AR072860A1 - Derivados de 3-(3-pirimidin-2-il-bencil)-[1,2,4]triazolo[4,3-b]piridazina - Google Patents

Derivados de 3-(3-pirimidin-2-il-bencil)-[1,2,4]triazolo[4,3-b]piridazina

Info

Publication number
AR072860A1
AR072860A1 ARP090102184A ARP090102184A AR072860A1 AR 072860 A1 AR072860 A1 AR 072860A1 AR P090102184 A ARP090102184 A AR P090102184A AR P090102184 A ARP090102184 A AR P090102184A AR 072860 A1 AR072860 A1 AR 072860A1
Authority
AR
Argentina
Prior art keywords
nhet
hal
nhet1
het1
nhconh
Prior art date
Application number
ARP090102184A
Other languages
English (en)
Inventor
Frank Stieber
Oliver Schadt
Dieter Dorsch
Andree Blaukat
Original Assignee
Merck Patent Gmbh
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 Merck Patent Gmbh filed Critical Merck Patent Gmbh
Publication of AR072860A1 publication Critical patent/AR072860A1/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/02Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Neurosurgery (AREA)
  • Cardiology (AREA)
  • Immunology (AREA)
  • Vascular Medicine (AREA)
  • Ophthalmology & Optometry (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Urology & Nephrology (AREA)
  • Oncology (AREA)
  • Neurology (AREA)
  • Rheumatology (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Los compuestos de la formula (1), en donde: R1es Ar, Het o A; R2 es H, A, Hal, OR5, N(R5)2, N=CR5N(R5)2, SR5, NO2, CN, COOR5, CON(R5)2, NR5COA, NR5SO2A, SO2N(R5)2, S(O)mA, Het, -[C(R5)2]nN(R5)2, -[C(R5)2]nHet, O[C(R5)2]nN(R5)2, O[C(R5)2]nHet, S[C(R5)2]nN(R5)2, S[C(R5)2]nHet, -NR5[C(R5)2]nN(R5)2, -NR5[C(R5)2]nHet, NHCON(R5)2, NHCONH[C(R5)2]nN(R5)2, NHCONH[C(R5)2]nHet, NHCO[C(R5)2]nN(R5)2, NHCO[C(R5)2]nHet, CON(R5)2, CONR5[C(R5)2]nN(R5)2, CONR5[C(R5)2]nHet, COHet o COA; R3, R3' son cada uno, de modo independiente entre sí, H, F o A, también juntos son alquileno C2-5; R4 es H, A o Hal; R5 es H o A; A es alquilo C1-10 no ramificado o ramificado, en donde 1-7 átomos de H pueden estar reemplazados por OH, F, Cl y/o Br, y/o en donde uno o dos grupos CH2 pueden estar reemplazados por O, NH, S, SO, SO2 y/o grupos CH=CH, o es alquilo cíclico C3-7; Ar es fenilo, naftilo o bifenilo no sustituido o mono-, di- o trisustituido con Hal, A, OR5, N(R5)2, SR5, NO2, CN, COOR5, CON(R5)2, NR5COA, NR5SO2A, SO2N(R5)2 y/o S(O)mA; Het es un heterociclo saturado, insaturado o aromático mono-, di- o tricíclico 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, OR5, N(R5)2, SR5, NO2, CN, COOR5, CON(R5)2, NR5COA, NR5SO2A, SO2N(R5)2, S(O)mA, CO-Het1, Het1, [C(R5)2]nN(R5)2, -[C(R5)2]nHet1, O[C(R5)2]nN(R5)2, O[C(R5)2]nHet1, NHCOOA, NHCON(R5)2, NHCOO[C(R5)2]nN(R5)2, NHCOO[C(R5)2]nHet1, NHCONH[C(R5)2]nN(R5)2, NHCONH[C(R5)2]nHet1, OCONH[C(R5)2]nN(R5)2, OCONH[C(R5)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, Hal y/u =O (oxígeno del carbonilo); Hal es F, Cl, Br o I; m es 0, 1 o 2; n es 1, 2, 3 o 4; así como sus sales, tautomeros y estereoisomeros farmacéuticamente aceptables, incluyendo sus mezclas en todas las proporciones. Son inhibidores de la tirosina quinasa, en especial de la Met-quinasa, y pueden utilizarse, por ejemplo, para el tratamiento de tumores.
ARP090102184A 2008-06-18 2009-06-17 Derivados de 3-(3-pirimidin-2-il-bencil)-[1,2,4]triazolo[4,3-b]piridazina AR072860A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE102008028905A DE102008028905A1 (de) 2008-06-18 2008-06-18 3-(3-Pyrimidin-2-yl-benzyl)-[1,2,4]triazolo[4,3-b]pyridazinderivate

