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AR094537A1 - COMPUESTOS DE PIRIDILO SUSTITUIDOS CON ALQUILAMIDA ÚTILES COMO MODULADORES DE LAS RESPUESTAS DE IL-12, IL-23 Y/O IFNa - Google Patents

COMPUESTOS DE PIRIDILO SUSTITUIDOS CON ALQUILAMIDA ÚTILES COMO MODULADORES DE LAS RESPUESTAS DE IL-12, IL-23 Y/O IFNa

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Publication number
AR094537A1
AR094537A1 ARP130104090A ARP130104090A AR094537A1 AR 094537 A1 AR094537 A1 AR 094537A1 AR P130104090 A ARP130104090 A AR P130104090A AR P130104090 A ARP130104090 A AR P130104090A AR 094537 A1 AR094537 A1 AR 094537A1
Authority
AR
Argentina
Prior art keywords
substituted
alkyl
case
heteroatoms selected
carbon atoms
Prior art date
Application number
ARP130104090A
Other languages
English (en)
Inventor
M Moslin Ryan
S Weinstein David
T Wrobleski Stephen
Zhang Yanlei
S Tokarski John
E Mertzman Michael
Liu Chunjian
Original Assignee
Bristol Myers Squibb Co
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
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Priority to TW102140574A priority Critical patent/TWI582077B/zh
Priority to ARP130104090A priority patent/AR094537A1/es
Priority to RS20191041A priority patent/RS59125B1/sr
Priority to AU2014347275A priority patent/AU2014347275B2/en
Priority to PE2016000603A priority patent/PE20160961A1/es
Priority to MYPI2016701601A priority patent/MY174453A/en
Priority to MA39001A priority patent/MA39001A1/fr
Priority to BR112016010172-3A priority patent/BR112016010172B1/pt
Priority to NZ720710A priority patent/NZ720710A/en
Priority to SI201431231T priority patent/SI3066078T1/sl
Priority to EP14702707.2A priority patent/EP3066078B1/en
Priority to CN201480072423.2A priority patent/CN106660960B/zh
Priority to TN2016000153A priority patent/TN2016000153A1/en
Priority to ES14702707T priority patent/ES2738826T3/es
Priority to HUE14702707A priority patent/HUE046052T2/hu
Priority to US15/034,915 priority patent/US9663467B2/en
Priority to LTEP14702707.2T priority patent/LT3066078T/lt
Priority to DK14702707.2T priority patent/DK3066078T3/da
Priority to CA2930060A priority patent/CA2930060C/en
Priority to EP19173861.6A priority patent/EP3590926A1/en
Priority to PL14702707T priority patent/PL3066078T3/pl
Priority to JP2016528221A priority patent/JP6312823B2/ja
Priority to PT14702707T priority patent/PT3066078T/pt
Priority to KR1020167014612A priority patent/KR102186633B1/ko
Priority to PCT/US2014/011769 priority patent/WO2015069310A1/en
Priority to EA201690865A priority patent/EA033272B1/ru
Priority to MX2016005853A priority patent/MX369394B/es
Publication of AR094537A1 publication Critical patent/AR094537A1/es
Priority to PH12016500779A priority patent/PH12016500779A1/en
Priority to IL245448A priority patent/IL245448B/en
Priority to CL2016001101A priority patent/CL2016001101A1/es
Priority to HK16114678A priority patent/HK1226400A1/zh
Priority to US15/480,787 priority patent/US9987266B2/en
Priority to HRP20191368 priority patent/HRP20191368T1/hr
Priority to CY20191100878T priority patent/CY1122065T1/el

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    • AHUMAN NECESSITIES
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • 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
