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AR108179A2 - Compuestos de pirrolo[2,3-d]pirimidina y sus usos para el tratamiento de diversos tipos de cáncer por medio de la modulación de la actividad de la cinasa de proteína tirosina - Google Patents

Compuestos de pirrolo[2,3-d]pirimidina y sus usos para el tratamiento de diversos tipos de cáncer por medio de la modulación de la actividad de la cinasa de proteína tirosina

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Publication number
AR108179A2
AR108179A2 ARP170100874A ARP170100874A AR108179A2 AR 108179 A2 AR108179 A2 AR 108179A2 AR P170100874 A ARP170100874 A AR P170100874A AR P170100874 A ARP170100874 A AR P170100874A AR 108179 A2 AR108179 A2 AR 108179A2
Authority
AR
Argentina
Prior art keywords
substituted
alkyl
cycloalkyl
heterocyclyl
heteroaryl
Prior art date
Application number
ARP170100874A
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English (en)
Original Assignee
Novartis Ag
Astex Therapeutics Ltd
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Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=38779335&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR108179(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag, Astex Therapeutics Ltd filed Critical Novartis Ag
Publication of AR108179A2 publication Critical patent/AR108179A2/es

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    • 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
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/18Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine
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    • 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
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
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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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • A61K31/522Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/24Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one nitrogen and one sulfur atom

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Abstract

La presente solicitud describe compuestos orgánicos que son útiles para el tratamiento, la prevención, y/o el alivio de enfermedades; en particular se describen compuestos de pirrolo-pirimidina y sus derivados, que inhiben a las cinasas de proteína. Los compuestos orgánicos son útiles en el tratamiento de enfermedades proliferativas. Reivindicación 1: Un compuesto de la fórmula (1), o una sal farmacéuticamente aceptable o solvato del mismo, caracterizado porque: la línea punteada indica un enlace doble; A es N o CR⁵, en donde R⁵ es hidrógeno o alquilo C₁₋₃; R² y R³ se seleccionan cada uno independientemente a partir del grupo que consiste en hidrógeno, hidroxilo, alquilo C₁₋₃, cicloalquilo C₃₋₈, heterociclilo, arilo, heteroarilo, alquilo C₁₋₃ sustituido, cicloalquilo C₃₋₈ sustituido, heterociclilo sustituido, arilo sustituido, y heteroarilo sustituido; R⁴ es seleccionado del grupo que consiste de C(H)(CH₂CH₃)₂, C(H)(CH₂CH₃)Ph, CH₂CH₃, ciclopropilo, ciclopentilo o ciclohexilo; X es N o CR¹¹, e Y es CR¹²; R¹¹ es seleccionado del grupo que consiste de halógeno, hidrógeno, alquilo C₁₋₃, alcoxi C₁₋₃, CN, C=NOH, C=NOCH₃, C(O)H, C(O)alquilo C₁₋₃, cicloalquilo C₃₋₈, heterociclilo, arilo, heteroarilo, alquilo C₁₋₃ substituido, cicloalquilo C₃₋₈ substituido, heterociclilo substituido, arilo substituido, heteroarilo substituido, -BNR¹³R¹⁴, -BOR¹³, -BC(O)R¹³, -BC(O)OR¹³, -BC(O)NR¹³R¹⁴; donde B es un enlace, alquilo C₁₋₃ o alquilo C₁₋₃ ramificado; donde R¹³ y R¹⁴ son cada uno, independientemente, seleccionados del grupo que consiste de hidrógeno, alquilo C₁₋₃, cicloalquilo C₃₋₈, heterociclilo, arilo, heteroarilo, alquilo substituido, cicloalquilo substituido, heterociclilo substituido, arilo substituido, y heteroarilo substituido y R¹² es -BC(O)NR¹³R¹⁴; donde B es un enlace, alquilo C₁₋₃ o alquilo C₁₋₃ ramificado; donde R¹³ y R¹⁴ son cada una, independientemente, seleccionados del grupo que consiste de hidrógeno, alquilo C₁₋₃, cicloalquilo C₃₋₈, heterociclilo, arilo, heteroarilo, alquilo substituido, cicloalquilo substituido, heterociclilo substituido, arilo substituido, y heteroarilo substituido.
ARP170100874A 2006-05-26 2017-04-05 Compuestos de pirrolo[2,3-d]pirimidina y sus usos para el tratamiento de diversos tipos de cáncer por medio de la modulación de la actividad de la cinasa de proteína tirosina AR108179A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US80860506P 2006-05-26 2006-05-26

Publications (1)

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AR108179A2 true AR108179A2 (es) 2018-07-25

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ID=38779335

Family Applications (2)

Application Number Title Priority Date Filing Date
ARP070102252A AR061124A1 (es) 2006-05-26 2007-05-24 Compuestos de pirrolo[2, 3 - d]pirimidina y sus usos para el tratamiento de diversos tipos de cancer por medio de la modulacion de la actividad de la cinasa de proteina tirosina.
ARP170100874A AR108179A2 (es) 2006-05-26 2017-04-05 Compuestos de pirrolo[2,3-d]pirimidina y sus usos para el tratamiento de diversos tipos de cáncer por medio de la modulación de la actividad de la cinasa de proteína tirosina

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Application Number Title Priority Date Filing Date
ARP070102252A AR061124A1 (es) 2006-05-26 2007-05-24 Compuestos de pirrolo[2, 3 - d]pirimidina y sus usos para el tratamiento de diversos tipos de cancer por medio de la modulacion de la actividad de la cinasa de proteina tirosina.

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US (2) US8324225B2 (es)
EP (1) EP2029145B1 (es)
JP (2) JP2009538341A (es)
KR (1) KR101466412B1 (es)
CN (1) CN101594871B (es)
AR (2) AR061124A1 (es)
AU (1) AU2007267645C1 (es)
BR (1) BRPI0712816B8 (es)
CA (1) CA2652044C (es)
CL (1) CL2007001504A1 (es)
CR (1) CR10433A (es)
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EA (1) EA016301B1 (es)
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ES (1) ES2623133T3 (es)
GE (1) GEP20115283B (es)
GT (1) GT200800258A (es)
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ME (1) ME00486B (es)
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NZ (1) NZ572549A (es)
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