AR086236A1 - Inhibidores de la tirosina quinasa de bazo (syk) que contienen aminopiridina - Google Patents

Inhibidores de la tirosina quinasa de bazo (syk) que contienen aminopiridina

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Publication number
AR086236A1
AR086236A1 ARP120101538A ARP120101538A AR086236A1 AR 086236 A1 AR086236 A1 AR 086236A1 AR P120101538 A ARP120101538 A AR P120101538A AR P120101538 A ARP120101538 A AR P120101538A AR 086236 A1 AR086236 A1 AR 086236A1
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Argentina
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alkyl
group
halo
fluoroalkyl
phenyl
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ARP120101538A
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English (en)
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Merck Sharp & Dohme
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Publication of AR086236A1 publication Critical patent/AR086236A1/es

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    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • 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
    • 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
    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/66Phosphorus compounds
    • A61K31/675Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/69Boron compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • 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
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
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    • C07F5/025Boronic and borinic acid compounds
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    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6558Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
    • C07F9/65583Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/66Phosphorus compounds
    • A61K31/662Phosphorus acids or esters thereof having P—C bonds, e.g. foscarnet, trichlorfon
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/04Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
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    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02Boron compounds
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    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/38Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Rheumatology (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Dermatology (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

También proporciona composiciones farmacéuticas que comprende dichos compuestos y procedimientos para usar los compuestos para tratar enfermedades o afecciones mediadas por la tirosina quinasa de bazo (Syk).Reivindicación 1: Un compuesto de fórmula (1) o una de sus sales farmacéuticamente aceptables, en la que: R1 se selecciona del grupo que consiste en: (i) -alquilo C1-3; (ii) fluoroalquilo; (iii) -CH2OR1a, en la que R1a se selecciona del grupo que consiste en H y alquilo C1-6; (iv) -N(R1b)2, en la que cada aparición de R1b se selecciona del grupo que consiste en H y alquilo C1-3 o dos R1b junto con el átomo de N al que están unidos forman un grupo de fórmula (2), en la que r es 1, 2, 3 ó 4; (v) -O-(alquilo C1-3); (vi) -N(H)C(O)-(alquilo C1-3); (vii) halo; (viii) H; y (ix) morfolinilo; R2 es -OH, -O-(alquilo C1-3), -N(R2a)2, -N(R2a)C(O)-R2b o -F; en la que R2a se selecciona del grupo que consiste en H, alquilo C1-3; y R2b es alquilo C1-6; R3 es -CO2R3a, -CH2CO2R3a, -CH2CH2CO2R3a, tetrazol, -C(O)N(R3b)2, -CH2OH, H, halo, -OH-alquilo C1-6, -O-(alquilo C1-3), -N(R3b)2, -CN, -C(O)N(H)S(O)2R3c, -C(O)-N(H)(R3d), -C(O)N(H)C(O)R3a, -P(O)(OR3b)2 o -B(OH)2; donde R3a se selecciona entre el grupo que cosiste en H y alquilo C1-6; donde cada R3b se selecciona independientemente entre el grupo que consiste en H y alquilo C1-3; donde R3c se selecciona entre el grupo que consiste en alquilo C1-3, fluoroalquilo C1-3, cicloalquilo C3-6 y fenilo, donde dicho fenilo está sin sustituir o sustituido con uno o dos alquilo C1-3; donde R3d se selecciona entre el grupo que consiste en -CN, -O-(alquilo C1-3) y tetrazol; R4 es -CO2R4a, CH2CO2R4a, -CH2CH2CO2R4a, tetrazol, -C(O)N(R4b)2, -CH2OH, H, halo, -OH, alquilo C1-6, -O-(alquilo C1-3), -N(R4b)2, -CN, C(O)N(H)S(O)2R4c, -C(O)-N(H)(R4d), C(O)N(H)C(O)R4a, -P(O)(OR4b)2 o -B(OH)2; donde R4a se selecciona entre el grupo que consiste en H y alquilo C1-6; donde cada R4b se selecciona independientemente entre el grupo que consiste en H y alquilo C1-3; donde R4c se selecciona entre el grupo que consiste en alquilo C1-3, fluoroalquilo C1-3, cicloalquilo C3-6 y fenilo, donde dicho fenilo está sin sustituir o sustituido con uno o dos alquilo C1-3; donde R4d se selecciona entre el grupo que consiste en -CN, -O-(alquilo C1-3) y tetrazol; R5 es -CO2R5a, CH2CO2R5a, -CH2CH2CO2R5a, tetrazol, -C(O)N(R5b)2, -CH2OH, H, halo, -OH, alquilo C1-6, -O-(alquilo C1-3), -N(R5b)2, -CN, C(O)N(H)S(O)2R5c, -C(O)-N(H)(R5d), -C(O)N(H)C(O)R5a, -P(O)(OR5b)2 o -B(OH)2; donde R5a se selecciona entre el grupo que consiste en H y alquilo C1-6; donde cada R5b se selecciona independientemente entre el grupo que consiste en H y alquilo C1-3; donde R5c se selecciona entre el grupo que consiste en alquilo C1-3, fluoroalquilo C1-3, cicloalquilo C3-6 y fenilo, donde dicho fenilo está sin sustituir o sustituido con uno o dos alquilo C1-3; donde R5d se selecciona entre el grupo que consiste en -CN, -O-(alquilo C1-3) y tetrazol; R6 se selecciona entre el grupo que consiste en: (i) alquilo C1-6; (ii) fluoroalquilo C1-3; (iii) -O-(alquilo C1-6); (iv) -O-(fluoroalquilo C1-3); (v) -R6a, donde R6a se selecciona entre el grupo que consiste en: (a) cicloalquilo C3-6; (b) un grupo de la fórmula (3), en la que m es 1, 2, 3 ó 4; (c) un grupo de la formula (4), donde R6a1 es H, alquilo C1-3, o -CH2CH2NH2; y (d) un heteroarilo de 5 a 6 miembros que contiene 1 a 3 heteroátomos seleccionados entre el grupo que consiste en N, O y S; donde R6a está sin sustituir o sustituido con 1 a 3 restos R6a2 seleccionados entre el grupo que consiste en halo y alquilo C1-3; (vi) -O-R6b, donde R6b se selecciona entre el grupo que consiste en: (a) cicloalquilo C3-6; y (b) un grupo de la fórmula (5), en la que p es 0, 1 ó 2, y q es 1, 2 ó 3; donde R6b está sin sustituir o sustituido con 1 a 2 restos R6b1 seleccionados entre el grupo que consiste en flúor y alquilo C1-3; (vii) -N(R6c)2, donde cada aparición de R6c se selecciona entre el grupo que consiste en H y alquilo C1-3; (viii) -N(H)C(O)-(alquilo C1-3); (ix) -N(H)C(O)O-(alquilo C1-3); (x) -NHC(O)N(R6d)2, donde cada R6d es H o alquilo C1-3; (xi) halo; y (xii) H; R7 es H o halo; R8 es H o halo; R9 es H o halo; y n es 0, 1 ó 2.
ARP120101538A 2011-05-04 2012-05-02 Inhibidores de la tirosina quinasa de bazo (syk) que contienen aminopiridina AR086236A1 (es)

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US (2) US8796310B2 (es)
EP (1) EP2704571B1 (es)
JP (1) JP5934782B2 (es)
KR (1) KR20140025500A (es)
CN (1) CN103619170B (es)
AR (1) AR086236A1 (es)
AU (1) AU2012250958B8 (es)
BR (1) BR112013028430A2 (es)
CA (1) CA2834043A1 (es)
MX (1) MX2013012776A (es)
RU (1) RU2612217C2 (es)
TW (1) TW201247663A (es)
WO (1) WO2012151137A1 (es)

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CA2834043A1 (en) 2012-11-08
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