    • A61K31/455Nicotinic acids, e.g. niacin; Derivatives thereof, e.g. esters, amides
    • 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
    • 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
    • A61K31/435Heterocyclic 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
    • 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
    • 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]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon 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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    • 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
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    • 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
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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/54Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/56Amides

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  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

Son útiles para la modulación de IL-12, IL-23 y/o lFNa que actúan en Tyk-2 para generar la inhibición de la transducción de señal. Reivindicación 1: Un compuesto caracterizado porque tiene la fórmula (1), o un estereoisómero o una sal de aquel aceptable desde el punto de vista farmacéutico, en donde R¹ es alquilo C₁₋₃ opcionalmente sustituido con 0 - 7 R¹ᵃ; R¹ᵃ es, en cada caso, independientemente hidrógeno, deuterio, F, CI, Br, CF₃ o CN; R² es alquilo C₁₋₆ sustituido con 0 - 4 R²ᵃ, cicloalquilo C₃₋₆ sustituido con 0 - 4 R²ᵃ, arilo C₆₋₁₀ sustituido con 0 - 4 R²ᵃ, un heterociclo de 5 - 14 miembros que contiene 1 - 4 heteroátomos seleccionados de N, O y S, sustituido con 0 - 4 R²ᵃ, NR⁶R⁶ u ORᵇ; R²ᵃ es, en cada caso, independientemente hidrógeno, =O, halo, OCF₃, CN, NO₂, -(CH₂)ʳORᵇ, -(CH₂)ʳSRᵇ, -(CH₂)ʳC(O)Rᵇ, -(CH₂)ʳC(O)ORᵇ, -(CH₂)ʳOC(O)Rᵇ, -(CH₂)ʳNR¹¹R¹¹, -(CH₂)ʳC(O)NR¹¹R¹¹, -(CH₂)ʳNRᵇC(O)Rᶜ, -(CH₂)ʳNRᵇC(O)ORᶜ, -NRᵇC(O)NR¹¹R¹¹, -S(O)ₚNR¹¹R¹¹, -NRᵇS(O)ₚRᶜ, -S(O)ₚRᶜ, alquilo C₁₋₆ sustituido con 0 - 3 Rᵃ, haloalquilo C₁₋₆, -(CH₂)ʳ-carbociclo de 3 - 14 miembros sustituido con 0 - 1 Rᵃ o -(CH₂)ʳ-heterociclo de 5 - 7 miembros que comprende átomos de carbono o 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 2 Rᵃ; o un R²ᵃ y otro R²ᵃ, junto con los átomos a los que están unidos, se combinan para formar un anillo fusionado de 5 - 6 miembros, en donde el anillo fusionado se puede sustituir con 0 - 2 Rᵃ; R³ es -(CH₂)ʳ-carbociclo de 3 - 14 miembros sustituido 0 - 5 R³ᵃ; R³ᵃ es, en cada caso, independientemente hidrógeno, =O, halo (F), OCF₃, CF₃, CHF₂, CN, NO₂, -(CH₂)ʳORᵇ, -(CH₂)ʳSRᵇ, -(CH₂)ʳC(O)Rᵇ, -(CH₂)ʳC(O)ORᵇ, -(CH₂)ʳOC(O)Rᵇ, -(CH₂)ʳNR¹¹R¹¹, -(CH₂)ʳC(O)NR¹¹R¹¹, -(CH₂)ʳNRᵇC(O)Rᶜ, -(CH₂)ʳNRᵇC(O)ORᶜ, -NRᵇC(O)NR¹¹R¹¹, -S(O)ₚNR¹¹R¹¹, -NRᵇS(O)ₚRᶜ, -S(O)ₚRᶜ, alquilo C₁₋₆ sustituido con 0 - 3 Rᵃ, haloalquilo C₁₋₆, -(CH₂)ʳ-carbociclo de 3 - 14 miembros sustituido con 0 - 3 Rᵃ o -(CH₂)ʳ-heterociclo de 5 - 10 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᵃ; o dos R³ᵃ, junto con los átomos a los que están unidos, se combinan para formar un anillo fusionado, en donde el anillo se selecciona de fenilo y un heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, S u O, y ese