IP Library Granted Patent US 7,674,773
Granted Patent B2
US 7,674,773 · App. 11/155,109 · Granted Mar 9, 2010

Diphenylazetidinones, process for their preparation, medicaments comprising these compounds and their use

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Quick Facts
Patent No.
US 7,674,773
App. No.
11/155,109
Granted
Mar 9, 2010
Kind
B2
Abstract

Compounds of the formula I, in which R1, R2, R3, R4, R5, and R6 have the meanings given in the description, and their physiologically acceptable salts. The compounds are suitable for use, for example, as hypolipidemics.

Claims (32)

1. A pharmaceutical combination comprising at least one compound chosen from compounds of the formula II,

and pharmaceutically acceptable salts and esters thereof,

in which

R1, R2, R4, R5, R6 independently of one another are

H, F, Cl, Br, I, CF 3 , NO 2 , CN, COOH, COO(C 1 -C 6 )-alkyl, CONH 2 , CONH(C 1 -C 6 )-alkyl, CON[(C 1 -C 6 )-alky] 2 , (C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl or O—(C 1 -C 6 )-alkyl, where one, more or all hydrogens in the alkyl radicals may be replaced by fluorine; or

SO 2 —NH 2 , SO 2 NH(C 1 -C 6 )-alkyl, SO 2 N[(C 1 -C 6 )-alkyl] 2 , S—(C 1 -C 6 )-alkyl, S—(CH 2 ) n -phenyl, SO—(C 1 -C 6 )-alkyl, SO—(CH 2 ) n -phenyl, SO 2 —(C 1 -C 6 )-alkyl or SO 2 —(CH 2 ) n -phenyl, where n=0-6 and the phenyl radical may be substituted up to two times by F, Cl, Br, OH, CF 3 , NO 2 , CN, OCF 3 , O—(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkyl or NH 2 ; or

NH 2 , NH—(C 1 -C 6 )-alkyl, N((C 1 -C 6 )-alkyl) 2 , NH(C 1 -C 7 )-acyl, phenyl, O—(CH 2 ) n -phenyl, where n=0-6, where the phenyl ring may be mono- to trisubstituted by F, Cl, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , O—(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkyl, NH 2 , NH(C 1 -C 6 )-alkyl, N((C 1 -C 6 )-alkyl) 2 , SO 2 —CH 3 , COOH, COO—(C 1 -C 6 )-alkyl or CONH 2 ;

R7 is H or CH 3 ;

(LAG) is a sugar residue, disugar residue, trisugar residue, tetrasugar residue;

a sugar acid, an amino sugar;

an amino acid residue, an oligopeptide residue comprising 2 to 9 amino acids;

a trialkylammoniumalkyl radical; or —O—(SO 2 )—OH;

and

at least one further pharmacologically active compound, wherein said at least one further pharmacologically active compound is chosen from simvastatin, fluvastatin, pravastatin, lovastatin, atorvastatin, cerivastatin, and rosuvastatin.

2. A pharmaceutical combination according to claim 1 , wherein the at least one further pharmacologically active compound is atorvastatin.

3. A pharmaceutical combination according to claim 1 , wherein the at least one further pharmacologically active compound is rosuvastatin.

4. A pharmaceutical combination comprising at least one compound chosen from compounds of the formula

and pharmaceutically acceptable salts and esters thereof,

in which

R1, R2, R4, R5, R6 independently of one another are

H, F, Cl, Br, I, CF 3 , NO 2 , CN, COOH, COO(C 1 -C 6 )-alkyl, CONH 2 , CONH(C 1 -C 6 )-alkyl, CON[(C 1 -C 6 )-alky] 2 , (C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl or O—(C 1 -C 6 )-alkyl, where one, more or all hydrogens in the alkyl radicals may be replaced by fluorine; or

SO 2 —NH 2 , SO 2 NH(C 1 -C 6 )-alkyl, SO 2 N[(C 1 -C 6 )-alkyl] 2 , S—(C 1 -C 6 )-alkyl, S—(CH 2 ) n -phenyl, SO—(C 1 -C 6 )-alkyl, SO—(CH 2 ) n -phenyl, SO 2 —(C 1 -C 6 )-alkyl or SO 2 —(CH 2 ) n -phenyl, where n=0-6 and the phenyl radical may be substituted up to two times by F, Cl, Br, OH, CF 3 , NO 2 , CN, OCF 3 , O—(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkyl or NH 2 ; or

NH 2 , NH—(C 1 -C 6 )-alkyl, N((C 1 -C 6 )-alkyl) 2 , NH(C 1 -C 7 )-acyl, phenyl, O—(CH 2 ) n -phenyl, where n=0-6, where the phenyl ring may be mono- to trisubstituted by F, Cl, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , O—(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkyl, NH 2 , NH(C 1 -C 6 )-alkyl, N((C 1 -C 6 )-alkyl) 2 , SO 2 —CH 3 , COOH, COO—(C 1 -C 6 )-alkyl or CONH 2 ;

R7 is H or CH 3 ;

(LAG) is a sugar residue, disugar residue, trisugar residue, tetrasugar residue;

a sugar acid, an amino sugar;

an amino acid residue, an oligopeptide residue comprising 2 to 9 amino acids;

a trialkylammoniumalkyl radical; or —O—(SO 2 )—OH;

and

at least one further pharmacologically active compound, wherein said at least one further pharmacologically active compound is chosen from simvastatin, fluvastatin, pravastatin, lovastatin, atorvastatin, cerivastatin, and rosuvastatin.

5. A pharmaceutical combination according to claim 4 , wherein the at least one further pharmacologically active compound is atorvastatin.

6. A pharmaceutical combination according to claim 4 , wherein the at least one further pharmacologically active compound is rosuvastatin.

Assignments (1)
CHANGE OF NAME Recorded Nov 22, 2005
From: AVENTIS PHARMA DEUTSCHLAND GMBH
To: SANOFI-AVENTIS DEUTSCHLAND GMBH
Reel/Frame 016800/0538 →