Substituted bicyclic imidazole derivatives as gamma secretase modulators
The present invention is concerned with novel substituted bicyclic imidazole derivatives of Formula (I) wherein R 0 , R 1 , R 3 , R 4 , X, A 1 , A 2 , A 3 , A 4 , Y 1 , Y 2 and Y 3 have the meaning defined in the claims. The compounds according to the present invention are useful as gamma secretase modulators. The invention further relates to processes for preparing such novel compounds, pharmaceutical compositions comprising said novel compound as an active ingredient as well as the use of said compounds as a medicament.
1. A compound of formula (I)
or a stereoisomeric form thereof, wherein
R 0 is hydrogen, or C 1-4 alkyl;
R 1 is hydrogen, or C 1-4 alkyl;
X is CR 7 or N; wherein R 7 is hydrogen;
A 1 is CR 2 or N;
A 2 is CR 8 or N;
A 3 and A 4 each independently are CH or N;
provided that no more than two of A 1 , A 2 , A 3 and A 4 are N;
R 2 is hydrogen, halo or C 1-4 alkyloxy;
R 8 is hydrogen or halo;
R 3 is hydrogen; C 1-6 alkyl optionally substituted with one or more substituents each independently selected from the group consisting of hydroxyl, halo, morpholinyl, piperidinyl, pyrrolidinyl, tetrahydropyranyl, Ar, C 1-6 alkyloxy, cycloC 3-7 alkyloxy, and cycloC 3-7 alkyl; carboxyl; C 2-4 alkenyl; NR 5 R 6 -carbonyl; cycloC 3-7 alkyl; Ar; tetrahydropyranyl; C 1-6 alkylcarbonyl;
C 1-6 alkyloxycarbonyl; or Ar—O—CH 2 —;
wherein each Ar independently is phenyl optionally substituted with one or more substituents each independently selected from the group consisting of halo, C 1-4 alkyloxy, cyano, NR 5 R 6 , morpholinyl, C 1-4 alkyl, and C 1-4 alkyl substituted with one or more substituents each independently selected from the group consisting of halo, C 1-4 alkyloxy, and NR 5 R 6 ; benzimidazolyl optionally substituted with one or more substituents each independently selected from C 1-4 alkyl; or pyridinyl optionally substituted with one or more substituents each independently selected from the group consisting of halo, C 1-4 alkyloxy, cyano, C 1-4 alkyl, and C 1-4 alkyl substituted with one or more substituents each independently selected from halo;
each R 5 independently is hydrogen, C 1-4 alkyl, C 1-6 alkylcarbonyl,
or C 1-4 alkyloxy(CH 2 CH 2 O) n —CH 2 -carbonyl;
n is an integer selected from 1, 2, 3, 4, 5 or 6,
each R 6 independently is hydrogen or C 1-4 alkyl;
R 4 is hydrogen; cyano; halo; phenyl optionally substituted with one or more substituents each independently selected from the group consisting of halo and phenyl; phenylcarbonyl optionally substituted with one or more substituents each independently selected from halo; C 1-4 alkyloxy; C 1-6 alkyl optionally substituted with one or more substituents each independently selected from the group consisting of halo, NR 5 R 6 , C 1-4 alkyloxy, hydroxyl, and formylamino;
Y 1 is CH;
Y 2 is CR 9 ;
Y 3 is CH;
R 9 is hydrogen; halo; tetrahydropyranyl;
C 2-4 alkenyl; phenyl optionally substituted with one or more substituents each independently selected from C 1-4 alkyloxy; or C 1-4 alkyl optionally substituted with one or more substituents each independently selected from halo;
or a pharmaceutically acceptable addition salt or a solvate thereof.
