PE20130386A1 - Derivados de indolizina, su procedimiento de preparacion y su aplicacion en terapeutica - Google Patents

Derivados de indolizina, su procedimiento de preparacion y su aplicacion en terapeutica

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Publication number
PE20130386A1
PE20130386A1 PE2013000019A PE2013000019A PE20130386A1 PE 20130386 A1 PE20130386 A1 PE 20130386A1 PE 2013000019 A PE2013000019 A PE 2013000019A PE 2013000019 A PE2013000019 A PE 2013000019A PE 20130386 A1 PE20130386 A1 PE 20130386A1
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PE
Peru
Prior art keywords
alkyl
methylindolizin
rent
carbonyl
phenyl
Prior art date
Application number
PE2013000019A
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English (en)
Inventor
Chantal Alcouffe
Corentin Herbert
Gilbert Lassalle
Original Assignee
Sanofi Sa
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Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=43382527&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20130386(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sanofi Sa filed Critical Sanofi Sa
Publication of PE20130386A1 publication Critical patent/PE20130386A1/es

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    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
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    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2013—Organic compounds, e.g. phospholipids, fats
    • A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
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    • A61K9/2022—Organic macromolecular compounds
    • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
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    • C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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  • Animal Behavior & Ethology (AREA)
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  • Urology & Nephrology (AREA)
  • Obesity (AREA)
  • Cardiology (AREA)
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  • Pain & Pain Management (AREA)
  • Heart & Thoracic Surgery (AREA)
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Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE INDOLIZINA DE FORMULA (I) DONDE R1 ES H, HALOGENO, ALQUILO SUSTITUIDO OPCIONALMENTE CON -COOR5, ALQUENILO SUSTITUIDO OPCIONALMENTE CON -COOR5, ENTRE OTROS, EN DONDE R5 ES H, HALOGENOALQUILO, CICLOALQUILO, ENTRE OTROS; R2 ES H, ALQUILO O FENILO SUSTITUIDO OPCIONALMENTE CON ALQUILO; R3 Y R4 FORMAN JUNTO CON LOS ATOMOS DE CARBONO DEL NUCLEO FENILO AL QUE ESTAN UNIDOS UN HETEROCICLO NITROGENADO DE 6 MIEMBROS DE FORMULA (A), (B), ENTRE OTROS, DONDE Ra ES H, ALQUILO, HALOGENOALQUILO, ENTRE OTROS; Ra' ES H, ALQUILO, ENTRE OTROS; Rb ES H, ALQUILO, ENTRE OTROS; Rb' ES H, ALQUILO, CICLOALQUILO, FENILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 2-{6-[(1-METOXI-2-METILINDOLIZIN-3-IL)CARBONIL]-2,4-DIOXO-1,4-DIHIDROQUINAZOLIN-3(2H)-IL}-N,N'-DIMETILACETAMIDA; 6-[(1-METOXI-2-METILINDOLIZIN-3-IL)CARBONIL]-3-[(3-METIL-1,2,4-OXADIAZOL-5-IL)METIL]QUINAZOLINA-2,4(1H,3H)-DIONA; ACIDO 3-{3-(2,4-DIOXO-3-PROPIL-1,2,3,4-TETRAHIDROQUINAZOLIN-6-IL)CARBONIL}-2-METILINDOLIZIN-1-IL}BENZOICO; ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LOS FACTORES DE CRECIMIENTO DE FIBROBLASTOS (FGF) SIENDO UTILES EN EL TRATAMIENTO DE ATEROSCLEROSIS, FIBROSIS HEPATICA, CANCER
PE2013000019A 2010-07-06 2011-07-04 Derivados de indolizina, su procedimiento de preparacion y su aplicacion en terapeutica PE20130386A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR1055477A FR2962438B1 (fr) 2010-07-06 2010-07-06 Derives d'indolizines, procedes de preparation et application en therapeutique

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PE20130386A1 true PE20130386A1 (es) 2013-04-11

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JP (1) JP5863788B2 (es)
KR (1) KR101797795B1 (es)
CN (1) CN103080112B (es)
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US8754114B2 (en) 2010-12-22 2014-06-17 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
FR2985258A1 (fr) * 2011-12-28 2013-07-05 Sanofi Sa Composes dimeres agonistes des recepteurs des fgfs (fgfrs), leur procede de preparation et leur application en therapeutique
CN107383009B (zh) 2012-06-13 2020-06-09 因塞特控股公司 作为fgfr抑制剂的取代的三环化合物
US9388185B2 (en) 2012-08-10 2016-07-12 Incyte Holdings Corporation Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
US9266892B2 (en) 2012-12-19 2016-02-23 Incyte Holdings Corporation Fused pyrazoles as FGFR inhibitors
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