MXPA03004347A - Nuevos derivados de imidazol, metodo de produccion y uso de los mismos. - Google Patents

Nuevos derivados de imidazol, metodo de produccion y uso de los mismos.

Info

Publication number
MXPA03004347A
MXPA03004347A MXPA03004347A MXPA03004347A MXPA03004347A MX PA03004347 A MXPA03004347 A MX PA03004347A MX PA03004347 A MXPA03004347 A MX PA03004347A MX PA03004347 A MXPA03004347 A MX PA03004347A MX PA03004347 A MXPA03004347 A MX PA03004347A
Authority
MX
Mexico
Prior art keywords
compound
production method
imidazole derivatives
novel imidazole
mixture
Prior art date
Application number
MXPA03004347A
Other languages
English (en)
Inventor
Isao Aoki
Original Assignee
Takeda Chemical Industries Ltd
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 Takeda Chemical Industries Ltd filed Critical Takeda Chemical Industries Ltd
Publication of MXPA03004347A publication Critical patent/MXPA03004347A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • 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
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • 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
    • 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
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/24Drugs for disorders of the endocrine system of the sex hormones
    • A61P5/28Antiandrogens
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • 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

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Endocrinology (AREA)
  • Diabetes (AREA)
  • Reproductive Health (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Steroid Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicinal Preparation (AREA)

Abstract

La presente invencion proporciona un compuesto que tiene una actividad inhibidora sobre la esteroide C17,20-liasa, y util para el tratamiento y la profilaxis de un tumor, tal como prostatismo, cancer mamario y similares, y un metodo para separar eficientemente un compuesto opticamente activo de este compuesto de una mezcla de isomeros opticos del mismo, un compuesto de la formula:(Ver formula),en donde cada simbolo es como se definio en la especificacion, una sal del mismo o un profarmaco del mismo, y un metodo para obtener un compuesto opticamente activo separando opticamente una mezcla de isomeros opticos mediante el uso de un agente de separacion, tal como acido tartranilico y similares.
MXPA03004347A 2000-11-17 2001-11-16 Nuevos derivados de imidazol, metodo de produccion y uso de los mismos. MXPA03004347A (es)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2000351780 2000-11-17
JP2001247618 2001-08-17
JP2001336880 2001-11-01
PCT/JP2001/010002 WO2002040484A2 (en) 2000-11-17 2001-11-16 Novel imidazole derivatives, production method thereof and use thereof

Publications (1)

Publication Number Publication Date
MXPA03004347A true MXPA03004347A (es) 2004-05-04

Family

ID=27345219

Family Applications (1)

Application Number Title Priority Date Filing Date
MXPA03004347A MXPA03004347A (es) 2000-11-17 2001-11-16 Nuevos derivados de imidazol, metodo de produccion y uso de los mismos.

Country Status (27)

