DK2788349T3 - Kinasehæmmere - Google Patents

Kinasehæmmere Download PDF

Info

Publication number
DK2788349T3
DK2788349T3 DK12809140.2T DK12809140T DK2788349T3 DK 2788349 T3 DK2788349 T3 DK 2788349T3 DK 12809140 T DK12809140 T DK 12809140T DK 2788349 T3 DK2788349 T3 DK 2788349T3
Authority
DK
Denmark
Prior art keywords
tert
yloxy
butyl
tetrahydro
urea
Prior art date
Application number
DK12809140.2T
Other languages
English (en)
Inventor
Niel Monique Bodil Van
Nicholas Charles Ray
Lilian Alcaraz
Terry Aaron Panchal
Andrew Stephen Robert Jennings
Elisabetta Armani
Andrew Peter Cridland
Christopher Hurley
Original Assignee
Chiesi Farm Spa
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=47471708&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DK2788349(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Chiesi Farm Spa filed Critical Chiesi Farm Spa
Application granted granted Critical
Publication of DK2788349T3 publication Critical patent/DK2788349T3/da

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • 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
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C53/00Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
    • C07C53/02Formic acid
    • C07C53/06Salts thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/38Nitrogen atoms
    • C07D231/40Acylated on said nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56Benzopyrazoles; Hydrogenated benzopyrazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • 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
    • C07D487/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic 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 two hetero rings
    • C07D498/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Hydrogenated Pyridines (AREA)

Claims (12)

