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AR074688A1 - Derivados de piridazinona, procedimiento para prepararlos, medicamentos que los contienen y uso de los mismos para el tratamiento de tumores. - Google Patents

Derivados de piridazinona, procedimiento para prepararlos, medicamentos que los contienen y uso de los mismos para el tratamiento de tumores.

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Publication number
AR074688A1
AR074688A1 ARP090104911A ARP090104911A AR074688A1 AR 074688 A1 AR074688 A1 AR 074688A1 AR P090104911 A ARP090104911 A AR P090104911A AR P090104911 A ARP090104911 A AR P090104911A AR 074688 A1 AR074688 A1 AR 074688A1
Authority
AR
Argentina
Prior art keywords
piperidin
nhet
nhet1
hal
nor2
Prior art date
Application number
ARP090104911A
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English (en)
Inventor
Dieter Dorsch
Andree Blaukat
Frank Stieber
Oliver Schadt
Original Assignee
Merck Patent Gmbh
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Filing date
Publication date
Application filed by Merck Patent Gmbh filed Critical Merck Patent Gmbh
Publication of AR074688A1 publication Critical patent/AR074688A1/es

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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom 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
    • A61K31/495Heterocyclic 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
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    • 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
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    • A61K47/02Inorganic compounds
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    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0014Skin, i.e. galenical aspects of topical compositions
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    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
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    • A61K9/0048Eye, e.g. artificial tears
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    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2013Organic compounds, e.g. phospholipids, fats
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07D403/08Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing alicyclic rings
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    • C07D453/00Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C07D453/02Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/19Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/28Dragees; Coated pills or tablets, e.g. with film or compression coating
    • A61K9/2806Coating materials
    • A61K9/282Organic compounds, e.g. fats
    • A61K9/2826Sugars or sugar alcohols, e.g. sucrose; Derivatives thereof

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  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
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  • Veterinary Medicine (AREA)
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  • Dermatology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Diabetes (AREA)
  • Immunology (AREA)
  • Hematology (AREA)
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  • Inorganic Chemistry (AREA)
  • Urology & Nephrology (AREA)
  • Oncology (AREA)
  • Heart & Thoracic Surgery (AREA)
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  • Cardiology (AREA)
  • Obesity (AREA)
  • Endocrinology (AREA)
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Los compuestos de la fórmula (1) en donde R1 es Ar, Het, A, OR2, O[C(R2)2]nAr, O[C(R2)2]nHet, N(R2)2, NR2[C(R2)2]nAr o NR2[C(R2)2]nHet; R2 es H o A'; R3, R3' son, en cada caso de modo independiente entre sí, H, Hal, A, OR2, CN, COOR2, CON(R2)2, NR2COA, NR2SO2A, SO2N(R2)2 o S(O)mA, Y es [C(R2)2]nNR2COZ, [C(R2)2]nNR2COHet1, [C(R2)2]nCyc[C(R2)2]nN(R2)2, [C(R2)2]nCyc[C(R2)2]nOR2, [C(R2)2]nCyc[C(R2)2]nHet1, [C(R2)2]n-C(CH2)-((CH2)p)-[C(R2)2]nN(R2)2, [C(R2)2]n-C(CH2-(CH2)p)[C(R2)2]nOR2, [C(R2)2]n-C(CH2-(CH2)p)-[C(R2)2]nHet, [C(R2)2]nHet2, [C(R2)2]nCR2(NR2)2COOR2, [C(R2)2]nNR2CO[C(R2)2]nNR2COA, [C(R2)2]nNR2COOA, [C(R2)2]nCO-NR2-A, [C(R2)2]nCO-NR2-[C(R2)2]nHet1, [C(R2)2]nCONH2, [C(R2)2]nCONHA, [C(R2)2]nCONA2, [C(R2)2]nCO-NR2-[C(R2)2]nN(R2)2 o COOA; ; Z es CR2(NR2)2CR2(OR2)A, Ar es fenilo, naftilo o bifenilo no sustituido o mono-, di- o trisustituido con Hal, A, [C(R2)2]nOR2, [C(R2)2]nN(R2)2, SR2, NO2, CN, CO-OR2, CON(R2)2, NR2COA, NR2SO2A, SO2N(R2)2, S(O)mA, CO-Het, Het, O[C(R2)2]nN(R2)2, O[C(R2)2]nHet, NHCOOA, NHCON(R2)2, NHCOO[C(R2)2]nN(R2)2, NHCOO[C(R2)2]nHet, NHCONH[C(R2)2]nN(R2)2, NHCONH[C(R2)2]nHet, OCONH[C(R2)2]nN(R2)2, OCONH[C(R2)2]nHet, CONR2[C(R2)2]nN(R2)2, CONR2[C(R2)2]nHet, y/o COA, Het es un heterociclo mono-, bi- o tricíclico saturado, insaturado o aromático con 1 a 4 átomos de N, O y/o S, que puede no estar sustituido o que puede estar mono-, di- o trisustituido con Hal, A, [C(R2)2]nOR2, [C(R2)2]n(R2)2, SR2, NO2, CN, COOR2, CON(R2)2, NR2COA, NR2SO2A, SO2N(R2)2, S(O)mA, CO-Het1, [C(R2)2]nHet1, O[C(R2)2]nN(R2)2, O[C(R2)2]nHet1, NHCOOA, NHCON(R2)2, NHCOO[C(R2)2]nN(R2)2, NHCOO[C(R2)2]nHet1, NHCONH[C(R2)2]nN(R2)2, NHCONH[C(R2)2]nHet1, OCONH[C(R2)2]nN(R2)2, OCONH[C(R2)2]nHet1, CO-Het1, CHO, COA, =S, =NH, =NA y/u =O (oxígeno del carbonilo), Het1 es un heterociclo saturado monocíclico con 1 a 2 átomos de N y/u O, que puede estar mono- o disustituido con A, OA, OH, COOH, COOA, Hal y/u =O (oxígeno del carbonilo), Het2 es 2-metoxicarbonil-pirrolidin-4-ilo, 2-carboxi-pirrolidin-4-ilo, 1-ciclopropilmetil-piperidin-4-ilo, piperidin-4-ilo, morfolin-2-o 4-ilo, 1-isopropil-piperidin-4-ilo, 1-metil-piperidin-4-ilo, 4-piperazinilo, 1-metil-pirrolidin-2-ilo, 1-ter.-butoxicarbonil-piperidin-4-ilo, 1-etil-piperidin-2-ilo, 1-(2-metoxi-etil)-piperidin-4-ilo, 1-[2-(N,N-dimetilamino)-etil]-piperidin-4-ilo, 1,2,2,6,6-pentametil-piperidin-4-ilo, 1-aza-biciclo[2,2,2]oct-3-ilo, tetrahidropiran-4-ilo, 1-formil-piperidin-4-ilo o 1-metil-1-oxi-piperidin-4-ilo, A es alquilo no ramificado o ramificado C1-10, en donde 1-7 átomos de H pueden estar reemplazados por F, y/o en donde uno o dos grupos CH2 no adyacentes pueden estar reemplazados por O, NH, S, SO, SO2 y/o grupos CH=CH, o es alquilo cíclico C3-7, A' es alquilo no ramificado o ramificado C1-6 en donde 1-5 átomos de H pueden estar reemplazados por F; CyC es cicloalquileno C3-7; Hal es F, Cl, Br o I; m es 0, 1 o 2, n es 1, 2, 3 o 4, p es 1, 2, 3, 4, o 5; así como sus sales, tautómeros y estereoisómeros farmacéuticamente aceptables, incluyendo sus mezclas en todas las proporciones. Son inhibidores de las tirosina quinasas, en especial de la Met-quinasa, y pueden utilizarse, por ejemplo, para el tratamiento de tumores.
ARP090104911A 2008-12-23 2009-12-16 Derivados de piridazinona, procedimiento para prepararlos, medicamentos que los contienen y uso de los mismos para el tratamiento de tumores. AR074688A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE102008062826A DE102008062826A1 (de) 2008-12-23 2008-12-23 Pyridazinonderivate

