AR118043A1 - DERIVADOS DE INDAZOLIL-ISOXAZOL COMO INHIBIDORES DE c-KIT QUINASA - Google Patents

DERIVADOS DE INDAZOLIL-ISOXAZOL COMO INHIBIDORES DE c-KIT QUINASA

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Publication number
AR118043A1
AR118043A1 ARP200100351A ARP200100351A AR118043A1 AR 118043 A1 AR118043 A1 AR 118043A1 AR P200100351 A ARP200100351 A AR P200100351A AR P200100351 A ARP200100351 A AR P200100351A AR 118043 A1 AR118043 A1 AR 118043A1
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Argentina
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denotes
hal
atoms
unsubstituted
substituted
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ARP200100351A
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English (en)
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Blum Andreas Dr
Dorsch Dieter Dr
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Merck Patent Gmbh
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Publication of AR118043A1 publication Critical patent/AR118043A1/es

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    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero 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
    • A61K31/41Heterocyclic 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
    • 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
    • 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
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/541Non-condensed thiazines containing further heterocyclic rings
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P35/00Antineoplastic agents
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    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/48Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom
    • C07C311/49Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom to nitrogen atoms
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    • C07F7/0812Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
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  • Veterinary Medicine (AREA)
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  • Pharmacology & Pharmacy (AREA)
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  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Compuestos derivados de indazolil-isoxazol con actividad inhibidora de c-KIT quinasa, un proceso para su preparación, intermediarios utilizados en dicho proceso, medicamentos y un kit que los comprenden y el uso de los mismos para el tratamiento del cáncer. Reivindicación 1: Los compuestos de la fórmula (1) caracterizados porque R¹ denota Hal, CF₃, OA, Het¹, COOR³ o CON(R³)₂, R² denota H, Hal o CN, R³ denota H o A, X denota fenileno, piridin-diilo, 1,3-tiazol-diilo o pirazol-diilo, cada uno de los cuales está sin sustituir o sustituido una, dos o tres veces con Hal y/o A, Y está ausente o denota CO, O[C(R³)₂]ₙ, NR³CO, CONR³, CONR³[C(R³)₂]ₙ, CONHCH₂C(CH₃)₂, SO₂, SO₂N(R³), -N= o S(=O, =NR³), Z denota H, A, Hal, OA, [C(R³)₂]ₙHet² o N=S(=O)A₂, A denota alquilo ramificado o no ramificado con 1 - 10 átomos de C, donde uno o dos grupos CH y/o CH₂ no adyacentes pueden ser reemplazados con átomos de O y donde 1 - 7 átomos de H pueden ser reemplazados con R⁵, o denota (CH₂)ₙCyc, Cyc denota alquilo cíclico que tiene de 3 - 7 átomos de C, R⁵ denota F, Cl, OH, SO₂A o N(R³)₂, Het¹ denota pirazolilo el cual puede estar sustituido una o dos veces con A, Het² denota un heterociclo saturado o insaturado, aromático, monocíclico, de 4 a 7 miembros que tiene de 1 a 4 átomos de N, O y/o S, el cual puede estar sin sustituir o sustituido una, dos o tres veces con A, Hal, CN, OR³, [C(R³)₂]ₙN(R³)₂, [C(R³)₂]ₙSO₂A, [C(R³)₂]ₙNR³SO₂A, Het³, =NR³ y/o =O, o denota un heterociclo saturado o insaturado, aromático, bicíclico, de 7 a 10 miembros que tiene de 1 a 4 átomos de N, O y/o S, el cual puede estar sin sustituir o sustituido una, dos o tres veces con A, Hal, CN, OR³, [C(R³)₂]ₙN(R³)₂, [C(R³)₂]ₙSO₂A, [C(R³)₂]ₙNR³SO₂A, Het³, =NR³ y/o =O, Het³ denota un heterociclo saturado o insaturado, aromático, monocíclico, de 4 a 7 miembros que tiene de 1 a 4 átomos de N, O y/o S, el cual puede estar sin sustituir o puede estar sustituido una o dos veces con A, Hal, OR³, oxetanilo y/o =O, o denota un heterociclo saturado o insaturado, aromático, bicíclico, de 7 a 10 miembros que tiene de 1 a 4 átomos de N, O y/o S, el cual puede estar sin sustituir o puede estar sustituido una o dos veces con A, Hal, OR³, oxetanilo y/o =O, Hal denota F, Cl, Br o I, n denota 0, 1, 2 ó 3, y sus solvatos, sales, tautómeros y estereoisómeros farmacéuticamente aceptables, incluyendo las mezclas de los mismos en todas las proporciones.
ARP200100351A 2019-02-11 2020-02-10 DERIVADOS DE INDAZOLIL-ISOXAZOL COMO INHIBIDORES DE c-KIT QUINASA AR118043A1 (es)

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US (1) US20220127254A1 (es)
EP (1) EP3924340A1 (es)
JP (1) JP2022520374A (es)
KR (1) KR20210129674A (es)
CN (1) CN113474334B (es)
AR (1) AR118043A1 (es)
AU (1) AU2020220333A1 (es)
BR (1) BR112021014466A2 (es)
CA (1) CA3129601A1 (es)
IL (1) IL285421A (es)
MX (1) MX2021009426A (es)
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AU2019212959A1 (en) 2018-01-29 2020-09-17 Capulus Therapeutics, Llc SREBP inhibitors comprising a 6-membered central ring
KR20220128335A (ko) * 2019-11-13 2022-09-20 카풀루스 테라퓨틱스, 엘엘씨 티오펜 중심 고리를 포함하는 srebp 저해제
CN114000167B (zh) * 2021-11-25 2024-02-06 南京先进生物材料与过程装备研究院有限公司 一种电化学合成吡唑类化合物的方法
WO2024073560A2 (en) * 2022-09-28 2024-04-04 The Trustees Of Columbia University In The City Of New York Novel gpx4 inhibitors and uses thereof

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NZ565255A (en) * 2005-06-22 2010-04-30 Plexxikon Inc Pyrrolo[2,3-b] pyridine derivatives as protein kinase inhibitors
HUE029617T2 (en) * 2010-12-20 2017-03-28 Merck Serono Sa Indazolyl triazole derivatives as IRAK inhibitors
HUE057043T2 (hu) * 2016-01-11 2022-04-28 Merck Patent Gmbh Kinolin-2-on származékok
WO2019051199A1 (en) * 2017-09-08 2019-03-14 Incyte Corporation 6-CYANO-INDAZOLE COMPOUNDS AS HEMATOPOIETIC PROGENITOR KINASE 1 (HPK1) MODULATORS

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MX2021009426A (es) 2021-09-10
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BR112021014466A2 (pt) 2021-09-21
CA3129601A1 (en) 2020-08-20
JP2022520374A (ja) 2022-03-30
IL285421A (en) 2021-09-30
CN113474334B (zh) 2024-08-06
EP3924340A1 (en) 2021-12-22
CN113474334A (zh) 2021-10-01
AU2020220333A1 (en) 2021-09-30
SG11202108636SA (en) 2021-09-29
US20220127254A1 (en) 2022-04-28

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