1. Forbindelse med formel (I) eller et farmaceutisk acceptabelt salt deraf:
hvor; WerNH; Y er O; R1 er en gruppe udvalgt blandt (Ila) - (Ile):
R8 og R9 hver især uafhængigt er hydrogen eller CrC6-alkyl, eller R8 og R9 sammen med det nitrogenatom, som de er bundet til, kan danne et 5-11-leddet mættet monocyklisk eller et kondenseret eller spiro bicyklisk ringsystem eventuelt indeholdende et yderligere heteroatom, som er oxygen eller nitrogen, hvor nitrogenatomet eventuelt er substitueret med CrC6-alkyl; hvor sådanne CrC6-alkylgrupper kan være eventuelt substitueret med en gruppe C-i-Ce-alkyl, C3-Cs-cycloalkyl, hydroxyl eller halo; X1, X2, X3, X4 og X5 hver især uafhængigt er et carbonatom, et nitrogenatom, en -(CH)-gruppe eller en -NH-gruppe; således at hver kombination deraf danner et aromatisk ringsystem; R10 er udvalgt fra en gruppe bestående af: Hydrogen, -CN, -NRARB, -N(Rc)(C2-C6alkylen)-NRARB, -N(Rc)(C3-C7cycloalkylen)-NRARB, -(CrC6alky-len)-NRARB, -(C3-C7cycloalkylen)-NRARB, -0-(C2-C6alkylen)-NRARB, -0-(C3-C7cycloalkylen)-NRARB, -S-(C2-C6alkylen)-NRARB, -S-(C3-C7cycloalkylen)-NRaRb, -N(Rc)C(0)-(CrC6alkylen)-NRARB, -N(RG)C(0)-(C3-C7cycloalkylen)-NRaRb, -C(0)N(Rc)-(C2-C6alkylen)-NRARB, -C(0)N(RC)-(C3-C7cycloalkylen)-NRaRb, -C(0)N(Rc)-(C2-C6alkylen)-0RD, -C(0)N(Rc)-(C3-C7cycloalkylen)- 0Rd, -N(Rc)C(0)NRaRb, -C(0)NRaRb, -N(Rc)C(0)N(Rc)-(C2-C6alkylen)-NRaRb, -N(Rc)C(0)N(Rc)-(C3-C7cycloalkylen)-NRARB, -(C2-C6alkylen)-ORD, -(C3-C7cycloalkylen)-ORD, -0-(C2-C6alkylen)-0RD, -0-(C3-C7cycloalkylen)-0Rd, -S-(C2-C6alkylen)-ORD, -S-(C3-C7cycloalkylen)-ORD, -N(Rc)S(0)2-(Cr C6alkylen)-NRARB, -N(Rc)S(0)2-(C3-C7cycloalkylen)-NRARB, -S(0)2N(Rc)-(C2-C6alkylen)-NRARB, -S(0)2N(Rc)-(C3-C7cycloalkylen)-NRARB, -S(0)2N(Rc)-(C2-C6alkylen)-ORD, -S(0)2N(Rc)-(C3-C7cycloalkylen)-ORD, -N(Rc)S(0)2-(C2-C6alkylen)-ORD, -N(Rc)S(0)2-(C3-C7cycloalkylen)-ORD,-S(0)2N(RARB), -N(Rc)S(0)2Rd, -N(Rc)C(0)Rc, -0Rc, -SRc, -(C3-C7heterocycloalkyl), (C5-C7heterocycloalkyl)-(CrC6alkyl), (C5-C7heterocycloalkyl)(C3-C6cycloalkyl)-, og C3-C7heterocycloalkylcarbonyl; hvor en hvilken som helst af en sådan Cr C6alkyl, C3-C6cycloalkyl, -(CrC6alkylen)-, -(C2-C6alkylen)-, -(C3-C7cycloalky-len)-, -(C3-C7heterocycloalkyl), (C5-C7heterocycloalkyl)-(CrC6alkyl), (C5-C7. heterocycloalkyl)-(C3-C6cycloalkyl) og (C3-C7heterocycloalkyl)carbonyl-del i de ovenfor angivne grupper kan være eventuelt substitueret med en gruppe C-|-C6-alkyl, C3-C7-cycloalkyl, hydroxyl eller halo; R11 er bundet til X4 og er udvalgt fra en gruppe bestående af: Hydrogen; -CN; C-|-Cs-alkyl, som er substitueret med en gruppe udvalgt blandt -CN, -ORc, -SRC, halo; C3-C6cycloalkyl, som er substitueret med en gruppe udvalgt blandt CrC4-alkyl, -CN, -ORc, -SR°, halo; -NRARB, -N(Rc)(C2-C6alkylen)-NRARB, -N(RG)(C3-C7cycloalkylen)-NRARB, -(CrC6alky-len)-NRARB, -(C3-C7cycloalkylen)-NRARB, -0-(C2-C6alkylen)-NRARB, -0-(C3-C7cycloalkylen)-NRARB, -S-(C2-C6alkylen)-NRARB, -S-(C3-C7cycloalkylen)-NRARB, -N(Rc)C(0)-(CrC6alkylen)-NRARB, -N(Rc)C(0)-(C3-C7cycloalkylen)-NRaRb, -C(0)N(RG)-(C2-C6alkylen)-NRARB, -C(0)N(RG)-(C3-C7cycloalkylen)-NRaRb, -C(0)N(Rc)-(C2-C6alkylen)-0RD, -C(0)N(RG)-(C3-C7cycloalkylen)-ORd, -N(Rc)C(0)N(RaRb), -C(0)N(RaRb), -N(Rc)C(0)N(Rc)-(C2-C6alkylen)-NRaRb, -N(Rc)C(0)N(Rc)-(C3-C7cycloalkylen)-NRARB, -0-(C2-C6alkylen)-ORd, -0-(C3-C7cycloalkylen)-ORD, -S-(C2-C6alkylen)-ORD, -S-(C3-C7cyclo-alkylen)-OR°, -N(Rc)S(0)2-(CrC6alkylen)-NRARB, -N(Rc)S(0)2-(C3-C7cyclo-alkylen)-NRARB, -S(0)2N(Rc)-(C2-C6alkylen)-NRARB, -S(0)2N(Rc)-(C3-C7cy-cloalkylen)-NRARB, -S(0)2N(Rc)-(C2-C6alkylen)-0RD, -S(0)2N(Rc)-(C3-C7cy-cloalkylen)-ORD, -N(Rc)S(0)2-(C2-C6alkylen)-0RD, -N(Rc)S(0)2(C3-C7cyclo-alkylen)-OR°, -S(0)2N(RARB), -N(Rc)S(0)2RD, -N(Rc)C(0)Rc, ORc, SRC, -(C3-C7heterc>cycloalkyl), (C5-C7heterocycloalkyl)-(Ci-C6alkyl), (C5-C7hetero-cycloalkyl)(C3-C6cycloalkyl) og (C3-C7heterocycloalkyl)carbonyl, hvor en hvilken som helst af en sådan CrC6alkyl, C3-C6cycloalkyl, -(CrCealkylen)-, -(C2-C6alkylen)-, -(C3-C7cycloalkylen)-, -(C3-C7heterocycloalkyl), (C5-C7hete-rocycloalkyl)-(CrC6alkyl), (C5-C7heterocycloalkyl)-(C3-C6cycloalkyl) og (C3-C7heterocycloalkyl)carbonyl-del i de ovenfor angivne grupper kan være eventuelt substitueret med en, to eller tre R25-grupper, som er uafhængigt udvalgt i listen bestående af: CrC6-alkyl, (CrC3)-haloalkyl, (CrC4)hydroxyalkyl, C3-C7-cycloalkyl, hydroxyl og halo; eller R11 er bundet til X4 og er phenyl eller 5- eller 6-leddet monocyklisk heteroaryl, hvor en sådan phenyl eller 5- eller 6-leddet monocyklisk heteroaryl er substitueret med en gruppe udvalgt i listen bestående af: CrC6-alkyl, som er substitueret med en -CN-gruppe; C3-C6-cycloalkyl, som er substitueret med en gruppe udvalgt blandt: -CN, -ORc, -SRC eller halo; -N(Rc)(C2-C6alkylen)-NRaRb, -N(Rc)(C3-C7cycloalkylen)-NRARB, -(CrC6alkylen)-NRARB, -(C3-C7cy-cloalkylen)-NRARB, -0-(C3-C7cycloalkyien)-NRARB, -S-(C2-C6alkylen)-NRARB, -S-(C3-C7cycloalkylen)-NRARB, -N(Rc)C(0)-(CrC6alkylen)-NRARB, -N(Rc)C(0)-(C3-C7cycloaikylen)-NRARB, -C(0)N(Rc)-(C2-C6alkylen)-NRARB, -C(0)N(Rc)-(C3-C7cycloaikylen)-NRARB, -C(0)N(Rc)-(C2-C6alkylen)-0RD, -C(0)N(Rc)-(C3-C7cycloalkylen)-ORD, -N(Rc)C(0)N(Rc)-(C2-C6alkylen)-NRaRb, -N(Rc)C(0)N(Rc)-(C3-C7cycloalkylen)-NRARB, -0-(C3-C7cycloalky-len)-OR°, -S-(C3-C7cycloalkylen)-ORD,-N(Rc)S(0)2-(CrC6alkylen)-NRARB, -N(Rc)S(0)2-(C3-C7cycloalkylen)-NRARB, -S(0)2N(Rc)-(C2-C6alkylen)-NRARB, -S(0)2N(Rc)-(C3-C7cycloalkylen)-NRARB,-S(0)2N(Rc)-(C2-C6alkylen)-0RD, -S(0)2N(RC)-(C3-C7cycloalkylen)-ORD, -N(Rc)S(0)2-(C2-C6alkylen)-0RD, -N(Rc)S(0)2-(C3-C7cycloalkylen)-ORD, -N(Rc)S(0)2RD, -(C3-C7heterocyclo-alkyl), (C5-C7heterocycloalkyl)-(Ci-C6alkyl), (C5-C7heterocycloalkyl)(C3-C6cy-cloalkyl) og (C3-C7heterocycloalkyl)carbonyl, hvor en hvilken som helst af en sådan CrC6alkyl, C3-C6cycloalkyl, -(CrC6alkylen)-, -(C2-C6alkylen)-, -(C3-C7cycloalkylen)-, -(C3-C7heterocycloalkyl), (C5-C7heterocycloalkyl)-(Cr Ce-alkyl), (C5-07-heterocycloalkyl)-(C3-C6-cycloalkyl) og (C3-C7heterocyclo-alkyl)carbonyl-del i de ovenfor angivne grupper kan være eventuelt substitueret med en, to eller tre R25-grupper, som er uafhængigt udvalgt fra gruppen bestående af: CrC6-alkyl, (CrC3)-haloalkyl, (CrC4)hydroxyalkyl, C3-C7cyclo-alkyl, hydroxyl og halo; Ra og Rb ved hver forekomst uafhængigt er hydrogen, CrC6-alkyl eller C3-C7-cycloalkyl, hvor en sådan CrC6-alkyl og C3-C7-cycloalkyl eventuelt er substitueret med en gruppe CrC3-alkyl, C3-C7cycloalkyl, -ORD, -CN eller halo; alternativt, RA og RB, sammen med det nitrogenatom, som de er bundet til, kan danne et 5-11-leddet mættet heterocyklisk monocyklisk eller bicyklisk ringsystem, som eventuelt er substitueret med en eller flere grupper -OR°, -CN, halo, CrC6-alkyl eller C3-C7-cycloalkyl, hvor en sådan CrC6-alkyl og C3-C7-cycloalkyl eventuelt er substitueret med en gruppe Ci-C3-alkyl, C3-C7cycloalkyl, -OR°, -CN eller halo; og hvilken 5-11-leddet mættet heterocyklisk monocyklisk eller bicyklisk ring eventuelt indeholder et yderligere hetero-atom, som er oxygen eller nitrogen, hvor nitrogenatomet eventuelt er substitueret med CrC6-alkyl eller C3-C6-cycloalkyl, hvor en hvilken som helst af en sådan Ci-C6-alkyl eller C3-C6-cycloalkyl kan være eventuelt substitueret med en gruppe CrC6-alkyl, C3-C7-cycloalkyl, -OR°, -CN eller halo; og/eller RA og Rb kan være bundet til et carbonatom af -(CrC6alkylen)-, -(C2-C6alkylen)-eller -(C3-C7cycloalkylen)-delen af gruppen bundet til det nitrogen, som de er forbundet med, for at danne en mættet cyklus på op til 6 ringatomer; Rc ved hver forekomst uafhængigt er hydrogen, CrC6-alkyl eller C3-C6-cycloalkyl, hvor en sådan CrC6-alkyl og C3-C6-cycloalkyl eventuelt er substitueret med en gruppe C-i-C3-alkyl, -OR°, -CN eller halo; Rd ved hver forekomst uafhængigt er hydrogen, -CH3 eller -C2H5; R12 og R13 uafhængigt er hydrogen, CrC6-alkyl eller halogen; A er et divalent cycloalkylen-radikal med 5 eller 6 ringatomer; hvor cycloalky-lenringen er bundet til W og Y, og kondenseret til en phenylring, hvor en sådan phenylring er eventuelt substitueret med en eller to R24-grupper; og hvor det divalente cycloalkylen-radikal har formlen
