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PE20090741A1 - Derivados de 1,1,1-trifluor-2-hidroxi-3-fenilpropano - Google Patents

Derivados de 1,1,1-trifluor-2-hidroxi-3-fenilpropano

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Publication number
PE20090741A1
PE20090741A1 PE2008001670A PE2008001670A PE20090741A1 PE 20090741 A1 PE20090741 A1 PE 20090741A1 PE 2008001670 A PE2008001670 A PE 2008001670A PE 2008001670 A PE2008001670 A PE 2008001670A PE 20090741 A1 PE20090741 A1 PE 20090741A1
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PE
Peru
Prior art keywords
trifluor
alkyl
hydroxy
phenylpropane
butan
Prior art date
Application number
PE2008001670A
Other languages
English (en)
Inventor
Jacques Bailly
Cornelia Hertel
Daniel Hunziker
Christian Lerner
Ulrike Bost Sander
Jens-Uwe Peters
Philippe Pflieger
Tanja Schulz-Gasch
Original Assignee
Hoffmann La Roche
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Publication date
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PE20090741A1 publication Critical patent/PE20090741A1/es

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    • C07D241/10Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/12Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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    • A61P3/06Antihyperlipidemics
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  • Pyridine Compounds (AREA)
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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
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Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE 1,1,1-TRIFLUOR-2-HIDROXI-3-FENILPROPANO DE FORMULA (I) DONDE A ES C-R1b O N; R1a, R1b, R1c, R1d Y R1e SON CADA UNO H, ALQUILO(C1-C7), CICLOALQUIL(C3-C7)-ALQUILO(C1-C7), HALOGENO, HIDROXI, ENTRE OTROS; R2 ES ALQUILO(C1-C7), CICLOALQUIL(C3-C7)-ALQUILO(C1-C7), CARBOXIL-ALQUILO(C1-C7), ENTRE OTROS; R3 ES H O ALQUILO(C1-C7); R4 ES PIRIDILO, PIRAZINILO, PIRIMIDINILO, ENTRE OTROS; R5 ES H O METILO; n ES 0 O 1. SON COMPUESTOS PREFERIDOS: 3-(2-CLORO-4-METOXI-FENIL)-1,1,1-TRIFLUOR-2-(5-METIL-PIRAZIN-2-IL)-BUTAN-2-OL, 1,1,1-TRIFLUOR-2-(2-METIL-PIRIDIN-4-IL)-3-FENIL-BUTAN-2-OL, 3-(2,4-DICLORO-FENIL)-1,1,1-TRIFLUOR-2-PIRIDIN-3-IL-BUTAN-2-OL, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON ANTAGONISTAS DEL RECEPTOR DE GLUCOCORTICOIDE SIENDO UTILES EN EL TRATAMIENTO DE LA DIABETES
PE2008001670A 2007-09-27 2008-09-25 Derivados de 1,1,1-trifluor-2-hidroxi-3-fenilpropano PE20090741A1 (es)

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US (2) US8143280B2 (es)
EP (1) EP2205562B1 (es)
JP (1) JP5242691B2 (es)
KR (1) KR101174982B1 (es)
CN (1) CN101808992B (es)
AR (1) AR068635A1 (es)
AT (1) ATE502012T1 (es)
AU (1) AU2008303600B8 (es)
BR (1) BRPI0817242A8 (es)
CA (1) CA2700277A1 (es)
CL (1) CL2008002863A1 (es)
DE (1) DE602008005634D1 (es)
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ES (1) ES2360272T3 (es)
IL (1) IL204052A (es)
MX (1) MX2010002893A (es)
PE (1) PE20090741A1 (es)
PL (1) PL2205562T3 (es)
PT (1) PT2205562E (es)
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TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
AU2011320565A1 (en) * 2010-10-28 2013-05-23 Innocrin Pharmaceuticals, Inc. Metalloenzyme inhibitor compounds
EP2567959B1 (en) 2011-09-12 2014-04-16 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
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