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AR086468A1 - Compuestos heterociclos biciclicos y sus usos en terapia - Google Patents

Compuestos heterociclos biciclicos y sus usos en terapia

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Publication number
AR086468A1
AR086468A1 ARP120101376A ARP120101376A AR086468A1 AR 086468 A1 AR086468 A1 AR 086468A1 AR P120101376 A ARP120101376 A AR P120101376A AR P120101376 A ARP120101376 A AR P120101376A AR 086468 A1 AR086468 A1 AR 086468A1
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AR
Argentina
Prior art keywords
alkyl
crxry
groups
heterocyclyl
alkenyl
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ARP120101376A
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English (en)
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Astex Therapeutics Ltd
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Publication of AR086468A1 publication Critical patent/AR086468A1/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
    • A61K31/4439Non 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
    • A61K31/33Heterocyclic 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
    • A61K31/33Heterocyclic 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
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
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    • 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/5025Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
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    • C07D401/14Heterocyclic 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 three or more hetero rings
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    • 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
    • C07D403/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
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    • 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
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    • 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
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    • 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
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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Composiciones farmacéuticas que comprenden dichos compuestos y el uso de dichos compuestos en el tratamiento de enfermedades, por ejemplo, el cáncer.Reivindicación 1: Un compuesto de fórmula (1), o sus formas tautoméricas o estereoquímicamente isoméricas, N-óxidos, sales farmacéuticamente aceptables o sus solvatos; en donde el anillo E representa un grupo carbocíclico o heterocíclico aromático de 6 miembros; G y J se seleccionan de manera independiente de C o N; Q es CR4 o N; R1 se selecciona de alquilo C1-4, alquenilo C2-4 y cicloalquilo C3-8-(CH2)s-, donde dicho alquilo C1-4, alquenilo C2-4, y cicloalquilo C3-8 pueden sustituirse opcionalmente por uno o más grupos Ra; Ra se selecciona entre halógeno, -OH y -O-alquilo C1-6; R2a y R2b se seleccionan de manera independiente de hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, -C(=O)NH(2-q)(alquilo C1-6)q, -(CH2)s-(heterociclilo de 3 - 12 miembros), y -(CH2)s-carbociclilo C3-12, o los grupos R2a y R2b, junto con el átomo de carbono al que se encuentran unidos, se pueden unir para formar un grupo carbociclilo o heterociclilo saturado de 3 - 10 miembros, donde dicho alquilo C1-6, alquenilo C2-6, alquinilo C2-6, los grupos heterociclilo y carbociclilo pueden estar opcionalmente sustituidos por uno o más grupos Rb; R3a y R3b se seleccionan de manera independiente de hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, -C(=O)NH(2-q)(alquilo C1-6)q, -(CH2)s-(heterociclilo de 3 - 12 miembros), -(CH2)s-carbociclilo C3-12, -C(=O)-(heterociclilo de 3 - 12 miembros), y -C(=O)-carbociclilo C3-12, o los grupos R3a y R3b, junto con el átomo de carbono al que se encuentran unidos, se pueden unir para formar un grupo carbociclilo o heterociclilo saturado de 3 - 10 miembros, donde dichos grupos alquilo C1-6, alquenilo C2-6, alquinilo C2-6, heterociclilo y carbociclilo pueden estar opcionalmente sustituidos por uno o más grupos Rb; R4 se selecciona entre hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, -C(=O)NH(2-q)(alquilo C1-6)q, -(CH2)s-(heterociclilo de 3 - 12 miembros), -(CH2)s-carbociclilo C3-12, -C(=O)-(heterociclilo de 3 - 12 miembros), y -C(=O)-carbociclilo C3-12, donde dichos grupos alquilo C1-6, alquenilo C2-6, alquinilo C2-6, heterociclilo y carbociclilo pueden estar opcionalmente sustituidos por uno o más grupos Rb; R5 se selecciona entre hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, -(CH2)s-cicloalquilo C3-8 y -(CH2)s-cicloalquenilo C3-8, donde dicho alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-8 y cicloalquenilo C3-8 pueden estar opcionalmente sustituidos por uno o más grupos Ra; R6 y R7 se seleccionan de manera independiente de hidrógeno, grupos alquilo C1-8, alquenilo C2-8, alquinilo C2-8, -Y-carbociclilo C3-12, -Z-(heterociclilo de 3 - 12 miembros), -(CRxRy)s-O-Rz, -O-(CRxRy)n-ORz, -(CH2)s-CN, -S(O)q-Rx, -C(=O)Rx, -C(=S)Rx, -C(=N)Rx, -(CRxRy)s-C(=O)ORz, -(CRxRy)s-O-C(=O)-Rz, -(CRxRy)s-C(=O)NRxRy, -(CH2)s-NRxC(=O)Ry, -(CH2)s-OC(=O)NRxRy, -(CH2)s-NRxC(=O)ORy, -(CH2)s-NRxRy, -NRx-(CH2)s-Rz, -(CRxRy)s-C(=S)NRz, -(CRxRy)s-C(=N)NRz, -(CH2)s-O-C(=O)-alquilo C1-4-NRxRy, -(CH2)s-NRx-(CH2)n-O-C(=O)-Rz, -(CH2)s-NRx-(CH2)s-SO2-Ry, -(CH2)s-NH-SO2-NRxRy y -(CH2)s-SO2NRxRy, o los grupos R6 y R7, junto con el átomo de carbono al que se encuentran unidos, se pueden unir para formar un grupo carbociclilo o heterociclilo parcial o completamente saturado de 3 - 10 miembros, y que pueden fusionarse opcionalmente a un anillo carbociclilo o heterociclilo aromático de 5 - 6 miembros, donde dichos grupos alquilo C1-8, alquenilo C2-8 y alquinilo C2-8 pueden sustituirse opcionalmente por uno o más grupos Rb y donde dichos grupos carbociclilo y heterociclilo pueden estar opcionalmente sustituidos por uno o más grupos Rb (por ejemplo, 1, 2 ó 3); R8 y R9 se seleccionan de manera independiente de hidrógeno, halógeno, grupos alquilo C1-8, alquenilo C2-8, alquinilo C2-8, -Y-carbociclilo C3-12, -Z-(heterociclilo de 3 - 12 miembros), -(CRxRy)s-O-Rz, -O-(CRxRy)n-ORz, =O, =S, nitro, Si(Rx)4, -(CH2)s-CN, -S(O)q-(CRxRy)s-Rz, -C(=O)Rx, -C(=S)Rx, -C(=N)Rx, -(CRxRy)s-C(=O)ORz, -(CRxRy)s-O-C(=O)-Rz, -(CRxRy)s-C(=O)NRxRy, -(CH2)s-NRxC(=O)Ry, -(CH2)s-OC(=O)NRxRy, -(CH2)s-NRxC(=O)ORy, -(CH2)s-NRxRy, -NRx-(CH2)s-Rz, -(CRxRy)s-C(=S)NRz, -(CRxRy)s-C(=N)NRx, -S(O)(=NRx)Ry, -(CH2)s-O-C(=O)-alquilo C1-4-NRxRy, -(CH2)s-NRx-(CH2)n-O-C(=O)-Rz, -(CH2)s-NRx-(CH2)s-SO2-Ry, -(CH2)s-NH-SO2-NRxRy, -(CH2)s-SO2NRxRy y -P(=O)(Rx)2, donde dichos grupos alquilo C1-8, alquenilo C2-8 y alquinilo C2-8 pueden estar opcionalmente sustituidos por uno o más grupos Rb y donde dichos grupos carbociclilo y heterociclilo pueden estar opcionalmente sustituidos por uno o más grupos Rb (por ejemplo, 1, 2 ó 3); Rb se selecciona independientemente de halógeno, grupos alquilo C1-6, alquenilo C2-6, alquinilo C2-6, -(CH2)s-cicloalquilo C3-8, -(CH2)s-cicloalquenilo C3-8, -(CH2)s-fenilo, -(CH2)s-(heterociclilo saturado de 4 - 7 miembros), -(CRxRy)s-O-Rz, -O-(CRxRy)n-ORz, haloalquilo C1-6, haloalcoxi C1-6, alcanol C1-6, =O, =S, nitro, Si(Rx)4, -(CH2)s-CN, -S(O)q-Rx, -C(=O)Rx, -(CRxRy)s-C(=O)ORz, -(CRxRy)s-O-C(=O)-Rz, -(CRxRy)s-C(=O)NRxRy, -(CH2)s-NRxC(=O)y, -(CH2)s-OC(=O)NRxRy, -(CH2)s-NRxC(=O)ORy, -(CH2)s-NRxRy, -NRx-(CH2)s-Rz, -(CH2)s-O-C(=O)-alquilo C1-4-NRxRy, -(CH2)s-NRx-(CH2)n-O-C(=O)-Rz, -(CH2)s-NRx-(CH2)s-SO2-Ry, -(CH2)s-NH-SO2-NRxRy, -(CH2)s-SO2NRxRy y -P(=O)(Rx)2, donde dichos grupos alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-8, cicloalquenilo C3-8 y heterociclilo pueden estar opcionalmente sustituidos por uno o más grupos Rx; Rx, Ry y Rz representan independientemente halógeno, hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, -(CH2)s-cicloalquilo C3-8, -(CH2)s-cicloalquenilo C3-8, -(CH2)s-fenilo, -(CH2)s-(heterociclilo saturado de 4 - 7 miembros), alcanol C1-6 opcionalmente sustituido con uno o más halo, -C(=O)O-alquilo C1-6, hidroxi, alcoxi C1-6, haloalquilo C1-6, -(CH2)n-O-alquilo C1-6, -C(=O)-(CH2)n-alcoxi C1-6, -C(=O)-alquilo C1-6, -(CH2)s-CN, alquilo C1-6-N(H)2-q(alquilo C1-6)q, -N(H)2-q(alquilo C1-6)q, -C(=O)N(H)2-q(alquilo C1-6)q, -(CH2)s-NH-SO2-N(H)2-q(alquilo C1-6)q, -(CH2)s-N(alquilo C1-4)-SO2-N(H)2-q(alquilo C1-6)q y -(CH2)s-O-C(=O)-alquilo C1-4-N(H)2-q(alquilo C1-6)q, y cuando se encuentran unidos a un átomo de nitrógeno, carbono, silicio o fósforo, Rx y Ry pueden unirse para formar un anillo de 3 - 7 miembros que contiene opcionalmente uno o dos heteroátomos adicionales seleccionados de O, N, S y las formas oxidadas de N o S; Y y Z se seleccionan de manera independiente de un enlace, -(CRxRy)m-, -C(=CRx)-, -C(=O)-, -NRx, -C(=O)NRx-, -NRxC(=O), -(CRxRy)q-O-, -O-(CRxRy)q-, -S(O)2-NH, NH-S(O)2- y -S(O)q-; s representa de manera independiente un número entero de 0 - 4; n representa de manera independiente un número entero de 1 - 4; p representa de manera independiente un número entero de 0 - 4; q representa un número entero de 0 - 2; y m representa un número entero de 1 - 2.
ARP120101376A 2011-04-21 2012-04-20 Compuestos heterociclos biciclicos y sus usos en terapia AR086468A1 (es)

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