 5-oxo-isoxazoles as inhibitors of lipases and phospholipases
专利摘要:
公开号:AU2008235071A1 申请号:U2008235071 申请日:2008-03-22 公开日:2008-10-16 发明作者:Karl-Heinz Baringhaus；Hubert Heuer；Gunter Muller；Stefan Petry；Manfred Seidel；Gerhard Zoller 申请人:Sanofi Aventis France； IPC主号:C07D261-12
专利说明:
WO 2008/122357 1 PCT/EP2008/002314 Description 5-Oxoisoxazoles as inhibitors of lipases and phospholipases 5 The present invention relates to 5-oxoisoxazoles of the formula I, the pharmaceutically usable salts thereof and the use thereof as medicinal substances. Certain 3-oxo-3H-benzo[c]isoxazole-1-carboxamides are described as acylpeptidase hydrolase inhibitors in WO 01/44211. 10 Lowe et al., Bioorg. Med. Chem. Lett. 14 (2004) 3155-3159 describe 3-oxoisoxazole 5-urea derivatives having activity on hormone-sensitive lipase. Mentioned examples having hydrogen on the urea amino group are described as having no activity on hormone-sensitive lipase. Said examples have no activity on 15 endothelial lipase either. Compounds with an inhibitory effect on endothelial lipase are described in the prior art, for example in W02004/094394, W02004/094393, W02004/093872 or W02006/111321. 20 The invention was based on the object of providing novel compounds which display a therapeutically utilizable effect. The object was in particular to find novel compounds which are suitable for the treatment of elevated blood lipid concentrations, the metabolic syndrome, diabetes, insulin resistance, dysregulation 25 of LDL, HDL or cardiovascular disorders. It is an object of the present invention to provide compounds which bring about an inhibition of endothelial lipase. 30 The invention relates to 5-oxoisoxazoles of the formula I WO 2008/122357 2 PCT/EP2008/002314 0 R2,4 5 R3- N IL H 2 /'NH 0 RI (I) in which the meanings are: 5 RI (C 5 -C 16 )-alkyl, Y-aryl, Y-heteroaryl, where aryl or heteroaryl may be substituted one or more times by F, CI, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , 0-(C1-C 6 )-alkyl, O-(C1-C 4 )-alkoxy (C 1 -C 4 )-alkyl, S-(C1-C 6 )-alkyl, (C1-C 6 )-alkyl, (C 2 -C 4 )-haloalkyl, 10 0-(C 2 -C 4 )-haloalkyl, (C 2 -C 6 )-alkenyl, (C 3 -C)-cycloalkyl, 0-(C3-C8) cycloalkyl, (C 2 -C 6 )-alkynyl, (Co-C 8 )-alkylene-aryl, 0-(Co-C 8 )-alkylene aryl, S-aryl, (Co-Ca)-alkylene-heteroaryl, N(R4)(R5), S0 2 -CH 3 , SO 2 NH 2 , SF 5 , COOH, COO-(C 1 -C)-alkyl, CON(R6)(R7), N(R8)CO(R9), N(R10)SO 2 (R11), CO(R12), (CR13R14)x-O(R15), O-CO-N(R16)(R17), 15 O-CO-(C1-C)-alkylene-CO-O-(C1-C 6 )-alkyl, O-CO-(C1-C)-alkylene CO-OH, O-CO-(C 1 -C 6 )-alkylene-CO-N(R1 8)(R1 9), where aryl or heteroaryl may in turn be substituted one or more times by F, Cl, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , O-(C 1 -C)-alkyl, 20 0-(C1-C 4 )-alkoxy-(C1-C 4 )-alkyl, S-(C1-C 6 )-alkyl, (C1-C)-alkyl, (C 2 -C 4 )-haloalkyl, (C 2 -C 6 )-alkenyl, (C 3 -C 8 )-cycloalkyl, 0-(C 3 -C 8 )-cycloalkyl, (C 2 -C 6 )-alkynyl, N(R4a)(R5a), S0 2 -CH 3 , SF 5 , COOH, COO-(C 1 -C)-alkyl, CON(R6a)(R7a), N(R8a)CO(R9a), N(R1Oa)SO 2 (RI 1 a), CO(R1 2a), 25 (CR13aR14a)x--O(R15a), O-CO-N(R16a)(R17a), O-CO-(C1-C 6 )-alkylene-CO-O-(C1-C 6 )-alkyl, O-CO-(C1-C6) alkylene-CO-OH, O-CO-(C1-C 6 )-alkylene-CO- WO 2008/122357 3 PCT/EP2008/002314 N(R18a)(R19a); x, x' 0, 1,2, 3,4, 5, 6; 5 R4, R5, R6, R7, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18, R19, R4a, R5a, R6a, R7a, R9a, R10a, R11a, R12a, R13a, R14a, R15a, R16a, R17a, R18a, R19a independently of one another hydrogen, (C-C)-alkyl; 10 or a radical of the formula la R20 R21 W R25 R22 R23 R24 ,with W -C(R26)(R27)-, -C(R26)(R27)-C(R28)(R29)-, -C(R26)(R27)-O-; 15 R20, R21, R22, R23, R24, R25, R26, R27, R28, R29 identically or differently hydrogen, F, Cl, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , SF 5 , 0-(C-C 6 )-alkyl, 0-(C 1 -C 4 )-alkoxy-(C-C 4 )-alkyl, S-(CrC 6 )-alkyl, (C-C)-alkyl, (C 2 -C4)-haloalkyl, 0-(C2-C4) 20 haloalkyl, (C 2 -C 6 )-alkenyl, (C 3 -C 8 )-cycloalkyl, 0-(C3-C8) cycloalkyl, (C 3 -C 8 )-cycloalkenyl, (C 2 -C 6 )-alkynyl, N(R30)(R31), S0 2 -CH 3 , COOH, COO-(O-C)-alkyl, CON(R32)(R33), N(R34)CO(R35), N(R36)SO 2 (R37), CO(R38), (CR39R40)x---O(R41), O-CO-N(R42)(R43), 0-CO 25 (C-C 6 )-alkylene-CO-O-(Cr-C 6 )-alkyl, O-CO-(0C)-alkylene CO-OH, O-CO-(CriC 6 )-alkylene-CO-N(R44)(R45); x'' 0, 1,2, 3,4, 5, 6; WO 2008/122357 4 PCT/EP2008/002314 R30, R31, R32, R33, R34, R35, R36, R37, R38, R39, R40, R41, R42, R43, R44, R45 identically or differently hydrogen, (C1-C)-alkyl; 5 or R20 and R26 or R21 and R27 together with the carbon atoms carrying them form a monocyclic, 5 or 6 membered saturated, partly unsaturated or aromatic ring system whose individual members may be replaced by -CHR46-, -CR46R47-, =(C-R46)-; 10 or R22 and R24, or R23 and R25 together with the carbon atoms carrying them form a monocyclic, 5 or 6 membered saturated, partly unsaturated or an aromatic ring system whose individual members may be replaced by -CHR46-, -CR46R47-, 15 =(C-R46)-; R46, R47 identically or differently F, Cl, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , SF 5 , O-(C1-Cs)-alkyl, 0-(C1-C4)-alkoxy-(C 1 -C 4 )-alkyl, S-(C 1 -C6) alkyl, (C 1 -C)-alkyl, (C 2 -C 4 )-haloalkyl, 0-(C 2 -C 4 )-haloalkyl, 20 (C 2 -C 6 )-alkenyl, (C 3 -C 8 )-cycloalkyl, 0-(C 3 -C8)-cycloalkyl, (C 2 -C 6 )-alkynyl, N(R48)(R49), S0 2 -CH 3 , COOH, COO (C 1 -C)-alkyl, CON(R50)(R51), N(R52)CO(R53), N(R54)SO 2 (R55), CO(R56), (CR57R58)x----O(R59), O-CO N(R60)(R61), O-CO-(C1-C 6 )-alkylene-CO-O-(C 1 -C 6 )-alkyl, 25 O-CO-(C1-Cs)-alkylene-CO-OH, O-CO-(C1-C)-alkylene-CO N(R62)(R63); x''' 0, 1, 2, 3, 4, 5, 6; 30 R48, R49, R50, R51, R52, R53, R54, R55, R56, R57, R58, R59, R60, R61, R62, R63 identically or differently hydrogen, (C 1 -C)-alkyl; WO 2008/122357 5 PCT/EP2008/002314 Y, Z identically or differently (C 1 -C 2 )-alkylene, which may be substituted once by F, CI, CH 3 or OH; 5 R2 hydrogen, (C 1 -C1 2 )-alkyl, Z-aryl, where aryl may optionally be substituted, (C 3 -C 1 2 )-cycloalkyl; R3 (C 1 -C 1 2 )-alkyl, aryl, heteroaryl, where aryl or heteroaryl may optionally be substituted, (C3-C 1 2 )-cycloalkyl; or 10 R2 and R3 together with the carbon atoms carrying them form a monocyclic, saturated or partly unsaturated 4- to 8-membered ring system whose individual members may be replaced by one to three atoms or atomic groups from the series -CHR64-, -CR64R65-, =(C-R66)-, -NR67-, 15 -C(=O)-, -0-, with the proviso that two units from the series -0- may not be adjacent; R64, R65, R66, R67 identically or differently hydrogen, F, Cl, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , SF 5 , O-(C 1 -C)-alkyl, 0-(Cl-C4)-alkoxy-(C 1 -C 4 ) 20 alkyl, S-(C1-C 6 )-alkyl, (C 1 -C)-alkyl, (C 2 -C 4 )-haloalkyl, 0-(C 2 -C 4 )-haloalkyl, (C 2 -C)-alkenyl, (C 3 -C 8 )-cycloalkyl, 0-(C 3 -CB)-cycloalkyl, (C 3 -C8)-cycloalkenyl, (C 2 -C 6 )-alkynyl, N(R68)(R69), S0 2 -CH 3 , COOH, COO-(C1-C)-alkyl, CON(R70)(R71), N(R72)CO(R73), N(R74)SO 2 (R75), 25 CO(R76), (CR77R78)x-----O(R79), O-CO-N(R80)(R81), O-CO-(C1-C 6 )-alkylene-CO-O-(C1-C 6 )-alkyl, O-CO-(C1-C6) alkylene-CO-OH, O-CO-(C 1 -C 6 )-alkylene-CO-N(R82)(R83); x'''' 0, 1, 2, 3, 4, 5, 6; 30 R68, R69, R70, R71, R72, R73, R74, R75, R76, R77, R78, R79, R80, R81, R82, R83 WO 2008/122357 6 PCT/EP2008/002314 identically or differently hydrogen, (C1-C 6 )-alkyl; with the proviso that the compound with R1 = cyclohexyl, R2=H and R3 = phenyl is excluded; 5 the tautomeric forms of the compounds and the physiologically tolerated salts thereof. Preference is given to compounds of the formula I in which 10 R1 (C 5 -C 1 2 )-alkyl, Y-phenyl, Y-heteroaryl, where heteroaryl comprises 1 heteroatom from the series N, 0, S, and where phenyl or heteroaryl may be substituted one or more times by F, Cl, Br, OH, CF 3 , NO 2 , CN, OCF 3 , O-(C1-C 6 )-alkyl, S-(C 1 -C)-alkyl, (C1-C)-alkyl, (C 2 -C 4 )-haloalkyl, (C 3 -C8)-cycloalkyl, (Co-C 6 )-alkylene-phenyl, 0-(Co-C 6 )-alkylene-phenyl, 15 S-phenyl, (Co-C 8 )-alkylene-heteroaryl, N(R4)(R5), COOH, COO (C1-C)-alkyl, CON(R6)(R7), CO(R12), where phenyl or heteroaryl may in turn be substituted one or more times by F, Cl, OH, CF 3 , NO 2 , CN, OCF 3 , 0-(C 1 -C 6 )-alkyl, S-(C1-CG) 20 alkyl, (C 1 -C)-alkyl, (C 2 -C 4 )-haloalkyl, (C 3 -Cs)-cycloalkyl, N(R4a)(R5a), COOH, COO-(C1-C)-alkyl, CON(R6a)(R7a) CO(R12a); x, x' 0,1,2,3,4,5,6; 25 R4, R5, R6, R7, R12, R4a, R5a, R6a, R7a, R12a, identically or differently hydrogen, (C 1 -C 8 )-alkyl; or a radical of the formula lb 30 WO 2008/122357 7 PCT/EP2008/002314 R20 R21 W with W -C(R26)(R27)-, -C(R26)(R27)-C(R28)(R29)-, -C(R26)(R27)-O-; 5 R20, R21, R26, R27, R28, R29 identically or differently hydrogen, F, Cl, OH, CF 3 , NO 2 , CN, OCF 3 , O-(C 1 -C)-alkyl, (C 1 -C)-alkyl, CO-(C1-C)-alkyl; or 10 R20, R21, R26 and R27 together with the carbon atoms carrying them form a fused benzene residue which may be substituted one or more times by F, Cl, CN, NO 2 , CF 3 , OCF 3 , (C 1 -C 6 )-alkyl, O-(C 1 -C 6 )-alkyl, CO-(C 1 -C 6 )-alkyl; Y, Z identically or differently -CH 2 - or -CH 2 -CH 2 -, which may be substituted 15 once byCH 3 orOH; R2 hydrogen, (C1-C 1 2 )-alkyl, Z-phenyl, where phenyl may optionally be substituted, (C 3 -C 1 2 )-cycloalkyl; 20 R3 (C1-C 1 2 )-alkyl, phenyl, heteroaryl, which comprises 1 heteroatom from the series N, 0, S, where phenyl or heteroaryl may optionally be substituted, (C3-C1 2 )-cycloalkyl; or R2 and R3 together with the carbon atoms carrying them form a monocyclic, 25 saturated 5- to 7-membered ring system whose individual members may be replaced by one to three atomic groups from the series -CHR64-, -CR64R65-, =(C-R66)-; WO 2008/122357 8 PCT/EP2008/002314 R64, R65, R66 identically or differently F, Cl, OH, CF 3 , 0-(C1-C 6 )-alkyl, 0-(C1-C 4 )-alkoxy-(C 1 -C4)-alkyl, (C1-C)-alkyl, (C 2 -C 4 ) haloalkyl, (C 3 -C 8 )-cycloalkyl, N(R68)(R69), S0 2 -CH 3 , COOH, COO-(C 1 -C)-alkyl, CON(R70)(R71), N(R72)CO(R73), 5 CO(R76), O-CO-N(R80)(R81), O-CO-(C1-C)-alkylene-CO O-(C 1 -C)-alkyl, O-CO-(C 1 -C)-alkylene-CO-OH, 0-CO (C1-C 6 )-alkylene-CO-N(R82)(R83); R68, R69, R70, R71, R72, R73, R76, R77, R78, R79, R80, R81, R82, R83 10 independently of one another hydrogen, (C 1 -C)-alkyl; the tautomeric forms of the compounds, and the physiologically tolerated salts thereof. 15 Particular preference is given to compounds of the formula I in which R1 is (C 5 -C 8 )-alkyl, Y-phenyl, Y-pyridyl, Y-thienyl, Y-furyl, Y-benzothienyl, Y-benzofuryl, where phenyl or the heteroaromatic radical may be substituted once, twice or three times by F, Cl, Br, CF 3 , CN, OCF 3 , 20 O-(C 1 -C)-alkyl, (C 1 -C)-alkyl, (C 3 -C 6 )-cycloalkyl, N(R4)(R5), COOH, COO-(C1-C)-alkyl, CON(R6)(R7), CO(R12), and may be substituted once by (Co-C 1 )-alkylene-phenyl, 0-(Co-C1)-phenyl, pyrazolyl, pyridyl, thienyl, furyl, benzothienyl, benzofuryl, where a heteroaromatic radical or phenyl may in turn be substituted once, twice or three times by F, C, 25 Br, CF 3 , CN, OCF 3 , O-(C 1 -C)-alkyl, (C 1 -C)-alkyl, (C 3 -C 6 )-cycloalkyl, N(R4a)(R5a), COOH, COO-(C 1 -C)-alkyl, CON(R6a)(R7a), CO(R12a); R4, R5, R6, R7, R12, R4a, R5a, R6a, R7a, R12a are independently of one another H, (C 1 -C)-alkyl; 30 or a radical from the group WO 2008/122357 9 PCT/EP2008/002314 R20 R21 R26 R20 R21R26 R21R26 R27 R -27 R20 R27 R28 0 -- R29 R20, R21, R26, R27, R28, R29 are identically or differently hydrogen, (C1-C6) alkyl, preferably hydrogen and methyl; 5 Y is -CH 2 - or -CH 2 -CH 2 -, which may be substituted once by CH 3 ; R2 is hydrogen, (C1-Cs)-alkyl, -CH 2 -phenyl, where phenyl may optionally be substituted, (C 3 -C 8 )-cycloalkyl; 10 R3 is (C1-C 8 )-alkyl, phenyl, pyridyl, thienyl, where phenyl, pyridyl or thienyl may optionally be substituted, (C 3 -C 8 )-cycloalkyl; or R2 and R3 together with the carbon atoms carrying them form a monocyclic, 15 saturated 6- to 7-membered ring system whose individual members may be replaced by one to three atoms or atomic groups from the series -CHR64-, -CR64R65-; R64, R65 are identically or differently F, Cl, CF 3 , OCF 3 , (C 1 -C)-alkyl, 0-(C1-C6) 20 alkyl, N(R68)(R69), COOH, COO-(C 1 -C)-alkyl, CO-N(R70)(R71), CO(R76); R68, R69, R70, R71, R76 are identically or differently hydrogen, (C 1 -C)-alkyl; 25 the tautomeric forms of the compounds, and the physiologically tolerated salts thereof. WO 2008/122357 10 PCT/EP2008/002314 In a particularly preferred embodiment of the compounds of the formula I, R2 is ispropyl and 5 R3 is methyl. In a further particularly preferred