AR077468A1 - Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa - Google Patents
Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasaInfo
- Publication number
- AR077468A1 AR077468A1 ARP100102489A ARP100102489A AR077468A1 AR 077468 A1 AR077468 A1 AR 077468A1 AR P100102489 A ARP100102489 A AR P100102489A AR P100102489 A ARP100102489 A AR P100102489A AR 077468 A1 AR077468 A1 AR 077468A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- ring
- optionally substituted
- independently selected
- halogen
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
- C07D453/04—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems having a quinolyl-4, a substituted quinolyl-4 or a alkylenedioxy-quinolyl-4 radical linked through only one carbon atom, attached in position 2, e.g. quinine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic 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
- C07D471/22—Heterocyclic 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 systems contains four or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic 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
- C07D487/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Tropical Medicine & Parasitology (AREA)
- Psychiatry (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Hospice & Palliative Care (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Inhibidores de las Trk quinasas y son de utilidad en el tratamiento de enfermedades que se pueden tratar con un inhibidor de Trk quinasa tales como dolor, cáncer, inflamacion, enfermedad neurodegenerativas y ciertas enfermedades infecciosas. Reivindicacion 1: Un compuesto que tiene la formula general (1) o una de sus sales, en donde R1 es H o alquilo C1-6; R2 es H, alquilo C1-6, -fluoroalquilo C1-6, -difluoroalquilo C1-6, -trifluoroalquilo C1-6, -cloroalquilo C1-6, -clorofluoroalquilo C2-6,-difluorocloroalquilo C2-6, -clorohidroxialquilo C2-6, -hidroxialquilo C1-6, -dihidroxialquilo C2-6, -(alquil C1-6)CN, -(alquil C1-6)SO2NH2, -(alquil C1-6)NHSO2(alquilo C1-3), -(alquil C1-6)NH2, -(alquil C1-6)NH(alquilo C1-4), -(alquil C1-6)N(alquilo C1-4)2, -(alquil C1-6)NHC(=O)O(alquilo C1-4), -(alquil C1-6)hetCyc1, -(alquil C1-6) hetAr1, hetAr2, hetCyc2, -O(alquilo C1-6) que está opcionalmente sustituido con halogeno, OH o alcoxi C1-4, -O(cicloalquilo C3-6), Cyc1, -(alquil C1-6)(cicloalquilo C3-6), -(alquil C1-6)(alcoxi C1-4), -(hidroxialquil C1-6)(alcoxi C1-4), un anillo cicloalquilo en puente de 7 miembros opcionalmente sustituido con hidroxialquilo C1-6 o un anillo heterocíclico en puente de 7-8 miembros que tiene 1-2 átomos de nitrogeno del anillo; o NR1R2 forma un anillo azacíclico de 4-6 miembros opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de alquilo C1-6, OH, CO2H, (alquil C1-3)CO2H, -O(alquilo C1-6) e hidroxialquilo C1-6; hetCyc1 es un anillo heterocíclico de 5-6 miembros que tiene 1-2 heteroátomos del anillo seleccionados, de modo independiente, de N y O, en donde hetCyc1 está opcionalmente sustituido con oxo, OH, halogeno o alquilo C1-6; hetCyc2 es un anillo heterocíclico ligado a carbono de 6 miembros que tiene 1-2 heteroátomos del anillo seleccionados, de modo independiente, de N y O, en donde hetCyc2 está opcionalmente sustituido con F, SO2NH2, SO2 (alquilo C1-3) o halogeno; hetAr1 es un anillo heteroarilo de 5 miembros que tiene 1-2 heteroátomos del anillo seleccionados, de modo independiente, de N y O y opcionalmente sustituido con alquilo C1-4; hetAr2 es un anillo