R24 ved hver forekomst uafhængigt er udvalgt fra gruppen bestående af: Cr C6-alkyl, halogen og cyano; R2 er et radikal med formel (Illa), (IMb), (IIle) eller (llld):
hvor R14 er udvalgt fra gruppen bestående af: -F, -CH3, -C2H5, -CH2OH, -CH2OMe, -CF2CF3, -CH2SCH3j -SCH3 og -SC2H5; R15 og R16 uafhængigt er -CFI3 eller -C2Fl5; R17 er udvalgt fra gruppen bestående af: ionelektronpar, hydrogen, -CF3, -NReRf, -(C3-C7cycloalkyl), -(C3-C7heterocycloalkyl), aryl eller heteroaryl, hvor en hvilken som helst af en sådan -(C3-C7cycloalkyl), -(C3-C7heterocy-cloalkyl), aryl eller heteroaryl kan være eventuelt substitueret med en gruppe CrC6-alkyl, C3-C7-cycloalkyl eller halo; eller R17 er en
pruppe med den almene formel (IV) hvor R20 er udvalgt fra gruppen bestående af: -F, -CH3, -C2H5, -CFI2OH, -CH2OMe, -CF2CF3, -CH2SCH3, -SCH3 og -SC2H5; R21 er -CH3 eller -C2H5; eller R20 og R21 som defineret ovenfor sammen med det carbonatom, som de er bundet til, kan danne en mættet 3-7-leddet monocyklisk ring; Re og Rf hver især uafhængigt er CrC6-alkyl, eventuelt substitueret med en gruppe CrC3alkyl, -OR°, -CN eller halo; alternativt, RE og RF sammen med det nitrogenatom, som de er bundet til, kan danne et 5-11-leddet mættet monocyklisk eller bicyklisk heterocyklisk ringsystem, som eventuelt er substitueret med en eller flere grupper -ORG, -CN, halo, Ci-C6alkyl eller C3-C7cyclo-alkyl, hvor en sådan CrC6alkyl og C3-C7cycloalkyl eventuelt er substitueret med en gruppe CrC3alkyl, C3-C7cycloalkyl, -ORG, -CN eller halo; og hvilken 5-11-leddet mættet monocyklisk eller bicyklisk heterocyklisk ring eventuelt indeholder et yderligere heteroatom, som er oxygen eller nitrogen, hvor nitrogenatomet eventuelt er substitueret med CrC6alkyl eller C3-C6cycloalkyl, hvor en hvilken som helst af en sådan CrCealkyl eller C3-C6cycloalkyl kan være eventuelt substitueret med en gruppe CrC6alkyl eller C3-C7cycloalkyl; Rg er hydrogen, -CH3 eller -C2H5; R18 er udvalgt fra gruppen bestående af: ionelektronpar, hydrogen, aryl, hete-roaryl, -(CrC6alkyl), -(C3-C7cycloalkyl), -(C3-C7heterocycloalkyl), (C5-C7hete-rocycloalkyl)-(CrC6alkyl) og (C5-C7heterocycloalkyl)-(C3-C6-cycloalkyl), hvor en hvilken som helst af en sådan aryl, heteroaryl, -(CrC6alkyl), -(C3-C7cyclo-alkyl), -(C3-C7heterocycloalkyl), (C5-C7heterocycloalkyl)-(Ci-C6alkyl) og (C5-C7heterocycloalkyl)-(C3-C6cycloalkyl) kan være eventuelt substitueret med en gruppe -CN, -OH, halo, -COORM, CrCealkyl, C3-C6cycloalkyl, -0-(Cr C6alkyl), -0-(C3-C6cycloalkyl), -S-(Ci-C6alkyl), -S-(C3-C6cycloalkyl), -NRHRJ, -N(RL)(C2-C6alkylen)-NRHRJ, -N(RL)(C3-C7cycloalkylen)-NRHRJ, -(CrC6alky-len)-NRHRJ, -(C3-C7cycloalkylen)-NRHRJ, -0-(C2-C6alkylen)-NRHRJ, -0-(C3-C7cycloalkylen)-NRHRJ, -S-(C2-C6alkylen)-NRHRJ, -S-(C3-C7cycloalkylen)-NRhRj, -N(RL)C(0)-(CrC6alkylen)-NRHRJ, -N(RL)C(0)-(C3-C7cycloalkylen)-NRhRj, -C(0)N(RL)-(C2-C6alkylen)-NRHRJ, -C(0)N(RL)-(C3-C7cycloalkylen)-NRhRj, -C(0)N(RL)-(C2-C6alkylen)-0RM, -C(0)N(RL)-(C3-C7cycloalkylen)-ORm, -N(Rl)C(0)N(RhRj), -C(0)N(RhRj), -N(RL)C(0)N(RL)-(C2-C6alkylen)-NRhRj, -N(RL)C(0)N(RL)-(C3-C7cycloalkylen)-NRHRJ, -0-(C2-C6alkylen)-0RM, -0-(C3-C7cycloalkylen)-ORM, -S-(C2-C6alkylen)-ORM, -S-(C3-C7cycloalkylen)-ORm, -N(Rl) S(0)2-(C1-C6alkylen)-NRHRJ, -N(RL)S(0)2-(C3-C7cycloalkylen)-NRhRj, -S(0)2N(RL)-(C2-C6alkylen)-NRHRJ, -S(0)2N(RL)-(C3-C7cycloalkylen)-NRhRj, -S(0)2N(RL)-(C2-C6alkylen)-0RM, -S(0)2N(RL)-(C3-C7cycloalkylen)-ORm, -N(RL)S(0)2-(C2-C6alkylen)-0RM, -N(RL)S(0)2-(C3-C7cycloalkylen)-ORm, -S(0)2N(RhRj), -N(Rl)S(0)2Rl, -N(Rl)C(0)Rl, ORl, SRl, -(C3-C7hete-rocycloalkyl), (C5-C7heterocycloalkyl)-(CrC6-alkyl) og (C5-C7-heterocyclo-alkyl)-(C3-C6-cycloalkyl), hvor en hvilken som helst af en sådan CrC6alkyl, C3-C6cycloalkyl, -(CrCealkylen)-, -(C2-C6alkylen)-, -(C3-C7cycloalkylen)-, -(C3-C7heterocycloalkyl), (C5-C7heterocycloalkyl)-(CrC6alkyl) og (C5-C7hete-rocycloalkyl)-(C3-C6cycloalkyl)-del i de ovenfor angivne grupper kan være eventuelt substitueret med en gruppe CrC6alkyl, C3-C7cycloalkyl, -ORL eller halo; Rh og RJ, ved hver forekomst uafhængigt er hydrogen, CrCealkyl eller C3-Cecycloalkyl, hvor en sådan CrC6alkyl eller C3-C6cycloalkyl eventuelt er substitueret med en gruppe CrC3alkyl, -ORM, CN eller halo; alternativt, RH og RJ sammen med det nitrogenatom, som de er bundet til, også kan danne et 5-11-leddet mættet monocyklisk eller bicyklisk heterocyk-lisk ringsystem, som eventuelt er substitueret med en eller flere grupper -ORm, -CN, halo, CrC6alkyl eller C3-C7Cycloalkyl, hvor en sådan CrC6alkyl og C3-C7cycloalkyl eventuelt er substitueret med en gruppe CrC3alkyl, C3-C7cycloalkyl, -ORM, CN eller halo; og hvilken 5-11-leddet mættet monocyklisk eller bicyklisk heterocyklisk ring eventuelt indeholder et yderligere hetero-atom, som er oxygen eller nitrogen, hvor nitrogenatomet eventuelt er substitueret med CrC6alkyl eller C3-C6cycloalkyl, hvor en hvilken som helst af en sådan CrC6alkyl eller C3-C6cycloalkyl kan være eventuelt substitueret med en gruppe CrC6alkyl, C3-C7cycloalkyl, -ORM, CN eller halo; og/eller RH og RJ kan være bundet til et carbonatom af -(CrC6alkylen)-, -(C2-C6alkylen)- eller -(C3-C7cycloalkylen)-delen af gruppen bundet til det nitrogen, som de er forbundet med, for at danne en mættet cyklus på op til 6 ringatomer; Rl ved hver forekomst uafhængigt er hydrogen, CrC6alkyl eller C3-C6cyclo-alkyl, hvor en sådan CrC6alkyl eller C3-C6cycloalkyl eventuelt er substitueret med en gruppe CrC3alkyl, -ORM, -CN eller halo; Rm ved hver forekomst uafhængigt er hydrogen, CrC6alkyl eller C3-C6cyclo-alkyl, hvor en sådan CrC6alkyl eller C3-C6cycloalkyl eventuelt er substitueret med en gruppe hydroxyl, -CN eller halo; z1, z2, z3 og z4 uafhængigt er udvalgt fra gruppen bestående af: C, N, S, O, en gruppe -CH- og en gruppe -NH-, i en sådan kombination, at den resulterende dannede ring er et aromatisk system; R19 er udvalgt fra gruppen bestående af: hydrogen, -CF3, -NRERF, -(C3-C7cycloalkyl), -(C3-C7heterocycloalkyl), aryl eller heteroaryl, hvor en hvilken som helst af en sådan -(C3-C7cycloalkyl), -(C3-C7heterocycloalkyl), aryl eller heteroaryl kan være eventuelt substitueret med en gruppe CrC6alkyl, C3-C7cycloalkyl eller halo; eller R19 er en gruppe med den almene formel (V) hvor R20, R21, Re og RF er som defineret ovenfor;
T er -N= eller -CR23=; R23 er H, halo, -CH3, eller -CN; R22 er H, halo, -CH3, eller -CN; q er 0, 1,2 eller 3.
2. Forbindelse med formel (I) ifølge krav 1, som er en forbindelse med formel (la), hvor det stereogene carboncenter på cycloalkylen-delen af ring A, som er bundet til gruppe W og er identificeret med nummer (1) nedenfor, har den absolutte konfiguration repræsenteret nedenfor:
(la) eller et farmaceutisk acceptabelt salt deraf.
3. Forbindelse med formel (I), ifølge krav 1 eller 2, som er en forbindelse med formel (Ib), hvor de stereogene carboncentre på cycloalkylen-delen af ring A, som er bundet til gruppe W og Y og er identificeret, respektivt, med numrene (1) og (2) nedenfor, har den absolutte konfiguration repræsenteret nedenfor:
(Ib) eller et farmaceutisk acceptabelt salt deraf.
4. Forbindelse med formel (I) ifølge et af kravene 1 til 3, hvor R1 er en gruppe med formel (Ile): eller et farmaceutisk acceptabelt salt deraf.
5. Forbindelse med formel (I) ifølge et af kravene 1 til 4, hvor R1 er en gruppe med formel (llca) som defineret ovenfor, som er forbundet med gruppen Y via carbonatomet grænsende op til X2
og hvor X4 er et carbonatom, X5 er et nitrogenatom, X3 er et nitrogenatom og X2 er en -CH-gruppe, og R13 er hydrogen; hvor R11 er en gruppe:
hvor R25 eventuelt er til stede og repræsenterer en, to eller tre substituenter uafhængigt udvalgt fra listen bestående af: CrC6alkyl, (CrC3)haloalkyl, (Cr C4)hydroxyalkyl, C3-C7cycloalkyl, hydroxyl og halo; og hvor stjernen betegner bindingspunktet for R11-gruppen til resten af molekylet via X4; hvor R2 er et radikal med formel (I I Ib): (Nib)