embodiment of the compounds of the formula I, 10 R2 is hydrogen and R3 is phenyl, which may be substituted once by Cl. In a further particularly preferred embodiment of the compounds of the formula 1, 15 R2 and R3 together are -CH 2 -CH 2 -CH 2 -CH 2 - or -CH 2 -CH 2 -CH 2 -CH 2 -CH 2 -. Very particular preference is given to compounds of the formula I in which 0 R1 is (C 5 -C 7 )-alkyl, Y-phenyl, Y-thienyl, Y-benzothienyl, where phenyl or the heteroaromatic radical may be substituted once, twice or three times by F, Cl, Br, CF 3 , 0-CH 3 , -CH 3 , -CH 2 CH 3 , -CH 2 -CH 2 -CH 2 -CH 3 , and be substituted once by phenyl, pyrazolyl or thienyl, where the heteroaromatic radical or phenyl may in turn be 5 substituted once, twice or three times by F, Cl, Br, CF 3 , 0-(C 1 -CB)-alkyl, (C-C 6 )-alkyl; or a radical from the group WO 2008/122357 11 PCT/EP2008/002314 R20 R21 R26 R20 R21R26 R21R26 - R27 R27 R20 R27 R28 0 - 7- R29 R20, R21, R26, R27, R28, R29 are identically or differently hydrogen, CH 3 ; 5 Y is -CH 2 -, which may be substituted once by CH 3 ; R2 is hydrogen, methyl, isopropyl, cyclopropyl, phenyl, -CH 2 -phenyl, where phenyl may be substituted by C in position 4; 10 R3 is methyl, phenyl, pyridyl, cyclopropyl, where phenyl may be substituted by Cl; or R2 and R3 are together -CH 2 --CH 2 -CH 2 -CH 2 - or -CH 2 -CH 2 -CH 2 -CH 2 -CH 2 ; 5 the tautomeric forms of the compounds, and the physiologically tolerated salts thereof. The invention relates to compounds of the formula I in the form of their salts, racemates, racemic mixtures and pure enantiomers, and to their diastereomers and 20 mixtures thereof. The alkyl radicals in the substituents R1, R2, R3, R4, R5, R6, R7, R9, R10, R1 1, R12, R13, R14, R15, R16, R17, R18, R19, R4a, R5a, R6a, R7a, R9a, R10a, R11a, R12a, R13a, R14a, R15a, R16a, R17a, R18a, R19a, R20, R21, R22, R23, R24, 5 R25, R26, R27, R28, R29, R30, R31, R32, R33, R34, R35, R36, R37, R38, R39, R40, R41, R42, R43, R44, R45, R46, R47, R48, R49, R50, R51, R52, R53, R54, R55, R56, R57, R58, R59, R60, R61, R62, R63, R64, R65, R66, R67, R68, R69, WO 2008/122357 12 PCT/EP2008/002314 R70, R71, R72, R73, R74, R75, R76, R77, R78, R79, R80, R81, R82, R83 may be either straight chain or branched. Halogen is fluorine, chlorine, bromine or iodine, preferably fluorine or chlorine. 5 Haloalkyl means an alkyl radical which is substituted one or more times by halogen. An aryl radical means a phenyl, naphthyl or biphenyl radical. The preferred aryl radical is phenyl. The aryl radicals may be substituted one or more times by suitable groups such as, 10 for example: F, Cl, Br, I, CF 3 , OH, OCF 3 , NO 2 , CN, COOH, COO(O,-C 6 )alkyl, CONH 2 , CONH(Cr-C 6 )alkyl, CON[(C-C 6 )alkyl] 2 , (C 3 -C1O)-cycloalkyl, (CrCo)-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, O-(O-C)-alkyl, CO-(O-C)-alkyl, O-CO-(Cr C6) alkyl, O-CO-(C-C 6 )-aryl, P0 3 H 2 , SO 3 H, S0 2 -NH 2 , SO 2 NH(C-C 6 )-alkyl, SO 2 N[(0 1 -C 6 )-alkyl] 2 , S-(0 1 C)-alkyl, 15 S-(CH 2 )n-aryl, S-(CH 2 )n-heterocycle, SO-(C-C 6 )-alkyl, SO-(CH 2 )n-aryl, SO-(CH 2 )n heterocycle, SO2-(C-C 6 )-alkyl, SO 2 -(CH 2 )n-aryl, SO 2 -(CH 2 )n-heterocycle, S02 NH(CH 2 )n-aryl, SO 2 -NH(CH 2 )n-heterocycle, SO 2 -N(CriC 6 )-alkyl)(CH 2 )n-aryl, S02 N(Cr-C 6 )-alkyl)(CH 2 )n-heterocycle, SO 2 -N((CH 2 )n-aryl) 2 , SO 2 -N((CH 2 )n-(heterocycle) 2 , NH-(CH 2 )n-aryl, NH-(CH 2 )n-heterocycle, N((C 1 -C 6 )-alkyl)(CH 2 )n-aryl, N((0 1 -C 6 ) 20 alkyl)(CH 2 )n-heterocycle, C(NH)(NH 2 ), NH 2 , NH-(Cr-C 6 )-alkyl, N((Cr-C 6 )-alkyl) 2 , NH-CO-(0 1 -C 6 )-alkyl, NH COO-(C-C 6 )-alkyl, NH-CO-aryl, NH-CO-heterocycle, NH-COO-aryl, NH-COO heterocycle, NH-CO-NH-(0 1 -C 6 )-alkyl, NH-CO-NH-aryl, NH-CO-NH-heterocycle, aryl, 0-(CH 2 )n-aryl, 0-(CH 2 )n-heterocycle, where n may be 0 - 6, where the aryl 5 radical or heterocyclic radical may be substituted one to 3 times by F, Cl, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , 0-(C-C 6 )-alkyl, (Ol-C 6 )-alkyl, NH 2 , NH(C-Ce)-alkyl, N((0 1 -C 6 ) alkyl) 2 , S0 2 -CH 3 , COOH, COO-(C-C 6 )-alkyl, CONH 2 . Heterocycle is a mono- or bicyclic ring system having 5 to 12 ring members in which 30 at least one atom in the ring system is a heteroatom from the series N, 0 and S. This definition also includes ring systems in which the heterocycle is fused to a benzene nucleus. (C 5 -C 7 )-heterocycle is a monocyclic, (C 8 -C 1 2 )-heterocycle a bicyclic, ring WO 2008/122357 13 PCT/EP2008/002314 system. Suitable "heterocyclic rings" or "heterocyclic radicals" are azocinyl, benzimidazolyl, benzofuryl, benzothienyl, benzothiophenyl, benzoxazolyl, benzthiazolyl, benztriazolyl, benztetrazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazalinyl, 5 carbazolyl, 4aH-carbazolyl, carbolinyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl, quinuclidinyl, chromanyl, chromenyl, cinnolinyl, decahydroquinolinyl, 2H,6H-1,5,2-dithiazinyl, dihydrofuro[2,3-b]-tetrahydrofuran, furyl, furazanyl, imidazolidinyl, imidazolinyl, imidazolyl, 1 H-indazolyl, indolinyl, indolizinyl, indolyl, 3H-indolyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl, 10 isoquinolinyl (benzimidazolyl), isothiazolyl, isoxazolyl, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, oxadiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, oxazolidinyl, oxazolyl, oxazolidinyl, pyrimidinyl, phenanthridinyl, phenanthrolinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, piperidinyl, pteridinyl, purynyl, pyranyl, 15 pyrazinyl, pyroazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridooxazoles, pyridoimidazoles, pyridothiazoles, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, 2H-pyrrolyl, pyrrolyl, tetrahydrofuranyl, tetra hydroisoquinolinyl, tetrahydroquinolinyl, 6H-1,2,5-thiadazinyl, thiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, thienyl, triazolyl, tetrazolyl and 20 xanthenyl. Pyridyl is both 2-, 3- and 4-pyridyl. Thienyl is both 2- and 3-thienyl. Furyl is both 2 and 3-furyl. Also included are the corresponding N-oxides of these compounds, i.e. for example 1-oxy-2-, 3- or 4-pyridyl. 25 Heteroaryl is a subgroup of heterocycle and is a mono- or bicyclic aromatic ring system having 5 to 12 ring members, in which at least one atom in the ring system is a heteroatom from the series N, 0 and S. Suitable "heteroaryl rings" or "heteroaryl radicals" are for example benzimidazolyl, 30 benzofuranyl, benzothienyl, benzoxazolyl, benzothiazolyl, benzotriazolyl, benzotetrazolyl, benzisoxazolyl, benzisothiazolyl, quinolinyl, furanyl, furazanyl, imidazolyl, 1H-indazolyl, indolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, WO 2008/122357 14 PCT/EP2008/002314 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, pyrimidinyl, pyrazinyl, pyrazolyl, pyridyl, pyrrolyl, thiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, thienyl. Preferred heteroaryl radicals are thienyl, pyridyl, furanyl, pyrazolyl, benzothienyl and 5 benzofuranyl. Particularly preferred heteroaryl radicals are thienyl, benzothienyl and furanyl, and thienyl is especially preferred. The heterocyclic radicals or the heteroaromatic radicals may be substituted one or more times by suitable groups such as, for example, F, Cl, Br, I, CF 3 , OH, OCF 3 , 10 NO 2 , CN, COOH, COO(C-C)alkyl, CONH 2 , CONH(Cr-C 6 )alkyl, CON[(CrC 6 )alkyl] 2 , (C 3 -C 1 o)-cycloalkyl, (CrC- 1 o)-alkyl, (C 2 -C)-alkenyl, (C 2 -C 6 )-alkynyl, O-(CrC 6 )-alkyl, CO-(Cr-Cs)-alkyl, 0-CO-(Cr-Cs)-alkyl, 0-CO-(CO-aryl, P0 3 H 2 , SO 3 H, S0 2 -NH 2 , SO 2 NH(C-C 6 )-alkyl, SO 2 N[(C-C)-alkyl] 2 , S-(C-C)-alkyl, S-(CH 2 )n-aryl, S-(CH 2 )n-heterocycle, SO-(C0)-alkyl, SO-(CH 2 )n-aryl, SO-(CH 2 )n 15 heterocycle, S0 2 -(CrC 6 )-alkyl, SO 2 -(CH 2 )n-aryl, SO 2 -(CH 2 )n-heterocycle, SO 2 -NH(CH 2 )n-aryl, SO 2 -NH(CH 2 )n-heterocycle, SO 2 -N(Cr-C 6 )-alkyl)(CH 2 )n-aryl, SO 2 -N(Cr-Cs)-alkyl)(CH 2 )n-heterocycle, SO 2 -N((CH 2 )n-aryl) 2 , SO 2 -N((CH 2 )a (heterocycle) 2 , NH-(CH 2 )n-aryl, NH-(CH 2 )n-heterocycle, N((-Cr)-alkyl)(CH 2 )n-aryl, N((CriC 6 )-alkyl)(CH 2 )n-heterocycle, 20 C(NH)(NH 2 ), NH 2 , NH-(Cr-C 6 )-alkyl, N((Cr 1 C 6 )-alkyl) 2 , NH-CO-(Cr-C 6 )-alkyl, NH COO-(Cr-C 6 )-alkyl, NH-CO-aryl, NH-CO-heterocycle, NH-COO-aryl, NH-COO heterocycle, NH-CO-NH-(0 1 -C 6 )-alkyl, NH-CO-NH-aryl, NH-CO-NH-heterocycle, aryl, 0-(CH 2 )n-aryl, 0-(CH 2 )n-heterocycle, where n may be 0 - 6, where the aryl radical or heterocyclic radical may be substituted one to 3 times by F, C, Br, I, OH, 5 CF 3 , NO 2 , CN, OCF 3 , 0-(Cr 1 C 6 )-alkyl, (Cr 1 C 6 )-alkyl, NH 2 , NH(Cr-C 6 )-alkyl, N((Cr-C 6 ) alkyl) 2 , S0 2 -CH 3 , COOH, COO-( 1 C 6 )-alkyl, CONH 2 . A cycloalkyl radical means a ring system which comprises one or more rings, which is saturated or partly unsaturated (having one or two double bonds) and which is 30 composed exclusively of carbon atoms, such as, for example, cyclopropyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl or adamantyl. The cycloalkyl radicals may be substituted one or more times by suitable groups WO 2008/122357 15 PCT/EP2008/002314 such as, for example: F, Cl, Br, I, CF 3 , OH, OCF 3 , NO 2 , CN, COOH, COO(C-C)alkyl, CONH 2 , CONH(C1-C)alkyl, CON[(C1-C 6 )alkyl] 2 , (C3-C0,) cycloalkyl, (C1-C1o)-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, O-(C 1 -C)-alkyl, CO-(C1-Ce)-alkyl, O-CO-(C 1 -Ce)-alkyl, O-CO-(C 1 -C 6 )-aryl, 5 P0 3 H 2 , SO 3 H, S0 2 -NH 2 , SO 2 NH(C1-C 6 )-alkyl, SO 2 N[(C1-C 6 )-alkyl] 2 , S-(C1-Cs)-alkyl, S-(CH 2 )n-aryl, S-(CH 2 )n-heterocycle, SO-(C1-C 6 )-alkyl, SO-(CH 2 )n-aryl, SO-(CH 2 )n heterocycle, S0 2 -(C1-C 6 )-alkyl, SO 2 -(CH 2 )n-aryl, SO 2 -(CH 2 )n-heterocycle, SO 2 -NH(CH 2 )n-aryl, SO 2 -NH(CH 2 )n-heterocycle, SO 2 -N(C1-C 6 )-alkyl)(CH 2 )n-aryl, SO 2 -N(C1-C 6 )-alkyl)(CH 2 )n-heterocycle, SO 2 -N((CH 2 )n-aryl) 2 , SO 2 -N((CH 2 )n 10 (heterocycle) 2 , NH-(CH 2 )n-aryl, NH-(CH 2 )n-heterocycle, N((C1-C 6 )-alkyl)(CH 2 )n-aryl, N((C1-C 6 )-alkyl)(CH 2 )n-heterocycle, C(NH)(NH 2 ), NH 2 , NH-(C1-C 6 )-alkyl, N((C1-C 6 )-alkyl) 2 , NH-CO-(C1-C 6 )-alkyl, NH-COO-(C1-C)-alkyl, NH-CO-aryl, NH-CO-heterocycle, NH-COO-aryl, NH-COO heterocycle, NH-CO-NH-(C 1 -C 6 )-alkyl, NH-CO-NH-aryl, NH-CO-NH-heterocycle, 15 aryl, 0-(CH 2 )n-aryl, 0-(CH 2 )n-heterocycle, where n may be 0 - 6, where the aryl radical or heterocyclic radical may be substituted one to 3 times by F, C, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , 0-(C1-C 6 )-alkyl, (C 1 -C)-alkyl, NH 2 , NH(C1-C 6 )-alkyl, N((C1-C 6 ) alkyl) 2 , SO 2 -CH 3 , COOH, COO-(C1-C)-alkyl, CONH 2 . 20 Pharmaceutically acceptable salts are, because their solubility in water is greater than that of the initial or basic compounds, particularly suitable for medical applications. These salts must have a pharmaceutically acceptable anion or cation. Suitable pharmaceutically acceptable acid addition salts of the compounds of the invention are salts of inorganic acids such as hydrochloric acid, hydrobromic, 25 phosphoric, metaphosphoric, nitric and sulfuric acid, and of organic acids such as, for example, acetic acid, benzenesulfonic, benzoic, citric, ethanesulfonic, fumaric, gluconic, glycolic, isethionic, lactic, lactobionic, maleic, malic, methanesulfonic, succinic, p-toluenesulfonic and tartaric acid. Suitable pharmaceutically acceptable basic salts are ammonium salts, alkali metal salts (such as sodium and potassium 30 salts) and alkaline earth metal salts (such as magnesium and calcium salts) and salts of trometamol (2-amino-2-hydroxymethyl-1,3-propanediol), diethanolamine, lysine or ethylenediamine. WO 2008/122357 16 PCT/EP2008/002314 Salts with a pharmaceutically unacceptable anion such as, for example, trifluoroacetate likewise belong within the framework of the invention as useful intermediates for the preparation or purification of pharmaceutically acceptable salts 5 and/or for use in nontherapeutic, for example in vitro, applications. The term "physiologically functional derivative" used herein refers to any physiologically tolerated derivative of a compound of the invention of the formula 1, for example an ester, which on administration to a mammal such as, for example, a 10 human is able to form (directly or indirectly) a compound of the formula I or an active metabolite thereof. Physiologically functional derivatives also include prodrugs of the compounds of the invention as, for example, described in H. Okada et al., Chem. Pharm. Bull. 1994, 15 42, 57-61. Such prodrugs can be metabolized