heteroarilo de 5-6 miembros que tiene 1-2 átomos de nitrogeno del anillo y está opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de alquilo C1-4, cicloalquilo C3-6, halogeno y OH; Cyc1 es un anillo cicloalquilo de 3-6 miembros que está opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de -alquilo C1-4, -OH, -OMe, -CO2H, -(alquil C1-4)OH, halogeno y CF3; Y es (i) fenilo opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de halogeno, alcoxi C1-4, -CF3, -CHF2, -O(alquil C1-4)hetCyc3, -(alquil C1-4) hetCyc3, -O(alquil C1-4)O(alquilo C1-3 ) y -Odihidroxialquilo C3-6 o (ii) un anillo heteroarilo de 5-6 miembros que tiene un heteroátomo del anillo seleccionado de N y S, en donde dicho anillo heteroarilo está opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de halogeno, -O(alquilo C1-4), alquilo C1-4 y NH2 o (iii) un anillo pirid-2-on-3-ilo opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de halogeno y alquilo C1-4; hetCyc3 es un anillo heterocíclico de 5-6 miembros que tiene 1-2 heteroátomos del anillo seleccionados, de modo independiente, de N y O y opcionalmente sustituido con alquilo C1-6; X es -CH2-, -CH2CH2-, -CH2O- o -CH2NRd-; Rd es H o -alquilo C1-4; R3 es H o -alquilo C1-4; cada R4 está seleccionado, de modo independiente, de halogeno, -alquilo C1-4, -OH, -alcoxi C1-4, -NH2, -NH(alquilo C1-4) y -CH2OH; y n es 0, 1, 2, 3, 4, 5 o 6.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US22419609P | 2009-07-09 | 2009-07-09 | |
US34676710P | 2010-05-20 | 2010-05-20 |
Publications (1)
Publication Number | Publication Date |
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AR077468A1 true AR077468A1 (es) | 2011-08-31 |
Family
ID=42732102
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP100102489A AR077468A1 (es) | 2009-07-09 | 2010-07-08 | Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa |
Country Status (22)
Country | Link |
---|---|
US (6) | US8791123B2 (es) |
EP (2) | EP2451812B1 (es) |
JP (3) | JP5716021B2 (es) |
KR (3) | KR101933123B1 (es) |
CN (3) | CN110003214B (es) |
AR (1) | AR077468A1 (es) |
AU (1) | AU2010271270C1 (es) |
CA (2) | CA3013618C (es) |
CL (1) | CL2012000059A1 (es) |
CO (1) | CO6612183A2 (es) |
CR (2) | CR20120065A (es) |
ES (2) | ES2655899T3 (es) |
IL (1) | IL217414A (es) |
MX (2) | MX2012000513A (es) |
MY (1) | MY162180A (es) |
NZ (1) | NZ598086A (es) |
RU (2) | RU2584157C2 (es) |
SG (2) | SG177553A1 (es) |
TW (1) | TWI503321B (es) |
UY (1) | UY32782A (es) |
WO (1) | WO2011006074A1 (es) |
ZA (1) | ZA201200982B (es) |
Families Citing this family (138)
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JP5503655B2 (ja) | 2008-09-22 | 2014-05-28 | アレイ バイオファーマ、インコーポレイテッド | Trkキナーゼ阻害剤としての置換イミダゾ[1,2b]ピリダジン化合物 |
SI3106463T1 (en) | 2008-10-22 | 2018-08-31 | Array Biopharma, Inc. | Compounds of substituted pyrazolo (1,5-) pyrimidine as inhibitors of TRK kinase |
RU2539568C2 (ru) | 2008-10-31 | 2015-01-20 | Дженентек, Инк. | Пиразолопиримидиновые соединения-ингибиторы jak и способы |
PT2376485T (pt) | 2008-12-19 | 2018-03-12 | Vertex Pharma | Derivados de pirazina úteis como inibidores da cinase atr |
UA110324C2 (en) | 2009-07-02 | 2015-12-25 | Genentech Inc | Jak inhibitory compounds based on pyrazolo pyrimidine |
AR077468A1 (es) | 2009-07-09 | 2011-08-31 | Array Biopharma Inc | Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa |
KR101852169B1 (ko) | 2010-05-20 | 2018-04-26 | 어레이 바이오파마 인크. | Trk 키나제 저해제로서의 매크로시클릭 화합물 |
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