Country Link
US (1) US7141598B2 (es)
EP (2) EP1334106B1 (es)
JP (2) JP3753971B2 (es)
KR (3) KR100809899B1 (es)
CN (3) CN100572363C (es)
AR (1) AR034854A1 (es)
AT (2) ATE327237T1 (es)
AU (3) AU1429602A (es)
BR (1) BR0115306B1 (es)
CA (1) CA2429133C (es)
CY (1) CY1105423T1 (es)
DE (1) DE60119963T2 (es)
DK (1) DK1334106T3 (es)
ES (1) ES2260303T3 (es)
HK (1) HK1056168A1 (es)
HU (1) HU229408B1 (es)
IL (2) IL155624A0 (es)
MX (1) MXPA03004347A (es)
MY (1) MY134929A (es)
NO (1) NO326366B1 (es)
NZ (1) NZ526387A (es)
PE (1) PE20020596A1 (es)
PL (1) PL204934B1 (es)
PT (1) PT1334106E (es)
SI (1) SI1334106T1 (es)
TW (1) TWI306099B (es)
WO (1) WO2002040484A2 (es)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2275411A3 (en) * 2002-01-10 2011-02-23 Takeda Pharmaceutical Company Limited Reformatsky Reagent in Stable Form and Process for Producing the Same
JP4745616B2 (ja) * 2003-02-26 2011-08-10 武田薬品工業株式会社 安定化されたイミダゾール誘導体含有医薬組成物、イミダゾール誘導体の安定化方法
WO2004075890A1 (ja) * 2003-02-26 2004-09-10 Takeda Pharmaceutical Company 安定化されたイミダゾール誘導体含有医薬組成物、イミダゾ-ル誘導体の安定化方法
JP4837895B2 (ja) * 2003-03-17 2011-12-14 武田薬品工業株式会社 放出制御組成物
CA2519211A1 (en) * 2003-03-17 2004-09-30 Takeda Pharmaceutical Company Limited Release control compositions
US7282507B2 (en) * 2004-05-03 2007-10-16 Janssen Pharmaceutica N.V. Indole derivatives as selective androgen receptor modulators (SARMS)
AR049125A1 (es) * 2004-05-28 2006-06-28 Speedel Experimenta Ag Heterociclos biciclicos nitrogenados inhibidores de la aromatasa.
EP1854463A4 (en) * 2005-03-03 2011-03-23 Takeda Pharmaceutical COMPOSITION WITH CONTROLLED RELEASE
GT200600381A (es) 2005-08-25 2007-03-28 Compuestos organicos
AR056888A1 (es) 2005-12-09 2007-10-31 Speedel Experimenta Ag Derivados de heterociclil imidazol
EP1991223B1 (en) * 2006-02-10 2010-07-14 Janssen Pharmaceutica, N.V. Novel imidazolopyrazole derivatives useful as selective androgen receptor modulators
TW200804284A (en) * 2006-03-31 2008-01-16 Speedel Experimenta Ag Process for preparing 6,7-dihydro-5H-imidazo[1,5-a]pyridin-8-one
KR20100088144A (ko) * 2007-10-29 2010-08-06 다케다 야쿠힌 고교 가부시키가이샤 공지된 암 치료법에 대해 난치성인 암의 예방 또는 치료에 사용하기 위한 피롤로 [1,2-c] 이미다졸 유도체
JOP20190231A1 (ar) * 2009-01-15 2017-06-16 Incyte Corp طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به
AR083916A1 (es) * 2010-11-18 2013-04-10 Takeda Pharmaceutical Metodo para tratar el cancer de mama y cancer de ovarios
US20150157609A1 (en) 2011-04-01 2015-06-11 Takeda Pharmaceutical Company Limited Solid preparation
WO2012173280A1 (en) * 2011-06-15 2012-12-20 Takeda Pharmaceutical Company Limited Production method of imidazole derivatives

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4728645A (en) * 1982-12-21 1988-03-01 Ciba-Geigy Corporation Substituted imidazo[1,5-A]pyridine derivatives and other substituted bicyclic derivatives, useful as aromatase inhibitors
NZ221729A (en) 1986-09-15 1989-07-27 Janssen Pharmaceutica Nv Imidazolyl methyl-substituted benzimidazole derivatives and pharmaceutical compositions
ZA882717B (en) 1987-04-22 1988-10-17 Merrell Dow Pharmaceuticals Inc. 17beta-(cyclopropylamino)-androst-5-eb-3beta-ol and related compounds useful as c17-20 lyase inhibitors
US5057521A (en) * 1988-10-26 1991-10-15 Ciba-Geigy Corporation Use of bicyclic imidazole compounds for the treatment of hyperaldosteronism
US4966898A (en) 1989-08-15 1990-10-30 Merrell Dow Pharmaceuticals Inc. 4-substituted 17β-(cyclopropylamino)androst-5-en-3β-ol and related compounds useful as C17-20 lyase inhibitors
JPH06507355A (ja) 1991-03-01 1994-08-25 エレクトロスタティック テクノロジー インコーポレーテッド 回路板用薄層板等を製造するための粉体コーティング法
CA2127689A1 (en) * 1992-01-27 1993-08-05 Marcel A. C. Janssen Pyrroloimidazolyl and imidazopyridinyl substituted 1h-benzimidazole derivatives as aromatase inhibitors
US5457102A (en) 1994-07-07 1995-10-10 Janssen Pharmaceutica, N.V. Pyrroloimidazolyl and imidazopyridinyl substituted 1H-benzimidazole derivatives
NZ249911A (en) 1992-03-31 1996-06-25 British Tech Group 17-(3-pyridyl) substituted steroids and use in pharmaceutical compositions
GB9310635D0 (en) 1993-05-21 1993-07-07 Glaxo Group Ltd Chemical compounds
NZ273681A (en) 1993-09-30 1996-09-25 Yamanouchi Pharma Co Ltd Fluoroenylmethylazole derivatives (including tricyclic ring systems where the middle ring is heterosubstituted)
WO1996014090A1 (en) 1994-11-07 1996-05-17 Janssen Pharmaceutica N.V. Compositions comprising carbazoles and cyclodextrins
WO1997000257A1 (fr) 1995-06-14 1997-01-03 Yamanouchi Pharmaceutical Co., Ltd. Derives d'imidazole fusionnes et composition medicinale les contenant
CA2281598A1 (en) 1997-02-21 1998-08-27 Tetsuya Aono Fused ring compounds, process for producing the same and use thereof
DK1028110T3 (da) 1997-10-02 2004-07-19 Daiichi Seiyaku Co Hidtil ukendte dihydronaphthalenforbindelser og fremgangsmåde til fremstilling deraf
ATE293102T1 (de) 1998-04-23 2005-04-15 Takeda Pharmaceutical Naphthalene derivate ,ihre herstellung und verwendung
PE20010781A1 (es) * 1999-10-22 2001-08-08 Takeda Chemical Industries Ltd Compuestos 1-(1h-imidazol-4-il)-1-(naftil-2-sustituido)etanol, su produccion y utilizacion