ί hvor z1 = -CH-, z2= C, z3 og z4 er N og R17 er en gruppe med den almene formel (IV)
(IV) og hvor R20 er -CH3 eller -CH2OH, R21 er -CH3 og R18 er som defineret i krav 1.
6. Forbindelse med formel (I) ifølge et af kravene 1 til 4, hvor R1 er en gruppe med formel (llca) som defineret ovenfor, som er forbundet med gruppen Y via carbonatomet grænsende op til X2
og hvor X4 er et carbonatom, X5 er et nitrogenatom, X3 er et nitrogenatom og X2 er en -CH-gruppe, og R13 er hydrogen; hvor R11 er en gruppe:
hvor R25 eventuelt er til stede og repræsenterer en, to eller tre substituenter uafhængigt udvalgt fra listen bestående af: CrCealkyl, (CrC3)haloalkyl, (Cr C4)hydroxyalkyl, C3-C7cycloalkyl, hydroxyl og halo; og hvor stjernen betegner bindingspunktet for R11-gruppen til resten af molekylet via X4; hvor R2 er et radikal med formel (lllb):
(Hib) . hvor z1 = -CH-, z2= C, z3 og z4 er N og R17 er en gruppe med den almene formel (IV)
og hvor R20 er -CH3 eller -CH2OH, R21 er -CH3 og R18 er som defineret krav 1.
7. Forbindelse ifølge krav 1 udvalgt blandt: 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-(2-pyrrolidin-1 -yl-ethyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-((1 S,4R)-4-{3-[2-(4-methyl-piperazin-1 -yl)-ethyl]-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy}-1,2,3,4-tetrahydro-naphthalen-1-yl)-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1 S,4R)-4-(3-piperidin-1 -yl)- [1.2.4] triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1S,4R)-4-(3-piperidin-4-yl)- [1.2.4] triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1 S,4R)-4-[3-((S)-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1S,4R)-4-((S)-3-pyrrolidin-2-yl- [1.2.4] triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1 S,4R)-4-(3-piperazin-1 -ylmethyl- [1.2.4] triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1S,4R)-4-(3-isopropylamino- [1.2.4] triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1S,4R)-4-((R)-3-pyrrolidin-2-yl- [1.2.4] triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-(4-methyl-piperazin-1 -ylmethyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1S,4R)-4-(3-morpholin-4-ylmethyl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1 S,4R)-4-(3-pyrrolidin-1 -ylmethyl- [1.2.4] triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-(4-morpholin-4-ylmethyl-phenyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-(3-morpholin-4-ylmethyl-phenyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-(2-morpholin-4-ylmethyl-phenyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-(1 -methyl-piperidin-4-ylmethyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-((1 S,4R)-4-{3-[1 -(2,2-difluor-ethyl)-piperidin-4-ylmethyl]-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy}-1,2,3,4-tetrahydro-naphthalen-1-yl)-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1S,4R)-4-[3-(4-hydroxypiperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(IS,4R)-4-{3-[(2-hydroxy-ethyl)-methyl-amino]-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; l-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-3-hydroxy-pyrrolidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-3-hydroxy-pyrrolidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((R)-2-hydroxymethyl-pyrrolidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-2-hydroxymethyl-pyrrolidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-[5-tert-Butyl-2-(3-hydroxymethyl-phenyl)-2H-pyrazol-3-yl]-3-[(1S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 3-[3-tert-Butyl-5-(3-{(1 S,4R)-4-[3-((S)-1 -methyl-pyrrolidin-2-yl)- [1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}- ureido)-pyrazol-1-yl]-benzoesyreethylester; 1-[5-tert-Butyl-2-(3-hydroxymethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((S)-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-[5-tert-Butyl-2-(4-hydroxymethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((S)-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}urea; 1-[5-tert-Butyl-2-(4-hydroxymethyl-phenyl)-2H-pyrazol-3-yl]-3-[(1S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1-{5-tert-Butyl-2-[3-(2-hydroxy-ethylsulfanyl)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -[5-(2-Hydroxy-1,1 -dimethyl-ethyl)-2-p-tolyl-2H-pyrazol-3-yl]-3-[(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1-[5-tert-Butyl-2-(4-hydroxymethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1S,3S)-3-[3-((S)-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-indan-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((R)-3-hydroxy-pyrrolidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-hydroxy-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-[(1S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1-{5-tert-Butyl-2-[3-(2-dimethylamino-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-[(1 S,4R)-4-(3-piperidin-1-yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1-{5-tert-Butyl-2-[3-(4-methyl-piperazin-1-ylmethyl)-phenyl]-2H-pyrazol-3-yl}- 3- [(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1-{5-tert-Butyl-2-[3-(2-hydroxy-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{(1S,4R)-4-[3-((S)-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-((1S,4R)-4-{3-[(2-dimethylamino-ethyl)-methyl-amino]-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy}-1,2,3,4-tetrahydro-naphthalen-1 -yl)-urea; 1 -[5-tert-Butyl-2-(3-piperidi n-1 -ylmethyl-phenyl)-2H-pyrazol-3-yl]-3-[(1 S,4R)- 4- (3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-((1S,4R)-4-{3-[methyl-(2- morpholin-4-yl-ethyl)-amino]-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy}-1,2,3,4- tetrahydro-naphthalen-1-yl)-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((R)-1 -morpholin-4-yl-ethyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-1 -morpholin-4-yl-ethyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-1,2-dimethyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-hydroxy-ethoxymethyl)-phenyl]-2H-pyrazol-3-yl}-3-[(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1 S,4R)-4-(3-[1,4]oxazepan-4-yl- [1.2.4] triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-{3-[4-(2-hydroxy-ethyl)-piperazin-1-ylmethyl]-phenyl}-2H-pyrazol-3-yl)-3-[(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1-{5-tert-Butyl-2-[3-(4-hydroxy-piperidin-1-ylmethyl)-phenyl]-2H-pyrazol-3-yl}-3-[(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1-{5-tert-Butyl-2-[3-(2-hydroxy-ethylsulfanyl)-phenyl]-2H-pyrazol-3-yl}-3-[(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-(4-hydroxymethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1 S,4S)-4-(3-piperidin-1 -yl- [1.2.4] triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-(3-hydroxymethyl-4-methyl-piperazin-1 -ylmethyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-[5-tert-Butyl-2-(4-hydroxymethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-(4-hydroxy-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-1 -isopropyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1S,4R)-4-(3-dimethylamino- [1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((R)-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-1 -ethyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-1 -methyl-piperidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-3-hydroxy-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((R)-3-hydroxy-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-[5-tert-Butyl-2-(4-hydroxymethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((S)-1 -methyl-piperidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-(4-hydroxyethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1 -[(1 S,4R)-4-(3-Azepan-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-3-(5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl)-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-(4-methyl-piperazine-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-(4-methyl- [1.4] diazepan-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}urea; 