IP Library Granted Patent US 8,008,488
Granted Patent B2
US 8,008,488 · App. 10/548,931 · Granted Aug 30, 2011

Pyrimidin-2-one compounds and their use as dopamine D

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,008,488
App. No.
10/548,931
Granted
Aug 30, 2011
Kind
B2
Abstract

The invention relates to pyrimidin 2-one compounds of general formula (I), in addition to the derivatives and tautomers of (I) and the physiologically acceptable salts of said compounds. In said formula, A represents linear or branched C 3 -C 6 alkene, which can have a double bond or triple bond and/or a group Z, which is not adjacent to the nitrogen atom of the pyrimidinone ring and is selected from O, S, C(O), NR 3 , C(O)NR 3 , NR 3 C(O), OC(O) and C(O)O; B represents a group of the formula (II), in which X stands for CH 2 or N and Y stands for CH 2 or CH 2 CH 2 , or X—Y can also jointly represent C═CH, C═CH—CH 2 or CH—CH═CH; R 1 and R 2 are defined as cited in the description and the claims; and Ar represents an optionally substituted aromatic group. The invention also relates to a pharmaceutical agent, containing at least one compound (I) and the tautomers, derivatives and/or acid addition salts of said compound, optionally together with physiologically acceptable carriers and/or auxiliary agents. The invention also relates to the use of compounds of formula (I), and their tautomers, derivatives and pharmacologically acceptable acid addition salts for producing a pharmaceutical agent for treating diseases which respond to the influence of dopamine D 3 receptor ligands.

Claims (45)

1. A pyrimidin-2-one compound of the formula I, or a tautomer thereof,

in which

A is —(CH 2 ) n —, in which n is 4, 5, or 6, or is trans-CH 2 —CH═CH—CH 2 —, trans-CH 2 —C(CH 3 )═CH—CH 2 —, —CH 2 —CH(CH 3 )—CH 2 —CH 2 —, or —CH 2 —CH 2 —CH 2 —CH(CH) 3 —,

B is a radical of the formula:

in which X is CH 2 or N, and Y is CH 2 or CH 2 CH 2 , or X—Y together may also be C═CH, C═CH—CH 2 or CH—CH═CH,

R 1 is selected from OR 3a , NR 4 R 5 , SR 6 , C 3 -C 6 -cycloalkyl, C 1 -C 4 -alkyl which is optionally substituted by OH, C 1 -C 4 -alkoxy, halogen or phenyl,

5- or 6-membered aromatic heterocyclyl having 1, 2 or 3 heteroatoms selected from O, S and N, which may be substituted by one or two radicals which are selected independently of one another from C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, NR 4 R 5 , CN, OH, C 1 -C 2 -fluoroalkyl or halogen, and

phenyl which may be substituted by one or two radicals which are selected independently of one another from C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, NR 4 R 5 , OH, CN, C 1 -C 2 -fluoroalkyl or halogen

R 2 is selected from H, C 1 -C 4 -alkyl, halogen, C 1 -C 2 -fluoroalkyl and cyano,

Ar is an aromatic radical which is selected from phenyl, pyridyl, pyrimidinyl and triazinyl, where the aromatic radical may have 1, 2 or 3 substituents which are selected independently of one another from C 1 -C 6 -alkyl which is optionally substituted by OH, C 1 -C 4 -alkoxy, halogen or phenyl, or C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl, C 5 -C 10 -bicycloalkyl, C 6 -C 10 -tricycloalkyl, where the last three groups mentioned may optionally be substituted by halogen or C 1 -C 4 -alkyl, or halogen, CN, OR 3c , NR 4 R 5 , NO 2 , SR 6 , SO 2 R 6 , SO 2 NR 4 R 5 , COOR 7 , COR 8 , 5- or 6-membered heterocyclyl having 1, 2 or 3 heteroatoms selected from O, S and N, and phenyl, where phenyl and heterocyclyl optionally have one or two substituents which are selected independently of one another from C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, NR 4 R 5 , CN, C 1 -C 2 -fluoroalkyl and halogen, and where 2 substituents bonded to adjacent C atoms of the aromatic radical may together be C 3 - or C 4 -alkylene, or may together with the C atoms to which they are bonded be a fused-on, unsaturated 5 or 6-membered carbocycle or a 5- or 6-membered heterocycle having 1 or 2 nitrogen atoms as ring members,

R 3 , R 3a , R 3b , R 3c , R 3d , R 4 , R 5 , R 6 , R 7 and R 8 are independently of one another H, C 1 -C 6 -alkyl which is optionally substituted by OH, C 1 -C 4 -alkoxy or phenyl, or C 1 -C 6 -haloalkyl or phenyl, where R 5 may also be a group COR 9 where R 9 is hydrogen, C 1 -C 4 -alkyl or phenyl which is optionally substituted by one or two radicals which are selected independently of one another from C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, NR 4 R 5 , CN, C 1 -C 2 -fluoroalkyl or halogen, where

R 4 with R 5 may also form together with the nitrogen atom to which they are bonded a 4-, 5- or 6-membered saturated or unsaturated heterocycle which may optionally have a further heteroatom selected from O, S and NR 10 as ring member, where R 10 is hydrogen or C 1 -C 4 -alkyl, and where the heterocycle may optionally carry 1, 2, 3 or 4 C 1 -C 4 -alkyl groups,

or a physiologically tolerated salt thereof.

