Diphenylazetidinone derivates possessing cholesterol absor tion inhibitor activit.

专利摘要:

公开号:AU2007243998A1
申请号:U2007243998
申请日:2007-04-25
公开日:2007-11-08
发明作者:Malin Lemurell；Ingemar Starke
申请人:AstraZeneca AB；
IPC主号:C07D205-08

专利说明:
WO 2007/126358 PCT/SE2007/000400 -1 Diphenylazetidinone Derivates Possessing Cholesterol Absorption Inhibitory Activity This invention relates to 2-azetidinone derivatives, or pharmaceutically acceptable salts, solvates, solvates of such salts and prodrugs thereof. These 2-azetidinones possess 5 cholesterol absorption inhibitory activity and are accordingly of value in the treatment of disease states associated with hyperlipidaemic conditions. They are therefore useful in methods of treatment of a warm-blooded animal, such as man. The invention also relates to processes for the manufacture of said 2-azetidinone derivatives, to pharmaceutical compositions containing them and to their use in the manufacture of medicaments to inhibit 10 cholesterol absorption in a warm-blooded animal, such as man. A further aspect of this invention relates to the use of the compounds of the invention in the treatment of dyslipidemic conditions. Atherosclerotic coronary artery disease is a major cause of death and morbidity in the western world as well as a significant drain on healthcare resources. It is well-known that 15 hyperlipidaemic conditions associated with elevated concentrations of total cholesterol and low density lipoprotein (LDL) cholesterol are major risk factors for cardiovascular atherosclerotic disease (for instance "Coronary Heart Disease: Reducing the Risk; a Worldwide View" Assman G., Carmena R. Cullen P. et al; Circulation 1999, 100, 1930-1938 and "Diabetes and Cardiovascular Disease: A Statement for Healthcare Professionals from the 20 American Heart Association" Grundy S, Benjamin I., Burke G., et al; Circulation, 1999, 100, 1134-46). The concentration of plasma cholesterol depends on the integrated balance of endogenous and exogenous pathways of cholesterol metabolism. In the endogenous pathway, cholesterol is synthesized by the liver and extra hepatic tissues and enters the circulation as 25 lipoproteins or is secreted into bile. In the exogenous pathway cholesterol from dietary and biliary sources is absorbed in the intestine and enters the circulation as component of chylomicrons. Alteration of either pathway will affect the plasma concentration of cholesterol. The precise mechanism by which cholesterol is absorbed from the intestine is however not clear. The original hypothesis has been that cholesterol is crossing the intestine by 30 unspecific diffusion. But more recent studies are suggesting that there are specific transporters involved in the intestinal cholesterol absorption. (See for instance New molecular targets for cholesterol-lowering therapy Izzat, N.N., Deshazer, M.E. and Loose-Mitchell D.S. JPET 293:315-320, 2000.) WO 2007/126358 PCT/SE2007/000400 -2 A clear association between reduction of total cholesterol and (LDL) cholesterol and decreased instance of coronary artery disease has been established, and several classes of pharmaceutical agents are used to control serum cholesterol. There major options to regulate 5 plasma cholesterol include (i) blocking the synthesis of cholesterol by agents such as HMG-CoA reductase inhibitors, for example statins such as simvastatin and fluvastatin, which also by up-regulation of LDL-receptors will promote the cholesterol removal from the plasma; (ii) blocking the bile acid reabsorption by specific agents resulting in increased bile acid excretion and synthesis of bile acids from cholesterol with agents such as bile acid 10 binders, such as resins e.g. cholestyramine and cholestipol; and (iii) by blocking the intestinal uptake of cholesterol by selective cholesterol absorption inhibitors. High density lipoprotein (HDL) elevating agents such as fibrates and nicotinic acid analogues have also been employed. Even with the current diverse range of therapeutic agents, a significant proportion of 15 the hypercholesterolaemic population is unable to reach target cholesterol levels, or drug interactions or drug safety preclude the long term use needed to reach the target levels. Therefore there is still a need to develop additional agents that are more efficacious and are better tolerated. Compounds possessing such cholesterol absorption inhibitory activity have been 20 described, see for instance the compounds described in WO 93/02048, WO 94/17038, WO 95/08532, WO 95/26334, WO 95/35277, WO 96/16037, WO 96/19450, WO 97/16455, WO 02/50027, WO 02/50060, WO 02/50068, WO 02/50090, WO 02/66464, WO 04/000803, WO 04/000804, W004/000805,WO04/01993, W004/010948, W004/043456 WO 04/043457, WO 04/081002, W005/000353, W005/021495, WO05/021497, W005/033100, 25 W005044256, W005044248, WO 05/062824, W005061451, W005061452, US 5756470, US 5767115, US 20040180860, US20040180861, US20050267049 and US RE37721. The present invention is based on the discovery that certain 2-azetidinone derivatives surprisingly inhibit cholesterol absorption. Such properties are expected to be of value in the treatment of disease states associated with hyperlipidaemic conditions. The compounds of the 30 present invention are not disclosed in any of the above applications and we have surprisingly found that the compounds of the present invention possess beneficial efficacious, metabolic and toxicological profiles that make them particularly suitable for in vivo administration to a warm blooded animal, such as man. In particular certain compounds of the present invention WO 2007/126358 PCT/SE2007/000400 -3 have a low degree of absorption whilst retaining their ability to inhibit cholesterol absorption. Accordingly there is provided a compound of formula (I): 5 0 Ri R6 0 OH 0 N N ~ OH R3 H O R2 R5 R3- N 0 H O N- - R4 0 (I) wherein: 10 R 1 is hydrogen, CI 6 alkyl, C 3 -6cycloalkyl or aryl;
R
2 and Rare independently hydrogen, a branched or unbranched C1- 6 alkyl, C 3
-
6 cycloalkyl or aryl; wherein said CI.
6 alkyl may be optionally substituted by one or more hydroxy, amino, guanidino, cyano, carbamoyl, carboxy, C1- 6 alkoxy, aryl CI- 6 alkoxy,(C-C 4
)
3 Si, N (C1- 6 alkyl)amino, NN-(C1- 6 alkyl) 2 amino, CI- 6 alkylS(O)a,, C 3
-
6 cycloalkyl, aryl or aryl C1-6 15 alkylS(O)a, wherein a is 0-2; and wherein any aryl group may be optionally substituted by one or two substituents selected from halo, hydroxy, CI- 6 alkyl, Ci- 6 alkoxy, or cyano;
R
3 is hydrogen, alkyl, halo, C1- 6 alkoxy or CI- 6 alkylS-;
R
4 is methyl or aryl;
R
6 is hydrogen, C1.
6 alkyl, or arylC- 6 alkyl; 20 wherein R 5 and R 2 may form a ring with 2-7 carbon atoms and wherein R 6 and R 2 may form a ring with 3-6 carbon atoms; n=0 or 1; or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. 25 WO 2007/126358 PCT/SE2007/000400 -4 In one aspect of the invention it is provided for a compound of formula (12): 5 0 R1 R6 0 OH O N 4OH R3 H O R2 R5 N H I I H- -- R4 0 (12) wherein: 10 R' is hydrogen, CI 6 alkyl, C 3
-
6 cycloalkyl or aryl; R 2 and
R
5 are independently hydrogen, a branched or unbranched C1.
6 alkyl, hydroxy, amino, guanidino, cyano, carbamoyl, carboxy, C1- 6 alkoxy, aryl C 1 6 alkoxy,(C1-C 4
)
3 Si, N (C1- 6 alkyl)amino, NN-(C 1
.
6 alkyl) 2 amino, C1.
6 alkylS(O)a, , C 3
-
6 cycloalkyl, aryl or aryl C 1
.
6 15 alkylS(O)a, wherein a is 0-2; and wherein any aryl group may be optionally substituted by one or two substituents selected from halo, hydroxy, C1.
6 alkyl, CI 6 alkoxy, or cyano;
R
3 is hydrogen, alkyl, halo, CI 6 alkoxy or C 1
-
6 alkylS-;
R
4 is methyl or aryl;
R
6 is hydrogen, C 1
-
6 alkyl, or arylC1.
6 alkyl; 20 wherein R 5 and R 2 may form a ring with 2-7 carbon atoms and wherein R 6 and R 2 may form a ring with 3-6 carbon atoms; n= 0 or 1 or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. (12) 25 WO 2007/126358 PCT/SE2007/000400 -5 wherein variable groups are defined above as for formula (I). What is said further for formula (I) will, apart from the process schemes below, apply also to formula (12). According to one aspect of the invention R 1 is hydrogen. According to one aspect of the 5 invention, R 2 and R 5 are hydrogen or a branched or unbranched C1.
6 alkyl, C 3
-
6 cycloalkyl or aryl; wherein said CI 6 alkyl may be optionally substituted by one or more hydroxyl or amino. According to one aspect of the invention, R 3 is halo. According to one aspect of the invention, R3 is fluorine. According to one aspect of the invention, R 6 is hydrogen. According to one aspect of the invention, R' is hydrogen; R 2 and R 5 are hydrogen or a branched or unbranched 10 CI 6 alkyl, C 3
-
6 cycloalkyl or aryl; wherein said C1.
6 alkyl may be optionally substituted by one or more hydroxyl or amino and R 3 and R 6 are halo. According to an aspect of the invention, a compound according to the invention is chosen from one of the following compounds: 15 N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2-yl]phenoxy}acetyl)glycyl-3 cyclohexyl-D-alanine; 20 N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2-yl]phenoxy}acetyl)glycyl D-valine; N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2-yl]phenoxy}acetyl)glycyl-3 25 methyl-D-valine; N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2-yl]phenoxy}acety)glycyl D-lysine; 30 N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2 yl]phenoxy}acetyl)glycylglycine; and WO 2007/126358 PCT/SE2007/000400 -6 N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)amino]prop-1-yn-1 -yl}phenyl)-4-oxoazetidin-2-yl]phenoxy} acetyl)glycine. 5 In this specification the term "alkyl" includes both straight and branched chain alkyl groups but references to individual alkyl groups such as "propyl" are specific for the straight chain version only. For example, "C1.
6 alkyl" and "Cp 4 alkyl" include propyl, isopropyl and t-butyl. However, references to individual alkyl groups such as 'propyl' are specific for the straight-chained version only and references to individual branched chain alkyl groups such as 10 'isopropyl' are specific for the branched chain version only. A similar convention applies to other radicals, for example "phenylC1-6alkyl" would include benzyl, 1-phenylethyl and 2-phenylethyl. The term "halo" refers to fluoro, chloro, bromo and iodo. Where optional substituents are chosen from "one or more" groups it is to be understood that this definition includes all substituents being chosen from one of the specified 15 groups or the substituents being chosen from two or more of the specified groups.
"C
3
.
6 cycloalkyl" refers to cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. A suitable pharmaceutically acceptable salt of a compound of the invention, or other compounds disclosed herein, is, for example, an acid-addition salt of a compound of the 20 invention which is sufficiently basic, for example, an acid-addition salt with, for example, an inorganic or organic acid, for example hydrochloric, hydrobromic, sulphuric, phosphoric, trifluoroacetic, citric, acetate or maleic acid. In addition a suitable pharmaceutically acceptable salt of a compound of the invention which is sufficiently acidic is an alkali metal salt, for example a sodium or potassium salt, an alkaline earth metal salt, for example a 25 calcium or magnesium salt, an ammonium salt or a salt with an organic base which affords a physiologically-acceptable cation, for example a salt with methylamine, dimethylamine, trimethylamine, piperidine, morpholine or tris-(2-hydroxyethyl)amine. The compounds of the formula (I), or other compounds disclosed herein, may be administered in the form of a pro-drug which is broken down in the human or animal body to 30 give a compound of the formula (I). Examples of pro-drugs include in vivo hydrolysable esters and in vivo hydrolysable amides of a compound of the formula (I). An in vivo hydrolysable ester of a compound of the formula (I), or other compounds disclosed herein, containing carboxy or hydroxy group is, for example, a pharmaceutically WO 2007/126358 PCT/SE2007/000400 -7 acceptable ester which is hydrolysed in the human or animal body to produce the parent acid or alcohol. Suitable pharmaceutically acceptable esters for carboxy include C 16 alkoxymethyl esters for example methoxymethyl, C 1
-
6 alkanoyloxymethyl esters for example pivaloyloxymethyl, phthalidyl esters, C 3 .. cycloalkoxycarbonyloxyC1- 6 alkyl esters for example 5 1-cyclohexylcarbonyloxyethyl; 1,3-dioxolen-2-onylmethyl esters for example 5-methyl-1,3-dioxolen-2-onylmethyl; and C 1
.
6 alkoxycarbonyloxyethyl esters for example 1-methoxycarbonyloxyethyl and may be formed at any carboxy group in the compounds of this invention. An in vivo hydrolysable ester of a compound of the formula (I), or other compounds 10 disclosed herein, containing a hydroxy group includes inorganic esters such as phosphate esters and a-acyloxyalkyl ethers and related compounds which as a result of the in vivo hydrolysis of the ester breakdown to give the parent hydroxy group. Examples of c-acyloxyalkyl ethers include acetoxymethoxy and 2,2-dimethylpropionyloxy-methoxy. A selection of in vivo hydrolysable ester forming groups for hydroxy include alkanoyl, benzoyl, 15 phenylacetyl and substituted benzoyl and phenylacetyl, alkoxycarbonyl (to give alkyl carbonate esters), dialkylcarbamoyl and N-(dialkylaminoethyl)-N-alkylcarbamoyl (to give carbamates), dialkylaminoacetyl and carboxyacetyl. Examples of substituents on benzoyl include morpholino and piperazino linked from a ring nitrogen atom via a methylene group to the 3- or 4- position of the benzoyl ring. 20 A suitable value for an in vivo hydrolysable amide of a compound of the formula (I), or other compounds disclosed herein, containing a carboxy group is, for example, a N-C1.
