ATE397600T1 - Diastereoselektives syntheseverfahren zur herstellung vn imidazolverbindungen - Google Patents

Diastereoselektives syntheseverfahren zur herstellung vn imidazolverbindungen

Info

Publication number
ATE397600T1
ATE397600T1 AT05737841T AT05737841T ATE397600T1 AT E397600 T1 ATE397600 T1 AT E397600T1 AT 05737841 T AT05737841 T AT 05737841T AT 05737841 T AT05737841 T AT 05737841T AT E397600 T1 ATE397600 T1 AT E397600T1
Authority
AT
Austria
Prior art keywords
methyl
synthesis process
production
sub
imidazole compounds
Prior art date
Application number
AT05737841T
Other languages
English (en)
Inventor
Walter Ferdinand Mari Filliers
Rudy Laurent Maria Broeckx
Patrick Rene Angibaud
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Application granted granted Critical
Publication of ATE397600T1 publication Critical patent/ATE397600T1/de

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
    • C07D401/02Heterocyclic 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
    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • 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

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
AT05737841T 2004-05-03 2005-04-28 Diastereoselektives syntheseverfahren zur herstellung vn imidazolverbindungen ATE397600T1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP04076319 2004-05-03

Publications (1)

Publication Number Publication Date
ATE397600T1 true ATE397600T1 (de) 2008-06-15

Family

ID=34966069

Family Applications (1)

Application Number Title Priority Date Filing Date
AT05737841T ATE397600T1 (de) 2004-05-03 2005-04-28 Diastereoselektives syntheseverfahren zur herstellung vn imidazolverbindungen

Country Status (10)

Country Link
US (1) US7456287B2 (de)
EP (1) EP1751137B1 (de)
JP (1) JP5008554B2 (de)
CN (1) CN100567292C (de)
AT (1) ATE397600T1 (de)
AU (1) AU2005238223B2 (de)
CA (1) CA2563807C (de)
DE (1) DE602005007346D1 (de)
ES (1) ES2308486T3 (de)
WO (1) WO2005105784A1 (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HRP20211976T1 (hr) 2015-08-17 2022-03-18 Kura Oncology, Inc. Postupci liječenja bolesnika od raka inhibitorima farnezil transferaze
EP3838275A1 (de) 2016-11-03 2021-06-23 Kura Oncology, Inc. Farnesyltransferase-inhibitoren zur verwendung bei der behandlung von krebs
CN110234639A (zh) 2016-12-08 2019-09-13 杭州领业医药科技有限公司 替吡法尼的晶型及其制备方法及药物组合物
AU2019270163A1 (en) 2018-05-18 2020-12-03 Kura Oncology, Inc. Synthesis of tipifarnib

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2175137T3 (es) * 1995-12-08 2002-11-16 Janssen Pharmaceutica Nv Derivados de (imidazol-5-il)metil-2-quinolinona como inhibidores de laproteina farnesil-transferasa.
HN2000000266A (es) 2000-01-21 2001-05-21 Pfizer Prod Inc Compuesto anticanceroso y metodo de separacion de enantiomeros util para sintetizar dicho compuesto.
CA2438421C (en) 2001-03-12 2010-05-18 Janssen Pharmaceutica N.V. Process for the preparation of imidazole compounds
WO2003104186A1 (ja) * 2002-06-11 2003-12-18 鐘淵化学工業株式会社 光学活性β−アミノアルコールの製造法

Also Published As

Publication number Publication date
WO2005105784A1 (en) 2005-11-10
EP1751137B1 (de) 2008-06-04
ES2308486T3 (es) 2008-12-01
CA2563807C (en) 2012-11-20
DE602005007346D1 (de) 2008-07-17
CN1946711A (zh) 2007-04-11
CN100567292C (zh) 2009-12-09
JP5008554B2 (ja) 2012-08-22
CA2563807A1 (en) 2005-11-10
EP1751137A1 (de) 2007-02-14
AU2005238223A1 (en) 2005-11-10
JP2007536335A (ja) 2007-12-13
US7456287B2 (en) 2008-11-25
US20070238880A1 (en) 2007-10-11
AU2005238223B2 (en) 2012-04-26
HK1101580A1 (zh) 2007-10-18

Similar Documents

Publication Publication Date Title
DK1713475T3 (da) 1,3,5-trisubstituerede 4,5-dihydro-1H-pyrazol-derivater med CB1-antagonistisk aktivitet
EA200800728A1 (ru) Полиморфы бензоатной соли 2-[[6-[(3r)-3-амино-1-пиперидинил]-3,4-дигидро-3-метил-2,4-диоксо-1(2н)-пиримидинил]метил]бензонитрила и способы их применения
WO2005070890A3 (en) Quinoline intermediates of receptor tyrosine kinase inhibitors and the synthesis thereof
EP4328223A3 (de) Substituierte diaminocarboxamid- und diaminocarbonitrilpyrimidine, zusammensetzungen davon und behandlungsverfahren damit
AU2018260844A1 (en) Processes of making and crystalline forms of a MDM2 inhibitor
EP1724262A4 (de) 1-(2h)-isochinolonderivat
EA200870336A1 (ru) Полициклические производные циннамида
SG170729A1 (en) Processes and intermediates for preparing steric compounds
RU2007147955A (ru) Способ получения дигидрохиназолинов
AR068115A1 (es) Derivado del acido pirazolcarboxilico metodo de produccion del mismo y fungicida
EA201100696A1 (ru) 1-(арилсульфонил)-4-(пиперазин-1-ил)-1h-бензимидазолы в качестве лигандов 5-гидрокситриптамина-6
DE602005008953D1 (de) Substituierte chinolinderivate als inhibitoren von mitotischem kinesin
EA200970793A1 (ru) Модуляторы рецепторов, активируемых пролифераторами пероксисом
WO2008032338A3 (en) Improved process for the preparation of ezetimibe and its intermediates
NZ600266A (en) Compound, certain novel forms thereof, pharmaceutical compositions thereof and methods for preparation and use
WO2008014360A3 (en) Modulators of chemokine receptor activity, crystalline forms and process
ATE397600T1 (de) Diastereoselektives syntheseverfahren zur herstellung vn imidazolverbindungen
NO20071817L (no) Fremgangsmate for a fremstille enantiomeriske imidazolforbindelser
DE602006014022D1 (de) 5-substituierte indol-2-carbonsäureamidderivate
DE602004031878D1 (de) Immunhemmende pyrazolon-verbindungen
MA31206B1 (fr) Dérivés cyclohexyl amide d'acide carboxylique aryle
EA200700767A1 (ru) Способ получения пиразолов
SE0400410D0 (sv) New compounds
ATE398612T1 (de) Diastereoselektive addition von lithiiertem n- methylimidazol an sulfinimine
TW200612944A (en) 4-(2,4-dichloro-5-methoxyphenyl)amino-6-methoxy-7-{[5-(substituted-amino)methyl]-3-furyl}-3-quinolinecarbonitriles as kinase inhibitors

Legal Events

Date Code Title Description
RER Ceased as to paragraph 5 lit. 3 law introducing patent treaties