Publications (1)

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AR074688A1 true AR074688A1 (es) 2011-02-02

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ARP090104911A AR074688A1 (es) 2008-12-23 2009-12-16 Derivados de piridazinona, procedimiento para prepararlos, medicamentos que los contienen y uso de los mismos para el tratamiento de tumores.

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US (1) US8637518B2 (es)
EP (1) EP2367815B1 (es)
JP (1) JP5592395B2 (es)
KR (1) KR20110098854A (es)
CN (1) CN102264727B (es)
AR (1) AR074688A1 (es)
AU (1) AU2009331991B2 (es)
BR (1) BRPI0923497A2 (es)
CA (1) CA2747863C (es)
CY (1) CY1116191T1 (es)
DE (1) DE102008062826A1 (es)
DK (1) DK2367815T3 (es)
EA (1) EA201100966A1 (es)
ES (1) ES2532139T3 (es)
HR (1) HRP20150375T1 (es)
HU (1) HUE025138T2 (es)
MX (1) MX2011006652A (es)
PL (1) PL2367815T3 (es)
PT (1) PT2367815E (es)
SI (1) SI2367815T1 (es)
WO (1) WO2010072296A1 (es)
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KR20110098854A (ko) 2011-09-01
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US8637518B2 (en) 2014-01-28
CY1116191T1 (el) 2017-02-08
HUE025138T2 (en) 2016-03-29
BRPI0923497A2 (pt) 2019-09-24
MX2011006652A (es) 2011-07-12
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PT2367815E (pt) 2015-02-20
DK2367815T3 (en) 2015-03-09
PL2367815T3 (pl) 2015-04-30
US20110257181A1 (en) 2011-10-20
CA2747863A1 (en) 2010-07-01
HRP20150375T1 (hr) 2015-05-22
ES2532139T3 (es) 2015-03-24
CA2747863C (en) 2016-08-23
SI2367815T1 (sl) 2015-05-29
DE102008062826A1 (de) 2010-07-01
AU2009331991A1 (en) 2011-08-11
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AU2009331991B2 (en) 2015-10-22
EP2367815B1 (de) 2015-01-14
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