in vivo to a compound of the invention. These prodrugs may themselves be active or not. The compounds of the invention may also exist in various polymorphous forms, for example as amorphous and crystalline polymorphous forms. All polymorphous forms 20 of the compounds of the invention belong within the framework of the invention and are a further aspect of the invention. All references to "compound(s) of formula I" hereinafter refer to compound(s) of the formula I as described above, and their salts, solvates and physiologically functional 25 derivatives as described herein. Use 30 The compounds of the invention of the formula I have a surprising inhibitory effect on endothelial lipase (EL). The preferred substrate for EL is HDL, which has antiatherosclerotic activity. A reduction in the HDL level leads to progression of WO 2008/122357 16 PCT/EP2008/002314 Salts with a pharmaceutically unacceptable anion such as, for example, trifluoroacetate likewise belong within the framework of the invention as useful intermediates for the preparation or purification of pharmaceutically acceptable salts 5 and/or for use in nontherapeutic, for example in vitro, applications. The term "physiologically functional derivative" used herein refers to any physiologically tolerated derivative of a compound of the invention of the formula 1, for example an ester, which on administration to a mammal such as, for example, a 10 human is able to form (directly or indirectly) a compound of the formula I or an active metabolite thereof. Physiologically functional derivatives also include prodrugs of the compounds of the invention as, for example, described in H. Okada et al., Chem. Pharm. Bull. 1994, 5 42, 57-61. Such prodrugs can be metabolized in vivo to a compound of the invention. These prodrugs may themselves be active or not. The compounds of the invention may also exist in various polymorphous forms, for example as amorphous and crystalline polymorphous forms. All polymorphous forms 0 of the compounds of the invention belong within the framework of the invention and are a further aspect of the invention. All references to "compound(s) of formula I" hereinafter refer to compound(s) of the formula I as described above, and their salts, solvates and physiologically functional 5 derivatives as described herein. Use 0 The compounds of the invention of the formula I have a surprising inhibitory effect on endothelial lipase (EL). The preferred substrate for EL is HDL, which has antiatherosclerotic activity. A reduction in the HDL level leads to progression of WO 2008/122357 17 PCT/EP2008/002314 atherosclerosis and its sequelae such as metabolic syndrome and coronary heart disease. An inhibition of EL should thus lead to prevention of atherosclerotic disorders. 5 It has further been found that the inhibitory effect of the compounds of the invention of the formula I is selective in relation to other lipases such as, for example, hormone-sensitive lipase (HSL). The compounds of the formula I additionally show an improved solubility in aqueous 0 media with an activity which is at least as high as that of compounds of similar structures. The compounds of the invention are further distinguished by further advantageous properties such as higher metabolic stability and serum stability compared with prior art compounds. 5 Compounds of this type are particularly suitable for the treatment and/or prevention of 1. Dyslipidemias and general disorders of lipid metabolism and their sequelae such as, for example, atherosclerosis, coronary heart disease, cerebrovascular disorders etc, especially those (but not restricted thereto) which are characterized by one or more of the following factors: 0 - high plasma triglyceride concentrations, high postprandial plasma triglyceride concentrations - low HDL cholesterol concentration - low apoA lipoprotein concentrations - high LDL cholesterol concentrations 5 - small dense LDL cholesterol particles - high apoB lipoprotein concentrations 2. Various other conditions which may be associated with the metabolic syndrome, such as: 0 - obesity (excess weight), including central obesity - thromboses, hypercoagulable and prothrombotic stages (arterial and venous) WO 2008/122357 18 PCT/EP2008/002314 - high blood pressure - heart failure such as, for example (but not restricted thereto), following myocardial infarction, hypertensive heart disease or cardiomyopathy - diabetes mellitus, especially type 2 diabetes, including the prevention of the 5 sequelae associated therewith (hyperglycemia, glucose intolerance, loss of the pancreatic B cells, macro- and microvascular disorders 3. Other disorders or conditions in which inflammatory reactions or cell differentiation is for example involved are: 10 - atherosclerosis such as, for example (but not restricted thereto), coronary sclerosis including angina pectoris or myocardial infarction, stroke - vascular restenosis or reocclusion - chronic inflammatory bowel diseases such as, for example, Crohn's disease and ulcerative colitis 15 - pancreatitis - other inflammatory states - retinopathy - adipose cell tumors - adipose cell carcinomas such as, for example, liposarcomas 20 - solid tumors and neoplasms such as, for example (but not restricted thereto), carcinomas of the gastrointestinal tract, of the liver, of the biliary tract and of the pancreas, endocrine tumors, carcinomas of the lungs, of the kidneys and the urinary tract, of the genital tract, prostate carcinomas etc - acute and chronic myeloproliferative disorders and lymphomas 25 - angiogenesis - neurodegenerative disorders - Alzheimer's disease - multiple sclerosis - Parkinson's disease 30 - erythemato-squamous dermatoses such as, for example, psoriasis - acne vulgaris WO 2008/122357 19 PCT/EP2008/002314 - other skin disorders and dermatological conditions which are modulated by PPAR - eczemas and neurodermatitis - dermatitis such as, for example, seborrheic dermatitis or photodermatitis 5 - keratitis and keratoses such as, for example, seborrheic keratoses, senile keratoses, actinic keratosis, photo-induced keratoses or keratosis follicularis - keloids and keloid prophylaxis - warts, including condylomata or condylomata acuminata - human papilloma viral (HPV) infections such as, for example, venereal 10 papillomata, viral warts such as, for example, molluscum contagiosum, leukoplakia - papular dermatoses such as, for example, lichen planus - skin cancer such as, for example, basal-cell carcinomas, melanomas or cutaneous T-cell lymphomas 15 - localized benign epidermal tumors such as, for example, keratoderma, epidermal naevi - chilblains - high blood pressure - syndrome X 20 - polycystic ovary syndrome (PCOS) - asthma - osteoarthritis - lupus erythematosus (LE) or inflammatory rheumatic disorders such as, for example, rheumatoid arthritis 25 - vasculitis - wasting (cachexia) - gout - ischemia/reperfusion syndrome - acute respiratory distress syndrome (ARDS) 30 WO 2008/122357 20 PCT/EP2008/002314 Formulations The amount of a compound of the invention necessary to achieve the desired biological effect depends on a number of factors, for example the specific compound 5 chosen, the intended use, the mode of administration and the clinical condition of the patient. The daily dose is generally in the range from 0.3 mg to 100 mg (typically from 3 mg to 50 mg) per day and per kilogram of bodyweight, for example 3-10 mg/kg/day. An intravenous dose may be, for example, in the range from 0.3 mg to 1.0 mg/kg, which can suitably be administered as infusion of 10 ng to 100 ng per 10 kilogram and per minute. Suitable infusion solutions for these purposes may contain, for example, from 0.1 ng to 10 mg, typically from 1 ng to 10 mg, per milliliter. Single doses may contain, for example, from 1 mg to 10 g of the active ingredient. Thus, ampoules for injections may contain, for example, from 1 mg to 100 mg, and single dose formulations which can be administered orally, such as, for example, tablets or 15 capsules, may contain, for example, from 0.05 to 1000 mg, typically from 0.5 to 600 mg. For the therapy of the abovementioned conditions, the compounds of formula I may be used as the compound itself, but they are preferably in the form of a pharmaceutical composition with an acceptable carrier. The carrier must, of course, be acceptable in the sense that it is compatible with the other ingredients of 20 the composition and is not harmful for the patient's health. The carrier may be a solid or a liquid or both and is preferably formulated with the compound as a single dose, for example as a tablet, which may contain from 0.05% to 95% by weight of the active ingredient. Other pharmaceutically active substances may likewise be present, including other compounds of the invention. The pharmaceutical compositions of the 25 invention can be produced by one of the known pharmaceutical methods, which essentially consist of mixing the ingredients with pharmacologically acceptable carriers and/or excipients. Pharmaceutical compositions of the invention are those suitable for oral, rectal, 30 topical, peroral (for example sublingual) and parenteral (for example subcutaneous, intramuscular, intradermal or intravenous) administration, although the most suitable mode of administration depends in each individual case on the nature and severity of WO 2008/122357 21 PCT/EP2008/002314 the condition to be treated and on the nature of the compound of formula I used in each case. Coated formulations and coated slow-release formulations also belong within the framework of the invention. Preference is given to acid- and gastric juice resistant formulations. Suitable coatings resistant to gastric juice comprise cellulose 5 acetate phthalate, polyvinyl acetate phthalate, hydroxypropylmethylcellulose phthalate and anionic polymers of methacrylic acid and methyl methacrylate. Suitable pharmaceutical preparations for oral administration may be in the form of separate units such as, for example, capsules, cachets, suckable tablets or tablets, 10 each of which contain a defined amount of the compound of formula I; as powders or granules; as solution or suspension in an aqueous or nonaqueous liquid; or as an oil in-water or water-in-oil emulsion. These compositions may, as already mentioned, be prepared by any suitable pharmaceutical method which includes a step in which the active ingredient and the carrier (which may consist of one or more additional 15 ingredients) are brought into contact. The compositions are generally produced by uniform and homogeneous mixing of the active ingredient with a liquid and/or finely divided solid carrier, after which the product is shaped if necessary. Thus, for example, a tablet can be produced by compressing or molding a powder or granules of the compound, where appropriate with one or more additional ingredients. 20 Compressed tablets can be produced by tableting the compound in free-flowing form such as, for example, a powder or granules, where appropriate mixed with a binder, glidant, inert diluent and/or one (or more) surface-active/dispersing agent(s) in a suitable machine. Molded tablets can be produced by molding the compound, which is in powder form and is moistened with an inert liquid diluent, in a suitable machine. 25 Pharmaceutical compositions which are suitable for peroral (sublingual) administration comprise suckable tablets which contain a compound of formula I with a flavoring, normally sucrose and gum arabic or tragacanth, and pastilles which comprise the compound in an inert base such as gelatin and glycerol or sucrose and 30 gum arabic. Pharmaceutical compositions suitable for parenteral administration comprise WO 2008/122357 22 PCT/EP2008/002314 preferably sterile aqueous preparations of a compound of formula I, which are preferably isotonic with the blood of the intended recipient. These preparations are preferably administered intravenously, although administration may also take place by subcutaneous, intramuscular or intradermal injection. These preparations can 5 preferably be produced by mixing the compound with water and making the resulting solution sterile and isotonic with blood. Injectable compositions of the invention generally contain from 0.1 to 5% by weight of the active compound. Pharmaceutical compositions suitable for rectal administration are preferably in the 10 form of single-dose suppositories. These can be produced by mixing a compound of the formula I with one or more conventional solid carriers, for example cocoa butter, and shaping the resulting mixture. Pharmaceutical compositions suitable for topical use on the skin are preferably in the 15 form of ointment, cream, lotion, paste, spray, aerosol or oil. Carriers which can be used are petrolatum, lanolin, polyethylene glycols, alcohols and combinations of two or more of these substances. The active ingredient is generally present in a concentration of from 0.1 to 15% by weight of the composition, for example from 0.5 to 2%. 