6 alkyl or NN-di-C 1
-
6 alkyl amide such as N-methyl, N-ethyl, N-propyl, NN-dimethyl, N-ethyl-N-methyl or NN-diethyl amide. Some compounds of the formula (I) may have chiral centres and/or geometric 25 isomeric centres (E- and Z- isomers), and it is to be understood that the invention encompasses all such optical, diastereoisomers and geometric isomers that possess cholesterol absorption inhibitory activity. The invention relates to any and all tautomeric forms of the compounds of the formula (I) that possess cholesterol absorption inhibitory activity. 30 It is also to be understood that certain compounds of the formula (I) can exist in solvated as well as unsolvated forms such as, for example, hydrated forms. It is to be understood that the invention encompasses all such solvated forms which possess cholesterol absorption inhibitory activity.
WO 2007/126358 PCT/SE2007/000400 -8 Preferred aspects of the invention are those which relate to the compound of formula (I) or a pharmaceutically acceptable salt thereof. Another aspect of the present invention provides a process for preparing a compound 5 of formula (I) or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof which process (wherein variable groups are, unless otherwise specified, as defined in formula (I)) comprises of: Another aspect of the present invention provides a process for preparing a compound of formula (12) or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug 10 thereof which process (wherein variable groups are, unless otherwise specified, as defined in formula (I)) comprises of: Process 1) reacting a compound of formula (II): OH OH R3 N SOO O 15 R4 (II) with a compound of formula (III): R6 O R 1 0 L N N OH o
R
2
R
5 (III) 20 wherein L is a displaceable group; Process 2) reacting an acid of formula (IV): WO 2007/126358 PCT/SE2007/000400 -9 0 OH 0 CI OH R3 N 0 S=O R4 (IV) or an activated derivative thereof; with an amine of formula (V):
R
6 R1 0
H
2 N OH O R 2
R
5 5 (V) Process 3): reacting an acid of formula (VI): 0 RI OH o OH R3 )-7 O 0 HN/ S=0 R4 (VI) or an activated derivative thereof, with an amine of formula (VII): 10 WO 2007/126358 PCT/SE2007/000400 - 10 R6 1 0 HN OH
R
2
R
5 (VII) Process 4): reducing a compound of formula (VIII): R6 0 R' 0 O N OH 3 ISH R 2
R
5 R R N"1 iI~ H4 5 (VIII) Process 5): reacting a compound of formula (IX):
R
6 O R I1 O N O N N OH HS H 0 R 2
R
5 N 0 0 N O H4 R4 (IX) with a compound of formula (X): OH 3 L 10
MX
WO 2007/126358 PCT/SE2007/000400 - 11 wherein L is a displaceable group; Process 6): reacting a compound of formula (XI): 0 R 1 RO N 0 0 H0 NsO R4 (XI) 5 wherein L is a displaceable group; with a compound of formula (XII): OH 3 SH R (XII) Process 7): De-esterifying a compound of formula (XIII) O R1 R 6 0 OH O N OR NN 3/ SIH 0 R2 R 5 RR 10 (XIII) wherein the group C(0)OR is an ester group; and thereafter if necessary or desirable: i) converting a compound of the formula (I) into another compound of the formula (I); ii) removing any protecting groups; 15 iii) forming a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug; or WO 2007/126358 PCT/SE2007/000400 - 12 iv) separating two or more enantiomers. L is a displaceable group, suitable values for L are for example, a halogeno or sulphonyloxy group, for example a chloro, bromo, methanesulphonyloxy or toluene-4-sulphonyloxy group. 5 C(O)OR is an ester group, suitable values for C(O)OR are methoxycarbonyl, ethoxycarbonyl, t-butoxycarbonyl and benzyloxycarbonyl. The starting materials used in the present invention can be prepared by modifications of the routes described in EP 0 792 264 B1, W005062824 and WO 05061452. Alternatively they can be prepared by the following reactions. 10 Process 1): Alcohols of formula (II) may be reacted with compounds of formula (III) in the presence of a base for example an inorganic base such as sodium carbonate, or an organic base such as Hunigs base, in the presence of a suitable solvent such as acetonitrile, dichloromethane or tetrahydrofuran at a temperature in the range of 0 0 C to reflux, preferably 15 at or near reflux. Another aspect of the present invention provides a process for preparing a compound of formula (12) or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof which process (wherein variable groups are, unless otherwise specified, as defined in 20 formula (I)) comprises of: Process 1) reacting a compound of formula (112): OH OH R3 N 0 SO R4 25 (112) WO 2007/126358 PCT/SE2007/000400 - 13 with a compound of formula (III):
R
6 O R1 0 L N OH 0 R 2
R
5 (III) wherein L is a displaceable group; 5 Process 2) reacting an acid of formula (IV2): 0 OH OH R3 O N 0 N~ /=0 S-0 R4 (IV2) or an activated derivative thereof; with an amine of formula (V):
R
6 R1 0
H
2 N OH 0
R
2
R
5 10 (V) Process 3): reacting an acid of formula (V12): WO 2007/126358 PCT/SE2007/000400 - 14 0 R1 OH 0 OH H N R3R N 0 0 S=O R4 (V12) or an activated derivative thereof, with an amine of formula (VII):
R
6 1 0 HN OH
R
2
R
5 5 (VII) Process 4): reducing a compound of formula (VII12): R6 0 R1 0 3 -"ON OH R S H R 2
R
5 R4 (VIII2) 10 Process 5): reacting a compound of formula (IX2): WO 2007/126358 PCT/SE2007/000400 -15 R6 0 R1 0 N N OH H HS,, 0 R 2
R
5 N 0 j N 0 O N - ::-O H II R4 (IX2) with a compound of formula (X): OH 3 L R' 5 (X) wherein L is a displaceable group; Process 6): reacting a compound of formula (X12):
R
6 O R0 O N N OH L o R2 R 5 N O L 0 H O R4 (X12) 10 wherein L is a displaceable group; with a compound of formula (XII): OH 3 SH R (XII) Process 7): De-esterifying a compound of formula (X1112) WO 2007/126358 PCT/SE2007/000400 - 16 0 R1 R 6 0 OH o N N OR 3S H 0 R 2
R
5 N 0 R4 (XII12) wherein the group C(O)OR is an ester group; 5 and thereafter if necessary or desirable: i) converting a compound of the formula (12) into another compound of the formula (I2); ii) removing any protecting groups; iii) forming a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug; or iv) separating two or more enantiomers. 10 L is a displaceable group, suitable values for L are for example, a halogeno or sulphonyloxy group, for example a chloro, bromo, methanesulphonyloxy or toluene-4-sulphonyloxy group. C(O)OR is an ester group, suitable values for C(O)OR are methoxycarbonyl, ethoxycarbonyl, t-butoxycarbonyl and benzyloxycarbonyl. 15 The starting materials used in the present invention can be prepared by modifications of the routes described in EP 0 792 264 B1, W005062824 and WO. Alternatively they can be prepared by the following reactions. Process 1): Alcohols of formula (II) or (112) may be reacted with compounds of formula (III) 20 in the presence of a base for example an inorganic base such as sodium carbonate, or an organic base such as Hunigs base, in the presence of a suitable solvent such as acetonitrile, dichloromethane or tetrahydrofuran at a temperature in the range of 0 0 C to reflux, preferably at or near reflux. 25 WO 2007/126358 PCT/SE2007/000400 - 17 Process 2) and Process 3): Acids and amines may be coupled together in the presence of a suitable coupling reagent. Standard peptide coupling reagents known in the art can be employed as suitable coupling reagents, for example carbonyldiimidazole and dicyclohexyl-carbodiimide, optionally in the presence of a catalyst such as 5 dimethylaminopyridine or 4-pyrrolidinopyridine, optionally in the presence of a base for example triethylamine, pyridine, or 2,6-di-alkyl-pyridines such as 2,6-lutidine or 2,6-di-tert-butylpyridine. Suitable solvents include dimethylacetamide, dichloromethane, benzene, tetrahydrofuran and dimethylformamide. The coupling reaction may conveniently be performed at a temperature in the range of -40 to 40'C. 10 Suitable activated acid derivatives include acid halides, for example acid chlorides, and active esters, for example pentafluorophenyl esters. The reaction of these types of compounds with amines is well known in the art, for example they may be reacted in the presence of a base, such as those described above, and in a suitable solvent, such as those described above. The reaction may conveniently be performed at a temperature in the range of 15 -40 to 40*C. Acids of formula (IV) or (IV2)and (VI) or (V12) may be prepared from compounds of formula (II) or (112) by reacting them with the appropriate, optionally protected, side chain using the conditions of Process 1). Amines of formula (V) and (VII) are commercially available compounds, or they are known in the literature, or they are prepared by standard 20 processes known in the art. Process 4): Reduction of compounds of formula (VIII) or (VII12) could be performed with a hydride reagent such as sodium borohydride in a solvent such as methanol at temperatures suitable between -20-40*C. Compounds of formula (VIII) or (VII12) can be prepared using the conditions of 25 Process 1, Process 2 or Process 3 and appropriate modifications of descriptions in EP 0 792 264 B1, W005062824 and WO 05061452. Process 5) and Process 6): these compounds may be reacted together in the presence of a base for example an inorganic base such as sodium carbonate, or an organic base such as 30 Hunigs base, in the presence of a suitable solvent such as acetonitrile, dichloromethane or tetrahydrofuran at a temperature in the range of 0 0 C to reflux, preferably at or near reflux. Compounds of formula (IX) or (IX2) and (XI) or (X12) may be prepared by appropriate modifications of descriptions in EP 0 792 264 B 1, W005062824 and WO WO 2007/126358 PCT/SE2007/000400 - 18 05061452. Compounds of formula (X) and (XII) are commercially available compounds, or they are known in the literature, or they are prepared by standard processes known in the art. Process 7): Esters of formula (XIII) or (XII12) may be deprotected under standard conditions such as those described below, for example a methyl or ethyl ester may be deprotected with 5 sodium hydroxide in methanol at room temperature. Compounds of formula (XIII) or (XII12) may be prepared by a modification of any of the processes described herein for the preparation of compounds of formula (I) or (12). It will also be appreciated that in some of the reactions mentioned herein it may be 10 necessary/desirable to protect any sensitive groups in the compounds. The instances where protection is necessary or desirable and suitable methods for protection are known to those skilled in the art. Conventional protecting groups may be used in accordance with standard practice (for illustration see T.W. Green, Protective Groups in Organic Synthesis, John Wiley and Sons, 1999). Thus, if reactants include groups such as amino, carboxy or hydroxy it may 15 be desirable to protect the group in some of the reactions mentioned herein. A suitable protecting group for an amino or alkylamino group is, for example, an acyl group, for example an alkanoyl group such as acetyl, an alkoxycarbonyl group, for example a methoxycarbonyl, ethoxycarbonyl or t-butoxycarbonyl group, an arylmethoxycarbonyl group, for example benzyloxycarbonyl, or an aroyl group, for example benzoyl. The deprotection 20 conditions for the above protecting groups necessarily vary with the choice of protecting group. Thus, for example, an acyl group such as an alkanoyl or alkoxycarbonyl group or an aroyl group may be removed for example, by hydrolysis with a suitable base such as an alkali metal hydroxide, for example lithium or sodium hydroxide. Alternatively an acyl group such as a t-butoxycarbonyl group may be removed, for example, by treatment with a suitable acid 25 as hydrochloric, sulphuric or phosphoric acid or trifluoroacetic acid and an arylmethoxycarbonyl group such as a benzyloxycarbonyl group may be removed, for example, by hydrogenation over a catalyst such as palladium-on-carbon, or by treatment with a Lewis acid for example boron tris(trifluoroacetate). A suitable alternative protecting group for a primary amino group is, for example, a phthaloyl group which may be removed by 30 treatment with an alkylamine, for example dimethylaminopropylamine, or with hydrazine. A suitable protecting group for a hydroxy group is, for example, an acyl group, for example an alkanoyl group such as acetyl, an aroyl group, for example benzoyl, or an arylmethyl group, for example benzyl. The deprotection conditions for the above protecting WO 2007/126358 PCT/SE2007/000400 - 19 groups will necessarily vary with the choice of protecting group. Thus, for example, an acyl group such as an alkanoyl or an aroyl group may be removed, for example, by hydrolysis with a suitable base such as an alkali metal hydroxide, for example lithium or sodium hydroxide. Alternatively an arylmethyl group such as a benzyl group may be removed, for example, by 5 hydrogenation over a catalyst such as palladium-on-carbon. A suitable protecting group for a carboxy group is, for example, an esterifying group, for example a methyl or an ethyl group which may be removed, for example, by hydrolysis with a base such as sodium hydroxide, or for example a t-butyl group which may be removed, for example, by treatment with an acid, for example an organic acid such as trifluoroacetic 10 acid, or for example a benzyl group which may be removed, for example, by hydrogenation over a catalyst such as palladium-on-carbon. The protecting groups may be removed at any convenient stage in the synthesis using conventional techniques well known in the chemical art. 15 As stated hereinbefore the compounds defined in the present invention possess cholesterol absorption inhibitory activity. These properties may be assessed, using the following biological tests. In vivo testing of cholesterol absorption inhibitors (A) 20 C57BL/6 female mice were maintained on regular chow diet and housed in individual cages to collect faeces. Mice were fasted for 3 hours and then gavaged with vehicle or compound. Half an hour later the mice were gavaged with radiolabelled cholesterol. Six hours after the 14 C-cholesterol gavage blood samples were taken via the tail and plasma prepared to determine how much cholesterol were absorbed. 24 hours after the gavage of 14 C-cholesterol 25 the mice were bled and plasma were prepared for analysis. Faeces were collected for 24 hours to assess absorption efficiency. In vivo testing of cholesterol absorption inhibitors (B). C57BL/6 female mice were maintained on regular chow diet and housed in individual cages to collect faeces. Mice were fasted for 3 hours and then gavaged with vehicle or 30 compound. One to ten hours later the mice were gavaged with radiolabelled cholesterol. Six hours after the 1 4 C-cholesterol gavage blood sample was taken via the tail and plasma prepared to determine how much cholesterol was absorbed. 24 hours after the gavage of 1 4