1-[5-tert-Butyl-2-(4-hydroxy-phenyl)-2H-pyrazol-3-yl]-3-[(1S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-2-(4-cyano-phenyl)-2H-pyrazol-3-yl]-3-[(1S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4S)-4-[3-((S)-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -[5-tert-Butyl-2-(4-hydroxy-phenyl)-2H-pyrazol-3-yl]-3-{(1 S,4R)-4-[3-((S)-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-((1 S,4R)-4-{3-[4-(1 -hydroxy-1 -methyl-ethyl)-piperidin-1 -yl]-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy}-1,2,3,4-tetrahydro-naphthalen-1-yl)-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[(1 S,4R)-4-(3-pyrrolidin-1 -yl- [1.2.4] triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-(1 -dimethylamino-1 -methyl-ethyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((R)-3-hydroxymethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-3-hydroxymethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-(4-hydroxy-4-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-(1 -methyl-1 -pyrrolidin-1 -yl-ethyl)-[l,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((R)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-4-methyl-morpholin-3-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-((1 S,4R)-4-{3-[(S)-1 -(3-hydroxy-propyl)-pyrrolidin-2-yl]-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy}-1,2,3,4-tetrahydro-naphthalen-1 -yl)-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-2-hydroxy-methyl-1 -methyl-pyrrolidi n-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-(1,4-dimethyl-piperazin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-1,4,4-trimethyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-1 -methyl-piperidin-3-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((R)-1 -methyl-piperidin-3-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((R)-1 -methyl-pyrrolidin-3-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((2S,4R)-4-fluor-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-3-hydroxymethyl-pyrrolidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((R)-3-hydroxymethyl-pyrrolidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-((1S,4R)-4-{3-[4-(2-hydroxy-ethyl)-piperazin-1 -yl]-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy}-1,2,3,4-tetrahydro-naphthalen-1-yl)-urea; 1-{5-tert-Butyl-2-[3-(2-dimethylamino-ethoxy)-phenyl]-2H-pyrazol-3-yl-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydronaphthalen-1 -yl]-urea; 1-{5-tert-Butyl-2-[3-(2-dimethylamino-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-(cis-2,6-dimethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-[5-tert-Butyl-2-(3-rnorpholin-4-ylmethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-{5-tert-Butyl-2-[3-(4-methyl-piperazin-1-ylmethyl)-phenyl]-2H-pyrazol-3-yl}-3-{1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-(1 -dimethylamino-cyclopentyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1 -[(1 S,4R)-4-(3-Amino-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-3-(5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl)-urea; 1-[5-tert-Butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[(1S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1-{5-tert-Butyl-2-[3-(2-dimethylamino-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-[(1 S,4R)-4-(3-diisopropylamino-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; N-(5-tert-Butyl-2-methoxy-3-{3-[(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3- a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-ureido}-phenyl)- methansulfonamid; 1 -(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[8-methyl-3-((S)-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-{5-tert-Butyl-2-[4-(4-methyl-piperazin-1-ylmethyl)-phenyl]-2H-pyrazol-3-yl}- 3- [(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1 -(3-tert-Butyl-1 '-methyl-1 'H-[1,4']bipyrazolyl-5-yl)-3-[(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1 -yl]-urea; 1 -[3-tert-Butyl-1 '-(2-dimethylamino-ethyl)-1 'H-[1,4']bipyrazolyl-5-yl]-3-[(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; N-[5-tert-Butyl-2-methoxy-3-(3-{(1S,4R)-4-[3-((S)-1-methyl-pyrrolidin-2-yl)- [1.2.4] triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-ureido)-phenyl]-methansulfonamid; 1-[5-tert-Butyl-2-(2-hydroxy-ethyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-isoxazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)- [1.2.4] triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-[3-tert-Butyl-1 '-(2-morpholin-4-yl-ethyl)-1 Ή-[1,4']bipyrazolyl-5-yl]-3- [(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1 -[3-tert-Butyl-1 '-(3-dimethylamino-propyl)-1 Ή-[1,4']bipyrazolyl-5-yl]-3-[(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1 -[3-tert-Buty I-1 '-(3-morpholin-4-yl-propyl)-1 Ή-[1,4']bipyrazolyl-5-yl]-3-[(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1 -{(1 S,4R)-4-[3-((2S,6R)-2,6-Dimethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-3-(3-fluor-5-morpholin- 4- yl-phenyl)-urea; 1-[5-tert-Butyl-2-(2-morpholin-4-yl-ethyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea;
1 -Cyclopropyl-3-{(1 S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1 -yl)- [1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-[5-tert-Butyl-2-(2-hydroxy-ethyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-{5-tert-Butyl-2-[-(2-dimethylamino-ethyl)-1 H-imidazol-4-yl]-2H-pyrazol-3-yl}-3-[(1 S,4R)-4-(3-piperidin-1 -yl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-yl]-urea; 1 -[5-tert-Butyl-2-(2-hydroxy-ethyl)-2H-pyrazol-3-yl]-3-{(1 S,4R)-4-[3-((S)-1 -methyl-piperidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-[5-tert-Butyl-2-(2-morpholin-4-yl-ethyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]- 1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{(1S,4R)-4-[3-(8-Aza-bicyclo[3.2.1]oct-8-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-3-{5-tert-butyl-2-[3-(2-dimethylamino-ethoxy)-phenyl]-2H-pyrazol-3-yl}-urea; 1-{5-tert-Butyl-2-[3-(2-dimethylamino-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((R)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -[3-tert-Butyl-1 '-(2-morpholin-4-yl-ethyl)-1 Ή-[1,4']bipyrazolyl-5-yl]-3-{(1 S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -[3-tert-Butyl-1 '-(2-dimethylamino-ethyl)-1 'H-[1,4']bipyrazolyl-5-yl]-3-{(1 S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydronaphthalen-1-yl]-urea; 1-[5-tert-Butyl-2-(2-dimethylamino-ethyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1 -[5-tert-Butyl-2-(2-piperidin-1 -yl-ethyl)-2H-pyrazol-3-yl]-3-{(1 S,4R)-4-[3-((S)- 2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-{5-tert-Butyl-2-[2-(4-methyl-piperazin-1-yl)-ethyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-[5-tert-Butyl-2-(3-morpholin-4-ylmethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]- 1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-morpholin-4-yl-ethyl)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -{5-tert-Butyl-2-[3-(2-pyrrolidin-1 -yl-ethyl)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-{3-[2-(ethyl-methyl-amino)-ethyl]-phenyl}-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-dimethylamino-ethyl)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-piperidin-1-yl-ethyl)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-{3-[2-(4-methyl-piperazin-1-yl)-ethyl]-phenyl}-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l-yl}-urea; 1-{5-tert-Butyl-2-[3-(2-[1,4]oxazepan-4-yl-ethyl)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -(5-tert-Butyl-2-{3-[2-(4-methyl-[1,4]diazepan-1 -yl)-ethyl]-phenyl}-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-[5-tert-Butyl-2-(2-hydroxy-ethyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((S)-3-methyl-morpholin-4-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-{2-[(2-dimethylamino-ethyl)-methyl-amino]-pyrimidin-4-yl}-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1-yl)- [1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-dimethylamino-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{(1S,4R)-4-[3-((S)-3-methyl-morpholin-4-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-[5-tert-Butyl-2-(2-morpholin-4-yl-ethyl)-2H-pyrazol-3-yl]-3-{1S,4R)-4-[3-((S)- 