Derivatives of dicarboxylic acid having pharmaceutical properties

1. A compound of the general formula (I)

in which

R 1 is located in the meta- or para-position to the radical W and represents a radical selected from the group consisting of H, halogen and OCF 3 ;

R 2 represents H, or halogen;

R 3 represents H or halogen;

R 4 represents C 1-6 -alkyl, C 3-8 -cycloalkyl, CF 3 , OCF 3 , F, Cl, OMe or phenyl, where the phenyl radical may additionally carry a substituent selected from the group consisting of halogen, CN, C 1-6 -alkoxy, CF 3 , C 1-6 -alkyl;

V is located in the ortho- or meta-position to the radical W and represents O, CH 2 O, OCF 2 or O—C 1-6 -alkyl-O;

W represents CH 2 or CH 2 CH 2 ;

or a pharmaceutically acceptable salt or stereoisomer thereof.

2. The compound as claimed in claim 1 , wherein

R 1 is located in the meta-position to the radical W and represents H or halogen;

R 2 represents H or halogen;

R 3 represents H or halogen;

R 4 represents C 1-6 -alkyl, C 3-8 -cycloalkyl or phenyl, where the phenyl radical may additionally carry a substituent selected from the group consisting of halogen, CN, C 1-6 -alkoxy, CF 3 , C 1-6 -alkyl;

V is located in the ortho- or meta-position to the radical W and represents O, CH 2 O, OCF 3 or O—C 1-6 -alkyl-O;

W represents CH 2 or CH 2 CH 2 ;

or a pharmaceutically acceptable salt or stereoisomer thereof.

3. The compound as claimed in claim 1 , wherein

R 1 is located in the meta-position to the radical W and represents a radical selected from the group consisting of H, F, Cl and Br;

R 2 represents H,

R 3 represents H;

R 4 represents methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or phenyl, where the phenyl radical may additionally carry a substituent from the group consisting of F, Cl, Br, CN, methoxy, ethoxy, n-propoxy, i-propoxy, n-butyloxy, i-butyloxy, t-butyloxy, CF 3 , methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl;

V is located in the ortho- or meta-position to the radical W and represents O, CH 2 O, OCF 2 or O—C 1-6 -alkyl-O;

W represents CH 2 or CH 2 CH 2 ;

or a pharmaceutically acceptable salt or stereoisomer thereof.

4. The compound as claimed in claim 1 , wherein

R 1 is located in the meta-position to the radical W and represents H;

R 2 represents H;

R 3 represents H;

R 4 represents cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or phenyl, where the phenyl radical may additionally carry a substituent from the group consisting of F, Cl, Br, CF 3 ;

V is located in the meta-position to the radical W and represents O;

W represents CH 2 ;

or a pharmaceutically acceptable salt or stereoisomer thereof.

5. The compound as claimed in claim 1 , characterized in that wherein

R 1 is located in the meta-position to the radical W and represents H;

R 2 represents H;

R 3 represents H;

R 4 represents phenyl, where the phenyl radical may additionally carry a substituent from the group consisting of F, Cl, Br, OMe, CF 3 , methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl;

V is located in the ortho-position to the radical W and represents OCF 2 ;

W represents CH 2 CH 2 ;

or a pharmaceutically acceptable salt or stereoisomer thereof.

6. The compound as claimed in claim 1 , wherein

R 1 is located in the meta-position to the radical W and represents a radical selected from the group consisting of H, F, Cl and Br;

R 2 represents H;

R 3 represents H;

R 4 represents methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or phenyl, where the phenyl radical may additionally carry a substituent selected from the group consisting of F, Cl, Br, CN, OMe, CF 3 , methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl;

V is located in the ortho-position to the radical W and represents CH 2 O;

W represents CH 2 CH 2 ;

or a pharmaceutically acceptable salt or stereoisomer thereof.

7. A process for preparing compounds of the general formula (I), comprising the following steps:

compounds of the formula (II)

 in which

R 1 , V and W are as defined in claim 1 and

L, if V is O, represents methyl or otherwise represents a radical of the formula

 where R 2 , R 3 and R 4 are as defined in claim 1 ,

with a C 1-6 -alkyl 4-formylbenzoate in an organic solvent, to give a compound of the formula (III)

in which R 1 , V, W and L are as defined above and Q represents a C 1-6 -alkyl radical, then reacting with a C 1-6 -alkyl ω-halovalerate in an organic solvent in the presence of a base with heating to give compounds of the formula (IV)

in which R 1 , V, W, and Q are as defined above, Q′ represents a C 1-6 -alkyl radical and L represents H— if V is O— or a radical of the formula II-A,

then—if V is O and L represents H—reacting the compound of the formula (IV) with a compound of the formula IV-A in an organic solvent with heating

where R 2 and R 3 are as defined in claim 1 and X and X′ each represent halogen,

followed by palladium-catalyzed substitution of the radical X with a benzene boronic acid derivative to give compounds of the formula (V)

and subsequent hydrolysis of the compounds of the formula (IV) or (V) under alkaline conditions to give the compounds of the formula (I).

8. The process of claim 7 wherein the step of reacting the compound of formula (II) with a C 1-6 -alkyl 4-formylbenzoate is carried out with heating and simultaneous or subsequent addition of a reducing agent.

9. The process of claim 7 wherein in the step of reacting the compound of formula (III) with a C 1-6 -alkyl ω-haolvalerate, the compound of formula (III) is first subjected to prior cleavage of the ether to give the free hydroxyl group, if V represents O and L represents methyl.

10. A pharmaceutical composition comprising a compound according to claim 1 and a pharmaceutically acceptable carrier.

11. A method for treating a cardiovascular disorder selected from angina pectoris, ischemias, hypertension, and arteriosclerosis comprising administering to a subject in need thereof an effective amount of a compound of claim 1 .

12. A method for treating fibrosis of the liver comprising administering to a subject in need thereof an effective amount of a compound of claim 1 .