Publications (1)

Publication Number Publication Date
AR072860A1 true AR072860A1 (es) 2010-09-29

Family

ID=40973097

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP090102184A AR072860A1 (es) 2008-06-18 2009-06-17 Derivados de 3-(3-pirimidin-2-il-bencil)-[1,2,4]triazolo[4,3-b]piridazina

Country Status (19)

Country Link
US (1) US8497266B2 (es)
EP (1) EP2285811B1 (es)
JP (1) JP5662311B2 (es)
KR (1) KR101661777B1 (es)
CN (1) CN102066378B (es)
AR (1) AR072860A1 (es)
AU (1) AU2009259764B2 (es)
BR (1) BRPI0915417B8 (es)
CA (1) CA2728194C (es)
DE (1) DE102008028905A1 (es)
DK (1) DK2285811T3 (es)
EA (1) EA019534B1 (es)
ES (1) ES2400117T3 (es)
IL (1) IL210063A (es)
MX (1) MX2010013649A (es)
PL (1) PL2285811T3 (es)
PT (1) PT2285811E (es)
WO (1) WO2009152920A1 (es)
ZA (1) ZA201100437B (es)

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DE102008037790A1 (de) * 2008-08-14 2010-02-18 Merck Patent Gmbh Bicyclische Triazolderivate
DE102008063667A1 (de) * 2008-12-18 2010-07-01 Merck Patent Gmbh 3-(3-Pyrimidin-2-yl-benzyl)-°[1,2,4]triazolo[4,3-b]pyrimidin-derivate
PL2361250T3 (pl) 2008-12-22 2014-01-31 Merck Patent Gmbh Nowe polimorficzne formy diwodorofosforanu 6-(1-metylo-1H-pirazolo-4-ylo)-2-{3-[5-(2-morfolino-4-ylo-etoksy)-pirymidyno-2-ylo]-benzylo}2H-pirydazyno-3-onowego oraz sposoby ich otrzymywania
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BRPI0915417B8 (pt) 2021-05-25
EA201100031A1 (ru) 2011-08-30
CA2728194A1 (en) 2009-12-23
EA019534B1 (ru) 2014-04-30
EP2285811B1 (de) 2012-12-05
WO2009152920A1 (de) 2009-12-23
EP2285811A1 (de) 2011-02-23
JP2011524385A (ja) 2011-09-01
JP5662311B2 (ja) 2015-01-28
AU2009259764B2 (en) 2013-09-26
PL2285811T3 (pl) 2013-04-30
BRPI0915417B1 (pt) 2020-02-11
US20110092498A1 (en) 2011-04-21
DK2285811T3 (da) 2013-03-11
DE102008028905A1 (de) 2009-12-24
KR20110031329A (ko) 2011-03-25
CN102066378A (zh) 2011-05-18
IL210063A0 (en) 2011-02-28
KR101661777B1 (ko) 2016-09-30
ZA201100437B (en) 2011-09-28
CN102066378B (zh) 2014-04-16
ES2400117T3 (es) 2013-04-05
IL210063A (en) 2015-06-30
PT2285811E (pt) 2013-03-05
BRPI0915417A2 (pt) 2015-11-03
US8497266B2 (en) 2013-07-30
CA2728194C (en) 2016-11-29
AU2009259764A1 (en) 2009-12-23
MX2010013649A (es) 2010-12-21

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