PE20081344A1 - Inhibidores del virus de la hepatitis c - Google Patents

Inhibidores del virus de la hepatitis c

Info

Publication number
PE20081344A1
PE20081344A1 PE2007001545A PE2007001545A PE20081344A1 PE 20081344 A1 PE20081344 A1 PE 20081344A1 PE 2007001545 A PE2007001545 A PE 2007001545A PE 2007001545 A PE2007001545 A PE 2007001545A PE 20081344 A1 PE20081344 A1 PE 20081344A1
Authority
PE
Peru
Prior art keywords
alkyl
cyclopropylsulfonil
carbamoil
prolinamide
isoquinolinyl
Prior art date
Application number
PE2007001545A
Other languages
English (en)
Inventor
Ny Sin
Brian Lee Venables
Li-Qiang Sun
Sing-Yuen Sit
Yan Chen
Paul Michael Scola
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
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of PE20081344A1 publication Critical patent/PE20081344A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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 three or more hetero rings
    • 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
    • A61K31/435—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
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
    • 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
    • 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
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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 chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides
    • C07K5/0802—Tripeptides with the first amino acid being neutral
    • C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides
    • C07K5/0827—Tripeptides containing heteroatoms different from O, S, or N

Abstract

REFERIDA A UN DERIVADO DE ISOQUINOLINA DE FORMULA (I), DONDE m ES 1, 2 O 3; R1 ES OH O NHSO2R6; R6 ES ALQUILO, ARILO, CICLOALQUILO, ENTRE OTROS; R2 ES H, ALQUENILO, ALQUILO, CICLOALQUILO, ENTRE OTROS; R3 ES ALQUENILO, ALCOXIALQUILO, ALQUILO, ENTRE OTROS; R4 ES FENILO O UN ANILLO PARCIALMENTE O COMPLETAMENTE INSATURADO DE CINCO O SEIS MIEMBROS QUE CONTIENE OPCIONALMENTE DE UNO A CUATRO HETEROATOMOS SELECCIONADOS DE N, O Y S, DONDE CADA ANILLO PUEDE ESTAR SUSTITUIDO CON ALQUILO, ALCOXI, CARBOXI, ENTRE OTROS; R5A, R5B, R5C, R5D, R5E Y R5F SON H, ALCOXI, ALQUILO, ALCOXICARBONILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: N-(4,6-DIMETIL-2-PIRIDIL)-L-VALIL-(4R)-N-((1R,2S)-1-((CICLOPROPILSULFONIL)CARBAMOIL)-2-VINILCICLOPROPIL)-4-((6-METOXI-1-ISOQUINOLINIL)OXI)-L-PROLINAMIDA, N-(4,6-DIMETIL-2-PIRIDIL)-D-VALIL-(4R)-N-((1R,2S)-1-((CICLOPROPILSULFONIL)CARBAMOIL)-2-VINILCICLOPROPIL)-4-((6-METOXI-1-ISOQUINOLINIL)OXI)-L-PROLINAMIDA, N-(5-(TRIFLUOROMETIL)-2-PIRIDIL)VALIL-(4R)-N-((1R,2S)-1-((CICLOPROPILSULFONIL)CARBAMOIL)-2-VINILCICLOPROPIL)-4-((6-METOXI-1-ISOQUINOLINIL)OXI)-L-PROLINAMIDA, ENTRE OTROS. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA PROTEASA NS3 CODIFICADA POR EL VIRUS DE LA HEPATITIS C
PE2007001545A 2006-11-09 2007-11-09 Inhibidores del virus de la hepatitis c PE20081344A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US86503406P 2006-11-09 2006-11-09
US11/934,840 US7772180B2 (en) 2006-11-09 2007-11-05 Hepatitis C virus inhibitors

Publications (1)

Publication Number Publication Date
PE20081344A1 true PE20081344A1 (es) 2008-09-18

Family

ID=39304590

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2007001545A PE20081344A1 (es) 2006-11-09 2007-11-09 Inhibidores del virus de la hepatitis c

Country Status (18)

Country Link
US (1) US7772180B2 (es)
EP (1) EP2086963B1 (es)
JP (1) JP2010509359A (es)
KR (1) KR20090082467A (es)
CN (1) CN101541784B (es)
AR (1) AR063653A1 (es)
AU (1) AU2007319435A1 (es)
BR (1) BRPI0718625A2 (es)
CA (1) CA2669310A1 (es)
CL (1) CL2007003250A1 (es)
EA (1) EA200900676A1 (es)
IL (1) IL198248A0 (es)
MX (1) MX2009004888A (es)
NO (1) NO20091591L (es)
NZ (1) NZ576817A (es)
PE (1) PE20081344A1 (es)
TW (1) TW200826938A (es)
WO (1) WO2008060927A2 (es)

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MX2009004888A (es) 2009-05-19
CN101541784B (zh) 2013-04-24
JP2010509359A (ja) 2010-03-25
AR063653A1 (es) 2009-02-04
NZ576817A (en) 2011-08-26
WO2008060927A3 (en) 2008-07-03
CN101541784A (zh) 2009-09-23
EP2086963A2 (en) 2009-08-12
KR20090082467A (ko) 2009-07-30
WO2008060927A2 (en) 2008-05-22
TW200826938A (en) 2008-07-01
US7772180B2 (en) 2010-08-10
NO20091591L (no) 2009-07-28
EP2086963B1 (en) 2015-09-16
EA200900676A1 (ru) 2010-02-26
IL198248A0 (en) 2009-12-24
CA2669310A1 (en) 2008-05-22
CL2007003250A1 (es) 2008-05-23
BRPI0718625A2 (pt) 2014-04-01
US20080119461A1 (en) 2008-05-22

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