anillo fenilo fusionado también se puede sustituir con Rᵃ; R⁴ y R⁵ son independientemente hidrógeno, alquilo C₁₋₄ sustituido con 0 - 1 Rᶠ, (CH₂)ʳ-fenilo sustituido con 0 - 3 Rᵈ o -(CH₂)-heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ; R⁶ y R¹¹ son, en cada caso, independientemente hidrógeno, alquilo C₁₋₄ sustituido con 0 - 3 Rᶠ, CF₃, cicloalquilo C₃₋₁₀ sustituido con 0 - 1 Rᶠ, (CH)ʳ-fenilo sustituido con 0 - 3 Rᵈ o (CH₂)ʳ-heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᵈ; Rᵃ es, en cada caso, hidrógeno, F, CI, Br, OCF₃, CF₃, CHF₂, CN, NO₂, -(CH₂)ʳORᵇ, -(CH₂)ʳSRᵇ, -(CH₂)ʳC(O)Rᵇ, -(CH₂)ʳC(O)ORᵇ, -(CH₂)ʳOC(O)Rᵇ, -(CH₂)ʳNR¹¹R¹¹, -(CH₂)ʳC(O)NR¹¹R¹¹, -(CH₂)ʳNRᵇC(O)Rᶜ, -(CH₂)ʳNRᵇC(O)ORᶜ, -NRᵇC(O)NR¹¹R¹¹, -S(O)ₚNR¹¹R¹¹, -NRᵇS(O)Rᶜ, -S(O)Rᶜ, -S(O)₂Rᶜ, alquilo C₁₋₆ sustituido con 0 - 3 Rᶠ, haloalquilo C₁₋₆, -(CH₂)ʳ-carbociclo de 3 - 14 miembros o -(CH₂)ʳ-heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᶠ; Rᵇ es, en cada caso, hidrógeno, alquilo C₁₋₆ sustituido con 0 - 3 Rᵈ, haloalquilo C₁₋₆, cicloalquilo C₃₋₆ sustituido con 0 - 2 Rᵈ, o -(CH₂)ʳ-heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᶠ o (CH₂)ʳ-fenilo sustituido con 0 - 3 Rᵈ; Rᶜ es alquilo C₁₋₆ sustituido con 0 - 3 Rᶠ, (CH₂)ʳ-cicloalquilo C₃₋₆ sustituido con 0 - 3 Rᶠ o (CH₂)ʳ-fenilo sustituido con 0 - 3 Rᶠ; Rᵈ es, en cada caso, independientemente hidrógeno, F, CI, Br, OCF₃, CF₃, CN, NO₂, -ORᵉ, -(CH₂)ʳ-C(O)Rᶜ, -NRᵉRᵉ, -NRᵉC(O)ORᶜ, alquilo C₁₋₆ o (CH₂)ʳ-fenilo sustituido con 0 - 3 Rᶠ; Rᵉ se selecciona, independientemente en cada caso, de hidrógeno, alquilo C₁₋₆, cicloalquilo C₃₋₆ y (CH₂)ʳ-fenilo sustituido con 0 - 3 Rᶠ; Rᶠ es, en cada caso, independientemente hidrógeno, halo, CN, NH₂, OH, cicloalquilo C₃₋₆, CF₃, O(alquilo C₁₋₆) o -(CH₂)ʳ-heteroarilo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ; p es 0, 1 ó 2; y r es 0, 1, 2, 3 ó 4.
ARP130104090A 2013-11-07 2013-11-07 COMPUESTOS DE PIRIDILO SUSTITUIDOS CON ALQUILAMIDA ÚTILES COMO MODULADORES DE LAS RESPUESTAS DE IL-12, IL-23 Y/O IFNa AR094537A1 (es)

Priority Applications (34)

Application Number Priority Date Filing Date Title
TW102140574A TWI582077B (zh) 2013-11-07 2013-11-07 作爲IL-12、IL-23及/或IFNα反應調節劑之經烷基-醯胺取代之吡啶化合物
ARP130104090A AR094537A1 (es) 2013-11-07 2013-11-07 COMPUESTOS DE PIRIDILO SUSTITUIDOS CON ALQUILAMIDA ÚTILES COMO MODULADORES DE LAS RESPUESTAS DE IL-12, IL-23 Y/O IFNa
DK14702707.2T DK3066078T3 (da) 2013-11-07 2014-01-16 Alkyl-amid-substituerede pyridylforbindelser, der er anvendelige som modulatorer af il-12-, il-23- og/eller ifn-alpha-responser
EP19173861.6A EP3590926A1 (en) 2013-11-07 2014-01-16 Alkyl-amide-substituted pyridyl compounds useful as modulators of il-12, il-23 and/or ifnalpha responses
PE2016000603A PE20160961A1 (es) 2013-11-07 2014-01-16 Compuestos de piridilo sustituidos con alquilamida utiles como moduladores de respuestas de citocinas heterodimericas interleucina 12 y 23 (il-12 e il-23) y/o interferon alfa (ifnalfa)
CA2930060A CA2930060C (en) 2013-11-07 2014-01-16 Alkyl-amide-substituted pyridyl compounds useful as modulators of il-12, il-23 and/or ifnalpha responses
MA39001A MA39001A1 (fr) 2013-11-07 2014-01-16 Composés pyridyle substitués par alkyl-amide, utiles comme modulateurs d'il-12, il-23 et/ou de réponses à l'ifn?
