4,4-disubstituted-1,4-dihydropyrimidines and the use thereof as medicaments for the treatment of hepatitis B
View Patent ↗Inhibitors of HBV replication of formula (I) including stereochemically isomeric forms, and salts, hydrates, solvates thereof, wherein R 1 -R 5 , B and Z have the meaning as defined herein. The present invention also relates to processes for preparing said compounds, pharmaceutical compositions containing them and their use, alone or in combination with other HBV inhibitors, in HBV therapy.
1. A compound of Formula I
including any possible stereoisomers or tautomeric forms thereof, wherein:
B is selected from the group consisting of C 1 -C 3 alkyl and C 1 -C 3 alkyl substituted with one or more Fluoro atoms;
Z is selected from H or halogen;
Or B and Z together with the carbons to which they are attached form a 4-7 membered ring, optionally containing one or more heteroatoms, wherein the 4-7 membered ring optionally is substituted with one or more substituents selected from the group consisting of C 1 -C 3 alkyl, oxo, OH and halogen;
R 1 is selected from the group comprising heteroaryl and phenyl, optionally substituted with one or more substituents selected from the group consisting of halogen and C 1 -C 3 alkyl;
R 2 is selected from the group consisting of —R 6 -R 7 , C≡N, cyclopropyl and CF 3 ;
R 3 is selected from the group consisting of C 1 -C 3 alkoxycarbonyl and C≡N;
R 4 and R 5 independently are selected from the group consisting of H, methyl and halogen;
R 6 is C 1 -C 3 alkyl or C 2 -C 3 alkenyl, both optionally substituted with one or more Fluoro;
R 7 is selected from the group consisting of hydrogen, a hetero C 3-7 cycloalkyl, cyclopropyl, C 1 -C 3 alkoxy and CF 3 ;
or a pharmaceutically acceptable salt or a solvate thereof.
2. A compound according to claim 1 wherein B is selected from the group consisting of C 1 -C 3 alkyl optionally substituted with one or more Fluoro atoms;
Z is selected from H or halogen;
Or B and Z together with the carbons to which they are attached form a 4-7 membered ring, optionally containing one or more heteroatoms, wherein the 4-7 membered ring optionally is substituted with one or more substituents selected from the group consisting of C 1 -C 3 alkyl oxo and halogen; and
R 1 is selected from the group consisting of heteroaryl and phenyl, optionally substituted with one or more halogen atoms.
3. A compound according to claim 1 , wherein B and Z together with the carbons to which they are attached form a 5- or 6-membered ring, optionally substituted with one or more substituents selected from the group consisting of C 1 -C 3 alkyl, oxo and halogen.
4. A compound according to claim 1 , wherein B and Z together with the carbons to which they are attached form a 5- or 6-membered ring, optionally substituted with one or more CH 3 substituents.
5. A compound according to claim 1 , wherein R 1 is selected from pyridinyl optionally substituted with one ore two Fluoro, or thiazolyl.
6. A compound according to claim 1 , wherein R 3 is C 1 - or C 2 -alkyloxycarbonyl.
7. A compound according to claim 1 , wherein R 6 is CH 2 and R 7 is selected from morpholinyl or piperidinyl.
8. The compound according to claim 1 , wherein formula I is formula (Ia)
9. A compound according to claim 1 wherein R 4 and R 5 independently are selected from the group H and Fluoro.
10. A pharmaceutical composition comprising a compound according to claim 1 , and a pharmaceutically acceptable carrier.
11. A product containing (a) a compound of claim 1 , and (b) another HBV inhibitor, as a combined preparation for simultaneous, separate or sequential use in the treatment of HBV infections.
12. The compound according to claim 1 , wherein R 2 is Cl.
13. A method of treating an HBV infection in a mammal, comprising administering to said mammal the compound of claim 1 .