2. A pyrimidinone compound as claimed in claim 1 , in which Ar is selected from a radical of the general formula:

in which at least one of the variables D 1 to D 3 is N and the other variables D 1 to D 3 are CH, and R a and R b have independently of one another the following meanings: OR 3c , NR 4 R 5 , CN, C 1 -C 6 -alkyl which is optionally substituted by OH, C 1 -C 4 -alkoxy, halogen or phenyl, or C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl, C 5 -C 10 -bicycloalkyl, C 6 -C 10 -tricycloalkyl, where the last three groups mentioned may optionally be substituted by halogen or C 1 -C 4 -alkyl, or halogen, CN, C 1 -C 4 -alkoxy, 5- or 6-membered heterocyclyl having 1, 2 or 3 heteroatoms selected from O, S and N, and phenyl, where phenyl and heterocyclyl optionally have one or two substituents which are selected independently of one another from C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, NR 4 R 5 , CN, C 1 -C 2 -fluoroalkyl and halogen.

3. A pyrimidinone compound as claimed in claim 2 , in which R a is C 1 -C 6 -alkyl and R b is selected from C 1 -C 6 -alkyl, C 3 -C 6 -cycloalkyl and C 1 -C 2 -fluoroalkyl.

4. A pyrimidinone compound as claimed in claim 1 , in which R 1 is OR 3a in particular OH.

5. A pyrimidinone compound as claimed in claim 1 , in which R 2 is selected from H, C 1 -C 4 -alkyl, halogen or cyano.

6. A pyrimidinone compound as claimed in claim 1 , in which A is a group of the formula —(CH 2 ) n — in which n is 4.

7. A pyrimidinone compound as claimed in claim 1 , in which B in formula I is selected from bivalent radicals of the general formulae:

8. A pyrimidinone compound of the formula I.1, or a tautomer thereof,

in which Ar, R 1 and R 2 have the meanings stated in claim 1 ,

n is 4, 5 or 6,

or a physiologically tolerated acid addition salt thereof.

9. A pyrimidinone compound as claimed in claim 8 , in which Ar is selected from a radical of the general formula:

in which at least one of the variables D 1 to D 3 is N and the other variables D 1 to D 3 are CH, R b is C 1 -C 6 -alkyl, and R a is selected from C 1 -C 6 -alkyl, C 3 -C 6 -cycloalkyl and C 1 -C 2 -fluoroalkyl.

10. A pyrimidinone compound as claimed in claim 9 , in which D 1 and D 2 are N and D 3 is CH.

11. A pyrimidinone compound as claimed in claim 8 , in which R 1 is selected from C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl, OR 3a , in which R 3a has the aforementioned meanings, and

phenyl which may be substituted by one or two radicals which are selected independently of one another from C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, OH, CN, C 1 -C 2 -fluoroalkyl or halogen.

12. A pyrimidinone compound as claimed in claim 11 , in which R 1 is OR 3a and in particular OH.

13. A pyrimidinone compound as claimed in claim 11 , in which R 1 is C 1 -C 4 -alkyl and in particular methyl.

14. A pharmaceutical composition comprising at least one compound as claimed in claim 1 and/or the acid addition salt thereof, where appropriate together with physiologically acceptable carriers and/or excipients.

15. A method of treating Parkinson's disease, anxiety states, or addiction in a patient in need thereof comprising administering an effective amount of at least one compound of claim 1 .

16. A method of treating schizophrenia and/or depression in a patient in need thereof comprising administering an effective amount of at least one compound of claim 1 .

17. A compound of claim 1 having the general formula I.1a,

wherein

R 1 is OH, R 2 is H, R a is CHF 2 and A′ is (CH 2 ) 4 , or

R 1 is OH, R 2 is H, R a is CF 3 and A′ is (CH 2 ) 4 , or

R 1 is OH, R 2 is CH 3 , R a is CF 3 and A′ is (CH 2 ) 4 , or

R 1 is OH, R 2 is F, R a is CF 3 and A′ is (CH 2 ) 4 or

R 1 is OH, R 2 is H, R a is CH 2 CH 2 CH 3 and A′ is (CH 2 ) 4 or

R 1 is OH, R 2 is CH 3 , R a is CH 2 CH 2 CH 3 and A′ is (CH 2 ) 4 .

18. A pharmaceutical composition comprising at least one compound as claimed in claim 17 and/or the acid addition salt thereof, where appropriate together with physiologically acceptable carriers and/or excipients.

19. A method of treating Parkinson's disease, anxiety states, or addiction in a patient in need thereof comprising administering an effective amount of at least one compound of claim 17 .

20. A method of treating schizophrenia and/or depression in a patient in need thereof comprising administering an effective amount of at least one compound of claim 17 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 9, 2013
From: ABBOTT GMBH & CO KG
To: ABBVIE DEUTSCHLAND GMBH & CO KG
Reel/Frame 030763/0308 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2006
From: GENESTE, HERVE; KLING, ANDREAS; BRAJE, WILFRIED; HAUPT, ANDREAS; UNGER, LILIANE
To: ABBOTT GMBH & CO. KG
Reel/Frame 017840/0374 →