20 Transdermal administration is also possible. Pharmaceutical compositions suitable for transdermal uses can be in the form of single patches which are suitable for long term close contact with the patient's epidermis. Such patches suitably contain the active ingredient in an aqueous solution which is buffered where appropriate, 25 dissolved and/or dispersed in an adhesive or dispersed in a polymer. A suitable active ingredient concentration is about 1 % to 35%, preferably about 3% to 15%. A particular possibility is for the active ingredient to be released by electrotransport or iontophoresis as described, for example, in Pharmaceutical Research, 2(6): 318 (1986). 30 The compounds of the formula I are distinguished by favorable effects on metabolic disorders. They beneficially influence lipid and sugar metabolism, in particular they WO 2008/122357 23 PCT/EP2008/002314 lower the triglyceride level and are suitable for the prevention and treatment of type Il diabetes and arteriosclerosis and the diverse sequelae thereof. Combinations with other medicaments 5 The compounds of the invention can be administered alone or in combination with one or more further pharmacologically active ingredients. In particular the compounds of the invention can be administered with active ingredients, which have a similar pharmacological effect to themselves. For example, they can be 10 administered in combination with active ingredients which have favorable effects on metabolic disturbances or disorders frequently associated therewith.. Examples of such medicaments are 1. medicaments which lower blood glucose, antidiabetics, 15 2. active ingredients for the treatment of dyslipidemias, 3. antiatherosclerotic medicaments, 4. antiobesity agents, 5. antiinflammatory active ingredients 6. active ingredients for the treatment of malignant tumors 20 7. antithrombotic active ingredients 8. active ingredients for the treatment of high blood pressure 9. active ingredients for the treatment of heart failure and 10. active ingredients for the treatment and/or prevention of complications caused by diabetes or associated with diabetes. 25 11. active ingredients for the treatment of neurodegenerative diseases 12. active ingredients for the treatment of diseases of the central nervous system 13. active ingredients for the treatment of dependence on drugs, nicotine and alcohol 14. analgesics 30 They can be combined with the compounds of the invention of the formula I in particular for a synergistic improvement in the effect. Administration of the active WO 2008/122357 24 PCT/EP2008/002314 ingredient combination can take place either by separate administration of the active ingredients to the patient or in the form of combination products in which a plurality of active ingredients are present in one pharmaceutical preparation. 5 Further active ingredients particularly suitable for the combination products are: All antidiabetics which are mentioned in the Rote Liste 2006, chapter 12; all weight reducing agents/appetite suppressants which are mentioned in the Rote Liste 2006, chapter 1; all lipid-lowering agents which are mentioned in the Rote Liste 2006, chapter 58. They can be combined with the compound of the invention of the formula 10 I in particular for a synergistic improvement in the effect. Administration of the active ingredient combination can take place either by separate administration of the active ingredients to the patient or in the form of combination products in which a plurality of active ingredients are present in one pharmaceutical preparation. Most of the active ingredients mentioned hereinafter are disclosed in the USP Dictionary of USAN and 15 International Drug Names, US Pharmacopeia, Rockville 2001. Antidiabetics include insulin and insulin derivatives such as, for example, Lantus* (see www.lantus.com) or Apidra* or those described in WO 2005005477 (Novo Nordisk), fast-acting insulins (see US 6,221,633), inhalable insulins such as, for example, Exubera * or oral insulins such as, for example, IN-105 (Nobex) or Oral 20 lynTm (Generex Biotechnology), GLP-1 -derivatives such as, for example, exenatide, liraglutide or those which have been disclosed in WO 98/08871 or WO 2005/027978 of Novo Nordisk A/S, in WO 01/04156 of Zealand or in WO 00/34331 of Beaufour Ipsen, Pramlintide Acetate (Symlin; Amylin Pharmaceuticals), and orally effective hypoglycemic active ingredients. 25 The active ingredients include preferably sulfonylureas, biguanides, meglitinides, oxadiazolidinediones, 30 thiazolidinediones, WO 2008/122357 25 PCT/EP2008/002314 glucosidase inhibitors, inhibitors of glycogen phosphorylase, glucagon antagonists, glucokinase activators, 5 inhibitors of fructose-1,6-bisphosphatase, modulators of glucose transporter 4 (GLUT4), inhibitors of glutamine-fructose-6-phosphate amidotransferase (GFAT), GLP-1 agonists, potassium channel openers such as, for example, those which have been disclosed 10 in WO 97/26265 and WO 99/03861 of Novo Nordisk A/S, inhibitors of dipeptidylpeptidase IV (DPP-IV), insulin sensitizers, inhibitors of liver enzymes involved in stimulating gluconeogenesis and/or glycogenolysis, 15 modulators of glucose uptake, of glucose transport and of glucose reabsorption, inhibitors of 11 B-HSD1, inhibitors of protein tyrosine phosphatase 1 B (PTP1 B), modulators of the sodium-dependent glucose transporter 1 or 2 (SGLT1, SGLT2), compounds which alter lipid metabolism such as antihyperlipidemic active 20 ingredients and antilipidemic active ingredients, compounds which reduce food intake, compounds which increase thermogenesis, PPAR and RXR modulators and active ingredients which act on the ATP-dependent potassium channel of the beta 5 cells. In one embodiment of the invention, the compound of the formula I is administered in combination with an HMGCoA reductase inhibitor such as simvastatin, fluvastatin, pravastatin, lovastatin, atorvastatin, cerivastatin, rosuvastatin or L-659699. 30 In one embodiment of the invention, the compound of the formula I is administered in combination with a cholesterol absorption inhibitor such as, for example, ezetimibe, WO 2008/122357 26 PCT/EP2008/002314 tiqueside, pamaqueside, FM-VP4 (sitostanol/campesterol ascorbyl phosphate; Forbes Medi-Tech, WO 2005042692), MD-0727 (Microbia Inc., WO 2005021497) or with compounds as described in WO 2002066464 (Kotobuki Pharmaceutical Co. Ltd.), WO 2005062824 (Merck & Co.) or WO 2005061451 and WO 2005061452 5 (AstraZeneca AB). In one embodiment of the invention, the compound of the formula I is administered in combination with a PPAR gamma agonist such as, for example, rosiglitazone, pioglitazone, JTT-501, GI 262570, R-483 or CS-011 (rivoglitazone). 10 In one embodiment of the invention, the compound of the formula I is administered in combination with a PPAR alpha agonist such as, for example, GW9578, GW-590735, K-111, LY-674, KRP-101 or DRF-10945. 15 In one embodiment of the invention, the compound of the formula I is administered in combination with a mixed PPAR alpha/gamma agonist such as, for example, muraglitazar, tesaglitazar, naveglitazar, LY-510929, ONO-5129, E-3030 or as described in WO 00/64888, WO 00/64876, WO 03/020269, WO 2004075891, WO 2004076402, WO 2004075815, WO 2004076447, WO 2004076428, 20 WO 2004076401, WO 2004076426, WO 2004076427, WO 2006018118, WO 2006018115, and WO 2006018116 or in J.P. Berger et al., TRENDS in Pharmacological Sciences 28(5), 244-251, 2005. In one embodiment of the invention, the compound of the formula I is administered in 25 combination with a PPAR delta agonist such as, for example, GW-501516, or as described in WO 2005097762, WO 2005097786, WO 2005097763, WO 2006029699. In one embodiment of the invention, the compound of the formula I is administered in combination with metaglidasen or with MBX-2044 or other partial PPAR gamma 30 agonists/antagonists. In one embodiment of the invention, the compound of the formula I is administered in WO 2008/122357 27 PCT/EP2008/002314 combination with a fibrate such as, for example, fenofibrate, clofibrate or bezafibrate. In one embodiment of the invention, the compound of the formula I is administered in combination with an MTP inhibitor such as, for example, implitapide, BMS-201038, 5 R-1 03757 or those described in WO 2005085226. In one embodiment of the invention, the compound of the formula I is administered in combination with a CETP inhibitor such as, for example, torcetrapib or JTT-705. 10 In one embodiment of the invention, the compound of the formula I is administered in combination with a bile acid absorption inhibitor (see, for example, US 6,245,744, US 6,221,897 or WO 00/61568), such as, for example, HMR 1741 or those as described in DE 10 2005 033099.1 and DE 10 2005 033100.9. 15 In one embodiment of the invention, the compound of the formula I is administered in combination with a polymeric bile acid adsorbent such as, for example, cholestyramine or colesevelam. In one embodiment of the invention, the compound of the formula I is administered in 20 combination with an LDL receptor inducer (see US 6,342,512), such as, for example, HMR1 171, HMR1 586 or those as described in WO 2005097738. In one embodiment, the compound of the formula I is administered in combination with Omacor@ (Omega-3 fatty acids; highly concentrated ethyl esters of 25 eicosapentaenoic acid and of docosahexaenoic acid). In one embodiment of the invention, the compound of the formula I is administered in combination with an ACAT inhibitor such as, for example, avasimibe. 30 In one embodiment of the invention, the compound of the formula I is administered in combination with an antioxidant such as, for example, OPC-14117, probucol, tocopherol, ascorbic acid, R-carotene or selenium. WO 2008/122357 28 PCT/EP2008/002314 In one embodiment of the invention, the compound of the formula I is administered in combination with a vitamin such as, for example, vitamin B6 or vitamin B12. 5 In one embodiment of the invention, the compound of the formula I is administered in combination with a lipoprotein lipase modulator such as, for example, ibrolipim (NO 1886). In one embodiment of the invention, the compound of the formula I is administered in 10 combination with an ATP citrate lyase inhibitor such as, for example, SB-204990. In one embodiment of the invention, the compound of the formula I is administered in combination with a squalene synthetase inhibitor such as, for example, BMS-188494 or as described in WO 2005077907. 15 In one embodiment of the invention, the compound of the formula I is administered in combination with a lipoprotein(a) antagonist such as, for example, gemcabene (Cl 1027). 20 In one embodiment of the invention, the compound of the formula I is administered in combination with an HM74A receptor agonist such as, for example, nicotinic acid. In one embodiment of the invention, the compound of the formula I is administered in combination with a lipase inhibitor such as, for example, orlistat or cetilistat (ATL 25 962). In one embodiment of the invention, the compound of the formula I is administered in combination with insulin. In one embodiment of the invention, the compound of the formula I is administered in 30 combination with a sulfonylurea such as, for example, tolbutamide, glibenclamide, glipizide or glimepiride. WO 2008/122357 29 PCT/EP2008/002314 In one embodiment of the invention, the compound of the formula I is administered in combination with a biguanide such as, for example, metformin. In another embodiment of the invention, the compound of the formula I is 5 administered in combination with a meglitinide such as, for example, repaglinide or nateglinide. In one embodiment of the invention, the compound of the formula I is administered in combination with a thiazolidinedione such as, for example, troglitazone, ciglitazone, pioglitazone, rosiglitazone or the compounds disclosed in WO 97/41097 of 10 Dr. Reddy's Research Foundation, in particular 5-[[4-[(3,4-dihydro-3-methyl-4-oxo-2 quinazolinylmethoxy]phenyl]methyl]-2,4-thiazolidinedione. In one embodiment of the invention, the compound of the formula I is administered in combination with an a-glucosidase inhibitor such as, for example, miglitol or acarbose. 