Amide derivatives useful in the treatment of HBV infection or HBV-induced diseases
The application relates to amide derivatives, processes for their preparation, pharmaceutical compositions, and their uses, more particularly their uses in treating chronic hepatitis B virus (HBV) infection.
1. A compound of formula (I)
a stereoisomer or tautomeric form thereof, wherein:
represents a 6-membered aryl optionally containing one or more heteroatoms, the heteroatom or each of the heteroatoms being nitrogen;
R 1 , R 2 and R 3 are each independently selected from the group consisting of H, F, Cl, Br, CHF 2 , CH 2 F, CF 3 , CN, C 1 -C 4 alkyl and C 3 -C 6 cycloalkyl;
R 4 is selected from the group consisting of H and F;
R 5 is selected from the group consisting of H, C 1 -C 4 alkyl, and C 3 -C 6 cycloalkyl;
Q is selected from the group consisting of
C 2 -C 5 alkyl, optionally substituted with one or more substituents each independently selected from the group consisting of halogens and SO 2 Me,
C 2 -C 3 alkenyl substituted with halogens and more particularly one or more fluoro,
3- to 6-membered monocyclic saturated rings, wherein the 3- to 6-membered monocyclic saturated rings optionally contain one or more heteroatoms, the heteroatoms being each independently selected from N, O and S, and are optionally substituted with one or more substituents each independently selected from the group consisting of F, oxo, OH, C(═O)NHCH 3 and C 1-4 alkyl optionally substituted with one or more fluoro,
3- to 9-membered polycyclic saturated rings, wherein the 3- to 9-membered polycyclic saturated rings optionally contain one or more heteroatoms, the heteroatoms being each independently selected from N, O and S, and are optionally substituted with one or more substituents each independently selected from the group consisting of F, oxo, OH, C(═O)NHCH 3 and C 1 -C 4 alkyl optionally substituted with one or more fluoro;
R 6 is H;
R 7 is selected from the group consisting of phenyl, phenyl substituted with one or more substituents each independently selected from the group consisting of halo, CN, CF 3 , CF 2 H, CH 2 F, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, OH and OC 1 -C 4 alkyl, pyridyl, pyridyl substituted with one or more substituents each independently selected from the group consisting of halo, CN, CF 3 , CF 2 H, CH 2 F, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, OH and OC 1 -C 4 alkyl, pyrimidyl, pyrimidyl substituted with one or more substituents each independently selected from the group consisting of halo, CN, CF 3 , CF 2 H, CH 2 F, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, OH and OC 1 -C 4 alkyl, pyrazinyl, pyrazinyl substituted with one or more substituents each independently selected from the group consisting of halo, CN, CF 3 , CF 2 H, CH 2 F, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, OH and OC 1 -C 4 alkyl, pyridazinyl, pyridazinyl substituted with one or more substituents each independently selected from the group consisting of halo, CN, CF 3 , CF 2 H, CH 2 F, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, OH and OC 1 -C 4 alkyl, 5-membered unsaturated heterocycles containing one to 4 heteroatoms, the heteroatoms being each independently selected from N, O and S, 5-membered unsaturated heterocycles containing one to 4 heteroatoms, the heteroatoms being each independently selected from N, O and S, substituted with one or more substituents each independently selected from the group consisting of halogens, CN, CF 3 , CF 2 H, CH 2 F, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, OH and OC 1 -C 4 alkyl; and
X is CR 8 ; and
R 8 is selected from the group consisting of H, F, Cl, Br, CN, OC 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, C 2 -C 3 alkenyl and C 1 -C 4 alkyl optionally substituted with one or more F and OCH 3 , or a pharmaceutically acceptable salt or a solvate thereof.
2. The compound of claim 1 , wherein Q is a 3-6 membered monocyclic saturated ring containing one or more heteroatoms, the heteroatoms being each independently selected from N, O and S, and wherein Q is optionally substituted with one or more substituents each independently selected from the group consisting of F, oxo, OH, C(═O)NHCH 3 , and C 1 -C 4 alkyl optionally substituted with one or more fluoro.
3. The compound of claim 1 , wherein Q is a 3-6 membered monocyclic saturated ring optionally containing one or more heteroatoms, the heteroatoms being each independently selected from N, O and S, and wherein Q is substituted with one or more substituents each independently selected from the group consisting of F, oxo, OH, C(═O)NHCH 3 , and C 1 -C 4 alkyl optionally substituted with one or more fluoro.
4. The compound of claim 1 , wherein R 7 is a 5-membered unsaturated heterocycle containing one to four heteroatoms, the heteroatoms being each independently selected from N, O and S, and optionally substituted with one or more substituents each independently selected from the group consisting of halo, CN, CF 3 , CF 2 H, CHF 2 , C 1 -C 4 alkyl, C 3-6 cycloalkyl, OH and OC 1 -C 4 alkyl.
5. The compound of claim 1 , wherein each of R 1 and R 2 is H, R 3 is methyl, chloro or cyano, and R 4 is F.
6. The compound of claim 1 , wherein
represents phenyl carrying substituents in a meta position and in the para position, whereby one substituent is fluoro and the other substituent is selected from the group consisting of fluoro, chloro, cyano, and methyl.
7. The compound of claim 1 , wherein Q is cyclobutyl.
8. The compound of claim 7 , wherein the cyclobutyl is substituted with one or more fluoro, more particularly 3,3-difluorocyclobutyl.
9. The compound of claim 1 , wherein Q is C 2 -C 5 alkyl, particularly ethyl or isopropyl.
10. A pharmaceutical composition comprising at least one compound or pharmaceutically acceptable salt of claim 1 .
11. The pharmaceutical composition of claim 10 , further comprising at least one pharmaceutically acceptable carrier.
12. A method of treating an HBV infection or an HBV-induced disease in an individual in need thereof, comprising administering to the individual a therapeutically effective amount of the compound of claim 1 .
13. A pharmaceutical composition comprising a first compound and a second compound, wherein said first compound is the compound claim 1 .
14. A process for the preparation of a compound of Formula (I) of claim 1 , comprising the reaction between a compound of Formula (II), wherein Formula (II) is
and a compound of Formula (III), wherein Formula (III) is
in the presence of a base, and a coupling reagent to form a compound of Formula (I).
15. The process of claim 14 , wherein the base is Diisopropylethylamine (DIPEA).
16. The process of claim 14 , wherein the coupling reagent is Hexafluorophosphate Azabenzotriazole Tetramethyl Uronium (HATU).