BR112016010172-3A BR112016010172B1 (pt) 2013-11-07 2014-01-16 Compostos de piridila substituída por alquil- amida úteis no tratamento de uma doença inflamatória ou autoimune e composição farmacêutica que os compreende
NZ720710A NZ720710A (en) 2013-11-07 2014-01-16 Alkyl-amide-substituted pyridyl compounds useful as modulators of il-12, il-23 and/or ifnalpha responses
AU2014347275A AU2014347275B2 (en) 2013-11-07 2014-01-16 Alkyl-amide-substituted pyridyl compounds useful as modulators of IL-12, IL-23 and/or IFNalpha responses
EP14702707.2A EP3066078B1 (en) 2013-11-07 2014-01-16 Alkyl-amide-substituted pyridyl compounds useful as modulators of il-12, il-23 and/or ifnalpha responses
CN201480072423.2A CN106660960B (zh) 2013-11-07 2014-01-16 用作IL-12、IL-23和/或IFNα响应的调节剂的烷基-酰胺-取代的吡啶化合物
TN2016000153A TN2016000153A1 (en) 2013-11-07 2014-01-16 Alkyl-amide-substituted pyridyl compounds useful as modulators of il-12, il-23 and/or ifnalpha responses.
ES14702707T ES2738826T3 (es) 2013-11-07 2014-01-16 Compuestos de piridilo sustituidos con alquilamida útiles como moduladores de respuestas de IL-12, IL-23 y/o IFNalfa
HUE14702707A HUE046052T2 (hu) 2013-11-07 2014-01-16 Alkil-amid szubsztituált piridil vegyületek, amelyek hasznosak IL-12, IL-23 és/vagy IFN-alfa reakciók modulátoraiként
PL14702707T PL3066078T3 (pl) 2013-11-07 2014-01-16 Związki pirydylowe podstawione alkilo-amidami przydatne jako modulatory odpowiedzi il-12, il-23 i/lub ifn-alfa
LTEP14702707.2T LT3066078T (lt) 2013-11-07 2014-01-16 Alkilamidu-pakeisti piridilo junginiai, naudingi kaip il-12, il-23 ir (arba) ifn-alfa atsako moduliatoriai
RS20191041A RS59125B1 (sr) 2013-11-07 2014-01-16 Alkil-amid-supstituisana piridil jedinjenja korisna kao modulatori il-12, il-23 i/ili ifnalfa odgovora
MYPI2016701601A MY174453A (en) 2013-11-07 2014-01-16 Alkyl-amide-substituted pyridyl compounds useful as modulators of il-12, il-23 and/or ifnalpha responses
SI201431231T SI3066078T1 (sl) 2013-11-07 2014-01-16 Alkil-amid-substituirane spojine piridila uporabne kot modulatorji IL-12, IL-23 in/ali IFN-ALFA odgovorov
US15/034,915 US9663467B2 (en) 2013-11-07 2014-01-16 Alkyl-amide-substituted pyridyl compounds useful as modulators of IL-12, IL-23 and/or IFNα responses
JP2016528221A JP6312823B2 (ja) 2013-11-07 2014-01-16 Il−12、il−23および/またはifnアルファ応答の調節因子として有用なアルキル−アミド−置換ピリジル化合物
PT14702707T PT3066078T (pt) 2013-11-07 2014-01-16 Compostos de piridilo substitoidos com alqoil-amida uteis como modoladores de respostas de il-12, il-23 e/00 ifn-alfa
KR1020167014612A KR102186633B1 (ko) 2013-11-07 2014-01-16 Il-12, il-23 및/또는 ifn알파 반응의 조정제로서 유용한 알킬-아미드-치환된 피리딜 화합물
PCT/US2014/011769 WO2015069310A1 (en) 2013-11-07 2014-01-16 Alkyl-amide-substituted pyridyl compounds useful as modulators of il-12, il-23 and/or ifnalpha responses
EA201690865A EA033272B1 (ru) 2013-11-07 2014-01-16 АЛКИЛАМИД-ЗАМЕЩЕННЫЕ ПИРИДИЛЬНЫЕ СОЕДИНЕНИЯ, ПРИМЕНИМЫЕ В КАЧЕСТВЕ ИНГИБИТОРОВ ОТВЕТОВ IL-12, IL-23 И/ИЛИ IFNα
MX2016005853A MX369394B (es) 2013-11-07 2014-01-16 Compuestos de piridilo sustituidos con alquilamida utiles como muduladores de respuestas de citocinas heterodimericas interleucina 12 y 23 (il-12 e il-23) y/o interferon alfa (ifnalfa).