15 In one embodiment of the invention, the compound of the formula I is administered in combination with an active ingredient which acts on the ATP-dependent potassium channel of the beta cells, such as, for example, tolbutamide, glibenclamide, glipizide, glimepiride or repaglinide. In one embodiment of the invention, the compound of the formula I is administered in 20 combination with more than one of the aforementioned compounds, e.g. in combination with a sulfonylurea and metformin, a sulfonylurea and acarbose, repaglinide and metformin, insulin and a sulfonylurea, insulin and metformin, insulin and troglitazone, insulin and lovastatin, etc. 25 In one embodiment of the invention, the compound of the formula I is administered in combination with an inhibitor of glycogen phosphorylase, such as, for example, PSN 357 or FR-258900 or those as described in WO 2003084922, WO 2004007455, WO 2005073229-31 or WO 2005067932. WO 2008/122357 30 PCT/EP2008/002314 In one embodiment of the invention, the compound of the formula I is administered in combination with glucagon receptor antagonists such as, for example, A-770077, NNC-25-2504 or as described in WO 2004100875 or WO 2005065680. 5 In one embodiment of the invention, the compound of the formula I is administered in combination with activators of glucokinase, such as, for example, RO-4389620, LY-2121260 (WO 2004063179), PSN-105, PSN-1 10, GKA-50 or those as are described for example by Prosidion in WO 2004072031, WO 2004072066, WO 05103021 or WO 06016178, by Roche in WO 00058293, WO 00183465, 10 WO 00183478, WO 00185706, WO 00185707, WO 01044216, GB 02385328, WO 02008209, WO 02014312, WO 0246173, WO 0248106, DE 10259786, WO 03095438, US 04067939 or WO 04052869, by Novo Nordisk in EP 1532980, WO 03055482, WO 04002481, WO 05049019, WO 05066145 or WO 05123132, by Merck/Banyu in WO 03080585, WO 03097824, WO 04081001, WO 05063738 or 15 WO 05090332, by Eli Lilly in WO 04063194, or by Astra Zeneca in WO 01020327, WO 03000262, WO 03000267, WO 03015774, WO 04045614, WO 04046139, WO 05044801, WO 05054200, WO 05054233, WO 05056530, WO 05080359, WO 05080360 or WO 05121110. 20 In one embodiment of the invention, the compound of the formula I is administered in combination with an inhibitor of gluconeogenesis, such as, for example, FR-225654. In one embodiment of the invention, the compound of the formula I is administered in combination with inhibitors of fructose- 1,6-bisphosphatase (FBPase), such as, for 25 example, CS-917. In one embodiment of the invention, the compound of the formula I is administered in combination with modulators of glucose transporter 4 (GLUT4), such as, for example, KST-48 (D.-0. Lee et al.: Arzneim.-Forsch. Drug Res. 54 (12), 835 (2004)). 30 In one embodiment of the invention, the compound of the formula I is administered in combination with inhibitors of glutamine-fructose-6-phosphate amidotransferase WO 2008/122357 31 PCT/EP2008/002314 (GFAT), as are described for example in WO 2004101528. In one embodiment of the invention, the compound of the formula I is administered in combination with inhibitors of dipeptidylpeptidase IV (DPP-IV), such as, for example, 5 vildagliptin (LAF-237), sitagliptin (MK-0431), saxagliptin (BMS-477118), GSK 823093, PSN-9301, SYR-322, SYR-619, TA-6666, TS-021, GRC-8200, GW 825964X or as are described in WO 2003074500, WO 2003106456, WO 200450658, WO 2005058901, WO 2005012312, WO 2005/012308, PCT/EP2005/007821, PCT/EP2005/008005, PCT/EP2005/008002, 10 PCT/EP2005/008004, PCT/EP2005/008283, DE 10 2005 012874.2 or DE 10 2005 012873.4. In one embodiment of the invention, the compound of the formula I is administered in combination with inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 (11R-HSD1), 15 such as, for example, BVT-2733 or those as are described for example in WO 200190090-94, WO 200343999, WO 2004112782, WO 200344000, WO 200344009, WO 2004112779, WO 2004113310, WO 2004103980, WO 2004112784, WO 2003065983, WO 2003104207, WO 2003104208, WO 2004106294, WO 2004011410, WO 2004033427, WO 2004041264, WO 2004037251, 20 WO 2004056744, WO 2004065351, WO 2004089367, WO 2004089380, WO 2004089470-71, WO 2004089896, WO 2005016877 or WO 2005097759. In one embodiment of the invention, the compound of the formula I is administered in combination with inhibitors of protein tyrosine phosphatase 1 B (PTP1 B), as are 25 described for example in WO 200119830-31, WO 200117516, WO 2004506446, WO 2005012295, PCT/EP2005/005311, PCT/EP2005/005321, PCT/EP2005/007151, PCT/EP2005/01294 or DE 10 2004 060542.4. In one embodiment of the invention, the compound of the formula I is administered in 30 combination with modulators of the sodium-dependent glucose transporter 1 or 2 (SGLT1, SGLT2), such as, for example, KGA-2727, T-1095 and SGL-0010 or as are described for example in WO 2004007517, WO 200452903, WO 200452902, WO 2008/122357 32 PCT/EP2008/002314 WO 2005121161, WO 2005085237, JP2004359630 or by A. L. Handlon in Expert Opin. Ther. Patents (2005) 15(11), 1531-1540. In one embodiment of the invention, the compound of the formula I is administered in 5 combination with inhibitors of hormone-sensitive lipase (HSL) as described for example in WO 01/17981, WO 01/66531, WO 2004035550, WO 2005073199 or WO 03/051842. In one embodiment of the invention, the compound of the formula I is administered in 10 combination with inhibitors of acetyl-CoA carboxylase (ACC), such as, for example, those as described in WO 199946262, WO 200372197, WO 2003072197 or WO 2005044814. In one embodiment of the invention, the compound of the formula I is administered in 15 combination with an inhibitor of phosphoenolpyruvate carboxykinase (PEPCK), such as, for example, those as described in WO 2004074288. In one embodiment of the invention, the compound of the formula I is administered in combination with an inhibitor of glycogen synthase kinase 3 beta (GSK-3 beta), as 20 described for example in US2005222220, WO 2004046117, WO 2005085230, WO 2005111018, WO 2003078403, WO 2004022544, WO 2003106410, WO 2005058908, US2005038023, WO 2005009997, US2005026984, WO 2005000836, WO 2004106343, EP1460075, WO 2004014910, WO 2003076442, WO 2005087727 or WO 2004046117. 25 In one embodiment of the invention, the compound of the formula I is administered in combination with an inhibitor of protein kinase C beta (PKC beta), such as, for example, ruboxistaurin. 30 In one embodiment of the invention, the compound of the formula I is administered in combination with an endothelin A receptor antagonist such as, for example, avosentan (SPP-301). WO 2008/122357 33 PCT/EP2008/002314 In one embodiment of the invention, the compound of the formula I is administered in combination with inhibitors of "I-kappaB kinase" (IKK inhibitors), as are described for example in WO 2001000610, WO 2001030774, WO 2004022553 or 5 WO 2005097129. In one embodiment of the invention, the compound of the formula I is administered in combination with modulators of the glucocorticoid receptor, like those described for example in WO 2005090336. 10 In a further embodiment of the invention, the compound of the formula I is administered in combination with CART modulators (see "Cocaine-amphetamine regulated transcript influences energy metabolism, anxiety and gastric emptying in mice" Asakawa, A. et al.: Hormone and Metabolic Research (2001), 33(9), 554-558); 15 NPY antagonists such as, for example, naphthalene-1-sulfonic acid {4-[(4-amino quinazolin-2-ylamino)methyl]cyclohexylmethyl}amide hydrochloride (CGP 71683A); peptide YY 3-36 (PYY3-36) or analogous compounds, such as, for example, CJC 1682 (PYY3-36 conjugated with human serum albumin via Cys34), CJC-1643 (derivative of PYY3-36 which conjugates in vivo to serum albumin) or those as are 20 described in WO 2005080424; cannabinoid receptor 1 antagonists such as, for example, rimonabant, SR147778 or those as are described for example in EP 0656354, WO 00/15609, WO 02/076949, WO 2005080345, WO 2005080328, WO 2005080343, WO 2005075450, WO 2005080357, WO 200170700, WO 2003026647-48, WO 200302776, 5 WO 2003040107, WO 2003007887, WO 2003027069, US6,509,367, WO 200132663, WO 2003086288, WO 2003087037, WO 2004048317, WO 2004058145, WO 2003084930, WO 2003084943, WO 2004058744, WO 2004013120, WO 2004029204, WO 2004035566, WO 2004058249, WO 2004058255, WO 2004058727, WO 2004069838, US20040214837, 0 US20040214855, US20040214856, WO 2004096209, WO 2004096763, WO 2004096794, WO 2005000809, WO 2004099157, US20040266845, WO 2004110453, WO 2004108728, WO 2004000817, WO 2005000820, WO 2008/122357 34 PCT/EP2008/002314 US20050009870, WO 200500974, WO 2004111033-34, WO 200411038-39, WO 2005016286, WO 2005007111, WO 2005007628, US20050054679, WO 2005027837, WO 2005028456, WO 2005063761-62, WO 2005061509 or WO 2005077897; 5 MC4 agonists (e.g. 1-amino- 1,2,3,4-tetrahydronaphthalene-2-carboxylic acid [2-(3a benzyl-2-methyl-3-oxo-2,3,3a,4,6,7-hexahydropyrazolo[4,3-c]pyridin-5-yl)-1-(4 chlorophenyl)-2-oxoethyl]amide; (WO 01/91752)) or LB53280, LB53279, LB53278 or THIQ, MB243, RY764, CHIR-785, PT-141 or those that are described in WO 2005060985, WO 2005009950, WO 2004087159, WO 2004078717, 10 WO 2004078716, WO 2004024720, US20050124652, WO 2005051391, WO 2004112793, WOUS20050222014, US20050176728, US20050164914, US20050124636, US20050130988, US20040167201, WO 2004005324, WO 2004037797, WO 2005042516, WO 2005040109, WO 2005030797, US20040224901, WO 200501921, WO 200509184, WO 2005000339, EP1460069, 15 WO 2005047253, WO 2005047251, EP1538159, WO 2004072076, WO 2004072077 or WO 2006024390; orexin receptor antagonists (e.g. 1 -(2-methylbenzoxazol-6-yl)-3-[1,5]naphthyrid in-4 ylurea hydrochloride (SB-334867-A) or those as are described for example in WO 200196302, WO 200185693, WO 2004085403 or WO 2005075458); 20 histamine H3 receptor agonists (e.g. 3-cyclohexyl-1-(4,4-dimethyl-1, 4,6,7-tetrahydro imidazo[4,5-c]pyridin-5-yl)propan-1-one oxalic acid salt (WO 00/63208) or those as are described in WO 200064884, WO 2005082893); CRF antagonists (e.g. [2-methyl-9-(2,4,6-trimethylphenyl)-9H-1,3,9-triazafluoren-4 yl]dipropylamine (WO 00/66585)); 25 CRF BP antagonists (e.g. urocortin); urocortin agonists; p3 agonists (such as, for example, 1-(4-chloro-3-methanesulfonylmethylphenyl)-2-[2 (2,3-dimethyl-1H-indol-6-yloxy)ethylamino]ethanol hydrochloride (WO 01/83451)); MSH (melanocyte-stimulating hormone) agonists; 30 MCH (melanin-concentrating hormone) receptor antagonists (such as, for example, NBI-845, A-761, A-665798, A-798, ATC-0175, T-226296, T-71, GW-803430 or compounds such as are described in WO 2003/15769, WO 2005085200, WO 2008/122357 35 PCT/EP2008/002314 WO 2005019240, WO 2004011438, WO 2004012648, WO 2003015769, WO 2004072025, WO 2005070898, WO 2005070925, WO 2006018280, WO 2006018279, WO 2004039780, WO 2003033476, WO 2002006245, WO 2002002744, WO 2003004027 or FR2868780); 5 CCK-A agonists (such as, for example, {2-[4-(4-chloro-2,5-dimethoxyphenyl)-5-(2 cyclohexylethyl)thiazol-2-ylcarbamoyl]-5,7-dimethylindol-1-yl}acetic acid trifluoroacetic acid salt (WO 99/15525), SR-146131 (WO 0244150) or SSR-125180); serotonin reuptake inhibitors (e.g. dexfenfluramine); mixed serotoninergic and noradrenergic compounds (e.g. WO 00/71549); 10 5-HT receptor agonists, e.g. 1-(3-ethylbenzofuran-7-yl)piperazine oxalic acid salt (WO 01/09111); 5-HT2C receptor agonists (such as, for example, APD-356, BVT-933 or those as are described in WO 200077010, WO 20077001-02, WO 2005019180, WO 2003064423, WO 200242304 or WO 2005082859); 15 5-HT6 receptor antagonists as are described for example in WO 2005058858; bombesin receptor agonists (BRS-3 agonists); galanin receptor antagonists; growth hormone (e.g. human growth hormone or AOD-9604); growth hormone releasing compounds (tertiary butyl 6-benzyloxy-1-(2-diisopropyl 20 aminoethylcarbamoyl)-3,4-dihydro-1 H-isoquinoline-2-carboxylate (WO 01/85695)); growth hormone secretagogue receptor antagonists (ghrelin antagonists) such as, for example, A-778193 or those as are described in WO 2005030734; TRH agonists (see, for example, EP 0 462 884); uncoupling protein 2 or 3 modulators; 25 leptin agonists (see, for example, Lee, Daniel W.; Leinung, Matthew C.; Rozhavskaya-Arena, Marina; Grasso, Patricia. Leptin agonists as a potential approach to the treatment of obesity. Drugs of the Future (2001), 26(9), 873-881); DA agonists (bromocriptine or Doprexin); lipase/amylase inhibitors (like those described for example in WO 00/40569); 30 inhibitors of diacylglycerol 0-acyltransferases (DGATs) as described for example in US2004/0224997, WO 2004094618, WO 200058491, WO 2005044250, WO 2005072740, JP2005206492 or WO 2005013907; WO 2008/122357 36 PCT/EP2008/002314 inhibitors of fatty acid synthase (FAS) such as, for example, C75 or those as described in WO 2004005277; oxyntomodulin; oleoyl-estrone 5 or thyroid hormone receptor agonists such as, for example: KB-2115 or those as described in WO 20058279, WO 200172692, WO 200194293, WO 2003084915, WO 2004018421 or WO 2005092316. 