3-methyl-morpholin-4-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-{5-tert-Butyl-2-[3-(4-methyl-piperazin-1-ylmethyl)-phenyl]-2H-pyrazol-3-yl}- 3- {(1 S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -[5-tert-Butyl-2-(3-pyrrolidin-1 -ylmethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1 S,4R)- 4- [3-((2S,6R)-2,6-dimethyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]- 1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-{3-[2-(4-methyl-piperazin-1-yl)-ethoxy]-phenyl}-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-{3-[2-(ethyl-methyl-amino)-ethoxy]-phenyl}-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -{(1 S,4R)-4-[3-(4-Aza-spiro[2.5]oct-4-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2J3,4-tetrahydro-naphthalen-1-yl}-3-{5-tert-butyl-2-[3-(2-dimethylamino-ethoxy)-phenyl]-2H-pyrazol-3-yl}-urea; 1-[5-tert-Butyl-2-(3-morpholin-4-yl-methyl-phenyl)-2H-pyrazol-3-yl]-3-{(1 S,4R)-4-[3-((S)-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydronaphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-{3-[(2-dimethylamino-ethyl)-methyl-amino]-phenyl}-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-((R)-2-dimethylamino-1-methyl-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-((S)-2-dimethylamino-1-methyl-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -[2-[3-(2-Dimethylamino-ethoxy)-phenyl]-5-(2-hydroxy-1,1 -dimethyl-ethyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1-yl)- [1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-diethylamino-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-morpholin-4-yl-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-piperidin-1-yl-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{(1 SJ4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1-(5-tert-Butyl-2-{3-[2-(4-methyl-piperazin-1-yl)-ethoxy]-phenyl}-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1-{5-tert-Butyl-2-{3-[2-(4-fluorpiperidin-1-yl)-ethoxy]-phenyl}-2H-pyrazol-3-yl}-3-{1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1 -(5-tert-Butyl-2-{3-[2-(4-methyl-[1,4]-diazepan-1 -yl)-ethoxy]-phenyl}-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-[1,4]oxazepan-4-yl-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1 -(2-{3-[2-(8-Aza-bicyclo[3.2.1 ]oct-8-yl)-ethoxy]-phenyl}-5-tert-butyl-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-{3-[2-(ethyl-methyl-amino)-ethoxy]-phenyl}-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1-{5-tert-Butyl-2-(3-{2-[(2-methoxy-ethyl)-methyl-amino]-ethoxy}-phenyl}-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1-(5-tert-Butyl-2-{3-[2-(4-methoxy-piperidin-1-yl-ethoxy]-phenyl}-2H-pyrazol-3-yl)-3-(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1-(5-tert-Butyl-2-{3-[2-(3-oxa-8-aza-bicyclo[3.2.1]oct-8-yl)-ethoxy]-phenyl}-2H-pyrazol-3-yl)-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1-yl)- [1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l-yl}-urea; 1-{5-tert-Butyl-2-[3-(4-methoxy-piperidin-1-ylmethyl)-phenyl]-2H-pyrazol-3-yl}- 3- {(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1-[5-tert-Butyl-2-(3-{[(2-methoxy-ethyl)-methyl-amino]-methyl}-phenyl)-2H-pyrazol-3-yl]-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1-{5-tert-Butyl-2-[3-(4-fluor-piperidin-1-ylmethyl)-phenyl]-2H-pyrazol-3-yl}-3-{1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1-[5-tert-Butyl-2-(3-dimethylaminomethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1S,4R)- 4- [3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l-yl}-urea; 1 -[5-tert-Butyl-2-(3-pyrrolidin-1 -ylmethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l -yl}-urea; 1 -{(1 S,4R)-4-[3-(4-Aza-spiro[2.5]oct-4-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-3-{5-tert-butyl-2-[3-(2-morpholin-4-yl-ethoxy)-phenyl]-2H-pyrazol-3-yl}-urea; 1 -[5-tert-Butyl-2-(3-piperidi n-1 -ylmethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1 -{5-tert-Butyl-2-[3-(4-methyl-[1,4]diazepan-1 -ylmethyl)-phenyl]-2H-pyrazol-3-yl}-3-{1S,4R)-4-[3-((S)-2-methyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -{5-tert-Butyl-2-[3-((1 S,4S)-5-methyl-2,5-diaza-bicyclo[2.2.1 ]hept-2-ylmethyl)-phenyl]-2H-pyrazol-3-yl}-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-[5-tert-Butyl-2-(4-morpholin-4-ylmethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-[5-tert-Butyl-2-(4-dimethylaminomethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1 -15-tert-Butyl-2-[4-(4-methyl-piperazin-1 -ylmethyl)-phenyl]-2H-pyrazol-3-yl}-3-{1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -{5-tert-Butyl-2-[4-(4-methyl-[1,4]diazepan-1 -ylmethyl)-phenyl]-2H-pyrazol-3-yl}-3-{1S,4R)-4-[3-((S)-2-methyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[4-(4-methoxy-piperidin-1-ylmethyl)-phenyl]-2H-pyrazol-3-yl}- 3- {1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1 -[5-tert-Butyl-2-(4-pyrrolidin-1 -ylmethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1 S,4R)- 4- [3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1 -[5-tert-Butyl-2-(4-piperidin-1 -ylmethyl-phenyl)-2H-pyrazol-3-yl]-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea; 1-{5-tert-Butyl-2-[4-(4-fluor-piperidin-1-ylmethyl)-phenyl]-2H-pyrazol-3-yl}-3-{1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-(5-tert-Butyl-2-{4-[(ethyl-methyl-amino)-methyl]-phenyl}-2H-pyrazol-3-yl)-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -y|)-[l ,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-[5-tert-Butyl-2-(4-{[(2-methoxy-ethyl)-methyl-amino]-methyl}-phenyl)-2H-pyrazol-3-yl]-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-(2-dimethylamino-ethoxy)-phenyl]-2H-pyrazol-3-yl-3-{(1 S,4S)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydronaphthalen-1 -yl]-urea; 1 -[3-tert-Butyl-1 '-(2-dimethylamino-ethyl)-1 'H-[1,4']bipyrazolyl-5-yl]-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 yl}-urea; 1 -[3-tert-Butyl-1 '-(2-morpholin-4-yl-ethyl)-1 Ή-[1,4']bipyrazolyl-5-yl]-3-{(1 S,4R)-4-[3-((S)-2-methyl-piperidin-1 -yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1 -yl}-urea; 1-{5-tert-Butyl-2-[3-(4-methyl-piperazin-1-ylmethyl)-phenyl]-2H-pyrazol-3-yl}-3-{(1 S,4R)-4-[3-((S)-1 -methyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-l-yl}-urea; og farmaceutisk acceptable salte deraf.
8. Farmaceutisk sammensætning omfattende en forbindelse ifølge et af de foregående krav 1 til 7, sammen med en eller flere farmaceutisk acceptable bærere.
9. Forbindelse ifølge et af kravene 1 til 7 til anvendelse ved behandling af sygdomme eller tilstande, som drager fordel af hæmning af p38-MAP-kinase-aktivitet.
10. Forbindelser ifølge et af kravene 1 til 7 til anvendelse ved behandling af sygdomme eller tilstande, som drager fordel af hæmning af p38-MAP-kinase-aktivitet ifølge krav 9, hvor sygdommene eller tilstandene er kronisk eosinofil pneumoni, asthma, COPD, respiratorisk distress-syndrom hos voksne (ARDS), exacerbation af luftvejs-hyperreaktivitet som en følge af en anden behandling med lægemidler eller luftvejssygdom, som er associeret med pulmonal hypertension.
11. Anvendelse af en forbindelse ifølge et af kravene 1 til 7 ved fremstilling af et medikament til behandling af sygdomme eller tilstande, som drager fordel af hæmning af p38-MAP-kinaseaktivitet.
12. Anvendelse ifølge krav 11, hvor sygdommen eller tilstanden er kronisk eosinofil pneumoni, asthma, COPD, respiratorisk distress-syndrom hos voksne (ARDS), exacerbation af luftvejs-hyperreaktivitet som en følge af en anden behandling med lægemidler eller luftvejssygdom, som er associeret med pulmonal hypertension.
DK12809140.2T 2011-12-09 2012-12-05 Kinasehæmmere DK2788349T3 (da)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP11192871 2011-12-09
EP12187931 2012-10-10
PCT/EP2012/074446 WO2013083604A1 (en) 2011-12-09 2012-12-05 Kinase inhibitors

