AR088293A1 - Inhibidores de proteina cinasa - Google Patents

Inhibidores de proteina cinasa

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Publication number
AR088293A1
AR088293A1 ARP120103776A ARP120103776A AR088293A1 AR 088293 A1 AR088293 A1 AR 088293A1 AR P120103776 A ARP120103776 A AR P120103776A AR P120103776 A ARP120103776 A AR P120103776A AR 088293 A1 AR088293 A1 AR 088293A1
Authority
AR
Argentina
Prior art keywords
alkyl
heterocyclic ring
cycloalkyl
alkoxy
membered heterocyclic
Prior art date
Application number
ARP120103776A
Other languages
English (en)
Inventor
Linnanen Tero
Nanduri Srinivas
Rajagopalan Srinivasan
Mukherjee Subhendu
Wohlfahrt Gerd
Kotrabasaiah Ujjinamatada Ravi
Original Assignee
Orion Corp
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=54261175&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR088293(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Orion Corp filed Critical Orion Corp
Publication of AR088293A1 publication Critical patent/AR088293A1/es

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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41841,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41921,2,3-Triazoles
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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
    • A61K31/422Oxazoles not condensed and containing further heterocyclic rings
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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4245Oxadiazoles
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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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    • 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
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    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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    • 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
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    • 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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    • A61K31/495Heterocyclic 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
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    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Los compuestos de la fórmula (1) poseen utilidad como inhibidores FGFR y son útiles en el tratamiento de una afección, donde se desea la inhibición de la cinasa FGFR, tal como cáncer. Reivindicación 1: Un compuesto de la fórmula (1) caracterizado porque Z es CH o N; G es -C(O)NR¹⁵R¹⁶, -C(O)OR¹⁷, -C(CH₃)=NOH o un grupo de la fórmula (2) en donde A es un anillo fenilo o un anillo heterocíclico de 5 - 12 miembros, y R¹ es H, alquilo C₁₋₇, cicloalquilo C₃₋₇, cicloalquilo C₃₋₇-alquilo C₁₋₇, alcoxi C₁₋₇, alquilcarbonilo C₁₋₇, amino, hidroxi, hidroxialquilo C₁₋₇, alquilamino C₁₋₇-alquilo C₁₋₇, fenilo-alcoxi C₁₋₇, -NHC(O)-R²¹, -R¹²-C(O)-R¹³, -SO₂-R¹⁴ o -E-R⁶, y R² es H, halógeno o alquilo C₁₋₇; B es un anillo carbocíclico o heterocíclico de 5 - 12 miembros; R³ es H, halógeno, alquilo C₁₋₇, alcoxi C₁₋₇; R⁴ es H, halógeno, alquilo C₁₋₇ u oxo; R⁵ es H, -C(O)R⁷, -SO₂R⁸, -C(O)-D-R⁹ o un anillo heterocíclico de 5 - 6 miembros opcionalmente sustituido; R⁶ es un anillo heterocíclico de 5 - 6 miembros opcionalmente sustituido; R⁷ es alquilo C₁₋₇, alquenilo C₁₋₇, cicloalquilo C₃₋₇, alcoxi C₁₋₇, alcoxi C₁₋₇, alquilo C₁₋₇, carboxil-alquilo C₁₋₇, alcoxi C₁₋₇carbonil-alquilo C₁₋₇, alquilamino C₁₋₇-alquilo C₁₋₇, -NH-R¹⁰ o NH-X¹-R¹¹; R⁸ es alquilo C₁₋₇, alquenilo C₂₋₇, cicloalquilo C₃₋₇, hidroxi-alquilo C₁₋₇, -NR¹⁸R¹⁹, -NH-X²-R²⁰, fenilo o un anillo heterocíclico de 5 - 6 miembros opcionalmente sustituido; R⁹ es fenilo o un anillo heterocíclico de 5 - 6 miembros opcionalmente sustituido; R¹⁰ es alquilo C₁₋₇ o cicloalquilo C₃₋₇; R¹¹ es fenilo o un anillo heterocíclico de 5 - 6 miembros opcionalmente sustituido; R¹² y R²¹ son alquilo C₁₋₇; R¹³ es alcoxi C₁₋₇ o amino; R¹⁴ es alquilo C₁₋₇ o cicloalquilo C₃₋₇; R¹⁵, R¹⁶, R¹⁷, R¹⁸ y R¹⁹ son, independientemente H, alquilo C₁₋₇ o cicloalquilo C₃₋₇; R²⁰ es fenilo o un anillo heterocíclico de 5 - 6 miembros opcionalmente sustituido; E es un enlace o un alquilo C₁₋₇; D es un enlace o un alquilo C₁₋₇; X¹ y X² son, independientemente, un enlace o alquilo C₁₋₇; y sales farmacéuticamente aceptables de los mismos.
ARP120103776A 2011-10-10 2012-10-10 Inhibidores de proteina cinasa AR088293A1 (es)

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