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PE20011118A1 - (+)-6-[amino-(6-cloro-piridin-3-il)-(3-metil-3h-imidazol-4-il)-metil]-4-(3-cloro-fenil)-1-ciclopropilmetil-1h-quinolein-2-ona como compuesto anticanceroso y metodo de separacion de enantiomeros util para sintetizar dicho compuesto - Google Patents

(+)-6-[amino-(6-cloro-piridin-3-il)-(3-metil-3h-imidazol-4-il)-metil]-4-(3-cloro-fenil)-1-ciclopropilmetil-1h-quinolein-2-ona como compuesto anticanceroso y metodo de separacion de enantiomeros util para sintetizar dicho compuesto

Info

Publication number
PE20011118A1
PE20011118A1 PE2001000041A PE2001000041A PE20011118A1 PE 20011118 A1 PE20011118 A1 PE 20011118A1 PE 2001000041 A PE2001000041 A PE 2001000041A PE 2001000041 A PE2001000041 A PE 2001000041A PE 20011118 A1 PE20011118 A1 PE 20011118A1
Authority
PE
Peru
Prior art keywords
chloro
methyl
compound
alkyl
cyclopropylmetil
Prior art date
Application number
PE2001000041A
Other languages
English (en)
Inventor
Bingwei Vera Yang
Original Assignee
Pfizer Prod Inc
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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of PE20011118A1 publication Critical patent/PE20011118A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • 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
    • 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)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Oncology (AREA)
  • Urology & Nephrology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Virology (AREA)
  • Communicable Diseases (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Hematology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Pyridine Compounds (AREA)

Abstract

SE REFIERE A (+)-6-[AMINO-(6-CLORO-PIRIDIN-3-IL)-(3-METIL-3H-IMIDAZOL-4-IL)-METIL]-4-(3-CLORO-FENIL)-1-CICLOPROPILMETIL-1H-QUINOLEIN-2-ONA. SE REFIERE TAMBIEN A UNA COMPOSICION QUE COMPRENDE ADEMAS AGENTE QUIMIOTERAPICO O INHIBIDORES DE METALOPROTEASA MMP2; INHIBIDORES DE MMP9, INHIBIDORES DE TRANSDUCCION DE SENALES, AGENTES ANTIPROLIFERATIVOS, AGENTES CAPACES DE BLOQUEAR CTL4; UN METODO PARA SEPARAR ENANTIOANMEROS (+) Y (-) DEL COMPUESTO DE FORMULA I DE LA MEZCLA RACEMICA, DONDE; R1 ES H, ALQUILO C1-C10; R2 ES HALO, CIANO, COOR15; R3 - R7 SON H, ALQUILO C1-C10, ALQUENILO C2-C10, ENTRE OTROS; Z ES HETEROCICLO AROMATICO DE 4-10 MIEMBROS; R9 ES -(CR13R14)t(IMIDAZOLILO), R9 ES (CR13R14)t(PIRIDINILO); R12 ES H, ALQUILO C1-C10, (CR13R14)t(CICLOALQUILO C3-C10), ENTRE OTROS; R13 Y R14 SON H, ALQUILO C1-C10; t ES 0-5; q ES 1-5; R15 NO ES H, R12; n ES 1-3 . UN METODO PARA SINTETIZAR ENANTIOMEROS (+), (-). EL COMPUESTO INHIBE FARNESIL TRANSFERASA ASI COMO EL DESARROLLO CELULAR ANORMAL Y PUEDE SER UTIL EN EL TRATAMIENTO DE CANCER DE PULMON, HUESO, PANCREAS, PIEL
PE2001000041A 2000-01-21 2001-01-17 (+)-6-[amino-(6-cloro-piridin-3-il)-(3-metil-3h-imidazol-4-il)-metil]-4-(3-cloro-fenil)-1-ciclopropilmetil-1h-quinolein-2-ona como compuesto anticanceroso y metodo de separacion de enantiomeros util para sintetizar dicho compuesto PE20011118A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US17771800P 2000-01-21 2000-01-21

Publications (1)

Publication Number Publication Date
PE20011118A1 true PE20011118A1 (es) 2001-11-06

Family

ID=22649709

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2001000041A PE20011118A1 (es) 2000-01-21 2001-01-17 (+)-6-[amino-(6-cloro-piridin-3-il)-(3-metil-3h-imidazol-4-il)-metil]-4-(3-cloro-fenil)-1-ciclopropilmetil-1h-quinolein-2-ona como compuesto anticanceroso y metodo de separacion de enantiomeros util para sintetizar dicho compuesto

Country Status (17)

Country Link
US (1) US6479513B2 (es)
EP (1) EP1248782A1 (es)
JP (2) JP2003520796A (es)
AR (1) AR029792A1 (es)
AU (1) AU2001214087A1 (es)
BR (1) BR0016986A (es)
CA (1) CA2398353C (es)
CO (1) CO5271702A1 (es)
GT (1) GT200100008A (es)
HN (1) HN2000000266A (es)
MX (1) MXPA02007153A (es)
MY (1) MY126069A (es)
PA (1) PA8508101A1 (es)
PE (1) PE20011118A1 (es)
SV (1) SV2002000291A (es)
TN (1) TNSN01009A1 (es)
WO (1) WO2001053289A1 (es)

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EA008501B1 (ru) * 2002-12-19 2007-06-29 Пфайзер Инк. 2-(1н-индазол-6-иламино)бензамидные соединения как ингибиторы протеинкиназ, полезные для лечения офтальмологических заболеваний
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WO2005105784A1 (en) * 2004-05-03 2005-11-10 Janssen Pharmaceutica N.V. Diastereoselective synthesis process for the preparation of imidazole compounds
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WO2009151683A2 (en) * 2008-03-12 2009-12-17 Link Medicine Corporation Quinolinone farnesyl transferase inhibitors for the treatment of synucleinopathies and other indications
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Also Published As

Publication number Publication date
MXPA02007153A (es) 2002-12-13
AU2001214087A1 (en) 2001-07-31
GT200100008A (es) 2001-10-19
WO2001053289A1 (en) 2001-07-26
TNSN01009A1 (fr) 2005-11-10
US6479513B2 (en) 2002-11-12
US20020004514A1 (en) 2002-01-10
SV2002000291A (es) 2002-07-16
PA8508101A1 (es) 2002-08-26
JP2003520796A (ja) 2003-07-08
CA2398353A1 (en) 2001-07-26
CA2398353C (en) 2007-07-31
EP1248782A1 (en) 2002-10-16
JP2007326868A (ja) 2007-12-20
MY126069A (en) 2006-09-29
HN2000000266A (es) 2001-05-21
BR0016986A (pt) 2002-10-08
CO5271702A1 (es) 2003-04-30
AR029792A1 (es) 2003-07-16

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