PH12016500779A PH12016500779A1 (en) 2013-11-07 2016-04-27 Alkyl-amide-substituted pyridyl compounds useful as modulators of il-12, il-23 and/or ifnalpha responses
IL245448A IL245448B (en) 2013-11-07 2016-05-03 Alkyl-amide substituted pyridyl compounds useful as modulators of responses to il-12, il-23, and/or ifnalpha
CL2016001101A CL2016001101A1 (es) 2013-11-07 2016-05-06 Compuestos de piridilo sustituidos con alquilamida útiles como moduladores de respuestas de il-12 e il-23 y/o ifnalfa
HK16114678A HK1226400A1 (zh) 2013-11-07 2016-12-23 作為il-12,il-23調節劑的烷基醯胺取代的吡啶基化合物
US15/480,787 US9987266B2 (en) 2013-11-07 2017-04-06 Alkyl-amide-substituted pyridyl compounds useful as modulators of IL-12, IL-23 and/or IFNα responses
HRP20191368 HRP20191368T1 (hr) 2013-11-07 2019-07-30 Alkil-amid supstituirani piridil spojevi korisni kao modulatori il-12, il-23 i/ili ifnalfa odgovora
CY20191100878T CY1122065T1 (el) 2013-11-07 2019-08-14 Ενωσεις αλκυλ-αμιδο-υποκατεστημενου πυριδυλιου χρησιμες ως διαμορφωτες των αποκρισεων il-12, il-23 και/η ιfναλφα

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TW102140574A TWI582077B (zh) 2013-11-07 2013-11-07 作爲IL-12、IL-23及/或IFNα反應調節劑之經烷基-醯胺取代之吡啶化合物
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Families Citing this family (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL3495358T3 (pl) 2012-11-08 2022-06-27 Bristol-Myers Squibb Company Podstawione amidem związki heterocykliczne przydatne jako modulatory odpowiedzi il-12, il-23 i/lub ifn-alfa
MX2015005561A (es) 2012-11-08 2015-07-23 Squibb Bristol Myers Co Compuestos de pirimidina sustituidos con alquil-amida utiles en la modulacion de interleucina 12 (il-12) interleucina 23 (il-23) y/o interferon alfa (ifn alfa).
EA029126B1 (ru) 2013-07-01 2018-02-28 Бристол-Майерс Сквибб Компани Ингибиторы ido
UA119050C2 (uk) 2013-11-11 2019-04-25 Ґілеад Саєнсиз, Інк. ПІРОЛО[1.2-f][1.2.4]ТРИАЗИНИ, ЯКІ ВИКОРИСТОВУЮТЬСЯ ДЛЯ ЛІКУВАННЯ РЕСПІРАТОРНО-СИНЦИТІАЛЬНИХ ВІРУСНИХ ІНФЕКЦІЙ
US10273237B2 (en) 2013-12-10 2019-04-30 Bristol-Myers Squibb Company Imidazopyridazine compounds useful as modulators of IL-12, IL-23 and/or IFN-α responses
CN107849039B (zh) 2015-06-24 2020-07-03 百时美施贵宝公司 经杂芳基取代的氨基吡啶化合物
CN108026099B (zh) 2015-06-24 2020-07-10 百时美施贵宝公司 经杂芳基取代的氨基吡啶化合物
ES2930198T3 (es) 2016-10-14 2022-12-07 Nimbus Lakshmi Inc Inhibidores de TYK2 y usos de los mismos
KR102477063B1 (ko) 2016-10-28 2022-12-12 브리스톨-마이어스 스큅 컴퍼니 Il-12, il-23 및/또는 ifn 알파 반응의 조정제로서 유용한 헤테로비시클릭 화합물
JP7012082B2 (ja) * 2016-11-17 2022-01-27 ブリストル-マイヤーズ スクイブ カンパニー Il-12、il-23および/またはifn-アルファのイミダゾピリダジン調節剤
AR110351A1 (es) * 2016-12-13 2019-03-20 Bristol Myers Squibb Co COMPUESTOS DE HETEROARILO SUSTITUIDOS CON FOSFINÓXIDO ALQUILAMIDA COMO MODULADORES DE RESPUESTAS DE IL-12, IL-23 Y/O IFNa