C-
WO 2007/126358 PCT/SE2007/000400 - 20 cholesterol the mice were bled and plasma analysed for radioactivity. Faeces were also collected for 24 hours to assess absorption efficiency. References 1. E. A. Kirk, G. L. Moe, M. T. Caldwell, J. A. Lernmark, D. L. Wilson, R. C. LeBoeuf. 5 Hyper- and hypo-responsiveness to dietary fat and cholesterol among inbred mice: searching for level and variability genes. J. Lipid Res. 1995 36:1522-1532. 2. C. P. Carter, P. N. Howles, D. Y. Hui. Genetic variation in cholesterol absorption efficiency among inbred strains of mice. J. Nutr. 1997 127:1344-1348. 3. C. D. Jolley, J. M. Dietschy, S. D. Turley. Genetic differences in cholesterol absorption in 10 129/Sv and C57BL/6 mice: effect on cholesterol responsiveness. Am. J. Physiol. 1999 276:G1117-G1124. Administration of 0.2 jimol/kg of Example 6 gave 90% inhibition of 14 C-cholesterol absorption (procedure A). 15 According to a further aspect of the invention there is provided a pharmaceutical composition which comprises a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, as defined hereinbefore in association with a pharmaceutically-acceptable diluent or carrier. 20 The composition may be in a form suitable for oral administration, for example as a tablet or capsule, for parenteral injection (including intravenous, subcutaneous, intramuscular, intravascular or infusion) as a sterile solution, suspension or emulsion, for topical administration as an ointment or cream or for rectal administration as a suppository. In general the above compositions may be prepared in a conventional manner using 25 conventional excipients. The compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, will normally be administered to a warm-blooded animal at a unit dose within the range of approximately 0.02-100 mg/kg, preferably 0.02 -50 mg/kg, and this normally provides a therapeutically-effective dose. A unit dose form such as a tablet 30 or capsule will usually contain, for example 1-250 mg of active ingredient. Preferably a daily dose in the range of 1-50 mg/kg, particularly 0.1-10 mg/kg is employed. In another aspect a daily dose in the rage of 0.01-20 mg/kg is employed. In one aspect of the invention the daily dose of a compound of formula (I) is less than or equal to 100mg. However the daily dose WO 2007/126358 PCT/SE2007/000400 - 21 will necessarily be varied depending upon the host treated, the particular route of administration, and the severity of the illness being treated. Accordingly the optimum dosage may be determined by the practitioner who is treating any particular patient. According to a further aspect of the present invention there is provided a compound of 5 the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, as defined hereinbefore for use in a method of prophylactic or therapeutic treatment of a warm-blooded animal, such as man. We have found that the compounds defined in the present invention, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, are 10 effective cholesterol absorption inhibitors, and accordingly have value in the treatment of disease states associated with hyperlipidaemic conditions. Thus according to this aspect of the invention there is provided a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, as defined hereinbefore for use as a medicament. 15 According to another feature of the invention there is provided the use of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, as defined hereinbefore in the manufacture of a medicament for use in the production of a cholesterol absorption inhibitory effect in a warm-blooded animal, such as man. 20 According to another feature of the invention there is provided the use of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, as defined hereinbefore in the production of a cholesterol absorption inhibitory effect in a warm-blooded animal, such as man. Herein, where the production of a cholesterol absorption inhibitory effect or a 25 cholesterol lowering effect is stated, suitably this relates to the treatment of hyperlipidaemic conditions in a warm-blooded animal, such as man. Additionally is relates to the treatment of dyslipidemic conditions and disorders such as hyperlipidaemia, hypertrigliceridemia, hyperbetalipoproteinemia (high LDL), hyperprebetalipoproteinemia (high VLDL), hyperchylomicronemia, hypolipoproteinemia, hypercholesterolemia, hyperlipoproteinemia 30 and hypoalphalipoproteinemia (low HDL) in a warm-blooded animal, such as man. Furthermore it relates to the treatment of different clinical conditions such as atherosclerosis, arteriosclerosis, arrhythmia, hyper-thrombotic conditions, vascular dysfunction, endothelial dysfunction, heart failure, coronary heart diseases, cardiovascular diseases, myocardial WO 2007/126358 PCT/SE2007/000400 -22 infarction, angina pectoris, peripheral vascular diseases, inflammation of cardiovascular tissues such as heart, valves, vasculature, arteries and veins, aneurisms, stenosis, restenosis, vascular plaques, vascular fatty streaks, leukocytes, monocytes and/or macrophage infiltration, intimal thickening, medial thinning, infectious and surgical trauma and vascular 5 thrombosis, stroke and transient ischaemic attacks in a warm-blooded animal, such as man. It also relates to the treatment of atherosclerosis, coronary heart diseases, myocardial infarction, angina pectoris, peripheral vascular diseases, stroke and transient ischaemic attacks in a warm-blooded animal, such as man. The production of a cholesterol absorption inhibitory effect or a cholesterol lowering 10 effect also relates to a method of treating and/or preventing atherosclerotic lesions, a method of preventing plaque rupture and a method of promoting lesion regression. Furthermore it relates to a method of inhibiting monocytes-macrophage accumulation in atherosclerotic lesions, a method of inhibiting expression of matrix metalloproteinases in atherosclerotic lesions, a method of inhibiting the destabilization of atherosclerotic lesions, a method for 15 preventing atherosclerotic plaque rupture and a method of treating unstable angina. The production of a cholesterol absorption inhibitory effect or a cholesterol lowering effect also relates to a method of treating sitosterolemia. Compounds of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof may also have value in the treatment or prevention of 20 Alzeheimer's Disease (see for example WO 02/096415). Therefore in a further aspect of the invention, there is provided a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, for use in the treatment or prevention of Alzheimer's Disease. Compounds of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a 25 salt or a prodrug thereof may also have value in the treatment or prevention of cholesterol associated tumors. Therefore in a further aspect of the invention, there is provided a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, for use in the treatment or prevention of cholesterol associated tumors. Compounds of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of 30 such a salt or a prodrug thereof may also have value in the treatment or prevention of vascular inflammation (see for example WO 03/026644). Therefore in a further aspect of the invention, there is provided a compound of formula (I), or a pharmaceutically acceptable salt, solvate, WO 2007/126358 PCT/SE2007/000400 -23 solvate of such a salt or a prodrug thereof, for use in the treatment or prevention of vascular inflammation. According to a further feature of this aspect of the invention there is provided a method for producing a cholesterol absorption inhibitory effect in a warm-blooded animal, 5 such as man, in need of such treatment which comprises administering to said animal an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. The cholesterol absorption inhibitory activity defined hereinbefore may be applied as a sole therapy or may involve, in addition to a compound of the invention, one or more other 10 substances and/or treatments. Such conjoint treatment may be achieved by way of the simultaneous, sequential or separate administration of the individual components of the treatment. According to this aspect of the invention there is provided a pharmaceutical product comprising a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, as defined hereinbefore and an additional 15 cholesterol absorption inhibitory substance as defined hereinbefore and an additional hypolipidaemic agent for the conjoint treatment of hyperlipidaemia. In another aspect of the invention, the compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, may be administered in association with cholesterol biosynthesis inhibitors, or pharmaceutically acceptable salts, 20 solvates, solvates of such salts or prodrugs thereof. Suitable cholesterol biosynthesis inhibitors include HMG Co-A reductase inhibitors, squalene synthesis inhibitors and squalene epoxidase inhibitors. Suitable squalene synthesis inhibitors are e.g squalestatin 1, TAK 475 and compounds described in W02005012284. A suitable squalene epoxidase inhibitor is NB 598. 25 In this aspect of the invention, the compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, may be administered in association with an HMG Co-A reductase inhibitor, or pharmaceutically acceptable salts, solvates, solvates of such salts or prodrugs thereof. Suitable HMG Co-A reductase inhibitors, pharmaceutically acceptable salts, solvates, solvates of such salts or prodrugs thereof are 30 statins well known in the art. Particular statins are fluvastatin, lovastatin, pravastatin, simvastatin, atorvastatin, cerivastatin, bervastatin, dalvastatin, mevastatin and rosuvastatin, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. A further particular statin is pitavastatin, or a pharmaceutically acceptable salt, solvate, solvate WO 2007/126358 PCT/SE2007/000400 -24 of such a salt or a prodrug thereof. A particular statin is atorvastatin, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. A more particular statin is atorvastatin calcium salt. A further particular statin is rosuvastatin, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. A preferable particular 5 statin is rosuvastatin calcium salt. Therefore in an additional feature of the invention, there is provided a combination of a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof and an HMG Co-A reductase inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. 10 Therefore in an additional feature of the invention, there is provided a method for producing a cholesterol lowering effect in a warm-blooded animal, such as man, in need of such treatment which comprises administering to said animal an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof in simultaneous, sequential or separate administration with an effective 15 amount of an HMG Co-A reductase inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. According to a further aspect of the invention there is provided a pharmaceutical composition which comprises a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and an HMG Co-A reductase 20 inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in association with a pharmaceutically acceptable diluent or carrier. According to a further aspect of the present invention there is provided a kit comprising a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and an HMG Co-A reductase inhibitor, or a 25 pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. According to a further aspect of the present invention there is provided a kit comprising: a) a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in a first unit dosage form; 30 b) an HMG Co-A reductase inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof; in a second unit dosage form; and c) container means for containing said first and second dosage forms.
