Diphenylazetidinones, process for their preparation, medicaments comprising these compounds and their use
View Patent ↗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.
1. A compound of the formula I,
or a pharmaceutically acceptable salt or ester thereof,
in which
R1, R2, R3, R4, R5, R6 independently of one another are (C 0 –C 30 )-alkylene-(LAG), where one or more carbon atoms of the alkylene radical may be replaced by —O—, —(C═O)—, —CH═CH—, —C≡C—, —N((C 1 –C 6 )-alkyl)-, —N((C 1 –C 6 )-alkylphenyl)- or —NH—; or
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 – 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 ;
(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;
wherein at least one of the radicals R1 to R6 has the meaning (C 0 –C 30 )-alkylene-(LAG), where one or more carbon atoms of the alkylene radical may be replaced by —O—, —(C═O)—, —CH═CH—, —C≡C—, —N((C 1 –C 6 )-alkyl)-, —N((C 1 –C 6 )-alkylphenyl)- or —NH—, and where the radicals R1 and R2 may not have the meaning —O-sugar residue or —O-sugar acid.
2. A compound as claimed in claim 1 , wherein
R1, R2, R3, R4, R5, R6 independently of one another are (C 0 –C 30 )-alkylene-(LAG), where one or more carbon atoms of the alkylene radical may be replaced by —O—, —(C═O)—, —N((C 1 –C 6 )-alkyl)- or —NH—; or
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 )-alkyl] 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 or O—(CH 2 ) n -phenyl, where n=0–6 and 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 ;
(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;
wherein at least one of the radicals R1 to R6 has the meaning (C 0 –C 30 )-alkylene-(LAG), where one or more carbon atoms of the alkylene radical may be replaced by —O—, —(C═O)—, —N((C 1 –C 6 )-alkyl)- or —NH—, and where the radicals R1 and R2 may not have the meaning —O-sugar residue or —O-sugar acid.
3. A compound as claimed in claim 1 , wherein
R1, R2, R3, R4, R5, R6 independently of one another are (C 0 –C 30 )-alkylene-(LAG), where one or more carbon atoms of the alkylene radical may be replaced by —O—, —(C═O)—, —N(C 3 )—or —NH—; or
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 )-alkyl] 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 or O—(CH 2 ) n -phenyl, where n=0–6 and 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 ;
(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;
wherein at least one of the radicals R1 or R6 has the meaning (C 0 –C 30 )-alkylene-(LAG), where one or more carbon atoms of the alkylene radical may be replaced by —O—, —(C═O)—, —N(CH 3 )— or —NH—, and where the radicals R1 and R2 may not have the meaning —O-sugar residue or —O-sugar acid.
4. A compound as claimed in claim 1 , wherein
R1, R2, R3, R4, R5, R6 independently of one another are —(CH 2 ) 0-1 —NH—(C═O) 0-1 —(C 3 –C 25 )-alkylene-(C═O) 0-1 —N(R7) 0-1 -LAG, where one or more carbon atoms of the alkylene radical may be replaced by oxygen atoms, or
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 )-alkyl] 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 or O—(CH 2 ) n -phenyl, where n=0–6 and 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;
where one of the radicals R1 or R3 has the meaning —(CH 2 ) 0-1 —NH—(C═O) 0-1 —(C 3 –C 25 )-alkylene-(C═O) 0-1 —N(R7) 0-1 -LAG, where one or more carbon atoms of the alkylene radical may be replaced by oxygen atoms.
5. A pharmaceutical composition comprising one or more of the compounds as claimed in claim 1 and a pharmaceutically acceptable carrier.
6. A method for the treatment of impaired lipid metabolism, which comprises administering to a host in need of the treatment an effective amount of at least one compound as claimed in claim 1 .
7. A method for the treatment of hyperlipidemia, which comprises administering to a host in need of the treatment an effective amount of at least one compound as claimed in claim 1 .
8. A method for lowering or maintaining a desired level of serum cholesterol concentration in a host, which comprises administering to the host in need of lowering or maintaining of serum cholesterol concentration an effective amount of at least one compound as claimed in claim 1 .
9. A method for treating insulin resistance, which comprises administering to a host in need of the treatment an effective amount of at least one compound as claimed in claim 1 .