ES2864450T3 (es) * 2017-03-30 2021-10-13 Bristol Myers Squibb Co Proceso para la preparación de 6-(ciclopropanamido)-4-((2-metoxi-3-(1-metil-1h-1,2,4-triazol-3-il)fenil)amino)-N-(metil-d3)piridazina-3-carboxamida
BR112019023290A2 (pt) 2017-05-11 2020-06-16 Bristol-Myers Squibb Company Tienopiridinas e benzotiofenos úteis como inibidores de irak4
EA202091269A1 (ru) * 2017-11-21 2020-08-07 Бристол-Маерс Сквибб Компани Сульфон-, пиридин-, алкил-, амид-замещенные гетероарильные соединения
US10508113B2 (en) 2018-03-12 2019-12-17 Abbvie Inc. Inhibitors of tyrosine kinase 2 mediated signaling
BR112021002642A2 (pt) * 2018-08-16 2021-05-04 Innate Tumor Immunity, Inc. compostos de 4-amino-1h-imidazo[4,5-c]quinolina substituídos e métodos aprimorados para a preparação dos mesmos
MX2021004538A (es) * 2018-10-22 2021-09-10 Esker Therapeutics Inc Inhibidores de tyk2 y sus usos.
IL282840B1 (en) * 2018-10-30 2024-11-01 Bristol Myers Squibb Company Substituted amide heterocyclic compounds for the treatment of conditions involving the regulation of IL-12, IL-23 AND/OR IFN-ALPHA
WO2020156311A1 (zh) * 2019-01-28 2020-08-06 江苏豪森药业集团有限公司 一种哒嗪类衍生物抑制剂、其制备方法和应用
KR20210121140A (ko) * 2019-01-30 2021-10-07 브리스톨-마이어스 스큅 컴퍼니 아미드-이치환된 피리딘 또는 피리다진 화합물
CN114269336A (zh) 2019-04-30 2022-04-01 细胞基因公司 包含阿普斯特和tyk2抑制剂的联合疗法
US20220204495A1 (en) * 2019-05-03 2022-06-30 Valo Health, Inc. Inhibiting trabid
US20230167082A1 (en) * 2019-07-16 2023-06-01 Bristol-Myers Squibb Company Prodrugs in the modulation of interleukin
PL4038063T3 (pl) * 2020-03-11 2024-07-15 Beijing Innocare Pharma Tech Co., Ltd. Związki heterocykliczne do hamowania aktywności tyk2
WO2021204626A1 (en) * 2020-04-06 2021-10-14 Almirall, S.A. Aryl and heteroaryl-carboxamide substituted heteroaryl compounds as tyk2 inhibitors
WO2021211741A1 (en) * 2020-04-14 2021-10-21 Gossamer Bio Services, Inc. Substituted pyridines for the treatment of inflammatory diseases
CN115715287A (zh) * 2020-04-28 2023-02-24 百时美施贵宝公司 作为IL-12、IL-23和/或IFNα调节剂的经取代的N-(甲基-d3)哒嗪-3-甲酰胺或N-(甲基-d3)-烟酰胺化合物
CN113563309A (zh) * 2020-04-28 2021-10-29 浙江海正药业股份有限公司 吡啶类衍生物及其制备方法和用途
WO2021237121A1 (en) * 2020-05-21 2021-11-25 Gossamer Bio Services, Inc. Substituted pyridines
EP3944859A1 (en) 2020-07-30 2022-02-02 Assistance Publique Hôpitaux de Paris Method for treating immune toxicities induced by immune checkpoint inhibitors
WO2022105771A1 (zh) * 2020-11-17 2022-05-27 江苏恒瑞医药股份有限公司 含氮杂环类衍生物、其制备方法及其在医药上的应用
CN112625030A (zh) * 2020-12-25 2021-04-09 杭州澳赛诺生物科技有限公司 一种一锅法合成n-保护3-溴代吡唑的合成方法
TW202233600A (zh) * 2021-02-06 2022-09-01 大陸商正大天晴藥業集團股份有限公司 含聯環的tyk2抑制劑化合物、藥物組合物及其用途
JP2024510274A (ja) * 2021-03-16 2024-03-06 アンルイ バイオメディカル テクノロジー (グァンヂョウ) カンパニー リミテッド アミノヘテロアリール化合物および組成物
AU2022268464A1 (en) * 2021-05-04 2023-12-21 Shanghai Zheye Biotechnology Co. Ltd. Nitrogen-containing heterocyclic pyridine compound