WO 2007/126358 PCT/SE2007/000400 -25 According to a further aspect of the present invention there is provided a kit comprising: a) a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, together with a pharmaceutically acceptable diluent or carrier, in a 5 first unit dosage form; b) an HMG Co-A reductase inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in a second unit dosage form; and c) container means for containing said first and second dosage forms. According to another feature of the invention there is provided the use of a compound 10 of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and an HMG Co-A reductase inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in the manufacture of a medicament for use in the production of a cholesterol lowering effect. According to a further aspect of the present invention there is provided a combination 15 treatment comprising the administration of an effective amount of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, optionally together with a pharmaceutically acceptable diluent or carrier, with the simultaneous, sequential or separate administration of an effective amount of an HMG Co-A reductase inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a 20 prodrug thereof, optionally together with a pharmaceutically acceptable diluent or carrier to a warm-blooded animal, such as man in need of such therapeutic treatment. According to an additional further aspect of the present invention there is provided a combination treatment comprising the administration of an effective amount of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a 25 prodrug thereof, optionally together with a pharmaceutically acceptable diluent or carrier, with the simultaneous, sequential or separate administration of a matrix metalloproteinase inhibitor. In another aspect of the invention, the compound of formula (I), or a 30 pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, may be administered in association with an ileal bile acid (IBAT) inhibitor or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. Suitable compounds possessing IBAT inhibitory activity for use in combination with WO 2007/126358 PCT/SE2007/000400 -26 compounds of the present invention have been described, see for instance the compounds described in WO 93/16055, WO 94/18183, WO 94/18184, WO 94/24087, WO 96/05188, WO 96/08484, WO 96/16051, WO 97/33882, WO 98/07749,WO 98/38182, WO 98/40375, WO 98/56757, WO 99/32478, WO 99/35135, WO 5 99/64409, WO 99/64410, WO 00/01687, WO 00/20392, WO 00/20393, WO 00/20410, WO 00/20437, WO 00/35889, WO 01/34570, WO 00/38725, WO 00/38726, WO 00/38727, WO 00/38728, WO 00/38729, WO 00/47568, WO 00/61568, WO 01/66533, WO 01/68096, WO 01/68637, WO 02/08211, WO 02/50051, WO 03/018024, WO 03/040127, WO 03/043992, WO 03/061604, 10 WO 04/020421, WO 04/076430,DE 19825804, JP 10072371, US 5070103, EP 251 315, EP 417 725, EP 489 423, EP 549 967, EP 573 848, EP 624 593, EP 624 594, EP 624 595, EP 864 582, EP 869 121 and EP 1070 703, WO 03/020710, WO 03/022825, WO 03/022830, WO 03/022286, WO 03/091232, WO 03/106482, and EP 597 107 15 and the contents of these patent applications are incorporated herein by reference. Particularly the named examples of these patent applications are incorporated herein by reference. More particularly claim 1 of these patent application are incorporated herein by reference. Other suitable classes of IBAT inhibitors for use in combination with compounds of the present invention are the benzothiepines, 1,2-benzothiazepines, 1,4-benzothiazepines and 20 1,5-benzothiazepines. A further suitable class of IBAT inhibitors is the 1,2,5 benzothiadiazepines. One particular suitable compound possessing IBAT inhibitory activity for use in combination with compounds of the present invention is (3R,5R)-3-butyl-3-ethyl-1,1-dioxido 5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl beta-D-glucopyranosiduronic acid (EP 25 864582). A further suitable compound possessing IBAT inhibitory activity for use in combination with compounds of the present invention is S-8921 (EP 597 107) and BARI 1741. A further suitable IBAT inhibitor for use in combination with compounds of the 30 present invention is the compound: WO 2007/126358 PCT/SE2007/000400 -27 0 -"S S (R) z :0 0
C'
N -N WO 99/32478 5 A particular BAT inhibitor for use in combination with compounds of the present invention is selected from any one of Examples 1-120 of WO 02/50051, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and the compounds of Examples 1-120 are incorporated herein by reference. Claims 1-15 of WO 02/50051 are also incorporated herein by reference. A particular IBAT inhibitor selected from WO 02/50051 for 10 use in combination with compounds of the present invention is selected from any one of: 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-1'-phenyl-1'-[N'-(carboxymethyl) carbamoyl]methyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-c-[N'-(carboxymethyl)carbamoyl]-4 hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 15 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-1'-phenyl-1'-[N'-(2 sulphoethyl)carbamoyl]methyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-(N-{ (R)-1'-phenyl-1'-[N'-(2 sulphoethyl)carbamoyl]methyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{(R)-a-[N'-(2-sulphoethyl)carbamoyl]-4 20 hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-(N-{(R)-a-[N'-(2-sulphoethyl) carbamoyl]-4-hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; WO 2007/126358 PCTSE2007OOO400 -28 1, 1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-(N- { (R)-cX-[N'-(2 carboxyethyl)carbamoyl]benzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 1, 1-.dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- I (R)-c.-[N'-(2-carboxyethy1)carbamoy1]-4 hydroxybenzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 5 1, 1 -dioxo-3--butyl-3-ethyl-5-phenyl-7-methylthio-8-(N- I (R)-ce4N'--(5-carboxypentyl) carbamoyl]benzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 1, 1-dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- {(R)-u-[N'-(2-carboxyethyl)carbamoyl] benzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 1, 1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N- I cx[N'-(2-sulphoethyl)carbamoyl]-2 10 fluorobenzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 1, 1-dioxo-3-butyl-3--ethyl-5-phenyl-7- methylthio-8-(N- {(R)-c- [N'-(R)-(2-hydroxy- 1 carboxyethyl)carbamoyl]benzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 1, 1-dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- {(R)-cX-[N'-(R)-(2-hydroxy-1 carboxyethyl)carbamoyl]benzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 15 1,1 -dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8- {N- [(R)-ca-(N'- {(R)-l1-IIN"-(R)-(2-hydroxy- 1 carboxyethyl)carbamoyl] -2-hydroxyethyl }carbamoyl)benzyl]carbamoylmethoxy} -2,3,4,5 tetrahydro- 1,5-benzothiazepine; 1, 1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio- 8-(N- { o-[N'-(carboxymethy1)carbainoyl] benzyl Icarbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 20 1, 1-dioxo-3-butyl-3.-ethyl-5-phenyl-7-methylthio-8-(N- x- [N'-((ethoxy)(methyl)phosphoryl methyl)carbamoyllbenzyl Icarbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 1,1 -dioxo-3-butyl-3-ethyl-5-phenyl-7-methyltlhio-8- {N-[(R)-oc-(N'- {2 [(hydroxy)(methyl)phosphoryl] ethyl)} carbamoyl)benzyll carbamoylmethoxy }-2,3,4,5 tetrahydro-1 ,5-benzothiazepine; 25 1,1 -dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- {(R)-oc-[N'-(2-methylthio- 1 carboxyethyl)carbamoyl]benzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 1,1 -dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8- {N-II(R)-u.-(N'-1{2- [(methyl)(ethyl) phosphoryl] ethyl I carbamoyl)-4-hydroxybenzyll carbamoylmethoxy}I -2,3 ,4,5-tetrahydro- 1,5 benzothiazepine; 30 1,1 -dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8- {N-[(R)-oc-(N'-1{2-I[(iethy1)(hydroxy) phosphoryl] ethyl I carb amoyl)-4-hydroxybenzyll carbamoylmethoxy I -2,3 ,4,5-tetrahydro- 1,5 benzothiazepine; WO 2007/126358 PCT/SE2007/000400 -29 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{(R)-a-[(R)-N'-(2-methylsulphinyl-1 carboxyethyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; and 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methoxy-8-[N-{ (R)-x-[N'-(2-sulphoethyl)carbamoyl]-4 5 hydroxybenzyl carbamoylmethoxy]-2,3,4,5-tetrahydro-1,5-benzothiazepine; or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. A particular IBAT inhibitor for use in combination with compounds of the present invention is selected from any one of Examples 1-44 of WO 03/0207 10, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and the compounds of 10 Examples 1-44 are incorporated herein by reference. Claims 1-10 of WO 03/020710 are also incorporated herein by reference. A particular IBAT inhibitor selected from WO 03/020710 for use in combination with compounds of the present invention is selected from any one of: 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-ca-[N-(2-(S)-3-(R)-4-(R)-5-(R) 2,3,4,5,6-pentahydroxyhexyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5 15 benzothiazepine; 1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-(N-{ (R)-a-[AP-(2-(S)-3-(R)-4-(R)-5-(R) 2,3,4,5,6-pentahydroxyhexyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5 benzothiazepine; 1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-(N-{ (R)-oa-[N-((S)-1-carbamoyl-2 20 hydroxyethyl)carbamoyl]benzyl carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-(N-{ (R)-a-[N-(hydroxycarbamoyl methyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-[N-((R)-a-{N-[2-(N-pyrimidin-2 ylureido)ethyl]carbamoyl }benzyl)carbamoylmethoxy]-2,3,4,5-tetrahydro-1,5 25 benzothiazepine; 1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-[N-((R)-x- {N-[2-(N-pyridin-2 ylureido)ethyl]carbamoyl }benzyl)carbamoylmethoxy]-2,3,4,5-tetrahydro-1,5 benzothiazepine; 1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-(N-{(R)-a-[N-(1-t 30 butoxycarbonylpiperidin-4-ylmethyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5 tetrahydro- 1,5-benzothiazepine; WO 2007/126358 PCT/SE2007/000400 -30 1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-(N-{(R)-ac-[N'-(2,3 dihydroxypropyl)carbamoyl]benzyl carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5 benzothiazepine; 1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-[N-((R)-c- {N-[2-(3,4-dihydroxyphenyl) 5 2-methoxyethyl]carbamoyl }benzyl)carbamoylmethoxy]-2,3,4,5-tetrahydro- 1,5 benzothiazepine 1, 1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-(N-{I(R)-ax-[NT-(2 aminoethyl)carbamoyl]benzyl } carbamoylmethoxy)-2,3,4,5-tetrahydro- 1,5-benzothiazepine; 1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-(N-{ (R)-x-[N-(piperidin-4-ylmethyl) 10 carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; or 1,1-dioxo-3-butyl-3-ethyl-5-phenyl-7-methylthio-8-(N-{(R)-a-[N-(2-N,N dimethylaminosulphamoylethyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro 1,5-benzothiazepine; or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. 15 A particular IBAT inhibitor for use in combination with compounds of the present invention is selected from any one of Examples 1-7 of WO 03/022825, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and the compounds of Examples 1-7 are incorporated herein by reference. Claims 1-8 of WO 03/022825 are also incorporated herein by reference. A particular BAT inhibitor selected from WO 03/022825 20 for use in combination with compounds of the present invention is selected from any one of: 1,1-dioxo-3(R)-3-butyl-3-ethyl-5-(R)-5-phenyl-8-[N-((R)-a-carboxybenzyl) carbamoylmethoxy]-2,3,4,5-tetrahydro-1,4-benzothiazepine; 1,1-dioxo-3(S)-3-butyl-3-ethyl-5-(S)-5-phenyl-8-[N-((R)-aX-carboxybenzyl) carbamoylmethoxy]-2,3,4,5-tetrahydro-1,4-benzothiazepine; 25 1,1-dioxo-3(R)-3-butyl-3-ethyl-5-(R)-5-phenyl-8-(N-{ (R)-a.-[N-(carboxymethyl)carbamoyl] benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,4-benzothiazepine; 1,1-dioxo-3(S)-3-butyl-3-ethyl-5-(S)-5-phenyl-8-(N-{ (R)-a-[N-(carboxymethyl)carbamoyl] benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,4-benzothiazepine; 3,5-trans-1,1-dioxo-3-ethyl-3-butyl-5-phenyl-7-bromo-8-(N-{ (R)-a-[N 30 (carboxymethyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,4 benzothiazepine; WO 2007/126358 PCT/SE2007/000400 - 31 3,5-trans-1, 1-dioxo-3-(S)-3-ethyl-3-butyl-4-hydroxy-5-(S)-5-phenyl-7-bromo-8-(N- { (R)-a [N-(carboxymethyl)carbamoyl]benzyl } carbamoylmethoxy)-2,3,4,5-tetrahydro- 1,4 benzothiazepine 3,5-trans-1,1-dioxo-3-(R)-3-ethyl-3-butyl-4-hydroxy-5-(R)-5-phenyl-7-bromo-8-(N-{(R)-a 5 [N-(carboxymethyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,4 benzothiazepine; 3,5-trans-1, 1-dioxo-3-ethyl-3-butyl-5-phenyl-7-methylthio-8-(N- { (R)-a-[N (carboxymethyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,4 benzothiazepine; 10 3,5-trans-1,1-dioxo-3-ethyl-3-butyl-5-phenyl-7-methylthio-8-(N- { (R)-a-[N-(2 sulphoethyl)carbamoyl]-4-hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,4 benzothiazepine ammonia salt; 1,1-dioxo-3-(S)-3-ethyl-3-butyl-5-(S)-5-phenyl-7-methylthio-8-(N-{(R)-X-[N (carboxymethyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,4 15 benzothiazepine diethylamine salt; and 1,1-dioxo-3-(R)-3-ethyl-3-butyl-5-(R)-5-phenyl-7-methylthio-8-(N-{(R)-a-[N (carboxymethyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,4 benzothiazepine diethylamine salt; or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. 20 A particular IBAT inhibitor for use in combination with compounds of the present invention is selected from any one of Examples 1-4 of WO 03/022830, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and the compounds of Examples 1-4 are incorporated herein by reference. Claims 1-8 of WO 03/022830 are also incorporated herein by reference. A particular IBAT inhibitor selected from WO 03/022830 25 for use in combination with compounds of the present invention is selected from any one of: 1,1-dioxo-3-butyl-3-ethyl-4-hydroxy-5-phenyl-7-(N-{ (R)-a-[N (carboxymethyl)carbamoyl]benzyl}carbamoylmethylthio)-2,3,4,5-tetrahydrobenzothiepine 1,1-dioxo-3-butyl-3-ethyl-4-hydroxy-5-phenyl-7-(N- { (R)-ax-[N-(2-sulphoethyl)carbamoyl]-4 hydroxybenzyl}carbamoylmethylthio)-2,3,4,5-tetrahydrobenzothiepine ammonia salt 30 1,1-dioxo-3-butyl-3-ethyl-4-hydroxy-5-phenyl-7- {N-[ca-(carboxy)-2-fluorobenzyl] carbamoylmethylthio}-2,3,4,5-tetrahydrobenzothiepine; and 1,1-dioxo-3-butyl-3-ethyl-4-hydroxy-5-phenyl-7-{N-[1-(carboxy)-1-(thien-2-yl)methyl] carbamoylmethylthio 1-2,3,4,5-tetrahydrobenzothiepine WO 2007/126358 PCT/SE2007/000400 -32 or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. A particular BAT inhibitor for use in combination with compounds of the present invention is selected from any one of Examples 1-39 of WO 03/022286, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and the compounds of 5 Examples 1-39 are incorporated herein by reference. Claims 1-10 of WO 03/022286 are also incorporated herein by reference. A particular IBAT inhibitor selected from WO 03/022286 for use in combination with compounds of the present invention is selected from any one of: 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{(R)-a-[N-((R)-1-carboxy-2-methylthio ethyl)carbamoyl]-4-hydroxybenzyl} carbamoylmethoxy)-2,3,4,5-tetrahydro-1,2,5 10 benzothiadiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-aX-[N-((S)-1-carboxy-2-(R) hydroxypropyl)carbamoyl]-4-hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,2,5 benzothiadiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-c-[N-((S)-1-carboxy-2 15 methylpropyl)carbamoyl]-4-hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,2,5 benzothiadiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-a-[N-((S)-1-carboxybutyl) carbamoyl]-4-hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,2,5 benzothiadiazepine; 20 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-ax-[N-((S)-1-carboxypropyl) carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,2,5-benzothiadiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-ax-[N-((S)-1-carboxyethyl) carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,2,5-benzothiadiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-oC-[N-((S)-1-carboxy-2-(R) 25 hydroxypropyl)carbamoyl]benzyl } carbamoylmethoxy)-2,3,4,5-tetrahydro- 1,2,5 benzothiadiazepine; 1,1 -dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N- { (R)-a-[N-(2-sulphoethyl)carbamoyl]-4 hydroxybenzyl } carbamoylmethoxy)-2,3,4,5-tetrahydro- 1,2,5-benzothiadiazepine; 1,1 -dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N- { (R)-c-[N-((S)- 1 30 carboxyethyl)carbamoyl]-4-hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,2,5 benzothiadiazepine; WO 2007/126358 PCT/SE2007/000400 -33 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-a-[N-((R)-1-carboxy-2 methylthioethyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,2,5 benzothiadiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{(R)-cx-[N-{(S)-1-[N-((S)-2-hydroxy-1 5 carboxyethyl)carbamoyl]propyl carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro 1,2,5-benzothiadiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{(R)-a-[N-((S)-1-carboxy-2 methylpropyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,2,5 benzothiadiazepine; 10 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{(R)-a-[N-((S)-1-carboxypropyl) carbamoyl]-4-hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,2,5 benzothiadiazepine; and 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-[N-((R)-a-carboxy-4 hydroxybenzyl)carbamoylmethoxy]-2,3,4,5-tetrahydro-1,2,5-benzothiadiazepine; 15 or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. A particular IBAT inhibitor for use in combination with compounds of the present invention is selected from any one of Examples 1-7 of WO 03/091232, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and the compounds of Examples 1-7 are incorporated herein by reference. Claims 1-10 of WO 03/091232 are also 20 incorporated herein by reference. A particular IBAT inhibitor selected from WO 03/091232 for use in combination with compounds of the present invention is selected from any one of: 1,1-Dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{(R)-ax-[N-(2-(S)-3-(R)-4-(R)-5-(R) 2,3,4,5,6-pentahydroxyhexyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro 1,2,5-benzothiadiazepine; 25 1,1-Dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{(R)-a-[N-(2-(S)-3-(R)-4-(R)-5-(R) 2,3,4,5,6-pentahydroxyhexyl)carbamoyl]-4-hydroxybenzyl carbamoylmethoxy)-2,3,4,5 tetrahydro-1,2,5-benzothiadiazepine; 1,1-Dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-[N-((R/S)-a-{N-[1-(R)-2-(S)-1-hydroxy-1 (3,4-dihydroxyphenyl)prop-2-yl]carbamoyl}-4-hydroxybenzyl)carbamoylmethoxy]-2,3,4,5 30 tetrahydro-1,2,5-benzothiadiazepine; 1,1-Dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-{N-[(R)-a-(N-{2-(S)-[N-(carbamoylmethyl) carbamoyl]pyrrolidin-1-ylcarbonylmethyl carbamoyl)benzyl]carbamoylmethoxyl-2,3,4,5 tetrahydro-1,2,5-benzothiadiazepine; WO 2007/126358 PCT/SE2007/000400 - 34 1,1-Dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-[N-((R)-a-{N-[2-(3,4,5 trihydroxyphenyl)ethyl]carbamoyl}benzyl)carbamoylmethoxy]-2,3,4,5-tetrahydro-1,2,5 benzothiadiazepine; and 1,1-Dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{(R)-ax-[N-(2-(R)-3-(S)-4-(S)-5-(R) 5 3,4,5,6-tetrahydroxytetrahydropyran-2-ylmethyl)carbamoyl]benzyl}carbamoylmethoxy) 2,3,4,5-tetrahydro-1,2,5-benzothiadiazepine; or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. Further suitable compounds possessing IBAT inhibitory for use in combination with compounds of the present invention are disclosed in WO 03/106482 10 Suitable IBAT inhibitors having the above structure for use in combination with compounds of the present invention are selected from any one of: 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-X-[N'-((S)-1-carboxyethyl) carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-X-[N'-((S)-1-carboxypropyl) 15 carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{(R)-a-[N'-((S)-1-carboxybutyl) carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N- { (R)-aX-[N'-((S)-1-carboxy-2 methylpropyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 20 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-aX-[N'-((S)-1-carboxy-2 methylbutyl)carbamoyl]benzyl carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-aX-[N'-((S)-1-carboxy-3 methylbutyl)carbamoyl]benzyl }carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-a-[N'-((S)-1-carboxy-2 25 hydroxypropyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5 benzothiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-a-[N'-((S)-1-carboxy-2 mesylethyl)carbamoyl]benzyl } carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-a-[N'-((S)-1-carboxy-3 30 methylsulphonylpropyl)carbamoyl]benzyl } carbamoylmethoxy)-2,3,4,5-tetrahydro- 1,5 benzothiazepine; 1, 1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N- { (R)-a-[N'-((S)- 1 -carboxy-3 mesylpropyl)carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine; WO 2007/126358 PCTISE2007OOO400 - 35 1, 1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N- I (R)-a-[N'-((S)- 1 -carboxyethyl) carbamoylll-4-hydroxybenzyl Icarbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 1, 1-dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- I (R)-cX-[N'-((S)- 1 -carboxypropyl) carbamoyl]-4-hydroxybenzyl lcarbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 5 1, 1-dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- I (R)-c-[N'-((S)- 1 -carboxybutyl) carbamoyl]-4-hydroxybenzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5-benzothiazepine; 1, 1-dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- I (R)-cc-IN'-((S)- 1-carboxy-2 methylpropyl)carbamoyl]-4-hydroxybenzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5 benzothiazepine; 10 1, 1-dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- I (R)-ce[N'-((S)-l1-carboxy-2 methylbutyl)carbamoyl]-4-hydroxybenzyl I carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5 benzothiazepine; 1,1 -dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- I (R)-oe4N'-((S)- 1 -carboxy-3 methylbutyl)carbamoyli-4-hydroxybenzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5 15 benzothiazepine; 1,1 -dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- {(R)-cL-IIN'-((S)-l1-carboxy-2 hydroxyethyl)carbamoyl]-4-hydroxybenzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5 benzothiazepine; 1, 1-dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- { (R)-oc-[N'-((S)-l1-carboxy-2 20 hydroxypropyl)carbamoyl]-4-hydroxybenzyl I carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5 benzothiazepine; 1,1 -dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- {(R)-c&{[N'-((S)-l1-carboxy-2 methylthioethyl)carbamoyl]-4-hydroxybenzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5 benzothiazepine; 25 1,1 -dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- I (R)-cL-[N'-((S)- 1 -carboxy-2 methylsulphinylethyl)carbamoyl]-4-hydroxybenzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro 1 ,5-benzothiazepine; 1, 1-dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- I (R)-cL-[N'-((S)-l1-carboxy-2 mesylethyl)carbamoyl]-4-hydroxybenzyl I carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5 30 benzothiazepine; 1, 1-dioxo-3 ,3-dibutyl-5-phenyl-7-methylthio-8-(N- I (R)-ce4N'-((S)-1 -carboxy-2 methoxyethyl)carbamoyl]-4-hydroxybenzyl }carbamoylmethoxy)-2,3 ,4,5-tetrahydro- 1,5 benzothiazepine; WO 2007/126358 PCT/SE2007/000400 -36 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N- { (R)-a-[N'-((S)-1-carboxy-3 methylthiopropyl)carbamoyl]-4-hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5 benzothiazepine; 1, 1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{ (R)-a-[N'-((S)-1-carboxy-3 5 methylsulphonylpropyl)carbamoyl]-4-hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro 1,5-benzothiazepine; 1, 1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N- { (R)-X-[N'-((S)-1-carboxy-3 mesylpropyl)carbamoyl]-4-hydroxybenzyl carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5 benzothiazepine; 10 1,1 -dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N- { (R)-a-[N'-((S)- 1 carboxypropyl)carbamoyl]-4-hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5 benzothiazepine; or 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{(R)-a-[N'-((S)-1-carboxyethyl) -carbamoyl]benzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,5-benzothiazepine. 15 or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. Further suitable IBAT inhibitors for use in combination with compounds of the present invention are those disclosed in WO 04/076430. In a particular aspect of the invention an IBAT inhibitor or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof is an IBAT inhibitor or a 20 pharmaceutically acceptable salt thereof. Therefore in an additional feature of the invention, there is provided a combination of a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof and an IBAT inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. 25 Therefore in an additional feature of the invention, there is provided a method for producing a cholesterol lowering effect in a warm-blooded animal, such as man, in need of such treatment which comprises administering to said animal an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof in simultaneous, sequential or separate administration with an effective 30 amount of an IBAT inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. According to a further aspect of the invention there is provided a pharmaceutical composition which comprises a compound of formula (I), or a pharmaceutically acceptable WO 2007/126358 PCT/SE2007/000400 -37 salt, solvate, solvate of such a salt or a prodrug thereof, and an IBAT inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in association with a pharmaceutically acceptable diluent or carrier. According to a further aspect of the present invention there is provided a kit 5 comprising a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and an IBAT inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. According to a further aspect of the present invention there is provided a kit comprising: 10 a) a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in a first unit dosage form; b) an IBAT inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof; in a second unit dosage form; and c) container means for containing said first and second dosage forms. 15 According to a further aspect of the present invention there is provided a kit comprising: a) a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, together with a pharmaceutically acceptable diluent or carrier, in a first unit dosage form; 20 b) an IBAT inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in a second unit dosage form; and c) container means for containing said first and second dosage forms. According to another feature of the invention there is provided the use of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a 25 prodrug thereof, and an IBAT inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in the manufacture of a medicament for use in the production of a cholesterol lowering effect in a warm-blooded animal, such as man. According to a further aspect of the present invention there is provided a combination treatment comprising the administration of an effective amount of a compound of the formula 30 (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, optionally together with a pharmaceutically acceptable diluent or carrier, with the simultaneous, sequential or separate administration of an effective amount of an IBAT inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug WO 2007/126358 PCT/SE2007/000400 -38 thereof, optionally together with a pharmaceutically acceptable diluent or carrier to a warm blooded animal, such as man in need of such therapeutic treatment. According to a further aspect of the present invention there is provided a combination 5 treatment comprising the administration of an effective amount of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, optionally together with a pharmaceutically acceptable diluent or carrier, with the simultaneous, sequential or separate administration of an effective amount of an IBAT inhibitor, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug 10 thereof, optionally together with a pharmaceutically acceptable diluent or carrier to a warm blooded animal, such as man in need of such therapeutic treatment. In another aspect of the invention, the compound of formula (I), or a pharmaceutically acceptable salt or solvate thereof, or a solvate of such a salt, may be administered in 15 association with a peroxisome proliferator-activated receptor (PPAR) modulating agent. PPAR modulating agents include a PPAR alpha and/or gamma and/or delta agonist, or pharmaceutically acceptable salts, solvates, solvates of such salts or prodrugs thereof. Suitable PPAR alpha and/or gamma and/or delta agonists, pharmaceutically acceptable salts, solvates, solvates of such salts or prodrugs thereof are well known in the art. These include the 20 compounds described in WO 01/12187, WO 01/12612, WO 99/62870, WO 99/62872, WO 99/62871, WO 98/57941, WO 01/40170, WO 04/000790, WO 04/000295, WO 04/000294, WO 03/051822, WO 03/051821, WO 02/096863, WO 04/056748, WO 03/051826, WO 02/085844, WO 01/40172, J Med Chem, 1996, 39, 665, Expert Opinion on Therapeutic Patents, 10 (5), 623-634 (in particular the compounds described in the patent applications 25 listed on page 634) and J Med Chem, 2000, 43, 527 which are all incorporated herein by reference. Particularly a PPAR alpha and/or gamma and/or delta agonist refers to muraglitazar (BMS 298585), rivoglitazone (CS-011), netoglitazone (MCC-555), balaglitazone (DRF-2593, NN-2344), clofibrate (Atromid-S* ), fenofibrate, bezafibrate (Oralipin* ), gemfibrozil (Lopid*), ciprofibrate (Ciprol* ), pioglitazone (Actos* ), rosiglitazone (Avandia*), AVE 30 0847, AVE-8134, CLX-0921, DRF-10945, DRF-4832, E-3030, K-111, KRP-101, LBM-642 (oxeglitazar), LY-518674, LY-674, naveglitazar (LY-818), LY-929, 641597, GW-590735, GW-677954, GW-501516, metaglidasan (MBX-102), MBX-2044, ONO-5129, PLX-204, R 483 (BM131258),.R-1 19702, , T-131 (AMG-13 1), TAK-559 or TAK-654. Particularly a WO 2007/126358 PCT/SE2007/000400 - 39 PPAR alpha and/or gamma and/or delta agonist refers to tesaglitazar ((S)-2-ethoxy-3-[4-(2 {4-methanesulphonyl-oxyphenyl I ethoxy)phenyl]propanoic acid) and pharmaceutically acceptable salts thereof. 5 For instance, a PPAR alpha and/or gamma and/or delta agonist refers to (S)-2-ethoxy-3-[4-(2 {4-methanesulphonyloxyphenyl}ethoxy) phenyl]propanoic acid (tesaglitazar) and pharmaceutically acceptable salts thereof. Therefore in an additional feature of the invention, there is provided a combination of a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a 10 salt or a prodrug thereof and a PPAR alpha and/or gamma agonist, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. Therefore in an additional feature of the invention, there is provided a method for producing a cholesterol lowering effect in a warm-blooded animal, such as man, in need of such treatment which comprises administering to said animal an effective amount of a 15 compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof in simultaneous, sequential or separate administration with an effective amount of a PPAR alpha and/or gamma and/or delta agonist, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. According to a further aspect of the invention there is provided a pharmaceutical 20 composition which comprises a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and a PPAR alpha and/or gamma and/or delta agonist, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in association with a pharmaceutically acceptable diluent or carrier. According to a further aspect of the present invention there is provided a kit 25 comprising a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and a PPAR alpha and/or gamma and/or delta agonist, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. According to a further aspect of the present invention there is provided a kit comprising: 30 a) a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in a first unit dosage form; b) a PPAR alpha and/or gamma and/or delta agonist, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof; in a second unit dosage form; and WO 2007/126358 PCT/SE2007/000400 -40 c) container means for containing said first and second dosage forms. According to a further aspect of the present invention there is provided a kit comprising: a) a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a 5 salt or a prodrug thereof, together with a pharmaceutically acceptable diluent or carrier, in a first unit dosage form; b) a PPAR alpha and/or gamma and/or delta agonist, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in a second unit dosage form; and c) container means for containing said first and second dosage forms. 