2. The compound according to claim 1 wherein the compound is a compound of formula (I-a)
or a stereoisomeric form thereof, wherein
R 0 is hydrogen or C 1-4 alkyl;
R 1 is hydrogen, or C 1-4 alkyl;
X is CR 7 or N; wherein R 7 is hydrogen;
A 1 is CR 2 or N;
A 2 , A 3 and A 4 each independently are CH or N;
provided that no more than two of A 1 , A 2 , A 3 and A 4 are N;
R 2 is hydrogen, halo or C 1-4 alkyloxy;
R 3 is hydrogen; C 1-6 alkyl optionally substituted with one or more substituents each independently selected from the group consisting of halo, morpholinyl, piperidinyl, pyrrolidinyl, Ar, C 1-6 alkyloxy, cycloC 3-7 alkyloxy, and
cycloC 3-7 alkyl; cycloC 3-7 alkyl; tetrahydropyranyl; Ar; or Ar—O—CH 2 —;
wherein each Ar independently is phenyl optionally substituted with one or more substituents each independently selected from the group consisting of halo, C 1-4 alkyloxy, cyano, NR 5 R 6 , morpholinyl, C 1-4 alkyl, and C 1-4 alkyl substituted with one or more substituents each independently selected from halo; benzimidazolyl optionally substituted with one or more substituents each independently selected from C 1-4 alkyl; or pyridinyl optionally substituted with one or more substituents each independently selected from the group consisting of halo, C 1-4 alkyloxy, cyano, C 1-4 alkyl, and C 1-4 alkyl substituted with one or more substituents each independently selected from halo;
wherein each R 5 independently is hydrogen or C 1-4 alkyl;
wherein each R 6 independently is hydrogen or C 1-4 alkyl;
R 4 is hydrogen; cyano; halo; phenyl optionally substituted with one or more substituents each independently selected from the group consisting of halo and phenyl; phenylcarbonyl optionally substituted with one or more substituents each independently selected from halo; C 1-6 alkyl optionally substituted with one or more substituents each independently selected from C 1-4 alkyloxy; or
C 1-4 alkyl substituted with one or more substituents each independently selected from halo;
or a pharmaceutically acceptable addition salt or a solvate thereof.
3. The compound according to claim 1 , or a stereoisomeric form thereof, wherein
R 0 is hydrogen or C 1-4 alkyl;
R 1 is hydrogen or C 1-4 alkyl;
X is CH or N;
R 3 is hydrogen; C 1-6 alkyl optionally substituted with one or more substituents each independently selected from the group consisting of hydroxyl, halo, morpholinyl, piperidinyl, tetrahydropyranyl, Ar, C 1-6 alkyloxy, and
cycloC 3-7 alkyl; carboxyl; C 2-4 alkenyl; NR 5 R 6 -carbonyl; cycloC 3-7 alkyl; Ar; tetrahydropyranyl; C 1-6 alkylcarbonyl; C 1-6 alkyloxycarbonyl; or Ar—O—CH 2 —;
wherein each Ar independently is phenyl optionally substituted with one or more substituents each independently selected from the group consisting of halo, C 1-4 alkyloxy, cyano, NR 5 R 6 , morpholinyl, C 1-4 alkyl, and C 1-4 alkyl substituted with one or more substituents each independently selected from the group consisting of halo and NR 5 R 6 ; benzimidazolyl optionally substituted with one or more substituents each independently selected from C 1-4 alkyl; or pyridinyl;
n is 2;
R 4 is hydrogen; cyano; halo; phenyl optionally substituted with one or more substituents each independently selected from the group consisting of halo and phenyl; phenylcarbonyl optionally substituted with one or more substituents each independently selected from halo; C 1-4 alkyloxy; C 1-6 alkyl optionally substituted with one or more substituents each independently selected from the group consisting of NR 5 R 6 , C 1-4 alkyloxy, hydroxyl, and formylamino;
Y 1 is CH;
y 2 is CR 9 ;
Y 3 is CH;
R 9 is hydrogen; halo; tetrahydropyranyl; C 2-4 alkenyl; phenyl optionally substituted with one or more substituents each independently selected from
C 1-4 alkyloxy; or
C 1-4 alkyl optionally substituted with one or more substituents each independently selected from halo;
or a pharmaceutically acceptable addition salt or a solvate thereof.
