Heterocyclic compounds and their use as glycogen synthase kinase-3 inhibitors
View Patent ↗The present invention relates to novel heterocyclic compounds which are useful for inhibiting glycogen synthase kinase 3 (GSK-3), methods of making the compounds, compositions containing the compounds, and methods of treatment using the compounds.
1. Heterocyclic compounds of the general formulae IA
the stereoisomers, N-oxides or physiologically tolerated acid addition salts thereof, wherein
A is a 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13- or 14-membered bicyclic or tricyclic saturated N-bound heterocyclic ring containing one nitrogen atom and optionally 1, 2 or 3 further heteroatoms or heteroatom-containing groups selected from N, O, S, SO and SO 2 as ring members and optionally carrying 1, 2, 3 or 4 substituents R 6 ;
X 1 , X 2 , X 3 and X 4 are independently of each other selected from the group consisting of CR 3 and N;
X 5 , X 6 and X 7 are independently of each other selected from the group consisting of CR 4 and N;
with the proviso that at most one of X 5 , X 6 and X 7 is N;
R 1 is hydrogen or a hydrolysable group;
each R 3 is independently selected from the group consisting of hydrogen, CN, NR a R b , OH, halogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 3 -C 7 -cycloalkyl, C 3 -C 7 -halocycloalkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -haloalkenyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, formyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -haloalkylcarbonyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 6 -haloalkoxycarbonyl, C 1 -C 6 -alkyl-NR a R b and an aromatic radical Ar, which is selected from the group consisting of phenyl and a 5- or 6-membered N- or C-bound heteroaromatic radical comprising one nitrogen atom and optionally 1, 2 or 3 further heteroatoms independently selected from O, S and N as ring members, wherein Ar is unsubstituted or carries one or two radicals R 7 and wherein Ar may also be bonded via a CH 2 group;
each R 4 is independently selected from the group consisting of hydrogen, CN, NR a R b , OH, halogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 3 -C 7 -cycloalkyl, C 3 -C 7 -halocycloalkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -haloalkenyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, formyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -haloalkylcarbonyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 6 -haloalkoxycarbonyl, C 1 -C 6 -alkyl-NR a R b and an aromatic radical Ar, which is selected from the group consisting of phenyl and a 5- or 6-membered N- or C-bound heteroaromatic radical comprising one nitrogen atom and optionally 1, 2 or 3 further heteroatoms independently selected from O, S and N as ring members, wherein Ar is unsubstituted or carries one or two radicals R 7 and wherein Ar may also be bonded via a CH 2 group; or
in case X 6 and X 7 are both CR 4 , then the two radicals R 4 of these groups X 6 and X 7 , together with the carbon atoms to which they are bound, may also form together a phenyl ring;
R 5 is hydrogen; or
in case X 6 is CR 4 , then R 4 of this group X 6 and R 5 , together with the carbon atoms to which they are bound, may also form together a phenyl ring;
each R 6 is independently selected from the group consisting of C 1 -C 4 -alkyl and C 1 -C 4 -haloalkyl;
each R 7 is independently selected from the group consisting of halogen, CN, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 3 -C 6 -cycloalkyl, C 3 -C 6 -halocycloalkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, NR a R b , a phenyl group and an aromatic 5- or 6-membered C-bound heteroaromatic radical comprising one nitrogen atom and optionally 1, 2 or 3 further heteroatoms independently selected from O, S and N as ring members, wherein phenyl and the heteroaromatic radical are, independently of each other, unsubstituted or substituted by 1, 2, 3 or 4 radicals selected from halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 -alkoxy and C 1 -C 4 haloalkoxy; and
R a and R b are independently of each other selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, C 1 -C 4 alkylcarbonyl and C 1 -C 4 -haloalkylcarbonyl; or
R a and R b form, together with the nitrogen atom to which they are bonded, a 3-, 4-, 5-, 6- or 7-membered saturated or unsaturated aromatic or non-aromatic N-heterocyclic ring, which may contain 1 further heteroatom or heteroatom-containing group selected from N, O, S, SO and SO 2 as a ring member.
2. The heterocyclic compounds of claim 1 , wherein A is a bi- or tricyclic saturated N-bound heterocyclic ring and either all of X 1 , X 2 , X 3 and X 4 are CR 3 or one of X 1 , X 2 , X 3 and X 4 is N and the other three are CR 3 .
3. The heterocyclic compounds of claim 1 , wherein A is a bicyclic saturated N-bound heterocyclic ring.
4. The heterocyclic compounds of claim 3 , wherein A is a 7-, 8-, 9- or 10-membered bicyclic saturated N-bound heterocyclic ring.
5. The heterocyclic compounds of claim 4 , wherein A is a 7-, 8-, 9- or 10-membered bicyclic saturated N-bound heterocyclic ring containing one nitrogen atom and 1 further heteroatom selected from O and N as ring members.
6. The heterocyclic compounds of claim 5 , wherein the bicyclic ring A is selected from one of the following formulae:
and the stereoisomers thereof;
where
Y 1 is O or NR 61 ;
each R 61 , independently of its occurrence, is hydrogen or has one of the meanings given in claim 1 for R 6 ; and
# is the attachment point to the remainder of the molecule.
7. The heterocyclic compounds of claim 6 , wherein A is selected from one of the following formulae:
8. The heterocyclic compounds of claim 6 , wherein R 61 is hydrogen.
9. The heterocyclic compounds of claim 1 , wherein X 7 is CR 4 .
10. The heterocyclic compounds of claim 1 , wherein X 5 , X 6 and X 7 are CR 4 .
11. The heterocyclic compounds of claim 1 , wherein R 1 is hydrogen.
12. The heterocyclic compounds of claim 1 , wherein each R 3 is independently selected from hydrogen, halogen, CN, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy and C 1 -C 6 -haloalkoxy.
13. The heterocyclic compounds of claim 12 , wherein R 3 is hydrogen, halogen or cyano.
14. The heterocyclic compounds of claim 1 , wherein each R 4 is independently selected from hydrogen, halogen, CN, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy and C 1 -C 6 -haloalkoxy.
15. The heterocyclic compounds of claim 1 , wherein R 4 is hydrogen.
16. The heterocyclic compounds of claim 1 , wherein R 5 is hydrogen.
17. A pharmaceutical composition comprising at least one heterocyclic compound of claim 1 , a stereoisomer, N-oxide or physiologically tolerated acid addition salt thereof and at least one physiologically acceptable carrier or auxiliary substance.
18. A method for treating a neurodegenerative disorder or an inflammatory disorder comprising administering to a subject in need thereof an effective amount of at least one heterocyclic compound as defined in claim 1 or of a stereoisomer, N-oxide or physiologically tolerated acid addition salt thereof, wherein the disorder is selected from the group consisting of schizophrenia, Alzheimer's disease, Parkinson's disease, tauopathies, vascular dementia, peripheral neuropathies, bipolar disorders, retinopathies, glaucoma, rheumatoid arthritis, and osteoarthritis.
19. The heterocyclic compounds of claim 1 , selected from the group consisting of:
3-(5-((dihydro-1H-furo[3,4-c]pyrrol-5(3H,6H,6aH)-yl)methyl)pyridin-2-yl)-2-hydroxy-1H-indole-5-carbonitrile; and
3-(5-(((3aS,6aS)-hexahydropyrrolo[3,4-b]pyrrol-1(2H)-yl)methyl)-pyridin-2-yl)-2-hydroxy-1H-indole-5-carbonitrile.