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PE20091957A1 - Compuestos triazina como inhibidores mtor y quinasa pi3 - Google Patents

Compuestos triazina como inhibidores mtor y quinasa pi3

Info

Publication number
PE20091957A1
PE20091957A1 PE2009000725A PE2009000725A PE20091957A1 PE 20091957 A1 PE20091957 A1 PE 20091957A1 PE 2009000725 A PE2009000725 A PE 2009000725A PE 2009000725 A PE2009000725 A PE 2009000725A PE 20091957 A1 PE20091957 A1 PE 20091957A1
Authority
PE
Peru
Prior art keywords
mtor
cor3
triazin
oxa
oct
Prior art date
Application number
PE2009000725A
Other languages
English (en)
Inventor
Aranapakam Mudumbai Venkatesan
Zecheng Chen
Christoph Martin Dehnhardt
Santos Osvaldo Dos
Santos Efren Guillermo Delos
Arie Zask
Jeroen Cunera Verheijen
Joshua Aaron Kaplan
David James Richard
Semiramis Ayral-Kaloustian
Tarek Suhayl Mansour
Ariamala Jay Gopalsamy
Kevin Joseph Curran
Mengxiao Shi
Original Assignee
Wyeth 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=40911929&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20091957(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Wyeth Corp filed Critical Wyeth Corp
Publication of PE20091957A1 publication Critical patent/PE20091957A1/es

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    • C—CHEMISTRY; METALLURGY
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    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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
    • A—HUMAN NECESSITIES
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    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic 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
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
    • C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
    • C07D251/18—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with nitrogen atoms directly attached to the two other ring carbon atoms, e.g. guanamines
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    • C07D401/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
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    • C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
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    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10—Spiro-condensed systems
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    • C07D498/08—Bridged systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
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  • Chemical Kinetics & Catalysis (AREA)
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  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Immunology (AREA)
  • Urology & Nephrology (AREA)
  • Cardiology (AREA)
  • Rheumatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Vascular Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Dermatology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

SE REFIERE A DERIVADOS DE [1,3,5] TRIAZINA 2,4,6-SUSTITUIDOS DE FORMULA (I) DONDE R1 ES (a) O (b), EN DONDE R6, R7, R8 Y R9 SON CADA UNO H, ALQUILO(C1-C6) OPCIONALMENTE SUSTITUIDO CON ALQUENILO(C2-C6), ALCADIENILO(C4-C6), ALQUINILO(C2-C6), ENTRE OTROS; ---- ES UN SEGUNDO ENLACE OPCIONAL; R2 ES ARILO(C6-C14) OPCIONALMENTE SUSTITUIDO CON -NH-COR3, HETEROARILO(C6-C9) OPCIONALMENTE SUSTITUIDO CON -NH-COR3, -CH=CH-ARILO(C6-C10)-NH-COR3, ENTRE OTROS, DONDE R3 ES OR5, NR5R5 O NHR5; R5 ES ALQUILO(C1-C6), ALQUENILO(C3-C6), ALQUINILO(C3-C6), ENTRE OTROS; R4 ES ALQUENILO(C3-C6), ALQUINILO(C3-C6), CICLOALQUILO(C3-C8), ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 1-{4-[4-MORFOLIN-4-IL-6-(8-OXA-3-AZABICICLO[3.2.1]OCT-3-IL)-1,3,5-TRIAZIN-2-IL]FENIL}-3-FENILUREA, 1-(4-FLUOROFENIL)-3-{4-[4-MORFOLIN-4-IL-6-(8-OXA-3-AZABICICLO[3.2.1]OCT-3-IL)-1,3,5-TRIAZIN-2-IL]FENIL}UREA, 1-(4-METILFENIL)-3-{4-[4-MORFOLIN-4-IL-6-(8-OXA-3-AZABICICLO[3.2.1]OCT-3-IL)-1,3,5-TRIAZIN-2-IL]FENIL}UREA, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA QUINASA FOSFATIDILINOSITOL-3 (PI3) Y mTOR SIENDO UTILES EN EL TRATAMIENTO DE CANCER, RESTENOSIS, ARTRITIS, SORIASIS
PE2009000725A 2008-05-23 2009-05-25 Compuestos triazina como inhibidores mtor y quinasa pi3 PE20091957A1 (es)

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US5566108P 2008-05-23 2008-05-23

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PE20091957A1 true PE20091957A1 (es) 2009-12-30

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PE2009000725A PE20091957A1 (es) 2008-05-23 2009-05-25 Compuestos triazina como inhibidores mtor y quinasa pi3

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