Also Published As

Publication number Publication date
EP1681290B9 (en) 2013-06-19
HK1056168A1 (en) 2004-02-06
AU2002214296B2 (en) 2005-09-29
NO20032234D0 (no) 2003-05-16
AU2005225035B2 (en) 2007-02-22
EP1681290B1 (en) 2011-11-16
BR0115306B1 (pt) 2013-12-24
PL204934B1 (pl) 2010-02-26
PE20020596A1 (es) 2002-08-13
KR20030048156A (ko) 2003-06-18
CN100572363C (zh) 2009-12-23
JP4427496B2 (ja) 2010-03-10
JP3753971B2 (ja) 2006-03-08
WO2002040484A3 (en) 2002-09-26
JP2006045239A (ja) 2006-02-16
DE60119963T2 (de) 2006-10-05
HUP0400549A2 (hu) 2004-06-28
KR100725442B1 (ko) 2007-06-07
CN1474819A (zh) 2004-02-11
IL155624A0 (en) 2003-11-23
JP2003201282A (ja) 2003-07-18
EP1334106B1 (en) 2006-05-24
DK1334106T3 (da) 2006-09-18
MY134929A (en) 2008-01-31
PL362766A1 (en) 2004-11-02
ATE533768T1 (de) 2011-12-15
HUP0400549A3 (en) 2004-09-28
CN1329394C (zh) 2007-08-01
NZ526387A (en) 2004-02-27
PT1334106E (pt) 2006-08-31
TWI306099B (en) 2009-02-11
BR0115306A (pt) 2004-02-10
CN1680336A (zh) 2005-10-12
NO326366B1 (no) 2008-11-17
NO20032234L (no) 2003-07-16
CA2429133C (en) 2009-08-18
HU229408B1 (hu) 2013-12-30
KR20080002929A (ko) 2008-01-04
AU1429602A (en) 2002-05-27
AR034854A1 (es) 2004-03-24
CY1105423T1 (el) 2010-04-28
US7141598B2 (en) 2006-11-28
ATE327237T1 (de) 2006-06-15
KR20050105287A (ko) 2005-11-03
AU2005225035A1 (en) 2005-11-10
CA2429133A1 (en) 2002-05-23
IL155624A (en) 2006-12-31
US20040033935A1 (en) 2004-02-19
CN1900079A (zh) 2007-01-24
EP1334106A2 (en) 2003-08-13
SI1334106T1 (sl) 2006-10-31
ES2260303T3 (es) 2006-11-01
WO2002040484A2 (en) 2002-05-23
EP1681290A2 (en) 2006-07-19
DE60119963D1 (de) 2006-06-29
AU2002214296C1 (en) 2006-04-13
EP1681290A3 (en) 2006-07-26
KR100809899B1 (ko) 2008-03-10

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