10 According to another feature of the invention there is provided the use of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and a PPAR alpha and/or gamma and/or delta agonist, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in the manufacture of a medicament for use in producing a cholesterol lowering effect in a warm-blooded animal, 15 such as man. According to a further aspect of the present invention there is provided a combination treatment comprising the administration of an effective amount of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, optionally together with a pharmaceutically acceptable diluent or carrier, with the 20 simultaneous, sequential or separate administration of an effective amount of a PPAR alpha and/or gamma and/or delta agonist, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, optionally together with a pharmaceutically acceptable diluent or carrier to a warm-blooded animal, such as man in need of such therapeutic treatment. 25 In another aspect of the invention, there is provided a combination treatment comprising the administration of an effective amount of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, optionally together with a pharmaceutically acceptable diluent or carrier, with the 30 simultaneous, sequential or separate administration of an -agonists to the receptor HM74A (nicotinic acid receptor). HM74A receptor agonists may be nicotine acid derivates. As used herein "nicotinic acid derivative" means a compounds comprising a pyridine-3-carboxylate WO 2007/126358 PCT/SE2007/000400 -41 structure or a pyrazine-2-carboxylate structure. Examples of nicotinic acid derivatives include nicotinic acid, niceritrol, nicofuranose, NIASPAN@ and acipimox. HM74A receptor agonists may be anthranilic acid derivatives described in WO-2005016867 5 and WO-2005016870. Other nicotinic receptor agonists are for example compounds described in W02005011677, W02004032928 and W02004033431. 10 Therefore, in an additional feature of the invention, there is provided a combination of a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof and a HM74A receptor agonists or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. Therefore in an additional feature of the invention, there is provided a method for 15 producing a cholesterol lowering effect in a warm-blooded animal, such as man, in need of such treatment which comprises administering to said animal an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof in simultaneous, sequential or separate administration with an effective amount of a HM74A receptor agonists, or a pharmaceutically acceptable salt, solvate, solvate 20 of such a salt or a prodrug thereof. According to a further aspect of the invention there is provided a pharmaceutical composition which comprises a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and a HM74A receptor agonists, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in 25 association with a pharmaceutically acceptable diluent or carrier. In another aspect of the invention, there is provided a combination treatment comprising the administration of an effective amount of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, 30 optionally together with a pharmaceutically acceptable diluent or carrier, with the simultaneous, sequential or separate administration of a mediator of reverse cholesterol transport i.e. a peptide ( Apo A-1 mimetic peptides) or small molecule mediator of reverse WO 2007/126358 PCT/SE2007/000400 -42 cholesterol transport e.g. those described in Circ. 2002;105:290, Circ. 2004.109:3215, Curr.Opinion in Lipidology 2004,15:645 or in W02004094471. In another aspect of the invention, the compound of formula I, or a pharmaceutically 5 acceptable salt or solvate thereof, or a solvate of such a salt, may be administered in association with an anti-obesity compound, or pharmaceutically acceptable salts, solvates, solvates of such salts or prodrugs thereof, for example a pancreatic lipase inhibitor e.g. orlistat (EP 129,748) or an appetite (satiety) controlling substance for example sibutramine (GB 2,184,122 and US 4,929,629), a cannabinoid 1 (CB1) antagonist or inverse agonist, or 10 pharmaceutically acceptable salts, solvates, solvates of such salts or prodrugs thereof, for example rimonabant (EP 656354 ) and as described in WOO1/70700 or a melanin concentrating hormone (MCH) antagonist, or pharmaceutically acceptable salts, solvates, solvates of such salts or prodrugs thereof, for example as described in WO 04/004726. 15 According to another feature of the invention there is provided the use of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and a nicotinic acid derivative, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in the manufacture of a medicament for use in the 20 production of a cholesterol lowering effect in a warm-blooded animal, such as man. In another aspect of the invention, the compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, may be administered in association with a bile acid sequestrant or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. Suitable bile acid sequestrants include cholestyramine, 25 cholestipol and cosevelam hydrochloride. Therefore, in an additional feature of the invention, there is provided a combination of a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof and a bile acid sequestrant or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. 30 Therefore in an additional feature of the invention, there is provided a method for producing a cholesterol lowering effect in a warm-blooded animal, such as man, in need of such treatment which comprises administering to said animal an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt WO 2007/126358 PCT/SE2007/000400 -43 or a prodrug thereof in simultaneous, sequential or separate administration with an effective amount of a bile acid sequestrant, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. According to a further aspect of the invention there is provided a pharmaceutical 5 composition which comprises a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and a bile acid sequestrant, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in association with a pharmaceutically acceptable diluent or carrier. According to another feature of the invention there is provided the use of a compound 10 of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and a bile acid sequestrant, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in the manufacture of a medicament for use in the production of a cholesterol lowering effect in a warm-blooded animal, such as man. 15 In another aspect of the invention, the compound of formula I, or a pharmaceutically acceptable salt or solvate thereof, or a solvate of such a salt, may be administered in association with a cholesteryl ester transfer protein (CETP) inhibitor, or pharmaceutically acceptable salts, solvates, solvates of such salts or prodrugs thereof, for example JTT-705, torcetrapib (CP-529414), Bay 194789 and those referenced and described in W005033082 or 20 WO 00/3 8725 page 7 line 22 - page 10, line 17 which are incorporated herein by reference. In another aspect of the invention, the compound of formula I, or a pharmaceutically acceptable salt or solvate thereof, or a solvate of such a salt, may be administered in association with a acyl coenzymA: cholesterol 0-acyltransferase (ACAT) inhibitor, or 25 pharmaceutically acceptable salts, solvates, solvates of such salts or prodrugs thereof, for example pactimibe (CS-505), eflucimibe (F-12511) and SMP-797, avasimibe or K604. In yet another aspect of the invention, the compound of formula I, association with modulators for example GW-4064 and INT-747of nuclear receptors such as farnesoid or a 30 pharmaceutically acceptable salt or solvate thereof, or a solvate of such a salt, may be administered in X receptor (FXR), or pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof .
WO 2007/126358 PCT/SE2007/000400 -44 In another aspect of the invention, the compound of formula I, or a pharmaceutically acceptable salt or solvate thereof, or a solvate of such a salt, may be administered in association with a phytosterol compound, or pharmaceutically acceptable salts, solvates, solvates of such salts or prodrugs thereof, for example stanols. An example of phytosterol 5 analogs is FM-VP4. In another aspect of the invention, the compound of formula I, or a pharmaceutically acceptable salt or solvate thereof, or a solvate of such a salt, may be administered in association with other therapies for the treatment of metabolic syndrome or type 2 diabetes 10 and its associated complications, these include biguanide drugs, for example metformin, phenformin and buformin, insulin (synthetic insulin analogues, amylin) and oral antihyperglycemics (these are divided into prandial glucose regulators and alpha-glucosidase inhibitors). An example of an alpha-glucosidase inhibitor is acarbose or voglibose or miglitol. An example of a prandial glucose regulator is repaglinide or nateglinide. 15 In another aspect of the invention, the compound of formula I, or a pharmaceutically acceptable salt or solvate thereof, or a solvate of such a salt, may be administered in association with a sulfonylurea for example: glimepiride, glibenclamide (glyburide), gliclazide, glipizide, gliquidone, chloropropamide, tolbutamide, acetohexamide, glycopyramide, carbutamide, glibonuride, glisoxepid, glybuthiazole, glibuzole, glyhexamide, 20 glymidine, glypinamide, phenbutamide, tolcylamide and tolazamide. Preferably the sulfonylurea is glimepiride or glibenclamide (glyburide). More preferably the sulfonylurea is glimepiride. Therefore the present invention includes administration of a compound of the present invention in conjunction with one, two or more existing therapies described in this paragraph. The doses of the other existing therapies for the treatment of type 2 diabetes and its 25 associated complications will be those known in the art and approved for use by regulatory bodies for example the FDA and may be found in the Orange Book published by the FDA. Alternatively smaller doses may be used as a result of the benefits derived from the combination. 30 According to an additional further aspect of the present invention there is provided a combination treatment comprising the administration of an effective amount of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, optionally together with a pharmaceutically acceptable diluent or carrier, WO 2007/126358 PCT/SE2007/000400 -45 with the simultaneous, sequential or separate administration one or more of the following agents selected from Group X: an antihypertensive compound (for example althiazide, benzthiazide, captopril, carvedilol, chlorothiazide sodium, clonidine hydrochloride, cyclothiazide, delapril 5 hydrochloride, dilevalol hydrochloride, doxazosin mesylate, fosinopril sodium, guanfacine hydrochloride, methyidopa, metoprolol succinate, moexipril hydrochloride, monatepil maleate, pelanserin hydrochloride, phenoxybenzemine hydrochloride, prazosin hydrochloride, primidolol, quinapril hydrochloride, quinaprilat, ramipril, terazosin hydrochloride, candesartan, candesartan cilexetil, 10 telmisartan, amlodipine besylate, amlodipine maleate and bevantolol hydrochloride); > an angiotensin converting enzyme inhibitor (for example alacepril, alatriopril, altiopril calcium, ancovenin, benazepril, benazepril hydrochloride, benazeprilat, benzoylcaptopril, captopril, captopril-cysteine, captopril-glutathione, ceranapril, ceranopril, ceronapril, cilazapril, cilazaprilat, delapril, delapril-diacid, enalapril, 15 enalaprilat, enapril, epicaptopril, foroxymithine, fosfenopril, fosenopril, fosenopril sodium, fosinopril, fosinopril sodium, fosinoprilat, fosinoprilic acid, glycopril, hemorphin-4, idrapril, imidapril, indolapril, indolaprilat, libenzapril, lisinopril, lyciumin A, lyciumin B, mixanpril, moexipril, moexiprilat, moveltipril, muracein A, muracein B, muracein C, pentopril, perindopril, perindoprilat, pivalopril, pivopril, 20 quinapril, quinapril hydrochloride, quinaprilat, ramipril, ramiprilat, spirapril, spirapril hydrochloride, spiraprilat, spiropril, spiropril hydrochloride, temocapril, temocapril hydrochloride, teprotide, trandolapril, trandolaprilat, utibapril, zabicipril, zabiciprilat, zofenopril and zofenoprilat); > an angiotensin II receptor antagonist (for example candesartan, candesartan cilexetil, 25 losartan, valsartan, irbesartan, tasosartan, telmisartan and eprosartan); > an andrenergic blocker (for example bretylium tosylate, dihydroergotamine so mesylate, phentolamine mesylate, solypertine tartrate, zolertine hydrochloride, carvedilol or labetalol hydrochloride); an alpha andrenergic blocker (for example fenspiride hydrochloride, labetalol hydrochloride, proroxan and alfuzosin 30 hydrochloride); a beta andrenergic blocker (for example acebutolol, acebutolol hydrochloride, alprenolol hydrochloride, atenolol, bunolol hydrochloride, carteolol hydrochloride, celiprolol hydrochloride, cetamolol hydrochloride, cicloprolol hydrochloride, dexpropranolol hydrochloride, diacetolol hydrochloride, dilevalol WO 2007/126358 PCT/SE2007/000400 -46 hydrochloride, esmolol hydrochloride, exaprolol hydrochloride, flestolol sulfate, labetalol hydrochloride, levobetaxolol hydrochloride, levobunolol hydrochloride, metalol hydrochloride, metoprolol, metoprolol tartrate, nadolol, pamatolol sulfate, penbutolol sulfate, practolol, propranolol hydrochloride, sotalol hydrochloride, 5 timolol, timolol maleate, tiprenolol hydrochloride, tolamolol, bisoprolol, bisoprolol fumarate and nebivolol); or a mixed alpha/beta andrenergic blocker; an andrenergic stimulant (for example combination product of chlorothiazide and methyldopa, the combination product of methyidopa hydrochlorothiazide and methyldopa, clonidine hydrochloride, clonidine, the combination product of 10 chlorthalidone and clonidine hydrochloride and guanfacine hydrochloride); > channel blocker, for example a calcium channel blocker (for example clentiazem maleate, amlodipine besylate, isradipine, nimodipine, felodipine, nilvadipine, nifedipine, teludipine hydrochloride, diltiazem hydrochloride, belfosdil, verapamil hydrochloride or fostedil); 15 > a diuretic (for example the combination product of hydrochlorothiazide and spironolactone and the combination product of hydrochlorothiazide and triamterene); > anti-anginal agents (for example amlodipine besylate, amlodipine maleate, betaxolol hydrochloride, bevantolol hydrochloride, butoprozine hydrochloride, carvedilol, cinepazet maleate, metoprolol succinate, molsidomine, monatepil maleate, primidolol, 20 ranolazine hydrochoride, tosifen or verapamil hydrochloride); > vasodilators for example coronary vasodilators (for example fostedil, azaclorzine hydrochloride, chromonar hydrochloride, clonitrate, diltiazem hydrochloride, dipyridamole, droprenilamine, erythrityl tetranitrate, isosorbide dinitrate, isosorbide mononitrate, lidoflazine, mioflazine hydrochloride, mixidine, molsidomine, 25 nicorandil, nifedipine, nisoldipine, nitroglycerine, oxprenolol hydrochloride, pentrinitrol, perhexiline maleate, prenylamine, propatyl nitrate, terodiline hydrochloride, tolamolol and verapamil); > anti-coagulants (selected from argatroban, bivalirudin, dalteparin sodium, desirudin, dicumarol, Iyapolate sodium, nafamostat mesylate, phenprocoumon, tinzaparin 30 sodium and warfarin sodium); > antithrombotic agents (for example anagrelide hydrochloride, bivalirudin, cilostazol, dalteparin sodium, danaparoid sodium, dazoxiben hydrochloride, efegatran sulfate, enoxaparin sodium, fluretofen, ifetroban, ifetroban sodium, lamifiban, lotrafiban WO 2007/126358 PCT/SE2007/000400 -47 hydrochloride, napsagatran, orbofiban acetate, roxifiban acetate, sibrafiban, tinzaparin sodium, trifenagrel, abciximab and zolimomab aritox); > fibrinogen receptor antagonists (for example roxifiban acetate, fradafiban, orbofiban, lotrafiban hydrochloride, tirofiban, xemilofiban, monoclonal antibody 7E3 and 5 sibrafiban) > platelet inhibitors (for example cilostezol, clopidogrel bisulfate, epoprostenol, epoprostenol sodium, ticlopidine hydrochloride, aspirin, ibuprofen, naproxen, sulindae, indomethacin, mefenamate, droxicam, diclofenac, sulfinpyrazone and piroxicam, dipyridamole); 10 > platelet aggregation inhibitors (for example acadesine, beraprost, beraprost sodium, ciprostene calcium, itezigrel, lifarizine, lotrafiban hydrochloride, orbofiban acetate, oxagrelate, fradafiban, orbofiban, tirofiban and xemilofiban) > hemorrheologic agents (for example pentoxifylline); > lipoprotein associated coagulation inhibitors; 15 > Factor Vlla inhibitors; > Factor Xa inhibitors; > low molecular weight heparins (for example enoxaparin, nardroparin, dalteparin, certroparin, parnaparin, reviparin and tinzaparin); > liver X receptor (LXR) agonists for example GW-3965 and those described in 20 W000224632, WO00103705, W002090375 and W000054759 (claim 1 and the named examples of these four application are incorporated herein by reference); > microsomal triglyceride transfer protein inhibitors for example implitapide ,CP 346086, JTT-130, BMS-201038, R-103757 and those described in W005/021486,WO03004020, W003002533, W002083658 and WO 00242291 25 (claim 1 and the named examples of these four application are incorporated herein by reference); > ApoAl expression inducer for example those described in W02005032559 or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, optionally together with a pharmaceutically acceptable diluent or carrier to a warm-blooded 30 animal, such as man in need of such therapeutic treatment. Therefore, in an additional feature of the invention, there is provided a combination of a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a WO 2007/126358 PCT/SE2007/000400 -48 salt or a prodrug thereof and a compound from Group X or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. Therefore in an additional feature of the invention, there is provided a method for producing a cholesterol lowering effect in a warm-blooded animal, such as man, in need of 5 such treatment which comprises administering to said animal an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof in simultaneous, sequential or separate administration with an effective amount of a compound from Group X, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. 