IP Library Granted Patent US 7,915,411
Granted Patent B2
US 7,915,411 · App. 11/613,825 · Granted Mar 29, 2011

Anti-viral compounds

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Quick Facts
Patent No.
US 7,915,411
App. No.
11/613,825
Granted
Mar 29, 2011
Kind
B2
Abstract

Compounds effective in inhibiting replication of Hepatitis C virus (“HCV”) or other viruses are disclosed. This invention is also directed to compositions comprising such compounds, co-formulation or co-administration of such compounds with other anti-viral or therapeutic agents, processes and intermediates for the syntheses of such compounds, and methods of using such compounds for the treatment of HCV or other viral infections.

Claims (21)

1. A compound, a tautomer of the compound, or a pharmaceutically acceptable salt of the compound or tautomer, wherein the compound has Formula II:

wherein:

R 6 is selected from the group consisting of hydrogen and cyano;

R 8 is selected from the group consisting of hydrogen and arylalkyl;

R 25 is selected from the group consisting of hydrogen and alkyl;

R 37 is selected from the group consisting of hydrogen, alkyl, hydroxyalkyl, and cycloalkyl;

R 42 is selected from the group consisting of arylsulfanyl, heteroarylsulfanyl, and aryloxy; wherein R 42 is optionally substituted with one or more substituents independently selected from R 46 ;

R 46 is one or more substituents selected from the group consisting of hydrogen, hydroxy, amino, halogen, dialkylamino, and alkoxycarbonylamino;

R 70 is selected from the group consisting of aryl, and heterocyclo; wherein R 70 is optionally substituted with R 75 ;

R 75 is one or more substituents independently selected from the group consisting of hydrogen, halogen, alkoxy, cyano, alkyl, haloalkyl, and aryl.

2. A compound, a tautomer of the compound, or a pharmaceutically acceptable salt of the compound or tautomer, wherein the compound has Formula III:

wherein R 80 is selected from the group consisting of hydrogen, alkylcarbonyl, and haloaryl.

3. A compound, a tautomer of the compound, or a pharmaceutically acceptable salt of the compound or tautomer, wherein the compound has Formula VII:

wherein:

A is selected from the group consisting of O and S;

R 21 is selected from the group consisting of hydrogen and hydroxy;

or R 21 taken together with R 39 form a 5-12 membered heterocycle containing at least two heteroatoms selected from the group consisting of O, N, and S; or

R 39 is selected from the group consisting of hydrogen, alkyl, arylalkenyl, dialkylamino, heteroaryl, haloheteroaryl, haloarylaminosulfonyl, arylsulfonyloxy, alkylcarbonyloxy, cycloalkylaminocarbonyl, arylalkoxycarbonylamino, alkoxycarbonyl, and NH—R 99 ;

R 99 is selected from the group consisting of hydrogen, arylalkyl, cycloalkylalkyl, aryl, heteroaryl, haloarylalkylamino, arylalkylamino, and alkylheteroaryl;

R 67 is selected from the group consisting of hydrogen, alkyl, cycloalkyl, and alkylcycloalkyl;

R 96 is selected from the group consisting of hydrogen, hydroxy, amino, alkoxy, arylsulfonyloxy, alkylcarbonylamino, alkoxy, halogen, alkoxycarbonyloxy, haloalkoxycarbonylamino, and arylalkoxy.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 17, 2013
From: ABBOTT LABORATORIES
To: ABBVIE INC.
Reel/Frame 030231/0808 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 3, 2007
From: BETEBENNER, DAVID A; DEGOEY, DAVID A; MARING, CLARENCE J; KRUEGAR, ALLAN C; IWASAKI, NOBUHIKO; ROCKWAY, TODD W; COOPER, CURT S; ANDERSON, DAVID D; DONNER, PAMELA L; GREEN, BRIAN E; KEMPF, DALE J; LIU, DACHUN; MCDANIEL, KEITH F; MADIGAN, DAROLD L; MOTTER, CHRISTOPHER E; PRATT, JOHN K; SHANLEY, JASON P; TUFANO, MICHAEL D; WAGNER, ROLF; ZHANG, RONG; MOLLA, AKHTERUZZAMAN; MO, HONGMEI; PILOT-MATIAS, TAMI J; MASSE, SHERIE VL; CARRICK, ROBERT J; HE, WENPING; LU, LIANGJUN; GRAMPOVNIK, DAVID J
To: ABBOTT LABORATORIES
Reel/Frame 019244/0328 →