10 In one embodiment of the invention, the further active ingredient is leptin; see, for example, "Perspectives in the therapeutic use of leptin", Salvador, Javier; Gomez Ambrosi, Javier; Fruhbeck, Gema, Expert Opinion on Pharmacotherapy (2001), 2(10), 1615-1622. 15 In one embodiment of the invention, the further active ingredient is dexamphetamine or amphetamine. In one embodiment of the invention, the further active ingredient is fenfluramine or dexfenfluramine. In another embodiment of the invention, the further active ingredient is sibutramine. 20 In one embodiment of the invention, the further active ingredient is mazindole or phentermine. In one embodiment of the invention, the compound of the formula I is administered in combination with bulking agents, preferably insoluble bulking agents (see, for 25 example, Carob/Caromax@ (Zunft H J; et al., Carob pulp preparation for treatment of hypercholesterolemia, ADVANCES IN THERAPY (2001 Sep-Oct), 18(5), 230-6)). Caromax is a carob-containing product from Nutrinova, Nutrition Specialties & Food Ingredients GmbH, Industriepark Hoechst, 65926 Frankfurt/Main. Combination with Caromax@ is possible in one preparation or by separate administration of WO 2008/122357 37 PCT/EP2008/002314 compounds of the formula I and Caromax@. Caromax@ can in this connection also be administered in the form of food products such as, for example, in bakery products or muesli bars. 5 In one embodiment of the invention, the compound of the formula I is administered in combination with PDE inhibitors (phosphodiesterase), like those described for example in WO 2003/077949 or WO 2005012485. In one embodiment of the invention, the compound of the formula I is administered in 10 combination with NAR-1 (nicotinic acid receptor) agonists like those described for example in WO 2004094429. In one embodiment of the invention, the compound of the formula I is administered in combination with CB2 (cannabinoid receptor) agonists like those described for 15 example in US2005/143448. In one embodiment of the invention, the compound of the formula I is administered in combination with histamine 1 agonists like those described for example in WO 2005101979. 20 In one embodiment of the invention, the compound of the formula I is administered in combination with bupropion as described in WO 2006017504. In one embodiment of the invention, the compound of the formula I is administered in 25 combination with opioid antagonists like those described for example in WO 2005107806 or WO 2004094429. In one embodiment of the invention, the compound of the formula I is administered in combination with neutral endopeptidase inhibitors like those described for example in 0 WO 200202513, WO 2002/06492, WO 2002040008, WO 2002040022 or WO 2002047670. WO 2008/122357 38 PCT/EP2008/002314 In one embodiment of the invention, the compound of the formula I is administered in combination with NPY inhibitors (neuropeptide Y) like those described for example in WO 2002047670. 5 In one embodiment of the invention, the compound of the formula I is administered in combination with sodium/hydrogen exchange inhibitors like those described for example in WO 2003092694. In one embodiment of the invention, the compound of the formula I is administered in 10 combination with modulators of the glucocorticoid receptor like those described for example in WO 2005090336. In one embodiment of the invention, the compound of the formula I is administered in combination with nicotine receptor agonists like those described for example in 15 WO 2004094429. In one embodiment of the invention, the compound of the formula I is administered in combination with NRIs (norepinephrine reuptake inhibitors) like those described for example in WO 2002053140. 20 In one embodiment of the invention, the compound of the formula I is administered in combination with MOA (E-beta-methoxyacrylate) such as, for example, segeline or like those described for example in WO 2002053140. 25 In one embodiment of the invention, the compound of the formula I is administered in combination with antithrombotic active ingredients such as, for example, clopidrogel. It will be appreciated that every suitable combination of the compounds of the invention with one or more of the aforementioned compounds and optionally one or 30 more other pharmacologically active substances is regarded as falling within the protection conferred by the present invention. WO 2008/122357 39 PCT/EP2008/002314 Some of the formulae for the development codes mentioned above are detailed hereinafter. WO 2008/122357 40 PCT/EP2008/0023 14 R CH,; CH-CH, "-H aH .- ,N 0 H 0 0~%- 0 0 No Na M-P JTT-501 o CH, OHN H N N 0 -N N~ S G262570 cs-oii1 Rivoglitazone HO S S NNNC H iOH GW-9578 cI 0-1 0 N 'N N -F ~N .H4 0 OH0 0 5LY-674 KRP-101 0 O0- OH F F 0 -0 HO Or> F "- N LY-51 0929 GW-501516 cI F F F - S 'Y"0 0 FX~N 0 NIY N ".. BMS-201038 R-103757N ' BMS-21 03 WO 2008/1 22357 41 PCT/EP2008/002314 H 3 C H 3 H 3 C CCH 3 (I), H H HN K) N OPC-14117 JTT-705 Br H 0 __/,CH, 0 N0 CHI CI ' - O SB-204990 HO NO0-1886 0 INH , H C ' C H 3 0 0 0 OH O XCH- 3 OH 0 CFI 0l HCO0 CH 3 3 C3 BMS-189494 H3 H 3 C0 CH 3 0 CI-1027 0, = HOIDN, HO,,O 0 00 ~O 0 OH ATL-962 FR-258900 0 N 0 N0 HO ~ N HO N' NNC-25-2504 N H , LY-2121260 5 - 0 0 OH 0 OH OH N N" -N HO, N IH GKA-50 o o OH H 0 H ON.~ oA 0 FR-225654 WO 2008/1 22357 42 PCT/EP2008/002314 cI-- 0'H HH 0N KST-48 /l CII0 HO BMS-4771 18 N N H-Cl Q 0 '- NS HO7 05;O OH H H I BVT-2733 HO ,OH NT.105 H N,, 0 HN 0 N N I kI 0'N s NN 010 SPP-301 THQCI HNI oHN~ 0 HN &0 N N N H 0 NH0 N N H F F A, 1 0N NN N 0 F H NH1 I a H 0 ' N r 0 5 CHIR-785 A-761 WO 2008/1 22357 43 PCT/EP2008/002314 N H NN NH Na N H 0 0'F N A-665798 Fe 0 0 ATC-0 175 0 011N N N H F'O T-226296 0 0 NH 2 H N OKN H:J Z .A 2 H Ni-PH r l 0 SH 0 NH N HNH 2 HS0T H'l H HN0 HO ;Ho HO 0 CI 004 14 GW-803430 HO NAOD-9604 Cl 5-11 NH A-778193 N OH H 2 N N 00' 7 0 H 0 5 OleoyI-estrone 00 HO Cl OH KB-2115 WO 2008/122357 44 PCT/EP2008/002314 The activity of the compounds of the invention of the formula I was tested in the following enzyme assay system: EL inhibition assay: 5 EL is released as secretory protein in high concentration into cell culture medium (conditioned medium) by recombinant cell lines (CHO, HEK293). This is employed as enzyme solution after concentration. 10 EL activity assay The phospholipase-specific substrate 1,2-bis(4,4-difluoro-5,7-dimethyl-4-bora-3a,4a diaza-s-indacene-3-undecanoyl)-sn-glycero-3-phosphocholine, (manufacturer Molecular Probes) is used to characterize the enzymatic activity of endothelial lipase 15 and the effect of inhibitors. Hydrolysis of the Al ester linkage of this phospholipid by the enzyme liberates a fatty acid labeled by the fluorescent dye Bodipy which can be detected after separation by thin-layer chromatography on an HPTLC plate (silica gel 60, Merck) or directly in the reaction vessel by measuring the fluorescence. The substrate solution is prepared by dissolving 100 pg of 1,2-bis(4,4-difluoro-5,7 20 dimethyl-4-bora-3a,4a-diaza-s-indacene-3-undecanoyl)-sn-glycero-3-phospho choline (manufacturer Molecular Probes) in 100 pl DMSO and taking it up in 2.4 mg of tripalmitin (Sigma) in 393 pl chloroform which contains 20 mg/ml DOP - choline (1,2-dioleoyl-sn-glycero-3-phosphocholine). 39.3 pl of this lipid mixture are transferred into a fresh reaction vessel and the solvent is evaporated. The lipid 25 mixture is dissolved in 4 ml of 200 mM TRIS-HCI, 150 mM sodium chloride, pH = 7.4, by sonication twice. The subsequent enzymic reaction takes place at 370C for 90 minutes. For this purpose, 20 pl of the substrate solution are incubated with 2 pl of inhibitor of appropriate concentration (dissolved in 10% DMSO, 10% strength DMSO solution is used as control) and 2 pl of enzyme solution (conditioned 30 medium). Then 4 pl of the assay mixture are loaded onto an HPTLC plate (silica gel 60, Merck), and the liberated fluorescent dye is separated for detection with an eluent (diethyl ether:petroleum benzine:acetic acid [78:22:1]). After evaporation of WO 2008/122357 45 PCT/EP2008/002314 the eluent, the plate is read in a fluorescence scanner. An increased release of the fluorescent dye in the uninhibited reaction is to be observed as a measure of the enzymic activity. 5 The enzymatic activity is reduced as a function of the inhibitor concentration used, and the inhibitor concentration at which a half-maximum enzymic activity is observed is called IC50. Example IC50 [M] EL 6 0.028 7 0.9 8 3.2 10 0.06 16 0.004 18 14.1 25 0.009 26 0.035 31 0.1 39 0.001 40 0.053 44 0.5 10 Other test models The suitability of the compounds of the invention as active pharmaceutical ingredient can be tested by means of various test models. Descriptions of such test models are 5 given below by way of example. Solubility in aqueous systems Adequate solubility of a substance in aqueous solvent systems is an important prerequisite for a (reproducible) pharmacological effect. Solubilities in aqueous WO 2008/122357 46 PCT/EP2008/002314 systems can be determined by various methods. Suitable examples are solution precipitation methods ("kinetic solubility") and methods which investigate the dissolution of a solid sample until an equilibrium is set up ("thermodynamic solubility"). 5 a) Kinetic solubility A DMSO solution of the test compound (2.5 mM; 0.5 pL) is pipetted into 200 pL of an aqueous test solution (e.g. phosphate-buffered saline, 1Ox, 1 M, Sigma, adjusted to 10 mM, pH 7.4) in a 96-well microtiter plate, and the turbidity is measured at the resulting theoretical concentration for the test compound of 6.25 pM using a 10 nephelometer (e.g. Nephelostar Galaxy, BMG Labtech). The concentration of the test compound in the aqueous test solution is then raised to a theoretical 12.5 pM by adding further DMSO solution (2.5 mM; 0.5 pL), and the turbidity measurement is repeated. Further additions of DMSO solutions (1 pL, 2.5 mM; 0.5 pL, 10 mM; then 9x 1 pL, 10 mM resulting in theoretical concentrations of 25 pM, 50 pM, 100 pM, 15 150 pM, 200 pM, 250 pM, 300 pM, 350 pM, 400 pM, 450 pM and 500 pM) with turbidity measurement in between complete the measurement process. Evaluation: The turbidity values from the nephelometer are plotted against the theoretical concentration of the test compound in the aqueous test solution. As soon as a significant turbidity is detected (e.g. 5 times above the control value of the 20 aqueous test solution) at a theoretical concentration, the level of concentration below this is stated to be the solubility limit of the test compound in the test solution. Thus, the maximum possible measurement range emerges as values <6.25 pM, 6.25 500 pM and >500 pM. Preferred compounds of the invention show a kinetic solubility in phosphate buffer 25 (pH 7.4) of at least 12.5 pM; more preferably of at least 50 pM and even more preferably of at least 250 pM. b) Thermodynamic solubility The integrated UV absorption from HPLC UV measurement of serial dilutions of the 30 test compound in DMSO (500 pM, 100 pM, 50 pM, 10 pM and 1 pM) shows a linear correlation with the concentration in a calibration line. The test compound (500 pg) is shaken together with the aqueous test solution (250 pL) in a closed vessel (capacity: WO 2008/122357 47 PCT/EP2008/002314 1.5 mL) for 16 hours (Eppendorf thermoshaker, 1400 rpm, 250C, covering to protect from light). The sample is then centrifuged at maximum rotational speed, and the supernatant is finally filtered. A sample of the filtered supernatant is analyzed directly by HPLC UV measurement (see above). A further sample is analyzed after dilution 5 (1 part by volume of supernatant, 39 parts by volume of test solution). Evaluation: The concentration of the test compound in the undiluted supernatant is calculated from the resulting integrated UV absorptions of the supernatant samples on the basis of the constructed calibration lines and stated as solubility of the test compound in the respective aqueous test solution. 