WO2022253335A1 (zh) * 2021-06-02 2022-12-08 南京明德新药研发有限公司 含磺酰基的芳基类化合物及其应用
IL311624A (en) * 2021-09-23 2024-05-01 Bristol Myers Squibb Co Methods for treating hair loss disorders with TYK2 inhibitors
AU2022378463A1 (en) 2021-10-25 2024-05-09 Kymera Therapeutics, Inc. Tyk2 degraders and uses thereof
TW202339749A (zh) * 2021-12-16 2023-10-16 大陸商凌科藥業有限公司 Tyk2抑制劑及其組合物和方法
WO2023108536A1 (en) * 2021-12-16 2023-06-22 Lynk Pharmaceuticals Co. Ltd. Tyk2 inhibitors and compositions and methods thereof
WO2023213308A1 (zh) * 2022-05-05 2023-11-09 苏州隆博泰药业有限公司 酰胺取代的杂环化合物及其医药用途
WO2024020221A1 (en) 2022-07-21 2024-01-25 Arvinas Operations, Inc. Modulators of tyk2 proteolysis and associated methods of use
WO2024042363A1 (en) * 2022-08-24 2024-02-29 Sudo Biosciences Limited Tyk2 inhibitors and uses thereof
WO2024042361A1 (en) * 2022-08-24 2024-02-29 Sudo Biosciences Limited Tyk2 inhibitors and uses thereof
WO2024165000A1 (zh) * 2023-02-07 2024-08-15 上海华汇拓医药科技有限公司 一种哒嗪类化合物、其制备方法和用途
CN118812511A (zh) * 2023-04-21 2024-10-22 浙江文达医药科技有限公司 作为tyk2抑制剂的杂环化合物及合成和应用

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7176214B2 (en) 2003-05-21 2007-02-13 Bristol-Myers Squibb Company Imidazo-fused oxazolo[4,5-β]pyridine and imidazo-fused thiazolo[4,5-β]pyridine based tricyclic compounds and pharmaceutical compositions comprising same
US20050049276A1 (en) 2003-07-23 2005-03-03 Warner-Lambert Company, Llc Imidazopyridines and triazolopyridines
AR076550A1 (es) * 2009-05-06 2011-06-22 Portola Pharm Inc Inhibidores de la janus tirosina kinasa (jak)
TW201103904A (en) 2009-06-11 2011-02-01 Hoffmann La Roche Janus kinase inhibitor compounds and methods
WO2013054351A1 (en) * 2011-08-08 2013-04-18 Cadila Healthcare Limited Heterocyclic compounds
JP5957537B2 (ja) 2011-12-21 2016-07-27 ビオタ ヨーロッパ リミテッドBiota Europe Ltd 複素環式ウレア化合物
EP2794598A1 (en) * 2011-12-23 2014-10-29 Cellzome Limited Pyrimidine-2,4-diamine derivatives as kinase inhibitors
PL3495358T3 (pl) 2012-11-08 2022-06-27 Bristol-Myers Squibb Company Podstawione amidem związki heterocykliczne przydatne jako modulatory odpowiedzi il-12, il-23 i/lub ifn-alfa
EA028526B1 (ru) 2012-11-08 2017-11-30 Бристол-Майерс Сквибб Компани АЛКИЛАМИДЗАМЕЩЕННЫЕ ПИРИДИЛЬНЫЕ СОЕДИНЕНИЯ, ПРИМЕНИМЫЕ В КАЧЕСТВЕ МОДУЛЯТОРОВ ОТВЕТОВ, ОПОСРЕДУЕМЫХ IL-12, IL-23 И/ИЛИ IFNα
MX2015005561A (es) 2012-11-08 2015-07-23 Squibb Bristol Myers Co Compuestos de pirimidina sustituidos con alquil-amida utiles en la modulacion de interleucina 12 (il-12) interleucina 23 (il-23) y/o interferon alfa (ifn alfa).
US10273237B2 (en) 2013-12-10 2019-04-30 Bristol-Myers Squibb Company Imidazopyridazine compounds useful as modulators of IL-12, IL-23 and/or IFN-α responses

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