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PE20090044A1 - Antagonistas del receptor de la hormona liberadora de gonadotropina y procedimientos relacionados con los mismos - Google Patents

Antagonistas del receptor de la hormona liberadora de gonadotropina y procedimientos relacionados con los mismos

Info

Publication number
PE20090044A1
PE20090044A1 PE2008000619A PE2008000619A PE20090044A1 PE 20090044 A1 PE20090044 A1 PE 20090044A1 PE 2008000619 A PE2008000619 A PE 2008000619A PE 2008000619 A PE2008000619 A PE 2008000619A PE 20090044 A1 PE20090044 A1 PE 20090044A1
Authority
PE
Peru
Prior art keywords
alkyl
phenyl
trifluoromethyl
methyl
cyane
Prior art date
Application number
PE2008000619A
Other languages
English (en)
Inventor
Mi Chen
Timothy Richard Coon
Todd Ewing
Wanlong Jiang
Richard Lowe
Willy Moree
Nicole Smith
Original Assignee
Neurocrine Biosciences 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 Neurocrine Biosciences Inc filed Critical Neurocrine Biosciences Inc
Publication of PE20090044A1 publication Critical patent/PE20090044A1/es

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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—Ortho-condensed systems
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • 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
    • A—HUMAN NECESSITIES
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    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Quinoline Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Steroid Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE AMIDA DE FORMULA (I) DONDE A ES PIRIDILO, FENILO, QUINOLINILO, NAFTIRIDINILO, ENTRE OTROS; R1a ES H, HALOGENO, ALQUILO(C1-C4), ALCOXI O TRIFLUOROMETILO; R1b Y R1c SON CADA UNO H, HALOGENO, HIDROXI, HALOALQUILO(C1-C4), ENTRE OTROS; R1d ES Cl, F, METILO, CF3 O CN; R2 ES ALQUIL(C1-C4)-(R5)p, EN DONDE R5 ES H, HIDROXI, -OC(O)-ALQUILO(C1-C6), -OC(O)O-ALQUILO(C1-C6), ENTRE OTROS; p ES DE 1 A 3; R2a ES FENILO, ALQUILO(C1-C6), ARIL-ALQUILO(C1-C4), ENTRE OTROS, OPCIONALMENTE SUSTITUIDOS CON R3, EN DONDE R3 ES HALOGENO, CN, HALOALQUILO(C1-C4), ENTRE OTROS. SON COMPUESTOS PREFERIDOS: ACIDO 4-{5-CLORO-4-(4-CIANO-6-TRIFLUOROMETIL-PIRIDIN-3-IL)-2-[(2-FLUORO-6-METOXI-FENIL)-METIL-CARBAMOIL]-FENOXI}-BUTIRICO, 4-CLORO-5-(4-CIANO-6-TRIFLUOROMETIL-PIRIDIN-3-IL)-N-(2-METOXI-FENIL)-N-METIL-2-[3-(2H-TETRAZOL-5-IL)-PROPOXI]-BENZAMIDA, 4-CLORO-3-(4-CIANO-6-TRIFLUOROMETIL-PIRIDIN-3-IL)-N-METIL-N-{2-[2-(1H-TETRAZOL-5-IL)-ETOXI]-FENIL}-BENZAMIDA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON ANTAGONISTAS DEL RECEPTOR DE LA HORMONA LIBERADORA DE GONADOTROPINA (GnRH) SIENDO UTILES EN EL TRATAMIENTO DE ENDOMETRIOSIS, FIBROIDES UTERINOS, DISMENORREA, ENFERMEDAD DEL OVARIO POLIQUISTICO
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