AR076002A1 - Derivados imidazolicos heterociclicos utiles como agentes antivirales para hepatitis c y composiciones farmaceuticas que los comprenden. - Google Patents

Derivados imidazolicos heterociclicos utiles como agentes antivirales para hepatitis c y composiciones farmaceuticas que los comprenden.

Info

Publication number
AR076002A1
AR076002A1 ARP100101038A ARP100101038A AR076002A1 AR 076002 A1 AR076002 A1 AR 076002A1 AR P100101038 A ARP100101038 A AR P100101038A AR P100101038 A ARP100101038 A AR P100101038A AR 076002 A1 AR076002 A1 AR 076002A1
Authority
AR
Argentina
Prior art keywords
alkyl
hydrogen
independently selected
nrarb
cycloalkyl
Prior art date
Application number
ARP100101038A
Other languages
English (en)
Inventor
John A Bender
John F Kadow
Piyasena Hewawasam
Jeffrey Lee Romine
Lawrence B Snyder
Van N Nguyen
Omar D Lopez
Nicholas A Meanwell
Makonen Belema
Gan Wang
Lauren Denis R St
Ningning Xu
Original Assignee
Bristol Myers Squibb Co
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=42320079&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR076002(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of AR076002A1 publication Critical patent/AR076002A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • A—HUMAN NECESSITIES
    • 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
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Virology (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Oncology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Communicable Diseases (AREA)
  • Molecular Biology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Reivindicacion 1: Un compuesto caracterizado porque tiene la formula (1) o una sal farmacéuticamente aceptable del mismo, en la que L se selecciona a partir de -O-, -CH2CH2-, -CH=CH-, -C:::C-, -OCH2-, -CH2O-, -CH2OCH2-, y grupo e formulas (2); X es hidrogeno (H) o halogeno y Z es hidrogeno; o X y Z, junto con los átomos de carbono a los que están unidos, forman un anillo condensado aromático o no aromático de cinco a ocho miembros que opcionalmente contiene uno o dos heteroátomos que se seleccionan independientemente a partir de nitrogeno, oxígeno, y azufre; en la que el anillo de cinco a ocho miembros está opcionalmente sustituido con uno, dos, o tres sustituyentes que se seleccionan independientemente a partir de alcoxi, alcoxialquilo, alcoxicarbonilo, alquilo, alquilsulfonilo, arilo, arilalquilo, arilsulfonilo, carboxi, formilo, halo, haloalcoxi, haloalquilo, hidroxi, hidroxialquilo, -NRaRb, (NRaRb)alquilo, (NRaRb)carbonilo, oxo, y espirociclo; X' es hidrogeno (H) o halogeno y Z' es hidrogeno; o X' y Z', junto con los átomos de carbono a los que están unidos, forman un anillo condensado aromático o no aromático de cinco a ocho miembros que opcionalmente contiene uno o dos heteroátomos que se seleccionan independientemente a partir de nitrogeno, oxígeno, y azufre; en los que el anillo de cinco a ocho miembros está opcionalmente sustituido con uno, dos, o tres sustituyentes que se seleccionan independientemente a partir de alcoxi, alcoxialquilo, alcoxicarbonilo, alquilo, alquilsulfonilo, arilo, arilalquilo, arilsulfonilo, carboxi, formilo, halo, haloalcoxi, haloalquilo, hidroxi, hidroxialquilo, -NRaRb, (NRaRb)alquilo, (NRaRb)carbonilo, oxo, y espirociclo; Y y Y' son cada uno independientemente -CH2-, -CH2CH2-, o -CH2O-, en los que el -CH2O- se dibuja de tal forma que el átomo de oxigeno esté unido al átomo de carbono sustituido con Rv y Rq o Rv' y Rq'; Rp es hidrogeno o alquilo C1-4; Rq es hidrogeno, alquilo, o halo; o Rp y Rq, junto con los átomos de carbono a los que están unidos, forman un anillo cicloalquilo; Rv se selecciona a partir de hidrogeno, alquilo, halo, e hidroxi; o Rv y Rq, junto con el átomo de carbono al que están unidos, forman un grupo