Publications (1)

Publication Number Publication Date
DK2788349T3 true DK2788349T3 (da) 2017-01-30

Family

ID=47471708

Family Applications (1)

Application Number Title Priority Date Filing Date
DK12809140.2T DK2788349T3 (da) 2011-12-09 2012-12-05 Kinasehæmmere

Country Status (34)

Country Link
US (5) US8907094B2 (da)
EP (1) EP2788349B1 (da)
JP (1) JP6128449B2 (da)
KR (1) KR101994381B1 (da)
CN (3) CN105503861B (da)
AR (1) AR089189A1 (da)
AU (1) AU2012347350C1 (da)
BR (1) BR112014013760A2 (da)
CA (1) CA2858447C (da)
CL (1) CL2014001486A1 (da)
CO (1) CO6970602A2 (da)
CY (1) CY1118340T1 (da)
DK (1) DK2788349T3 (da)
EA (1) EA025268B1 (da)
ES (1) ES2612259T3 (da)
GE (1) GEP201706735B (da)
HR (1) HRP20161714T1 (da)
HU (1) HUE029826T2 (da)
IL (1) IL232958A (da)
LT (1) LT2788349T (da)
ME (1) ME02624B (da)
MX (1) MX359200B (da)
MY (1) MY170656A (da)
PE (1) PE20141370A1 (da)
PH (1) PH12014501277A1 (da)
PL (1) PL2788349T3 (da)
PT (1) PT2788349T (da)
RS (1) RS55602B1 (da)
SG (1) SG11201402985VA (da)
SI (1) SI2788349T1 (da)
TW (1) TWI618703B (da)
UA (1) UA115320C2 (da)
WO (1) WO2013083604A1 (da)
ZA (1) ZA201404156B (da)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA115320C2 (uk) 2011-12-09 2017-10-25 К'Єзі Фармачеутічі С.П.А. Інгібітори кінази
MY167216A (en) * 2011-12-09 2018-08-14 Chiesi Farm Spa Kinase inhibitors
US9458154B2 (en) * 2011-12-09 2016-10-04 Chiesi Farmaceutici S.P.A. Kinase inhibitors
GB201214750D0 (en) 2012-08-17 2012-10-03 Respivert Ltd Compounds
US9783556B2 (en) 2012-08-29 2017-10-10 Respivert Limited Kinase inhibitors
US20150225373A1 (en) 2012-08-29 2015-08-13 Respivert Limited Kinase inhibitors
EP2890460B1 (en) 2012-08-29 2017-02-22 Respivert Limited Kinase inhibitors
US9732063B2 (en) 2012-11-16 2017-08-15 Respivert Limited Kinase inhibitors
WO2014140582A1 (en) 2013-03-14 2014-09-18 Respivert Limited Kinase inhibitors
AU2014246866B2 (en) 2013-04-02 2018-05-10 Oxular Acquisitions Limited Kinase inhibitor
EP2981534B1 (en) 2013-04-02 2017-07-19 Topivert Pharma Limited Kinase inhibitors based upon n-alkyl pyrazoles
RU2015151886A (ru) 2013-06-06 2017-06-08 КЬЕЗИ ФАРМАЧЕУТИЧИ С.п.А. Ингибиторы киназ
WO2014194956A1 (en) * 2013-06-06 2014-12-11 Chiesi Farmaceutici S.P.A. Derivatives of [1, 2, 4] triazolo [4, 3 - a] pyridine as p38 - map kinase inhibitors
EP3004098B1 (en) * 2013-06-06 2017-08-09 Chiesi Farmaceutici S.p.A. Kinase inhibitors
EP2818471A1 (en) * 2013-06-27 2014-12-31 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Nitrogen bicyclic compounds as inhibitors for Scyl1 and Grk5
CA2934199A1 (en) 2013-12-20 2015-06-25 Respivert Limited Urea derivatives useful as kinase inhibitors
PT3357919T (pt) 2014-02-14 2020-02-20 Respivert Ltd Compostos heterocíclicos aromáticos como compostos antiinflamatórios
MA40774A (fr) 2014-10-01 2017-08-08 Respivert Ltd Dérivés de diaryle-urée en tant qu'inhibiteurs de kinase p38
US10206949B2 (en) 2015-09-21 2019-02-19 Ofer Agam Composition that relieves heartburn, GERD and hangovers
WO2017108736A1 (en) 2015-12-23 2017-06-29 Chiesi Farmaceutici S.P.A. N-[3-(3-{4-[[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl} -ureido)-phenyl]-methanesulfonamide derivatives and their use as p38 mapk inhibitors
AR107165A1 (es) 2015-12-23 2018-03-28 Chiesi Farm Spa Inhibidores de quinasa
MA44131A (fr) 2015-12-23 2021-05-26 Chiesi Farm Spa Dérivés de 1-(3-tert-butyl-2h-pyrazol-5-yl or 5-tert-butyl-isoxaol-3-yl)-3-(4-([1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalenyl) urée et leur utlisation en tant qu'inhibiteurs de p38 mapk
EA201892213A1 (ru) 2016-04-06 2019-05-31 Топайверт Фарма Лимитед Ингибиторы киназ
US10364245B2 (en) * 2017-06-07 2019-07-30 Chiesi Farmaceutici S.P.A. Kinase inhibitors
US10342786B2 (en) 2017-10-05 2019-07-09 Fulcrum Therapeutics, Inc. P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD
BR112020006677A2 (pt) 2017-10-05 2020-10-06 Fulcrum Therapeutics, Inc. uso de inibidores p38 para reduzir a expressão de dux4
CN108424372B (zh) * 2018-05-11 2021-08-10 浙江华贝药业有限责任公司 2,2,2-三氟-n-[(s)-4-羰基四氢萘-1-基]-乙酰胺的纯化工艺
CN108707086B (zh) * 2018-05-15 2021-08-10 浙江华贝药业有限责任公司 一种(1s,4s)-n-(4-羟基四氢萘-1-基)叔丁氧基碳酰胺的纯化工艺
AR116628A1 (es) 2018-10-18 2021-05-26 Syngenta Crop Protection Ag Compuestos microbiocidas
EP4114184A1 (en) 2020-03-05 2023-01-11 Syngenta Crop Protection AG Fungicidal compositions
CN112174870B (zh) * 2020-10-12 2023-07-21 蔡霈 (r)-1-烷烃酰基-2-取代吡咯烷-2-甲酰胺的制备方法及其药用用途

