuticas que comprenden uno o más de dichos compuestos, y métodos de tratamiento, prevención, inhibición, o alivio de una o más enfermedades asociadas con las CDKs a través del uso de dichos compuestos o composiciones farmacéuticas. Reivindicación 1: Un compuesto representado por la fórmula estructural (1), en el cual: R es heteroarilo, donde dicho heteroarilo puede estar no sustituido o sustituido en forma opcional e independiente con uno o más restos que pueden ser iguales o diferentes, cada resto se selecciona en forma independiente del grupo formado por halógeno, arilo, cicloalquilo, CF3, OCF3, CN, -OR5, -NR5R6, C(R4R5)nOR5, -C(O)R5, -C(O)NR5R6, -SR6, -S(O2)R7, -S(O2)NR5R6, -N(R5)S(O)R7, -N(R5)C(O)R7 y -N(R5)C(O)NR5R6; R2 se selecciona del grupo formado por R9, alquilo, alquinilo, arilo, heteroarilo, CF3, heterociclilalquilo, alquinilalquilo, cicloalquilo, -C(O)OR4, alquilo sustituido con 1-6 grupos R9 que pueden ser iguales o diferentes y se seleccionan en forma independiente del listado de R9 que se muestra más adelante o es un resto del grupo de fórmula (2), donde el arilo en las definiciones indicadas precedentemente para R2 puede estar sustituido o sustituido en forma opcional con uno o más restos que pueden ser iguales o diferentes, cada resto se selecciona en forma del grupo formado por halógeno, CN, -OR5, SR5, -CH2OR5, -C(O)R5, -SO3H, -S(O2)R6, -S(O2)NR5R6, -NR5R6, -C(O)NR5R6, -CF3 y -OCF3; R3 se seleccionan del grupo formado por H, halógeno, -NR5R6, -C(O)OR4, -C(O)NR5R6, alquilo, alquinilo, cicloalquilo, cicloalquilalquilo, arilo, arilalquilo, heterociclilo, heterociclilalquilo, heteroarilo, o es un resto del grupo de fórmula (3), donde cada uno de dicho alquilo, cicloalquilo, arilo, arilalquilo, heterociclilo, heterociclilalquilo, heteroarilo y heteroarilalquilo para R3 y los restos heterociclilo cuyas estructuras se mostraron precedentemente para R3 pueden estar sustituidos o sustituidos en forma opcional e independiente con uno o más restos que pueden ser iguales o diferentes, cada resto se selecciona en forma independiente del grupo formado por halógeno, alquilo, arilo, cicloalquilo, CF3, CN, -OCF3,-(CR4R5)nOR5, -OR5, -NR5R6, -(CR4R5)nNR5R6, -C(O2)R5, -C(O)R5, -C(O)NR5R6, -SR6, -S(O2)R6, -S(O2)NR5R6, -N(R5)S(O2)R7, -N(R5)C(O)R7 y -N(R5)C(O)NR5R6; R4 es H, halo o alquilo; R5 es H o alquilo; R6 se selecciona del grupo formado por H, alquilo, arilo, arilalquilo, cicloalquilo, heterociclilo, heterociclilalquilo, heteroarilo, y heteroarilalquilo, donde cada uno de dichos alquilo, arilo, arilalquilo, cicloalquilo, heterociclilo, heterociclilalquilo, heteroarilo, y heteroarilalquilo puede estar sustituido o sustituido en forma opcional con uno o más restos que pueden ser iguales o diferentes, cada resto se selecciona en forma independiente del grupo formado por halógeno, alquilo, arilo, cicloalquilo, CF3, OCF3, CN, -OR5, -NR5R10, -N(R5)Boc, -(CR4R5)nOR5, -C(O2)R5, -C(O)R5, -C(O)NR5R10, -SO3H, -SR10, -S(O2)R7, -S(O2)NR5R10, -N(R5)S(O2)R7, -N(R5)C(O)R7 y -N(R5)C(O)NR5R10; R10 se selecciona del grupo formado por H, alquilo, arilo, arilalquilo, cicloalquilo, heterociclilo, heterociclilalquilo, heteroarilo, y heteroarilalquilo, donde cada uno de dichos alquilo, arilo, arilalquilo, cicloalquilo, heterociclilo, heterociclilalquilo, heteroarilo, y heteroarilalquilo puede estar no sustituido o sustituido en forma opcional con uno o más restos que pueden ser iguales o diferentes, cada resto se selecciona en forma independiente del grupo formado por halógeno, alquilo, arilo, cicloalquilo, CF3, OCF3, CN, -OR5, -NR4R5, -N(R5)Boc, -(CR4R5)nOR5, -C(O2)R5, -C(O)NR4R5, -C(O)R5, -SO3H, -SR5, -S(O2)R7, -S(O2)NR4R5, -N(R5)S(02)R7, -N(R5)C(O)R7 y -N(R5)C(O)NR4R5; o en forma opcional (i) R5 y R10 en el resto -NR5R10, o (ii) R5 y R6 en el resto -NR5R6, pueden estar unidos para formar un resto cicloalquilo o heterociclilo, con cada uno de dichos resto cicloalquilo o heterociclilo, con cada uno de dichos resto cicloalquilos o heterociclilos sustituidos o sustituido en forma opcional e independiente con uno o más grupos R9; R7 se selecciona del grupo formado por alquilo, cicloalquilo, arilo, heteroarilo, arilalquilo y heteroarilalquilo, donde cada uno de dichos alquilo, cicloalquilo, heteroarilalquilo, arilo, heteroarilo y arilalquilo para R7 puede ser no sustituido o sustituido en forma opcional e independiente con uno o más restos que pueden ser iguales o diferentes, cada resto se selecciona en forma independiente del grupo formado por halógeno, alquilo, arilo, cicloalquilo, CF3, OCF3, CN, -OR5, -NR5R10, -CH2OR5, -C(O2)R5, -C(O)NR5R10, -C(O)R5, -SR10, -S(O2)R10, -S(O2)NR5R10, -N(R5)S(02)R10, -N(R5)C(O)R10 y -N(R5)C(O)NR5R10; R8 se selecciona del grupo formado por R6, -C(O)NR5R10, -CH2OR4, -C(O)OR6, -C(O)R7 y -S(O2)R7; R9 se selecciona del grupo formado por, halógeno, -CN, -NR5R6, -(CH2)nOR4, -C(O2)R6, -C(O)NR5R6, -OR6, -SR6, -S(O2)R7, -S(O2)NR5R6, -N(R5)S(O2)R7, -N(R5)C(O)R7 y -N(R5)C(O)NR5R6; m es 0 hasta 4; y n es 1 hasta 4.
ARP030103189A 2002-09-04 2003-09-03 Pirazolopirimidinas como inhibidores de la quinasa dependiente de ciclina AR041134A1 (es)