etilenilo o un anillo cicloalquilo; Rp' es hidrogeno o alquilo C1-4; Rq' es hidrogeno, alquilo, o halo; o Rp' y Rq' junto con los átomos de carbono a los que están unidos, forman un anillo cicloalquilo; Rv' se seleccionan independientemente a partir de hidrogeno, alquilo, halo, e hidroxi; o Rv' y Rq', junto con el átomo de carbono al que están unidos, forman un grupo etilenilo o un anillo cicloalquilo; Rw y Rw' se seleccionan independientemente a partir de hidrogeno y alquilo; R1 es hidrogeno o -CO)Rx; R2 es hidrogeno o -C(O)Ry; Rx y Ry se seleccionan independientemente a partir de cicloalquilo, heteroarilo, heterociclilo, alcoxi, y alquilo, estando dicho alquilo sustituido por uno o más sustituyentes que se seleccionan independientemente a partir de arilo, alquenilo, cicloalquilo, heterociclilo, heteroarilo, -OR3, -C(O)OR4, NRaRb, y C(O)NRcRd, en los que cualquiera de dichos arilo y heteroarilo puede estar opcionalmente sustituido con uno o más sustituyentes que se seleccionan independientemente a partir de alquenilo, alquilo, haloalquilo, arilalquilo, heterociclilo, heterociclilalquilo, halogeno, ciano, nitro, -C(O)OR4, -OR5, NRaRb, (NRaRb)alquilo, y (MeO)(HO)P(O)O-, y en los que cualquiera de dichos cicloalquilo y heterociclilo puede opcionalmente estar condensado a un anillo aromático y puede estar opcionalmente sustituido con uno o más sustituyentes que se seleccionan independientemente a partir de alquilo, hidroxilo, halogeno, arilo, NRaRb, oxo, y -C(O)OR4; R3 es hidrogeno, alquilo, o arilalquilo; R4 es alquilo o arilalquilo; R5 es hidrogeno, alquilo, o arilalquilo; Ra y Rb se seleccionan independientemente a partir de hidrogeno, alquilo, cicloalquilo, arilalquilo, heteroarilo, -C(O)R6, -C(O)OR7, -C(O)NRcRd, y (NRcRd)alquilo, o de forma alternativa, Ra y Rb, junto con el átomo de nitrogeno al que están unidos, forman un anillo de cinco o seis miembros o estructura anular bicíclica con puente, en la que dicho anillo de cinco o seis miembros o estructura anular bicíclica con puente opcionalmente pueden contener uno o dos heteroátomos adicionales que se seleccionan independientemente a partir de nitrogeno, oxígeno, y azufre y pueden contener uno, dos, o tres sustituyentes que se seleccionan independientemente a partir de alquilo C1-6, haloalquilo C1-4, arilo, hidroxilo, alcoxi C1-6, haloalcoxi C1-4, y halogeno; R6 es alquilo; R7 es alquilo, arilalquilo, cicloalquilo, o haloalquilo; y Rc y Rd se seleccionan independientemente a partir de hidrogeno, alquilo, arilalquilo y cicloalquilo.
ARP100101038A 2009-03-30 2010-03-30 Derivados imidazolicos heterociclicos utiles como agentes antivirales para hepatitis c y composiciones farmaceuticas que los comprenden. AR076002A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16453109P 2009-03-30 2009-03-30
US12/729,940 US8796466B2 (en) 2009-03-30 2010-03-23 Hepatitis C virus inhibitors

Publications (1)

Publication Number Publication Date
AR076002A1 true AR076002A1 (es) 2011-05-11

Family

ID=42320079

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP100101038A AR076002A1 (es) 2009-03-30 2010-03-30 Derivados imidazolicos heterociclicos utiles como agentes antivirales para hepatitis c y composiciones farmaceuticas que los comprenden.

Country Status (19)

Country Link
US (1) US8796466B2 (es)
EP (1) EP2414350B1 (es)
JP (1) JP5612660B2 (es)
KR (1) KR20120034603A (es)
CN (1) CN102448956B (es)
AR (1) AR076002A1 (es)
AU (1) AU2010234970A1 (es)
BR (1) BRPI1013393A2 (es)
CA (1) CA2757269A1 (es)
CL (1) CL2011002426A1 (es)
CO (1) CO6430431A2 (es)
EA (1) EA022384B1 (es)
IL (1) IL215055A0 (es)
MX (1) MX2011009948A (es)
NZ (1) NZ595168A (es)
PE (1) PE20120546A1 (es)
SG (1) SG174521A1 (es)
WO (1) WO2010117635A1 (es)
ZA (1) ZA201106795B (es)

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