Cyclohexene benzotriazole derivatives
View Patent ↗The present invention is directed to cyclohexene benzotriazole derivatives which are potentiators of metabotropic glutamate receptors, particularly the mGluR2 receptor, and which are useful in the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction and diseases in which metabotropic glutamate receptors are involved. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which metabotropic glutamate receptors are involved.
1. A compound of Formula I
or a pharmaceutically acceptable salt thereof, wherein:
R 1 is selected from the group consisting of:
(1) C 2-8 alkyl,
(2) C 2-8 alkenyl,
(3) C 2-8 alkynyl,
(4) C 3-6 cycloalkyl-(CH 2 ) p —, wherein p is 1, 2, 3 or 4, and
(5) benzyl, wherein groups (1) to (5) above are optionally substituted with 1 to 3 R a groups;
each R a and R 2 is independently selected from the group consisting of: halo, OH, C 1-4 alkyl, C 1-4 alkoxy, CF 3 , —OCF 3 and —CN;
X is CH 2 or N(R), wherein R is H or C 1-4 alkyl;
Y is selected from the group consisting of: halo, CN, C 1-4 alkyl, C 2-4 alkenyl and CH 3 —S(O) k —, wherein said C 1-4 alkyl and C 2-4 alkenyl are optionally substituted with hydroxy, oxo and one or more fluoro groups as allowed by valence, and k is 0, 1 or 2;
R 3 is selected from the group consisting of: H, halogen, OH, CN, CF 3 , R 5 , OR 5 , SR 5 , SOR 5 , SO 2 R 5 , SO 2 N(R 4 ) 2 , COR 4 , CO 2 R 4 , CON(R 4 ) 2 , CON(R 4 )OR 5 , N(R 4 ) 2 , NO 2 , NR 4 COR 5 , NR 4 CO 2 R 5 , NR 4 —C 1-4 alkyl-CO 2 R 5 , —C 1-4 alkyl-N(R 4 ) 2 , —C 1-4 alkyl-NR 4 COR 5 and —C 1-4 alkyl-NR 4 CO 2 R 5 ;
each R 4 independently represents: (1) H, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-10 cycloalkyl, C 3-10 cycloalkylC 1-4 alkyl, C 3-10 cycloalkenyl or C 3-10 cycloalkenylC 1-4 alkyl, any of which except H optionally bear up to 5 halogen atoms or OH, CN, CF 3 and C 1-4 alkoxy; (2) phenyl, benzyl or heteroaryl, optionally bridged with a methylene, any of which optionally bear up to 3 substituents independently selected from halogen, OH, oxo, CN, CF 3 , C 1-4 alkyl, C 1-4 hydroxyalkyl, C 3-6 cycloalkyl, phenyl, heteroaryl, C 1-4 alkoxy, acetyl, amino, carbamoyl, CO 2 —C 1-4 alkyl, C 1-4 alkylamino and di(C 1-4 alkyl)amino; and (3) Het, optionally bridged with a methylene and said Het optionally bearing up to 3 substituents independently selected from halogen, OH, oxo, CN, CF 3 , C 1-4 alkyl, C 1-4 hydroxyalkyl, C 3-6 cycloalkyl, phenyl, heteroaryl, C 1-4 alkoxy, acetyl, amino, carbamoyl, CO 2 —C 1-4 alkyl, C 1-4 alkylamino and di(C 1-4 alkyl)amino;
and when two R 4 group are attached to the same nitrogen atom, they may be joined together with said nitrogen atom to form a non-aromatic monocyclic, a non-aromatic or partially aromatic bicyclic or a non-aromatic spiro-linked heterocyclic system of up to 12 ring atoms which optionally bears up to 4 substitutents independently selected from halogen, OH, oxo, CN, CF 3 , C 1-4 alkyl, C 3-6 cycloalkyl, phenyl, heteroaryl, C 1-4 alkoxy, acetyl, amino, C 1-4 alkylamino and di(C 1-4 alkyl)amino;
R 5 has the same definition as R 4 except that R 5 is not H;
each “heteroaryl” independently refers to 5- or 6-membered aromatic monocyclic or 9- or 10-membered aromatic bicyclic ring systems, in which at least one ring atom is selected from N or N-oxide, O and S; and
each “Het” independently refers to nonaromatic or partially aromatic mono- or bicyclic heterocyclic systems of up to 10 ring atoms, in which at least one ring atom is selected from N, O and S, where the sulfur atom may be in the form of the S-oxide or S,S-dioxide.
2. The compound according to claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 2 is not present.
3. The compound according to claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1 is selected from 2,2-dimethylpropyl, 1,2,2-trimethylpropyl, 4,4,4-trifluorobutyl, cyclopropylmethyl and cyclobutylmethyl.
4. The compound according to claim 3 , or a pharmaceutically acceptable salt thereof, wherein R 1 is selected from 2,2-dimethylpropyl and cyclopropylmethyl.
5. The compound according to claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 3 is CO 2 R 4 .
6. The compound according to claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 3 is C 1-6 alkyl substituted with hydroxyl.
7. The compound according to claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 3 is selected from H, hydroxy or CN.
8. The compound according to claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 3 is 3-methylimidazolidine-2,4-dione-CH 2 —.
9. The compound according to claim 1 , or a pharmaceutically acceptable salt thereof, wherein:
R 1 is selected from 2,2-dimethylpropyl and cyclopropylmethyl;
R 2 is not present; and
Y is Cl, Br or CF 3 ;
R 3 is selected from the group consisting of: H, hydroxy, CN, CO 2 R 4 , C 1-6 alkyl substituted with hydroxy, and 3-methylimidazolidine-2,4-dione-CH 2 —.
10. A compound according to claim 1 selected from the following group:
or a pharmaceutically acceptable salt of any of the foregoing compounds.
11. A pharmaceutical composition comprising a compound according to claim 1 , or a pharmaceutically acceptable salt thereof, in combination with a pharmaceutically acceptable carrier.
12. A method for treating a neurological or psychiatric disorder associated with glutamate dysfunction in a patient having said disorder comprising administering to the patient a therapeutically effective amount of a compound according to claim 1 , or a pharmaceutically acceptable salt thereof.
13. The method according to claim 12 wherein the neurological or psychiatric disorder associated with glutamate dysfunction is schizophrenia.