10 According to a further aspect of the invention there is provided a pharmaceutical composition which comprises a compound of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and a compound from Group X, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in association with a pharmaceutically acceptable diluent or carrier. 15 According to another feature of the invention there is provided the use of a compound of the formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, and a compound from Group X, or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, in the manufacture of a medicament for use in the production of a cholesterol lowering effect in a warm-blooded animal, such as man. 20 In addition to their use in therapeutic medicine, the compounds of formula (I), or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof, are also useful as pharmacological tools in the development and standardisation of in vitro and in vivo test systems for the evaluation of the effects of inhibitors of cholesterol absorption in laboratory animals such as cats, dogs, rabbits, monkeys, rats and mice, as part of the search 25 for new therapeutic agents. In the above other pharmaceutical composition, process, method, use and medicament manufacture features, the alternative and preferred embodiments of the compounds of the invention described herein also apply. 30 Examples WO 2007/126358 PCT/SE2007/000400 -49 The invention will now be illustrated in the following non limiting Examples, in which standard techniques known to the skilled chemist and techniques analogous to those described in these Examples may be used where appropriate, and in which, unless otherwise stated: (i) evaporations were carried out by rotary evaporation in vacuo and work up procedures were 5 carried out after removal of residual solids such as drying agents by filtration; (ii) all reactions were carried out under an inert atmosphere at ambient temperature, typically in the range 18-25'C, with solvents of HPLC grade under anhydrous conditions, unless otherwise stated; (iii) column chromatography (by the flash procedure) was performed on Silica gel 40-63 Pm 10 (Merck); (iv) yields are given for illustration only and are not necessarily the maximum attainable; (v) the structures of the end products of the formula (I) were generally confirmed by nuclear (generally proton) magnetic resonance (NMR) and mass spectral techniques; magnetic resonance chemical shift values were measured in deuterated CDCl 3 (unless otherwise stated) 15 on the delta scale (ppm downfield from tetramethylsilane); proton data is quoted unless otherwise stated; spectra were recorded on a Varian Mercury-300 MHz, Varian Unity plus 400 MHz, Varian Unity plus-600 MHz or on Varian Inova-500 MHz spectrometer unless otherwise stated data was recorded at 400MHz; and peak multiplicities are shown as follows: s, singlet; d, doublet; dd, double doublet; t, triplet; tt, triple triplet; q, quartet; tq, triple quartet; 20 m, multiplet; br, broad; ABq, AB quartet; ABd, AB doublet, ABdd, AB doublet of doublets; dABq, doublet of AB quartets; 25 Mass spectra were recorded on one of the following instruments: LCT, QTOF, ZQ Mass spectrometer, all from Waters. LC-MS: Separation was performed using Agilent 1100 Series Modules or Waters 1525 pump on a Synergi MAX-RP (Phenomenex) C12 3x50 mm 4pm with gradient elution. 30 Samples were injected using Waters 2700 Sample Manager. Mobile phases: Generic gradients were applied from 5% to 95% acetonitrile.
WO 2007/126358 PCT/SE2007/000400 - 50 Buffers containing 10 nM ammonium acetate or 5 mM ammonium formiate/5mM formic acid were used. The mass spectra were recorded with a Waters ZQ2000 or Waters ZMD equipped with an electrospray interface, swithing positive and negative ionization mode. UV spectra were 5 collected by a Aglent 1100 PDA or Waters 2996 DAD and the evaporative light scattering (ELS ) signal by a Sedere Sedex 55 or 75. Data collection and evaluation were performed using the MassLynx software. Accurate mass data were determined using either a LCT or QTOF MS (Waters) with leucine enkephaline (m/z 556.2771) as lockmass. Unless otherwise stated the mass ion quoted is 10 (MH*). Unless further details are specified in the text, analytical high performance liquid chromatography (HPLC) was performed on Prep LC 2000 (Waters), Cromasil C 8 , 7 pm, (Akzo Nobel); MeCN and de-ionised water 10 mM ammonium acetate as mobile phases, with 15 suitable composition; (vii) intermediates were not generally fully characterised and purity was assessed by thin layer chromatography (TLC), HPLC, infra-red (IR), MS or NMR analysis; (viii) where solutions were dried sodium sulphate was the drying agent; and (ix) the following abbreviations may be used hereinbefore or hereinafter: 20 DCM dichloromethane; DMF NN-dimethylformamide; TBTU o-Benzotriazol-1-yl-N,N,N'-tetramethyluronium tetrafluoroborate; EtOAc ethyl acetate; MeCN acetonitrile; 25 TFA trifluoroacetic acid; DMAP 4-(dimethylamino)pyridine; BSA N,0-Bis(trimethylsilyl)acetamide; and TBAF tetrabutylammonium fluoride; NMM N-methyl morpholine; 30 TEA triethylamine; DBN 1,5-diazabicyclo-[4,3,0]-non-5-ene. Examples WO 2007/126358 PCT/SE2007/000400 -51 Example 1 N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 5 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2 yl]phenoxylacetyl)glycyl-3-cyclohexyl-D-alanine N-({4-[(2R,3R)-3-{[(2R)-2-{ [tert-butyl(dimethyl)silylloxy}-2-(4-fluorophenyl)ethyllthio}-1 (4-{3-[(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin- 2 10 yl]phenoxylacetyl)glycyl-3-cyclohexyl-D-alanine (16.7 mg, 0.018 mmol) (Method 1) was dissolved in acetic acid (1 ml). Water (0.100 ml) and LiC1 (50 mg, 1.18 mmol) were added and the reaction mixture was stirred overnight. The acetic acid was co-evaporated with toluene. The residue was purified with preparative HPLC on a C8 column, UV 235/285 nm. A gradient from 20 to 60 % MeCN in 0.1M N1 4 OAc buffer was used as eluent. The pure 15 fractions were collected and some of MeCN was removed under reduced pressure. The residue was lyophilised to give the title compound. H-NMR (500 MHz, DMSO-d 6 ): 0.73-0.92 (m, 2H), 1.05-1.19 (m, 311), 1.30 (b, 1H), 1.40-1.70 (m, 7H), 2.93 (d, 2H), 2.97 (s, 3H), 3.76 (d, 2H), 4.00 (s, 2H), 4.14 (bs, 1H), 4.31 (d, 1H), 4.52 (s, 2H), 4.71 (t, 1H), 5.10 (d, 1H), 5.74 (bs, 1H), 6.99 (d, 2H), 7.08-7.13 (m, 2H), 7.20 (d, 2H), 7.32-7.41 (m, 6 H), 7.60 (b, 1H), 7.94 20 (b, 1H), 8.26 (t, 1H). M/z: 809 (M+1) and 807 (M-1). Example 2 N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 25 [(methylsulfonyl)amino]prop-1-yn-1-yll}phenyl)-4-oxoazetidin-2 yl]phenoxy}acetyl)glycyl-D-valine To a stirred solution of {4-[(2R,3R)-3-{[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4 fluorophenyl)ethyl]thio}-1-(4-{3-[(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4 30 oxoazetidin-2-yl]phenoxy} acetic acid (19.4 mg, 0.027 mmol), and N-methylmorpholine (9 pl, 0.082 mmol) in DMF (1 ml, dry) was added. TBTU (12 mg, 0.037 mmol) and the reaction mixture was stirred at 30'C for 1 hour. Glycyl-D-valine hydrochloride ( 8.0 mg, 0.038 mmol) was added and the reaction mixture was stirred for 1 hour. LC-MS showed the formation of WO 2007/126358 PCT/SE2007/000400 -52 the TBDMS-ether of the title compound, M/z: 868.68 (M-1). The reaction mixture was diluted with water and EtOAc. The solution was acidified with KHSO 4 (2M) to pH ca 3. The phases were separated and the organic phase was concentrated. The residue was dissolved in acetic acid (1 ml). Water (100 pl) and LiCl (51.4 mg, 1.21 mmol) were added and the reaction 5 mixture was stirred over the weekend. The acetic acid was co-evaporated with toluene. The residue was purified with preparative HPLC on a C8 column, UV 235/285 nm. A gradient from 20 to 80 % MeCN in 0.1M NH 4 OAc buffer was used as eluent. The pure fractions were collected and most of the MeCN was removed under reduced pressure. The residue was diluted with water and DCM. It was acidified with KHSO 4 (2M) to pH 3. The phases were 10 separated and the organic phase was passed through a phase separator. The organic phase was concentrated and the residue was dissolved in MeCN and water. After lyophilisation, the title compound was obtained. H-NMR (500 MHz, DMSO-d 6 ): 0.84 (d, 3H), 0.86 (d, 3H), 1.99 2.06 (m, 1H), 2.92 (d, 2H), 2.97 (s, 3H), 3.79-3.88 (m, 2H), 4.01 (d, 2H), 4.12-4.17 (m, 1H), 4.29 (d, 1H), 4.53 (s, 2H), 4.71 (t, 1H), 5.10 (d, 1H), 5.65 (bs, 1H), 6.99 (d, 2H), 7.08-7.13 15 (m, 2H), 7.20 (d, 2H), 7.30-7.40 (m, 6H), 7.58 (t, 1H), 8.02 (d, 1H), 8.24 (t, 1H), 12.65 (b, 1H). M/z: 753.52 (M-1). Example 3
N-({
4 -[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 20 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2 yl]phenoxy}acetyl)glycyl-3-methyl-D-valine To a stirred solution of {4-[(2R,3R)-3-{ [(2R)-2-{ [tert-butyl(dimethyl)silyl]oxy}-2-(4 fluorophenyl)ethyl]thio}-1-(4-{ 3 -[(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4 25 oxoazetidin-2-yl]phenoxy} acetic acid (19.4 mg, 0.027 mmol) and N-methylmorpholine (9 pl, 0.082 mmol) in DMF (1 ml, dry) was added TBTU (13.0 m, 0.040 mmol) and the reaction mixture was stirred at 30*C for 1 hour. Glycyl-3-methyl-D-valine (7.1 mg, 0.038 mmol) was added and the reaction mixture was stirred for 1 hour. LC-MS showed the formation of the TBDMS-ether of the title compound, M/z: 881.65 (M-1). The reaction mixture was diluted 30 with water and EtOAc. The solution was acidfied with KHSO 4 (2M) to pH 3. The phases were separated and the organic phase was concentrated. The residue was dissolved in acetic acid (1 ml). Water (100 pl) and LiCl (63 mg, 1.47 mmol) were added and the reaction mixture was stirred over the weekend. The acetic acid was co-evaporated with toluene. The residue WO 2007/126358 PCT/SE2007/000400 -53 was purified with preparative HPLC on a C8 column, UV 235/285 nm. A gradient from 20 to 60 % MeCN in 0.1M NH 4 OAc buffer was used as eluent. The pure fractions were collected and most of the MeCN was removed under reduced pressure. The residue was lyophilised to give the title compound. H-NMR (500 MHz, DMSO-d 6 ): 0.89 (s, 9H), 2.92 (d, 2H), 2.97 (s, 5 8H), 3.82 (d. 2H), 3.98-4.07 (b, 3H), 4.31 (d, 1H), 4.53 (s, 2H), 4.72 (t, 1), 5.09 (d, 1H), 6.99 (d, 2H), 7.07-7.13 (m, 2H), 7.20 (d, 2H), 7.32-7.40 (m, 6H), 7.59 (b, 1H), 7.81 (b, 1H), 8.23 (t, 1H).M/z: 769.39(M+1) and 767.58 (M-1). Example 4 10 N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)aminoprop-1-yn-1-yl}phenyl)-4-oxoazetidin- 2 yl]phenoxy}acetyl)glycyl-D-lysine 15 N-({4-[(2R,3R)-3-{[(2R)-2-{ [tert-butyl(dimethyl)silyl]oxy}-2-(4-fluorophenyl)ethyl]thio }-1 (4-{3-[(methylsulfonyl)aminolprop-1-yn-1-yl}phenyl)-4-oxoazetidin-2 yl]phenoxy}acetyl)glycyl-N 6 -(tert-butoxycarbonyl)-D-lysine (Method 2) (21.9, 0.022 mmol) was dissolved in MeCN (1.5 ml). Cerium(4+) tetranitrate - nitric acid (1:2) diammoniate (25.1 mg, 0.046 mmol) and water (50 pl) were added. The reaction mixture was heated at 45 'C for 20 6 h and 30 minutes and it was allowed to stand at room temperature over the weekend. The solution was purifed with preparative HPLC on a C8 column, UV 235/285 nm. A gradient from 10 to 90 % MeCN in 0.1M NH 4 OAc buffer was used as eluent. Most of the MeCN was removed under reduced pressure and the residue was lyophilised to give the title compound as a yellow solid. H-NMR (500 MHz, DMSO-d 6 ): 1.13-1.66 (m, 611), 2.64-2.71 (m, 2H), 2.90 25 2.96 (m, 2H), 2.97 (s, 3H), 3.62-3.80 (m, 3H), 4.00 (s, 2H), 4.34 (d, 1H), 4.53 (s, 2H), 4.72 (t, 1H), 5.09 (d, 1H), 6.99 (d, 2H), 7.07-7.13 (m, 2H), 7.20 (d, 2H), 7.32-7.40 (m, 6H), 7.46 (b, 1H), 8.42 (t, 1H). M/z: 782.58 (M-1) and 784.42 (M+1). Example 5 30 N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)- 4 -oxoazetidin- 2 yl]phenoxy}acetyl)glycylglycine WO 2007/126358 PCT/SE2007/000400 -54 {4-[(2R,3R)-3-{[(2R)-2-{ [tert-butyl(dimethyl)silyl]oxy}-2-(4-fluorophenyl)ethyl]thio}-1-(4 { 3-[(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2-yl]phenoxy} acetic acid (Method 8)(19.4 mg, 0.027 mmol) (9.7 mg, 0.014 mmol) was dissolved in DCM (1 ml, dry). 5 Methyl glycylglycinate hydrochloride (3.1 mg, 0.017 mmol ) followed by N methylmorpholine (4 il, 0.041 mmol) were added. TBTU (5.8 mg, 0.018 mmol) was added and the rection mixtutre was stirred for 2 hours. LC-MS confirmed the formation of the methylester and TBDMS-ether of the title compound, M/z: 839.58 (M-1). The solvent was removed under reduced pressure. The residue was dissolved in MeCN (1 ml). Triethyamine 10 (40 pl, 0.287 mmol), water (10 pl) and LiCl (23.6 mg, 0.55 mmol) were added and the reaction mixture was stirred over the weekend. LC-MS showed complete hydrolysis giving the TBDMS-ether of the title compound, M/z: 827.32 (M+1) and 825.56 (M-1). The solvent was removed under reduced pressure. The crude was dissolved in acetic acid (1 ml) and water (100 pl) and LiC1 (27 mg, 0.64 mmol) were added. The reaction mixture was stirred for 6 15 hours and 30 minutes. Additional LiCl (30 mg, 0.71 mmol) and water (40 Pl) were added and the reaction mixture was stirred overnight. The acetic acid was co-evporated with toluene and the residue was purified with preparative HPLC on a C8 column. A gradient from 20 to 60 % MeCN in a 0.1M NH 4 OAc buffer was used as fluent. The pure fractions were collected and most of the MeCN was removed under reduced pressure. The residue was lyophilised to give 20 a the title compound. 2.91-2.96 (m, 2H), 2.98 (s, 3H), 3.38 (d 2H), 3.74 (d, 2H), 4.01 (s, 2H), 4.33 (d, 1H), 4.55 (s, 2H), 4.72 (t, 1H), 5.10 (d, 1H), 7.01 (d, 2H), 7.11 (t, 2H), 7.21 (d, 2H), 7.32-7.42 (m, 6H), 7.47 (b, 1H), 8.37 (t, 1H). MIz: 713.33 (M+1) and 711.45 (M-1). 25 Example 6 N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2 yl]phenoxy}acetyl)glycine 30 {4-[(2R,3R)-3-{[(2R)-2-{ [tert-butyl(dimethyl)silyl]oxy}-2-(4-fluorophenyl)ethyl]thio}-1-(4 {3-[(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2-yl]phenoxy} acetic acid (Method 8) (19.4 mg, 0.027 mmol) (19.0 mg, 0.020 mmol) was dissolved in DCM (2 ml).