Family Cites Families (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU650953B2 (en) 1991-03-21 1994-07-07 Novartis Ag Inhaler
US5756533A (en) 1995-03-10 1998-05-26 G.D. Searle & Co. Amino acid hydroxyethylamino sulfonamide retroviral protease inhibitors
US6034057A (en) 1995-07-06 2000-03-07 Zeneca Limited Peptide inhibitors of fibronectine
US6248713B1 (en) 1995-07-11 2001-06-19 Biogen, Inc. Cell adhesion inhibitors
YU25500A (sh) 1999-05-11 2003-08-29 Pfizer Products Inc. Postupak za sintezu analoga nukleozida
GB0028383D0 (en) 2000-11-21 2001-01-03 Novartis Ag Organic compounds
EP1241176A1 (en) 2001-03-16 2002-09-18 Pfizer Products Inc. Purine derivatives for the treatment of ischemia
WO2002083628A1 (en) * 2001-04-13 2002-10-24 Boehringer Ingelheim Pharmaceuticals, Inc. 1,4-disubstituted benzo-fused compounds
DE60214428T2 (de) 2001-12-20 2007-09-20 Bayer Healthcare Ag 1, 4-dihydro-1, 4-diphenylpyridin-derivate
EP1549621A1 (en) * 2002-08-08 2005-07-06 Boehringer Ingelheim Pharmaceuticals Inc. Fluorinated phenyl-naphthalenyl-urea compounds as inhibitors of cytokines involved in inflammatory processes
EP1601672B1 (en) * 2003-02-14 2006-07-26 Pfizer Products Inc. Triazolo-pyridines as anti-inflammatory compounds
SE0302487D0 (sv) 2003-09-18 2003-09-18 Astrazeneca Ab Novel compounds
CA2564355C (en) * 2004-05-07 2012-07-03 Amgen Inc. Protein kinase modulators and method of use
PT1761520E (pt) 2004-06-23 2008-09-15 Lilly Co Eli Inibidores de quinase
EP1609789A1 (en) 2004-06-23 2005-12-28 Eli Lilly And Company Ureido-pyrazole derivatives and their use as kinase inhibitors
EA012119B1 (ru) 2004-08-12 2009-08-28 Пфайзер Инк. ПРОИЗВОДНЫЕ ТРИАЗОЛОПИРИДИНСУЛЬФАНИЛА В КАЧЕСТВЕ ИНГИБИТОРОВ p38 MAP КИНАЗЫ
GB0418015D0 (en) * 2004-08-12 2004-09-15 Pfizer Ltd New compounds
BRPI0514391A (pt) 2004-08-18 2008-06-10 Pharmacia & Upjohn Co Llc compostos de triazolopiridina para o tratamento de inflamação
GB0502258D0 (en) 2005-02-03 2005-03-09 Argenta Discovery Ltd Compounds and their use
CA2610509A1 (en) 2005-06-03 2006-12-14 Bayer Healthcare Ag 1-methyl-1h-pyrazole-4-carboxamides useful as cancer chemotherapeutic agents
US20090012079A1 (en) * 2006-02-09 2009-01-08 Russell Andrew Lewthwaite Triazolopyridine Compounds
CN101146029B (zh) * 2006-09-13 2011-12-28 华为技术有限公司 一种分组重排序方法和系统
US8188113B2 (en) 2006-09-14 2012-05-29 Deciphera Pharmaceuticals, Inc. Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
TW200837064A (en) 2006-10-04 2008-09-16 Pharmacopeia Inc 8-substituted 2-(benzimidazolyl)purine derivatives for immunosuppression
EP2068869A4 (en) 2006-10-06 2011-05-25 Abbott Lab NEW IMIDAZOTHIAZOLE AND IMIDAZOXAZOLE
WO2008125014A1 (fr) 2007-04-13 2008-10-23 Institute Of Pharmacology And Toxicology Academy Of Military Medical Sciences P.L.A. Composés d'urée, leurs procédés de préparation et leurs utilisations pharmaceutiques
WO2009015000A1 (en) 2007-07-25 2009-01-29 Array Biopharma Inc. Pyrazole urea derivatives used as kinase inhibitors
JP5569857B2 (ja) 2007-08-10 2014-08-13 アステラス製薬株式会社 二環式アシルグアニジン誘導体
TWI496779B (zh) 2008-08-19 2015-08-21 Array Biopharma Inc 作為pim激酶抑制劑之三唑吡啶化合物
PE20120121A1 (es) 2008-12-08 2012-02-20 Gilead Connecticut Inc Derivados de imidazopirazina como inhibidores de syk
MX2011006219A (es) * 2008-12-11 2011-06-28 Respivert Ltd Inhibidores de la proteina cinasa activada por el mitogeno p38.
US8629157B2 (en) 2009-01-05 2014-01-14 Boehringer Ingelheim International Gmbh Pyrrolidine compounds which modulate the CB2 receptor
CA2752693A1 (en) 2009-02-17 2010-08-26 Chiesi Farmaceutici S.P.A. Triazolopyridine derivatives as p38 map kinase inhibitors
US9127016B2 (en) 2009-03-20 2015-09-08 University of Pittsburgh—of the Commonwealth System of Higher Education Small molecule inhibitors of Dusp6 and uses therefor
US8721380B2 (en) 2009-08-12 2014-05-13 Konica Minolta Holdings, Inc. Method for manufacturing display panel
EP2308866A1 (de) 2009-10-09 2011-04-13 Bayer CropScience AG Phenylpyri(mi)dinylpyrazole und ihre Verwendung als Fungizide
GB0921731D0 (en) 2009-12-11 2010-01-27 Respivert Ltd Theraputic uses
GB201005589D0 (en) * 2010-04-01 2010-05-19 Respivert Ltd Novel compounds
US9024041B2 (en) * 2010-04-08 2015-05-05 Respivert Ltd. P38 MAP kinase inhibitors
GB201009731D0 (en) * 2010-06-10 2010-07-21 Pulmagen Therapeutics Inflamma Kinase inhibitors
US9458154B2 (en) 2011-12-09 2016-10-04 Chiesi Farmaceutici S.P.A. Kinase inhibitors
MY167216A (en) 2011-12-09 2018-08-14 Chiesi Farm Spa Kinase inhibitors
UA115320C2 (uk) * 2011-12-09 2017-10-25 К'Єзі Фармачеутічі С.П.А. Інгібітори кінази
RU2015151886A (ru) 2013-06-06 2017-06-08 КЬЕЗИ ФАРМАЧЕУТИЧИ С.п.А. Ингибиторы киназ
WO2014194956A1 (en) 2013-06-06 2014-12-11 Chiesi Farmaceutici S.P.A. Derivatives of [1, 2, 4] triazolo [4, 3 - a] pyridine as p38 - map kinase inhibitors
EP3004098B1 (en) 2013-06-06 2017-08-09 Chiesi Farmaceutici S.p.A. Kinase inhibitors

Also Published As

Publication number Publication date
MX359200B (es) 2018-09-19
US20140323470A1 (en) 2014-10-30
JP6128449B2 (ja) 2017-05-17
CN105503861A (zh) 2016-04-20
KR20140105516A (ko) 2014-09-01
CN104039787A (zh) 2014-09-10
HRP20161714T1 (hr) 2017-02-10
SI2788349T1 (sl) 2017-01-31
CN105968110A (zh) 2016-09-28
CY1118340T1 (el) 2017-06-28
US9139584B2 (en) 2015-09-22
PT2788349T (pt) 2017-02-02
TWI618703B (zh) 2018-03-21
US20150080375A1 (en) 2015-03-19
LT2788349T (lt) 2016-12-27
PH12014501277B1 (en) 2014-09-08
MY170656A (en) 2019-08-24
BR112014013760A2 (pt) 2017-06-13
CL2014001486A1 (es) 2014-11-14
CO6970602A2 (es) 2014-06-13
IL232958A (en) 2017-08-31
EP2788349B1 (en) 2016-10-26
AU2012347350C1 (en) 2017-01-19
HUE029826T2 (en) 2017-04-28
MX2014006724A (es) 2014-08-29
TW201336833A (zh) 2013-09-16
US20130150343A1 (en) 2013-06-13
IL232958A0 (en) 2014-08-03
PL2788349T3 (pl) 2017-04-28
PE20141370A1 (es) 2014-10-17
SG11201402985VA (en) 2014-08-28
RS55602B1 (sr) 2017-06-30
CN105503861B (zh) 2017-08-01
CA2858447A1 (en) 2013-06-13
CN104039787B (zh) 2016-06-29
EP2788349A1 (en) 2014-10-15
CA2858447C (en) 2020-10-27
ZA201404156B (en) 2016-07-27
US8907094B2 (en) 2014-12-09
HK1200828A1 (en) 2015-08-14
CN105968110B (zh) 2018-04-27
US9315503B2 (en) 2016-04-19
PH12014501277A1 (en) 2014-09-08
US9145413B2 (en) 2015-09-29
HK1222647A1 (zh) 2017-07-07
NZ625965A (en) 2016-08-26
EA201490949A1 (ru) 2014-11-28
UA115320C2 (uk) 2017-10-25
EA025268B1 (ru) 2016-12-30
JP2015500260A (ja) 2015-01-05
KR101994381B1 (ko) 2019-06-28
AU2012347350A1 (en) 2014-07-03
ES2612259T3 (es) 2017-05-16
AU2012347350B2 (en) 2016-09-08
ME02624B (me) 2017-06-20
US20160229852A1 (en) 2016-08-11
US9527846B2 (en) 2016-12-27
GEP201706735B (en) 2017-09-25
WO2013083604A1 (en) 2013-06-13
US20150344475A1 (en) 2015-12-03
AR089189A1 (es) 2014-08-06

Similar Documents

Publication Publication Date Title
DK2788349T3 (da) Kinasehæmmere
WO2014195402A1 (en) Kinase inhibitors
WO2014195400A1 (en) Kinase inhibitors
CA2885418A1 (en) Novel pyrazine derivatives as cb2 receptor agonists
CA2860479A1 (en) Kinase inhibitors
WO2015198045A1 (en) 3-substituted 2-amino-indole derivatives
CA2914457A1 (en) Kinase inhibitors
NZ625965B2 (en) Kinase inhibitors useful as anti-inflammatory agents
EP3634961A1 (en) (4-(([1,2,4]triazolo[4,3-a]pyridine-6-yl)oxy)-1,2,3,4-tetrahydronaphthalen-1-yl) ureido derivatives as anti-inflammatory p38 mapk inhibitors for treating diseases of the respiratory tract
WO2017108737A1 (en) 1-(3-tert-butyl-phenyl)-3-(4-([1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro- naphthalen-1-yl)-urea derivatives and their use as p38 mapk inhibitors
HK1222647B (en) Kinase inhibitors
HK1219277A1 (zh) 三唑并[4,5-d]嘧啶衍生物
HK1208030B (zh) 作为cb2受体激动剂的吡嗪衍生物