Amino-heteroaryl derivatives as HCN blockers
The invention relates to amino-heteroaryl derivatives having the general Formula I or a pharmaceutically acceptable salt thereof, to pharmaceutical compositions comprising the same, as well as to the use of these derivatives for the treatment of pain, such as neuropathic pain or inflammatory pain.
1. An amino-heteroaryl derivative according to general Formula 1:
wherein
Ar represents a 6-membered heteroaryl group containing 1 or 2 nitrogen atoms, which can be optionally substituted with one or more substituents selected from halogen, (C 1-4 )alkyl, halo(C 1-4 )alkyl, (C 1-4 )alkyloxy, halo(C 1-4 )alkyloxy, CN, (C 1-4 )alkylthio and halo(C 1-4 )alkylthio;
X is O, S, or NR 1 ;
R 1 is H or (C 1-4 )alkyl;
R 2 is (C 1-4 )alkyl, halo(C 1-4 )alkyl, (C 1-4 )alkyloxy(C 1-4 )alkyl or
halo(C 1-4 )alkyloxy(C 1-4 )alkyl;
R 3 is H, (C 1-4 )alkyl, halo(C 1-4 )alkyl, (C 1-4 )alkyloxy(C 1-4 )alkyl or halo(C 1-4 )alkyloxy(C 1-4 )alkyl; or
R 2 and R 3 form together with the carbon atom to which they are bonded a 3-7 membered saturated ring optionally containing an oxygen atom;
Y 1 , and Y 2 are N; and Y 3 is ═(CH)—;
R 4 and R 5 are independently H, (C 1-4 )alkyl, halo(C 1-4 )alkyl or
(C 1-4 )alkyloxy(C 1-4 )alkyl; or
R 4 and R 5 form together with the nitrogen atom to which they are bonded a 3-7 membered saturated ring optionally containing an oxygen atom; or a pharmaceutically acceptable salt thereof.
2. An amino-heteroaryl derivative of claim 1 or a pharmaceutically acceptable salt thereof, wherein Ar represents substituted pyridin-2-yl, pyridin-3-yl, pyridin-4-yl, pyrazin-2-yl or pyrimidin-2-yl.
3. The amino-heteroaryl derivative of claim 2 or a pharmaceutically acceptable salt thereof, wherein R 2 is CH 3 and R 3 is H.
4. The amino-heteroaryl derivative of claim 3 or a pharmaceutically acceptable salt thereof, wherein R 4 and R 5 are H.
5. An amino-heteroaryl derivative which is:
(R)-4-(1-(3-fluorophenoxy)ethyl)pyrimidin-2-amine;
(R)-4-(1-(2-chloro-5-fluorophenoxy)ethyl)pyrimidin-2-amine;
(R)-4-(1-(2,5-difluorophenoxy)ethyl)pyrimidin-2-amine;
(R)-4-(1-(2,4-difluorophenoxy)ethyl)pyrimidin-2-amine;
(R)-4-(1-(3-methoxypyridin-2-yloxy)ethyl)pyrimidin-2-amine;
(S)-4-(1-(3-fluorophenoxy)ethyl)pyrimidin-2-amine;
(S)-4-(1-(2,5-difluorophenoxy)ethyl)pyrimidin-2-amine;
4-(1-(3-(trifluoromethyl)pyridin-2-ylthio)ethyl)pyrimidin-2-amine;
(R)-4-(1-(3-(trifluoromethyl)pyridin-2-yloxy)ethyl)pyrimidin-2-amine;
(R)-4-(1-(4-(trifluoromethyl)pyrimidin-2-yloxy)ethyl)pyrimidin-2-amine; and
4-(1-(3-(trifluoromethyl)pyridin-2-ylamino)ethyl)pyrimidin-2-amine;
or a pharmaceutically acceptable salt thereof.
6. The amino-heteroaryl derivative of claim 5 which is selected from:
(R)-4-(1-(3-methoxypyridin-2-yloxy)ethyl)pyrimidin-2-amine;
(4-(1-(3-(trifluoromethyl)pyridin-2-ylthio)ethyl)pyrimidin-2-amine;
(R)-4-(1-(3-(trifluoromethyl)pyridin-2-yloxy)ethyl)pyrimidin-2-amine;
(R)-4-(1-(4-(trifluoromethyl)pyrimidin-2-yloxy)ethyl)pyrimidin-2-amine; and
4-(1-(3-(trifluoromethyl)pyridin-2-ylamino)ethyl)pyrimidin-2-amine;
or a pharmaceutically acceptable salt thereof.
7. A pharmaceutical composition comprising an amino-heteroaryl derivative of claim 1 or a pharmaceutically acceptable salt thereof in admixture with pharmaceutically acceptable auxiliaries.
8. A method of specifically inhibiting the I h HCN channel comprising administering to a patient in which the I h HCN channel is to be inhibited a therapeutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof.
9. The method according to claim 8 , wherein the patient is experiencing neuropathic pain arising from Ih HCN channel activity.
10. The method according to claim 8 , wherein the patient is experiencing inflammatory pain arising from Ih HCN channel activity.