Macrocyclic peptides active against the hepatitis c virus

C - Chemistry – Metallurgy – 07 – K

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C07K 5/08 (2006.01) A61K 38/06 (2006.01) A61K 38/00 (2006.01)

Patent

CA 2498572

Compounds of formula (I): wherein R1 is (C1-8)alkyl, (C3-7)cycloalkyl, {(C1- 6)alkyl-(C3-7)cycloalkyl} or Het, which are all optionally substituted from 1 to 3 times with halo, cyano, nitro, O-(C1-6)alkyl, amido, amino or phenyl, or R1 is C6 or C10 aryl which is optionally substituted from 1 to 3 times with halo, cyano, nitro, (C1-6)alkyl, O-(C1-6)alkyl, amido, amino or phenyl; or a pharmaceutically acceptable salt thereof, useful as an inhibitor of the HCV NS3 protease.

La présente invention concerne des composés représentés par la formule (I) dans laquelle R?1¿ représente alkyle (C¿1-8?), cycloalkyle (C¿3-7?), {alkyle (C¿1-6?)-cycloalkyle (C¿3-7?)} ou Het, qui, tous, sont facultativement substitués entre 1 et 3 fois par halo, cyano, nitro, O-alkyle (C¿1-6?), amido, amino ou phényle, ou bien R?1¿ représente aryle C¿6? ou C¿10? qui est facultativement substitué entre 1 et 3 fois par halo, cyano, nitro, alkyle (C¿1-6?), O-alkyle (C¿1-6?), amido, amino ou phényle. Ces composés ou un sel pharmaceutiquement acceptable de ces derniers sont utiles en tant qu'inhibiteur de la protéase NS3 VHC. Formule (I)

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