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US40803002P 2002-09-04 2002-09-04

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US (2) US7078525B2 (es)
EP (1) EP1534709B1 (es)
JP (2) JP2006501260A (es)
KR (1) KR20050058507A (es)
CN (1) CN1310918C (es)
AR (1) AR041134A1 (es)
AT (1) ATE364608T1 (es)
CA (1) CA2497444C (es)
DE (1) DE60314427T2 (es)
ES (1) ES2285164T3 (es)
HK (1) HK1071570A1 (es)
MX (1) MXPA05002573A (es)
MY (1) MY139336A (es)
NZ (1) NZ539162A (es)
PE (1) PE20041076A1 (es)
TW (1) TW200413377A (es)
WO (1) WO2004022559A1 (es)
ZA (1) ZA200501851B (es)

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EP1534709B1 (en) 2007-06-13
JP2010132704A (ja) 2010-06-17
EP1534709A1 (en) 2005-06-01
ZA200501851B (en) 2005-09-08
TW200413377A (en) 2004-08-01
MY139336A (en) 2009-09-30
WO2004022559A1 (en) 2004-03-18
ES2285164T3 (es) 2007-11-16
AU2003268357A1 (en) 2004-03-29
CN1738821A (zh) 2006-02-22
MXPA05002573A (es) 2005-09-08
KR20050058507A (ko) 2005-06-16
ATE364608T1 (de) 2007-07-15
DE60314427T2 (de) 2008-06-12
DE60314427D1 (de) 2007-07-26
US7078525B2 (en) 2006-07-18
US20040102451A1 (en) 2004-05-27
JP2006501260A (ja) 2006-01-12
PE20041076A1 (es) 2005-01-22
CA2497444A1 (en) 2004-03-18
CA2497444C (en) 2010-11-30
US20060235025A1 (en) 2006-10-19
CN1310918C (zh) 2007-04-18
HK1071570A1 (en) 2005-07-22
NZ539162A (en) 2006-07-28

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