10 Examples of aqueous test solutions are deionized water or aqueous phosphate buffer with various pH values (e.g. pH 1.2; pH 4.0; pH 6.8; pH 7.4; pH 9.0) which can be prepared from the commercial solution (phosphate buffered saline, 1 Ox, Sigma) by dilution and adjustment with phosphoric acid or sodium hydroxide solution by standard methods. 15 Preferred compounds of the invention show a solubility in phosphate buffer (pH 7.4) of at least 12.5 pM; more preferably of at least 50 pM and even more preferably of at least 250 pM. Metabolic stability 20 The metabolic stability is determined by incubating the test compound (5 pM) with microsomal liver fractions (1 mg/mL protein with 0.1% w/v BSA; 1 mM NADPH, 0.5% DMSO) at 370C. Analysis at an incubation time of 0 and 20 minutes takes place by means of LCMS/MS. Further descriptions of the test system and references for the 25 experimental procedure are to be found in Plant, N.; Drug Discovery Today 2004, 9(7), 328-336 and Lau, Y.Y. et al.; Pharmaceutical Res. 2002, 19(11), 1606-1610. Preparation processes 30 The compounds of the invention of the formula I are prepared by methods known per se in two steps. WO 2008/122357 48 PCT/EP2008/002314 Substituted isoxazolones can be prepared by reacting appropriately substituted acetoacetic ester derivatives Ila with hydroxylamine as described for example in Bowden K., Crank C., Ross WJ., J. Chem. Soc. C 1968, 172-185. The acetoacetic 5 ester derivatives Ila are on the one hand commercially available as marketed products or can be prepared from acetoacetic ester alkylation by methods known per se. O 0 R2 R2 OH + H '0 + HO'N" R3 0 R3 N H H Ila 10 In a further step, the compounds of the invention of the formula I are prepared by acylation of the unsubstituted or substituted isoxazolones II with carbamoyl chlorides Ill (method A), or in two stages by reaction of 3-oxoisoxazoles II with phosgene or equivalents such as trichloromethyl chlorocarbonate, ditrichloromethyl carbonate or 15 4-nitrophenyl chloroformate and further reaction of the resulting isoxazolonecarboxylic acid derivative with amines IV (method B), or by reacting the isoxazolone II with the appropriate isocyanates V R1-N=C=O. Since acids are ordinarily liberated in these reactions, it is advisable to add bases 20 such as pyridine, triethylamine, sodium hydroxide solution or alkali metal carbonates as promoters. The reactions can be carried out in wide temperature ranges. It has ordinarily proved advantageous to operate at from 0*C to the boiling point of the solvent used. Examples of solvents employed are methylene chloride, THF, DMF, toluene, ethyl acetate, n-heptane, dioxane, diethyl ether or pyridine. If anhydrous 5 conditions are employed, strong bases such as lithium hydride, sodium hydride or potassium tert-butoxide in aprotic solvents such as THF or DMF have also proved useful. WO 2008/122357 49 PCT/EP2008/002314 0 0 R2 C, R2 O + N. O R3 0 R3 N H R1 N/ II RI o 0 R2 R2) R2 0 + 0 + H I R3 N/ cici R3 H CR CI H R1 R RI 0 R2 R2 R + 0 N )NO R3 NR R3 H H 0 R1 5 V Examples 3-Cyclopropl-2H-isoxazol-5-one 5 0 4 3 N 0 2 A solution of methyl 3-cyclopropyl-3-oxopropionate (4.8 g, 34 mmol) in methanol (80 mL) is mixed with hydroxylamine hydrochloride (2.6 g, 38 mmol) and triethylamine (5.3 mL, 38 mmol), and the mixture is heated under reflux for 2 h. The solvent is distilled out in vacuo. The residue is taken up in EtOAc and filtered through 5 silica gel. Yield: 3.2 g (75.2%). WO 2008/122357 50 PCT/EP2008/002314 Isoxazolones having various substituents in position 3 or having additional substituents in position 4 were prepared analogously. In these cases, either commercially available substituted acetoacetic ester derivatives were employed, or 5 were prepared from acetoacetic ester by alkylation by methods known per se. 5-Oxo-5H-isoxazole-2-carboxam ides 5 0 4 3N1 N2 0 NH 2 10 3-Cyclopropyl-5-oxo-5H-isoxazole-2-thiophene-2-vlmethvlcarboxamide 0 0 0 IN N S A solution of phosgene in toluene (20%, 1 mL, 2 mmol) is diluted with THF (10 mL). A solution of 3-cyclopropyl-2H-isoxazol-5-one (125 mg, 1 mmol) in THF (5 mL) is 5 added to this solution, and triethylamine (140 pL, 1 mmol) is added to the mixture, which is stirred at 250C for 8 h. The precipitate is then filtered off, and the filtrate is concentrated in vacuo. The residue is taken up in THF (10 mL) and added to a solution of 2-thiophene-2-methylamine (113.2 mg, 1 mmol) in pyridine (10 mL). The mixture is stirred at 250C for 16 h. The solvent is then distilled out in vacuo, and the .0 residue is purified by HPLC. Yield: 66 mg (25%) Correspondingly, isoxazolones with various substituents in positions 3 and 4 were converted by reaction with various amines into the corresponding 5-oxo-5H- WO 2008/122357 51 PCT/EP2008/002314 isoxazole-2-carboxamides. The examples detailed below serve to illustrate the invention without, however, restricting it. WO 2008/122357 52 PCT/EP2008/002314 Ex. Chemical structure R1 0 1 ,1-Ethylpropyl 0 2 NH 4-Fluorobenzyl F 0 3 4-Trifluoromethylbenzyl 4 H Cyclohexyl 0 5 HN 4-Pyrazol-1 -ylbenzyl WO 2008/122357 53 PCT/EP2008/002314 6 - H2-Methylbenzyl 0 78 4ez-Me]th lbenz2ylm ty 0 80 0H / 0 Bnob]tIopn--ylmt 0 11 - HPyridin-4-ylmethyl WO 2008/122357 54 PCT/EP2008/002314 0-N 12 n-Hexyl 0 oN 13 H 3,3,5 Trimethylcyclohexyl 0 14 4[2,2'] Bith iophenyl-5-m ethyl 15 NH F 2-Fluorobenzyl ON 0 0 16 3,4-Dimethylbenzyl 17 2,4-Dimethoxybenzyl WO 2008/1 22357 55 PCT/EP2008/002314 0 0 ' 18 Thiophen-2-ylmethyl 0 F F 19 H 4-Trifluoromethylbenzyl 19 N N 0 'I 0 20 4-Methylbenzyl 20NYr ~0 21 SI- Thiophe n-2-yl methyl 0 22 N N 6-Methyl pyrid in-2-yl methyl 0 23 Hr f' Pyridin-3-ylmethyl WO 2008/122357 56 PCT/EP2008/002314 0 ~ FF o F 24 N N,_F 4-Trifl uorom ethyl benzyl 0N N N 0 25 N~j T N, 3,4-Di methyl benzyl 0 0 HH 26 H' 4-Methylbenzyl 0 27 - H /2,6-Dimethylbenzyl 0o F 28 H j F 4-Trifluoromethylbenzyl 0 29 N 4-Methylbenzyl 0 WO 2008/1 22357 57 PCT/EP2008/002314 o H S 30 N-_s Thiphen-2-ylmethyl 0 0 32 - HPyrid in-2-ylm ethyl N 33 0 4-Butylbenzyl 0 0, Nj 34 MI1 ,2,3,4-Tetrahydronaphthalen-1 -yI j CHIRAL 35 H /(S)-Indan-1-yl WO 2008/1 22357 58 PCT/EP2008/002314 0 O-IR&L 36 ::Nq (R)-Indan-1 -yI NH 37 2,2-Dimethyl-1 -chroman-4-yi 00 39 H A 2,6-ielenyl 0 0 0 0 0 410 3,-DMethylbenzyl WO 2008/1 22357 59 PCT/EP2008/0023 14 0 42 ~NH 2-Methylbenzy 0 0 43 IThiophen-2-ylmethyl o C IRAL 44 H /H (S)-Indan-1-y 0 0-iRAL 45 -~(S)-1 -Phenylethyl 0 H 0 46 - Benzyl - 0' 47 H - 2-N aphthyl WO 2008/122357 60 PCT/EP2008/002314 48 0Phenylethyl 0 49 H 0 3,5-Dichlorobenzyl QHA 00 0 0 50 Br -4biophenyl-yI l 0 0 53 2-Thiophe n-2-yl ethyl WO02008/122357 61 PCT/EP2008/00231 4 54 HN 0 1-Naphthalen-lyethyl 55 0 55 3,4-Dichiorophenyl 56 mlJ 0 4-Methyloxybenzyl N a,' Q 0 F F 57 H Pyridin-3-y - 0 58 0 Indan-5-y 0 59 0Benzo-1 ,3-dioxol-5-yi WO 2008/1 22357 62 PCT/EP2008/002314 60 ,1Dipenlmehy 0 0 61 Furan-2-ylmethyl 0 62 ~ -3-Methyloxybenzyl 63 1 ,2,3,4-Tetrahydronaphthalen-1 -yI 0 0 65 H 2-Bi phenyl-4-yl ethyl WO 2008/1 22351 63 PCT/EP2008/002314 0 N'0 66 Cyclohexylmethyl 0 0 0 67 H -I 2(,-Dimethyloxytphenylty 0 68 H12,34Dictrhyronphlthl- y 0 WO 2008/122357 64 PCT/EP2008/002314 72 MO(S)-Indan-1-yI 73/ 2-Methylbenzyl 0 0 0 74 N NHL 2-Methylbenzyl 0 0 0 76 Th4-iohnm ethyl ny 0 0 77 N / Th ioph en-2-ylm ethyl NH_" WO 2008/122357 65 PCT/EP2008/0023 14 0 CHIRAL 0 0 H7/ (S)-Indan-1-yI 0 CH1RAL 79 (R)-Indan-1 -yI HN 0 0 80 ~~~~~0 34Dmtybn 80 NO 3,- Dm etyl bnzy WO 2008/122357 66 PCT/EP2008/002314 Claims 5 1. A compound of the formula I 0 R2 R3 N N R1 (1) in which the meanings are: 10 R1 (Cs-C 1 6 )-alkyl, Y-aryl, Y-heteroaryl, where aryl or heteroaryl may be substituted one or more times by F, Cl, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , O-(C1-C)-alkyl, 0-(C 1 -C 4 )-alkoxy (C1-C 4 )-alkyl, S-(C1-Cs)-alkyl, (C 1 -C)-alkyl, (C 2 -C 4 )-haloalkyl, 0-(C 2 -C 4 )-haloalkyl, (C 2 -C 6 )-alkenyl, (C 3 -Cs)-cycloalkyl, 0-(C3-CB) 15 cycloalkyl, (C 2 -C 6 )-alkynyl, (Co-C 8 )-alkylene-aryl, 0-(Co-C 8 )-alkylene aryl, S-aryl, (Co-C 8 )-alkylene-heteroaryl, N(R4)(R5), S0 2 -CH 3 , SO 2 NH 2 , SF 5 , COOH, COO-(C 1 -C)-alkyl, CON(R6)(R7), N(R8)CO(R9), N(R1 0)SO 2 (R1 1), CO(R1 2), (CR1 3R1 4)x-O(R1 5), O-CO-N(R1 6)(R1 7), O-CO-(C1-C 6 )-alkylene-CO-O-(C1-C 6 )-alkyl, O-CO-(C1-C 6 )-alkylene 20 CO-OH, O-CO-(C 1 -C)-alkylene-CO-N(R18)(R19), where aryl or heteroaryl may in turn be substituted one or more times by F, Cl, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , O-(C 1 -C)-alkyl, 0-(C1-C4)-alkoxy-(C 1 -C 4 )-alkyl, S-(C 1 -Cs)-alkyl, (C 1 -Cs)-alkyl, 25 (C 2 -C4)-haloalkyl, (C 2 -C 6 )-alkenyl, (C 3 -Cs)-cycloalkyl, 0-(C 3 -C 8 )-cycloalkyl, (C 2 -C 6 )-alkynyl, N(R4a)(R5a), S0 2 -CH 3 , SF 5 , COOH, COO-(C1-Ce)-alkyl, CON(R6a)(R7a), WO 2008/122357 67 PCT/EP2008/002314 N(R8a)CO(R9a), N(R1 Oa)SO 2 (R1 1 a), CO(R1 2a), (CR13aR14a)x--O(R15a), O-CO-N(R16a)(R17a), O-CO-(CriC 6 )-alkylene-CO-O-(Cr-C 6 )-alkyl, O-CO-(Cr1C6) alkylene-CO-OH, O-CO-(CrO0)-alkylene-CO 5 N(R18a)(R19a); x, x' 0,1,2,3,4, 5,6; R4, R5, R6, R7, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18, R19, 10 R4a, R5a, R6a, R7a, R9a, R10a, R11a, R12a, R13a, R14a, R15a, R16a, R17a, R18a, R19a independently of one another hydrogen, (C-C 8 )-alkyl; or a radical of the formula la 15 R20 R21 W R25 R22 R23 R24 ,with W -C(R26)(R27)-, -C(R26)(R27)-C(R28)(R29)-, -C(R26)(R27)-O-; 0 R20, R21, R22, R23, R24, R25, R26, R27, R28, R29 identically or differently hydrogen, F, Cl, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , SF 5 , O-(C-C 6 )-alkyl, 0-(C 1 -C4)-alkoxy-(C-C 4 )-alkyl, S-(CO-alkyl, (CI-C6)-alkyl, (C2-C4)-haloalkyl, 0-(C2-C4) haloalkyl, (C 2 -C 6 )-alkenyl, (C 3 -C 8 )-cycloalkyl, 0-(C3-C8) .5 cycloalkyl, (C3-C8)-cycloalkenyl, (C 2 -C 6 )-alkynyl, N(R30)(R31), S0 2 -CH 3 , COOH, COO-(0 1 C)-alkyl, CON(R32)(R33), N(R34)CO(R35), N(R36)SO 2 (R37), CO(R38), (CR39R40)x---O(R41), O-CO-N(R42)(R43), 0-CO- WO 2008/122357 68 PCT/EP2008/002314 (CriC-)-alkylene-CO-O-( 1 -C 6 )-alkyl, O- (Cr0 6 )-alkylene CO-OH, O-CO-(C-C 6 )-alkylene-CO-N(R44)(R45); x'' 0, 1,2,3,4,5, 6; 5 R30, R31, R32, R33, R34, R35, R36, R37, R38, R39, R40, R41, R42, R43, R44, R45 identically or differently hydrogen, (CrO0)-alkyl; 10 or R20 and R26 or R21 and R27 together with the carbon atoms carrying them form a monocyclic, 5 or 6 membered saturated, partly unsaturated or aromatic ring system whose individual members may be replaced by -CHR46-, -CR46R47-, =(C-R46)-; 15 or R22 and R24, or R23 and R25 together with the carbon atoms carrying them form a monocyclic, 5 or 6 membered saturated, partly unsaturated or an aromatic ring system whose individual members may be replaced by -CHR46-, -CR46R47-, =(C-R46)-; 20 R46, R47 identically or differently F, Cl, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , SF 5 , O-(O-C)-alkyl, 0-(C-C 4 )-alkoxy-(C-C 4 )-alkyl, S-(CrC 6 ) alkyl, (Cr-0)-alkyl, (C 2 -C 4 )-haloalkyl, 0-(C 2 -C4)-haloalkyl, (C 2 -C 6 )-alkenyl, (C 3 -C 8 )-cycloalkyl, 0-(C 3 -C 8 )-cycloalkyl, 5 (C 2 -C 6 )-alkynyl, N(R48)(R49), S0 2 -CH 3 , COOH, COO (CrO0)-alkyl, CON(R50)(R51), N(R52)CO(R53), N(R54)SO 2 (R55), CO(R56), (CR57R58)x---O(R59), 0-CO N(R60)(R61), O-CO-(Cr-C-)-alkylene-CO-O-(Cr-C 6 )-alkyl, O-CO-(0 1 C)-alkylene-CO-OH, O-CO-(0C)-alkylene-CO 30 N(R62)(R63); x''' 0, 1, 2, 3, 4, 5, 6; WO 2008/122357 69 PCT/EP2008/002314 R48, R49, R50, R51, R52, R53, R54, R55, R56, R57, R58, R59, R60, R61, R62, R63 identically or differently hydrogen, (C1-C)-alkyl; 5 Y, Z identically or differently (C1-C 2 )-alkylene, which may be substituted once by F, Cl, CH 3 or OH; R2 hydrogen, (C1-C1 2 )-alkyl, Z-aryl, where aryl or heteroaryl may optionally 10 be substituted, (C3-C 1 2 )-cycloalkyl; R3 (C 1 -C1 2 )-alkyl, aryl, heteroaryl, where aryl or heteroaryl may optionally be substituted, (C3-C1 2 )-cycloalkyl; or 15 R2 and R3 together with the carbon atoms carrying them form a monocyclic, saturated or partly unsaturated 4- to 8-membered ring system whose individual members may be replaced by one to three atoms or atomic groups from the series -CHR64-, -CR64R65-, =(C-R66)-, -NR67-, -C(=O)-, -0-, with the proviso that two units from the series -0- may 20 not be adjacent; R64, R65, R66, R67 identically or differently hydrogen, F, Cl, Br, I, OH, CF 3 , NO 2 , CN, OCF 3 , SF 5 , O-(C1-C)-alkyl, O-(C1-C4)-alkoxy-(C1-C 4 ) alkyl, S-(C1-C 6 )-alkyl, (C1-Cs)-alkyl, (C 2 -C 4 )-haloalkyl, 25 0-(C 2 -C 4 )-haloalkyl, (C 2 -C 6 )-alkenyl, (C 3 -C 8 )-cycloalkyl, 0-(C 3 -Cs)-cycloalkyl, (C 3 -CB)-cycloalkenyl, (C2-C6)-alkynyl, N(R68)(R69), S0 2 -CH 3 , COOH, COO-(C 1 -C)-alkyl, CON(R70)(R71), N(R72)CO(R73), N(R74)SO 2 (R75), CO(R76), (CR77R78)x-----O(R79), O-CO-N(R80)(R81), 30 O-CO-(C1-C 6 )-alkylene-CO-O-(C1-C 6 )-alkyl, O-CO-(C1-C6) alkylene-CO-OH, O-CO-(C1-C 6 )-alkylene-CO-N(R82)(R83); WO 2008/122357 70 PCT/EP2008/002314 x'''' 0, 1, 2, 3, 4, 5, 6; R68, R69, R70, R71, R72, R73, R74, R75, R76, R77, R78, R79, R80, R81, R82, R83 5 identically or differently hydrogen, (-C)-alkyl; with the proviso that the compound with R1 = cyclohexyl, R2=H and R3 = phenyl is excluded; the tautomeric forms of the compound and the physiologically tolerated salts thereof. 