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AR102426A1 - Compuestos de indolcarboxamida como inhibidores de btk - Google Patents

Compuestos de indolcarboxamida como inhibidores de btk

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Publication number
AR102426A1
AR102426A1 ARP150103454A ARP150103454A AR102426A1 AR 102426 A1 AR102426 A1 AR 102426A1 AR P150103454 A ARP150103454 A AR P150103454A AR P150103454 A ARP150103454 A AR P150103454A AR 102426 A1 AR102426 A1 AR 102426A1
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Argentina
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zero
substituted
alkyl
group
formulas
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Application number
ARP150103454A
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English (en)
Inventor
A Tino Joseph
J Tebben Andrew
Ngu Khehyong
E Macor John
Guo Weiwei
Gong Hua
Beaudoin Bertrand Myra
Ahmad Saleem
G Batt Douglas
Hunter Watterson Scott
Liu Qingjie
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Bristol Myers Squibb Co
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Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of AR102426A1 publication Critical patent/AR102426A1/es

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    • 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
    • C07D401/10Heterocyclic 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 aromatic 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
    • A61K31/4045Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
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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
    • A61K31/435Heterocyclic 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
    • A61K31/445Non 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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    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/08Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
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    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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Abstract

También el uso de tales compuestos como inhibidores de la tirosina quinasa de Bruton (Btk) y composiciones farmacéuticas que comprenden tales compuestos. Estos compuestos son de utilidad en el tratamiento, prevención o lentificación de la progresión de enfermedades o trastornos en una variedad de áreas terapéuticas, tales como enfermedades autoinmunes y enfermedad vascular. Reivindicación 1: Un compuesto caracterizado por la fórmula (1), o una de sus sales, en donde: X es CR⁴ o N; A es (i) un resto del grupo de fórmulas (2); (ii) un resto del grupo de fórmulas (3); (iii) un resto del grupo de fórmulas (4); (iv) un resto del grupo de fórmulas (5); (v) un resto del grupo de fórmulas (6); (vi) -CHR⁸(piridinilo) en donde cada piridinilo está sustituido con R⁶ y R⁹; Q¹ es -NR⁷Q², -CR¹⁰R¹⁰NR⁷Q², -C(O)NR⁷(alquilo C₁₋₄ sustituido con cero o 1 R¹¹), -CH=CH₂, -CH=C(CN)S(O)₂CH₃, -S(O)₂CH=CR¹⁰R¹⁰, -NR⁷(diclorotriazinilo), -NR⁷(quinazolin-4-ilo sustituido con cero ó 1 R¹¹), 3-metilenpirrolidin-2-on-1-ilo, o un grupo cíclico seleccionado de 1H-pirrol-2(5H)-on-1-ilo, isoindolin-1-on-2-ilo, quinazolin-4(3H)-on-3-ilo, y quinazolin-2,4(1H,3H)-dion-3-ilo, cada grupo cíclico sustituido con cero a dos sustituyentes seleccionados, de modo independiente, de F, Cl, -CH₃, -CN, y -OCH₃; Q² es -CN, -C(O)(alquilo C₁₋₄ sustituido con cero ó 1 R¹¹), -C(O)(cicloalquilo C₃₋₆ sustituido con cero o 1 R¹¹), -C(O)(cicloalquenilo C₅₋₆), -C(O)CR¹⁰=CR¹⁰R¹⁰, -C(O)C(R¹⁰)=CHCH₂N(CH₃)₂, -C(O)CºCR⁷, -C(O)CºC(hidroxialquilo C₁₋₃), -C(O)CºC(fenilo), -C(O)CºCSi(CH₃)₃, o -S(O)₂CH=CHR¹⁰; R¹ es H, -CH₃, -CF₃, o fenilo sustituido con cero o 1 R¹²; R² es H, -CH₃, ciclopropilo, o fenilo sustituido con cero o 1 R¹², siempre que cero o uno de R¹ y R² es fenilo sustituido con cero o 1 R¹²; R³ es H, F, Cl, I, -CN, o -CH₃; R⁴ es H, F, -OH, -O(alquilo C₁₋₄), -O(alquil C₁₋₄)-O-(alquilo C₁₋₂), -O(CH₂)₁₋₃(fenilo), -O(CH₂)₁₋₃(metoxifenilo), o -O(CH₂)₁₋₃(morfolinilo); R⁵ es H, F, Cl, o -CH₃; R⁶ es H, F, Cl, -CF₃, o alcoxi C₁₋₃; cada R⁶ᵃ es, de modo independiente, H o F; R⁷, en cada aparición, es, de modo independiente, H, alquilo C₁₋₄, o ciclopropilo; R⁸ es H o alquilo C₁₋₄; R⁹ es -CH=CH₂, -CH=CHCH₂N(CH₃)₂, -CºCH, o -CºCCH₃; R¹⁰, en cada aparición, es, de modo independiente, H o -CH₃; R¹¹ es F, Cl, -CN, -CF₃, o alcoxi C₁₋₃; y R¹² es F, Cl, -CN, -CF₃, o alcoxi C₁₋₃.
ARP150103454A 2014-10-24 2015-10-23 Compuestos de indolcarboxamida como inhibidores de btk AR102426A1 (es)

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US201462068225P 2014-10-24 2014-10-24

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ARP150103454A AR102426A1 (es) 2014-10-24 2015-10-23 Compuestos de indolcarboxamida como inhibidores de btk
ARP200102971A AR120317A2 (es) 2014-10-24 2020-10-27 Compuestos de indolcarboxamida, composiciones farmacéuticas que los contienen y dichos compuestos para uso en el tratamiento de la enfermedad autoinmune o enfermedad inflamatoria crónica

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ARP200102971A AR120317A2 (es) 2014-10-24 2020-10-27 Compuestos de indolcarboxamida, composiciones farmacéuticas que los contienen y dichos compuestos para uso en el tratamiento de la enfermedad autoinmune o enfermedad inflamatoria crónica

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US (8) US9688629B2 (es)
EP (2) EP3209656B1 (es)
JP (1) JP6517928B2 (es)
KR (2) KR102030305B1 (es)
CN (2) CN107108583B (es)
AR (2) AR102426A1 (es)
AU (2) AU2015335694B2 (es)
CA (1) CA2965517C (es)
CL (1) CL2017000992A1 (es)
CO (1) CO2017004481A2 (es)
CY (2) CY1123401T1 (es)
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