4. The compound according to claim 1 , or a stereoisomeric form thereof, wherein
R 0 is hydrogen or C 1-4 alkyl;
R 1 is hydrogen, or C 1-4 alkyl;
X is CR 7 or N; wherein R 7 is hydrogen;
A 1 is CR 2 or N;
A 2 , A 3 and A 4 each independently are CH or N;
provided that no more than two of A 1 , A 2 , A 3 and A 4 are N;
R 2 is hydrogen, halo or C 1-4 alkyloxy;
R 3 is hydrogen; C 1-6 alkyl optionally substituted with one substituent selected from the group consisting of morpholinyl, piperidinyl, Ar, C 1-6 alkyloxy and
cycloC 3-7 alkyl; tetrahydropyranyl; Ar; or Ar—O—CH 2 —;
wherein each Ar independently is phenyl optionally substituted with one or more substituents each independently selected from the group consisting of halo, C 1-4 alkyloxy, cyano, NR 5 R 6 , morpholinyl, C 1-4 alkyl, and C 1-4 alkyl substituted with one or more substituents each independently selected from halo; benzimidazolyl optionally substituted with one or more substituents each independently selected from C 1-4 alkyl; or pyridinyl;
wherein each R 5 independently is C 1-4 alkyl;
wherein each R 6 independently is C 1-4 alkyl;
R 4 is hydrogen; cyano; halo; phenyl optionally substituted with one or more substituents each independently selected from the group consisting of halo and phenyl; phenylcarbonyl optionally substituted with one or more substituents each independently selected from halo; C 1-6 alkyl optionally substituted with one or more substituents each independently selected from C 1-4 alkyloxy;
or C 1-4 alkyl substituted with one or more substituents each independently selected from halo;
or a pharmaceutically acceptable addition salt or a solvate thereof.
5. The compound according to claim 1 , or a stereoisomeric form thereof, wherein
R 3 is phenyl;
R 4 is methyl; or
R 3 is phenyl substituted in a meta position and optionally further substituted in other positions;
R 4 is hydrogen or methyl; or
R 3 is phenyl substituted in an ortho position and optionally further substituted in other positions;
R 4 is hydrogen or methyl;
or a pharmaceutically acceptable addition salt or a solvate thereof.
6. The compound according to claim 1 , or a stereoisomeric form thereof, wherein
R 3 is methyl substituted with one or more phenyl groups, wherein phenyl is optionally substituted with one or more substituents each independently selected from the group consisting of halo, C 1-4 alkyloxy, cyano, NR 5 R 6 , morpholinyl,
C 1-4 alkyl, and C 1-4 alkyl substituted with one or more substituents each independently selected from halo;
R 4 is hydrogen;
or a pharmaceutically acceptable addition salt or a solvate thereof.
7. The compound according to claim 1 , or a stereoisomeric form thereof, wherein
X is N;
or a pharmaceutically acceptable addition salt or a solvate thereof.
8. The compound according to claim 1 , or a stereoisomeric form thereof, wherein
R 0 is hydrogen;
R 1 is C 1-4 alkyl;
X is CH or N;
A 1 is CR 2 ;
A 2 is N;
A 3 and A 4 are CH;
R 2 is C 1-4 alkyloxy;
R 3 is Ar; or C 1-4 alkyl optionally substituted with one or more substituents each independently selected from halo;
wherein Ar is phenyl optionally substituted with one or more substituents each independently selected from halo;
R 4 is hydrogen or C 1-6 alkyl;
or a pharmaceutically acceptable addition salt or a solvate thereof.
9. The compound according to any one of claims 1 and 3 to 8 , wherein
Y 1 is CH;
Y 2 is CH; and
Y 3 is CH.
10. The compound according to claim 1 , wherein the compound is 2-(2-chlorophenyl)-N-[6-methoxy-5-(3-methyl-1H-1,2,4-triazol-1-yl)-2-pyridinyl]-3-methyl-imidazo[1,2-a]pyridin-8-amine,
N-[6-methoxy-5-(4-methyl-1H-imidazol-1-yl)-2-pyridinyl]-2-(2,2,2-trifluoroethyl)-imidazo[1,2-a]pyridin-8-amine, or
N-[6-methoxy-5-(3-methyl-1H-1,2,4-triazol-1-yl)-2-pyridinyl]-2-(2,2,2-trifluoroethyl)-imidazo[1,2-a]pyridin-8-amine,
or any stereochemically isomeric form thereof or a pharmaceutically acceptable addition salt or a solvate thereof.
11. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and, as active ingredient, a therapeutically effective amount of a compound as defined in any one of claims 1 to 10 .
12. A method for the treatment of a disease or condition selected from Alzheimer's disease, traumatic brain injury, mild cognitive impairment, senility, dementia, dementia with Lewy bodies, cerebral amyloid angiopathy, multi-infarct dementia, Down's syndrome, dementia associated with Parkinson's disease and dementia associated with beta-amyloid comprising administering an effective amount of a compound as defined in claim 1 to a mammal in need thereof.
13. The method according to claim 12 wherein the disease is Alzheimer's disease.