10 2. A compound of the formula I as claimed in claim 1, wherein R1 is (C 5 -C1 2 )-alkyl, Y-phenyl, Y-heteroaryl, where heteroaryl comprises 1 heteroatom from the series N, 0, S, and where phenyl or heteroaryl 15 may be substituted one or more times by F, Cl, Br, OH, CF 3 , NO 2 , CN, OCF 3 , O-(0C)-alkyl, S-(PC)-alkyl, (Cr-C 6 )-alkyl, (C 2 -C 4 )-haloalkyl, (C 3 -C 8 )-cycloalkyl, (Co-C 6 )-alkylene-phenyl, 0-(Co-C 6 )-alkylene-phenyl, S-phenyl, (Co-C 8 )-alkylene-heteroaryl, N(R4)(R5), COOH, COO (C-C)-alkyl, CON(R6)(R7), CO(R12), where phenyl or heteroaryl may 20 in turn be substituted one or more times by F, C, OH, CF 3 , NO 2 , CN, OCF 3 , O-(0 1 C)-alkyl, S-(Cr 1 C 6 ) alkyl, (C-C)-alkyl, (C 2 -C 4 )-haloalkyl, (C 3 -C 8 )-cycloalkyl, N(R4a)(R5a), COOH, COO-(0 1 C)-alkyl, CON(R6a)(R7a) 25 CO(R12a); x, x' are 0, 1, 2, 3, 4, 5, 6; R4, R5, R6, R7, R12, R4a, R5a, R6a, R7a, R12a are 30 identically or differently hydrogen, (Cr-C 8 )-alkyl; or a radical of the formula lb WO 2008/122357 71 PCT/EP2008/002314 R20 R21 W with W is -C(R26)(R27)-, -C(R26)(R27)-C(R28)(R29)-, -C(R26)(R27)-O-; 5 R20, R21, R26, R27, R28, R29 are identically or differently hydrogen, F, Cl, OH, CF 3 , NO 2 , CN, OCF 3 , 0-(C1-C 6 )-alkyl, (C1-Cs)-alkyl, CO-(C1-Ce)-alkyl; 10 or R20, R21, R26 and R27 together with the carbon atoms carrying them form a fused benzene residue which may be substituted one or more times by F, Cl, CN, NO 2 , CF 3 , OCF 3 , (C 1 -C)-alkyl, 0-(C 1 -C 6 )-alkyl, CO-(C 1 -C)-alkyl; 15 Y, Z are identically or differently -CH 2 - or -CH 2 -CH 2 -, which may be substituted once by CH 3 or OH; R2 is hydrogen, (C 1 -C 1 2 )-alkyl, Z-phenyl, where phenyl may optionally be substituted, (C 3 -C 1 2 )-cycloalkyl; 20 R3 is (C 1 -C 1 2 )-alkyl, phenyl, heteroaryl, which comprises 1 heteroatom from the series N, 0, S, where phenyl or heteroaryl may optionally be substituted, (C 3 -C 1 2 )-cycloalkyl; or 25 R2 and R3 together with the carbon atoms carrying them form a monocyclic, saturated 5- to 7-membered ring system whose individual members may be replaced by one to three atomic groups from the series -CHR64-, -CR64R65-, =(C-R66)-; WO 2008/122357 72 PCT/EP2008/002314 R64, R65, R66 are identically or differently F, Cl, OH, CF 3 , 0-(Cr 1 C 6 )-alkyl, 0-(C-C 4 )-alkoxy-(C-C 4 )-alkyl, (C-C 6 )-alkyl, (C 2 -C 4 ) haloalkyl, (C 3 -C 8 )-cycloalkyl, N(R68)(R69), S0 2 -CH 3 , COOH, 5 COO-(,C0)-alkyl, CON(R70)(R71), N(R72)CO(R73), CO(R76), O-CO-N(R80)(R81), O-CO-(C-C 6 )-alkylene-CO 0-(Cr C 6 )-alkyl, O-CO-(OC 6 )-alkylene-CO-OH, 0-CO (C-C 6 )-alkylene-CO-N(R82)(R83); 10 R68, R69, R70, R71, R72, R73, R76, R77, R78, R79, R80, R81, R82, R83 are identically or differently hydrogen, (CrO0)-alkyl; the tautomeric forms of the compound, and the physiologically tolerated salts thereof. 15 3. A compound of the formula I as claimed in claim 1 or 2, wherein R1 is (C 5 -C 8 )-alkyl, Y-phenyl, Y-pyridyl, Y-thienyl, Y-furyl, Y-benzothienyl, Y-benzofuryl, where phenyl or the heteroaromatic radical may be 20 substituted once, twice or three times by F, Cl, Br, CF 3 , CN, OCF 3 , 0-(CrC 6 )-alkyl, (C-C)-alkyl, (C 3 -C 6 )-cycloalkyl, N(R4)(R5), COOH, COO-(CrCs)-alkyl, CON(R6)(R7), CO(R12), and may be substituted once by (Co-C1)-alkylene-phenyl, 0-(Co-C1)-phenyl, pyrazolyl, pyridyl, thienyl, furyl, benzothienyl, benzofuryl, where a heteroaromatic radical 25 or phenyl may in turn be substituted once, twice or three times by F, Cl, Br, CF 3 , CN, OCF 3 , 0-(C-C 6 )-alkyl, (0 1 -C 6 )-alkyl, (C 3 -C 6 )-cycloalkyl, N(R4a)(R5a), COOH, COO-(C-C6)-alkyl, CON(R6a)(R7a), CO(R12a); R4, R5, R6, R7, R12, R4a, R5a, R6a, R7a, R12a 30 are independently of one another H, (Cr-C 8 )-alkyl; or a radical from the group WO 2008/122357 73 PCT/EP2008/002314 R20 R21 R26 R20 R21R26 R21R26 R27 R27 R20 R27 R28 0 - R29 R20, R21, R26, R27, R28, R29 are identically or differently hydrogen, (CrC6) alkyl, preferably hydrogen and methyl; 5 Y is -CH 2 - or -CH 2 -CH 2 -, which may be substituted once by CH 3 ; R2 is hydrogen, (C-C 8 )-alkyl, -CH 2 -phenyl, where phenyl may optionally be substituted, (C 3 -C 8 )-cycloalkyl; I0 R3 is (C-C 8 )-alkyl, phenyl, pyridyl, thienyl, where phenyl, pyridyl or thienyl may optionally be substituted, (C 3 -C 8 )-cycloalkyl; or R2 and R3 together with the carbon atoms carrying them form a monocyclic, 5 saturated 6- to 7-membered ring system whose individual members may be replaced by one to three atoms or atomic groups from the series -CHR64-, -CR64R65-; R64, R65 are identically or differently F, Cl, CF 3 , OCF 3 , (C-C)-alkyl, 0-(Cr1C6) 0 alkyl, N(R68)(R69), COOH, COO-(OiC)-alkyl, CO-N(R70)(R71), CO(R76); R68, R69, R70, R71, R76 are identically or differently hydrogen, (OC)-alkyl; 5 the tautomeric forms of the compound, and the physiologically tolerated salts thereof. WO 2008/122357 74 PCT/EP2008/002314 4. A compound of the formula I as claimed in claims 1 to 3, wherein R2 is isopropyl and 5 R3 is methyl. 5. A compound of the formula I as claimed in claims 1 to 3, wherein R2 is hydrogen and 10 R3 is phenyl, which may be substituted once by Cl. 6. A compound of the formula I as claimed in claims 1 to 3, wherein 15 R2 and R3 together are -CH 2 -CH 2 -CH 2 -CH 2 - or -CH 2 -CH 2 -CH 2 -CH 2 -CH 2 -. 7. A compound of the formula I as claimed in claims 1 to 3, wherein R1 is (C 5 -C 7 )-alkyl, Y-phenyl, Y-thienyl, Y-benzothienyl, where phenyl or 20 the heteroaromatic radical may be substituted once, twice or three times by F, Cl, Br, CF 3 , 0-CH 3 , -CH 3 , -CH 2 CH 3 , -CH 2 -CH 2 -CH 2 -CH 3 , and be substituted once by phenyl, pyrazolyl or thienyl, where the heteroaromatic radical or phenyl may in turn be substituted once, twice or three times by F, Cl, Br, CF 3 , 5 O-(C1-C 6 )-alkyl, (C 1 -C)-alkyl; or a radical from the group WO 2008/122357 75 PCT/EP2008/002314 R20 21 R26 R20 R21R26 R21R26 R27 R '27 R20 R27 R28 0 - R29 R20, R21, R26, R27, R28, R29 are identically or differently hydrogen, CH 3 ; 5 Y is -CH 2 -, which may be substituted once by CH 3 ; R2 is hydrogen, methyl, isopropyl, cyclopropyl, phenyl, -CH 2 -phenyl, where phenyl may be substituted by C in position 4; 10 R3 is methyl, phenyl, pyridyl, cyclopropyl, where phenyl may be substituted by Cl; or R2 and R3 are together -CH 2 -CH 2 -CH 2 -CH 2 - or -CH 2 -CH 2 -CH 2 -CH 2 -CH 2 ; 15 the tautomeric forms of the compound, and the physiologically tolerated salts thereof. 8. A medicament comprising one or more compounds of the formula I as claimed in claims 1 to 7. 9. The use of the compounds of the formula I as claimed in claims 1 to 7 for the manufacture of a medicament for the treatment and/or prevention of disorders of fatty acid metabolism and glucose utilization disorders. 5 10. The use of the compounds of the formula I as claimed in claims 1 to 7 for the manufacture of a medicament for the treatment and/or prevention of disorders in which insulin resistance is involved. WO 2008/122357 76 PCT/EP2008/002314 11. The use of the compounds of the formula I as claimed in claims 1 to 7 for the manufacture of a medicament for the treatment and/or prevention of diabetes mellitus and the sequelae associated therewith. 5 12. The use of the compounds of the formula I as claimed in claims 1 to 7 for the manufacture of a medicament for the treatment and/or prevention of dyslipidemias and the sequelae thereof. 10 13. The use of the compounds of the formula I as claimed in claims 1 to 7 for the manufacture of a medicament for the treatment and/or prevention of conditions associated with the metabolic syndrome. 14. The use of the compounds of the formula I as claimed in claims 1 to 7 15 for the manufacture of a medicament for the treatment and/or prevention of conditions associated with reduced HDL level. 15. The use of the compounds of the formula I as claimed in claims 1 to 7 for the manufacture of a medicament for the treatment and/or prevention of 20 atherosclerotic disorders. 16. The use of the compounds of the formula I as claimed in claims 1 to 7 in combination with at least one further active ingredient for the manufacture of a medicament for the treatment and/or prevention of disorders in which insulin 25 resistance is involved. 17. A process for the manufacture of a medicament comprising one or more of the compounds of the formula I as claimed in claims 1 to 7, which comprises mixing the latter with a pharmaceutically suitable carrier, and converting this mixture 30 into a form suitable for administration. 18. A process for preparing compounds of the formula I as claimed in
权利要求:
Claims (1) [1] 4-nitrophenyl chloroformate and in a second step with amines of the formula IV, or c) being reacted with isocyanates of the formula V: O=C=N-R1, 10 in which the substituents have the abovementioned meanings. 0 0 R2)C R2 10 + CI NHI R3 N R3 N H H RI H R1 N. 0 II RI IlIlV 0 0 R2 Of R2 1N0 + O N -- N R3 1 CIR3 0HRR1 |RI 15 0 R2 0R2 1 I 0 + 0 N 10 R3 NNR HN 0 RI IIV I
类似技术:
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引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 DE19960917A1|1999-12-17|2001-06-21|Bayer Ag|New 3-oxo-2,1-benzisoxazol-1 -carboxamides for the treatment of CNS diseases| AT442139T|2003-03-31|2009-09-15|Lilly Co Eli|3-OXO-1,3-DIHYDRO-INDAZOLE-2-CARBOXYL ACID DERIVATIVES AS PHOSPHOLIPASE INHIBITORS| WO2004094394A1|2003-04-01|2004-11-04|Eli Lilly And Company|Benzisothiazol-3-one-carboxylic acid amides as phospholipase inhibitors| EP1613608A1|2003-04-01|2006-01-11|Eli Lilly And Company|Phospholipase inhibitors| DE102004005172A1|2004-02-02|2005-08-18|Aventis Pharma Deutschland Gmbh|Indazole derivatives as inhibitors of the hormone sensitive lipase| DE102005018389A1|2005-04-20|2006-10-26|Sanofi-Aventis Deutschland Gmbh|Azole derivatives as inhibitors of lipases and phospholipases|WO2011107494A1|2010-03-03|2011-09-09|Sanofi|Novel aromatic glycoside derivatives, medicaments containing said compounds, and the use thereof| WO2011157827A1|2010-06-18|2011-12-22|Sanofi|Azolopyridin-3-one derivatives as inhibitors of lipases and phospholipases| US8530413B2|2010-06-21|2013-09-10|Sanofi|Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments| TW201221505A|2010-07-05|2012-06-01|Sanofi Sa|Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament| TW201215387A|2010-07-05|2012-04-16|Sanofi Aventis|Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament| TW201215388A|2010-07-05|2012-04-16|Sanofi Sa|phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments| WO2013037390A1|2011-09-12|2013-03-21|Sanofi|6--3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors| WO2013045413A1|2011-09-27|2013-04-04|Sanofi|6--3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors|
法律状态:
2011-12-01| MK1| Application lapsed section 142(2)(a) - no request for examination in relevant period|
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申请号 | 申请日 | 专利标题 EP07007251.7||2007-04-05|| EP07007251||2007-04-05|| PCT/EP2008/002314|WO2008122357A1|2007-04-05|2008-03-22|5-oxo-isoxazoles as inhibitors of lipases and phospholipases| 相关专利
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