WO 2007/126358 PCT/SE2007/000400 - 55 Methyl glycinate hydrochloride (4.1 mg, 0.033 mmol) and N-methylmorpholine (6 pl, 0.059 mmol) were added and the reaction mixture was stirred for five minutes. TBTU (9.5 mg, 0.029 mmol) was added and the mixture was stirred for 2 hours. The solvent was removed under reduced pressure. LC-MS confirmed the formation of the methylester and TBDMS 5 ether of the title compound. M/z: 782.55 (M-1). The residue was suspended in MeCN (1 ml). Triethylamine (27 I, 0.19 mmol), water (7 g1) and LiC1 (24.8 mg, 0.58 mmol) were added and the reaction mixture was stirred at 35'C overnight. Additional triethylamine (15 pl, 0.11 mmol) and water (15 ptl) were added and the reaction mixture was stirred at 35'C for 5 hours. Additional MeCN (1 ml) was added and the reaction mixture was stirred overnight. The 10 mixture was purified with preparative HPLC on a C8 column, UV 235/285 nm. A gradient from 20 to 85 % MeCN in 0.1M NH 4 OAc buffer was used as eluent. Most of the MeCN was removed under reduced pressure and the residue was acidified to pH 3 and extracted from DCM. The phases were separated and the organic phase was passed through a phase separator. The solvent was removed under reduced pressure. The residue was dissolved in 15 water and MeCN and lyophilised. LC-MS confirmed the formation of the TBDMS-ether of the title compound, M/z: 768.60 (M-1). The residue was dissolved in acetic acid (1 ml). Water (100 pl) and LiCl (27.6 mg, 0.65 mmol) were added and the reaction mixture was stirred overnight. The acetic acid was co-evaporated with toluene. The residue was purified with preparative HPLC on a C8 column. A gradient from 20 to 75 % MeCN in 0.lM NLOAc 20 buffer was used as eluent. Most of the MeCN was removed under reduced pressure and the residue was lyophilised to give the title compound. H-NMR (400 MHz, DMSO-d 6 ) 2.93 (d, 2H), 2.98 (s, 3H), 3.47 (d, 2H), 4.01 (s, 2H), 4.32 (d, 1H), 4.50 (s, 2H), 4.72 8t, 1H), 5.10 (d, 1H), 7.00 (d, 2H), 7.11 (t, 2H), 7.21 (d, 2H), 7.32-7.42 (m, 6H), 7.79 (b, 1H). M/z: 654.43 (M-1). 25 Preparation of starting materials Method 1 30 N-({4-[(2R,3R)-3-{[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-fluorophenyl)ethyllthio} 1-(4-{3-[(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2 yl]phenoxy}acetyl)glycyl-3-cyclohexyl-D-alanine WO 2007/126358 PCT/SE2007/000400 -56 {4-[(2R,3R)-3-{[(2R)-2-{ [tert-butyl(dimethyl)silyl]oxy}-2-(4-fluorophenyl)ethyl]thio}-1-(4 {3-[(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2-yl]phenoxy} acetic acid (Method 8) (25.1 mg, 0.040 mmol) was dissolved in DMF (1 ml, dry). N-methylmorpholine 5 (13 pl, 121 mmol) was added and the reaction mixture was stirred at 30'C for five minutes. TBTU (20.1 mg, 0.063 mmol) was added and the reaction mixture was stirred at 30'C for 1 hour. Glycyl-3-cyclohexyl-D-alanine (12.5 mg, 0.055 mmol) was added and the reaction mixture was stirred for 2 hours. The reaction mixture was purified with preparative HPLC on a C8 column. A gradient from 10 to 100 % MeCN in 0.1M NH 4 OAc buffer was used as 10 eluent. Most of the MeCN was removed under reduced pressure. The residue was diluted with water and lyophilised to give the title compound, M/z: 921 (M-1). Method 2 15 N-({4-[(2R,3R)-3-{[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-fluorophenyl)ethyl]thio} 1-(4-{3-[(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2 yl]phenoxy}acetyl)glycyl-N 6 -(tert-butoxycarbonyl)-D-lysine 20 {4-[(2R,3R)-3-{[(2R)-2-{ [tert-butyl(dimethyl)silyl]oxy}-2-(4-fluorophenyl)ethyl]thio}-1-(4 {3-[(methylsulfonyl)amino]prop-1-yn-1-yl }phenyl)-4-oxoazetidin-2-yl]phenoxy} acetic acid (Method 8) (15.1 mg, 0.021 mmol) was dissolved in DMF (1 ml, dry). N-methylmorpholine (7 pl, 0.064 mmol) was added and the reaction mixture was stirred at 30'C for five minutes. 25 TBTU (10.8 mg, 0.034 mmol) was added and the reaction mixture was stirred at the same conditions for hour. Glycyl-N 6 -(tert-butoxycarbonyl)-D-lysine (10.0 mg 0.033 mmol) was added and the reaction mixture was stirred for 2 hours. The mixture was purified with preparative HPLC on a C8 column. A gradient from 10 to 100 % MeCN in a 0.1M NH 4 OAc buffer was used as eluent. The pure fractions were collected and most of the MeCN was 30 removed under reduced pressure. The residue was lyophilised to give the title compound. M/z: 996.74 (M-1).
WO 2007/126358 PCT/SE2007/000400 -57 Method 3
N-({
4
-[(
2 R,3R)-3-{[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4-fluorophenyl)ethyl]thio} 1-(4-{3-[(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2 5 yl]phenoxy}acetyl)glycine {4-[(2R,3R)-3-{[(2R)-2-{ [tert-butyl(dimethyl)silyl]oxy}-2-(4-fluorophenyl)ethyl]thio}-1-(4
{
3 -[(methylsulfonyl)amino]prop-1-yn-1-yllphenyl)-4-oxoazetidin-2-yl]phenoxy} acetic acid 10 (19.0 mg, 0.020 mmol) was dissolved in DCM (2 ml). Methyl glycinate hydrochloride (4.1 mg, 0.033 mmol) and N-methylmorpholine (6 ptl, 0.059 mmol) were added and the reaction mixture was stirred for five minutes. TBTU (9.5 mg, 0.029 mmol) was added and the reaction mixture was stirred for 2 hours. The solvent was removed under reduced pressure. The formation of the methylester of the titled compound was confirmed, M/z: 782.55 (M-1). The 15 residue was suspended in MeCN (1 ml). Triethylamine (27 pl, 0.19 mmol), water (7 pl) and LiCl (24.8 mg, 0.66 mmol) were added and the reaction mixture was stirred at 35*C overnight. Additional triethylamine (15 pl, 0.11 mmol) and water (15 pl) were added and the reaction mixture was stirred at 35'C for 5 hours. MeCN (1 ml) was added and the mixture was stirred overnight. The reaction mixture was purified with preparative HPLC on a C8 20 column. A gradient from 20 to 85 % MeCN in 0.1M NH 4 OAc buffer was used as eluent. Most of the MeCN was removed under reduced pressure and the residue was acidified to pH 3 with
KHSO
4 , (2M) and extracted from DCM. The phases were separated and the organic phase was passed through a phase separator. The solvent was removed under reduced pressure. The residue was diluted with water and MeCN and lyophilised to give the title compound. H 25 NMR (400 MHz, DMSO-d 6 ) 0.00 (s, 3H), 0.14 (s, 3H), 0.95 (s, 9H), 3.03-3.14 (m 2H), 3.16 (s, 3H), 3.97 (d, 2H), 4.19 (d, 2H), 4.48 (d, 2H), 4.70 (s, 2H), 5.10 (t, 1H), 5.30 8d, 1H), 7.18 (2H), 7.32 (t, 2H), 7.40 (d, 2H), 7.52-7.59 (m, 6H), 7.76 (t, 1H), 8.52 (t, 1H). M/z: 768.60 (M 1). 30 Method 4 Glycyl-3-cyclohexyl-D-alanine WO 2007/126358 PCT/SE2007/000400 - 58 N-(tert-butoxycarbonyl)glycine (2.0 g, 11.4 mmol) and DIPEA (4.0 g, 31 mmol) were dissolved in methylene chloride (25 ml). TBTU (4.1 g, 12.8 mmol) was added and the mixture was stirred for 15 min at room temperature. 3-cyclohexyl-D-alanine (2.1 g, 12.2 mmol) was added and the reaction mixture was stirred over night at room temperature. The 5 reaction mixture was transferred to a separation funnel and was then extracted with a water/acetic acid solution (100ml 5% acetic acid). The organic layer was separated and evaporated under reduced pressure. The residue was dissolved in formic acid (20 ml) and the mixture was stirred over night at 40 'C. The formic acid was removed under reduced pressure.The residue was washed with water (50 ml) and then stirred in aceton (25 ml) for 1 h 10 at room temperature. The solid material was filtered off and washed with aceton (20 ml). The title compound was obtained. 1 H-NMR, 300 MHz, CD3COOD): 0.8-1.9 (m, 13H), 3.9-4.1 (m, 2H), 4.55-4.65 (m, 1H). 15 Method 5 Methyl ( 4 -{(E)-[(4-iodophenyl)imino]methyl}phenoxy)acetate 20 Methyl (4-formylphenoxy)acetate ( 8.0 g, 40 mmol) was dissolved in 100 ml toluene and p iodoaniline (9.1 g, 40 mmol) was added. The mixture was refluxed over night using a Dean Stark apparatus. The reaction mixture was partly evaporated under reduced pressure. Methanol was added to the suspension and the mixture was stirred for a few minutes. The precipitate was filtered off, washed with methanol and dried under reduced pressure over 25 night to yield the title compound. 1 H-NMR (400 MHz, CDC1 3 ) 5: 3.83 (s, 3H), 4.72 (s, 2H), 6.95 (d, 2H), 7.00 (d, 2H), 7.69 (d, 2H), 7.86 (d, 2H), 8.35 (s, 1H). 30 Method 6 Methyl {4-[(2R,3R)-3-{[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4 fluorophenyl)ethy]thio}-1-(4-iodophenyl)-4-oxoazetidin-2-yl]phenoxy}acetate WO 2007/126358 PCT/SE2007/000400 -59 5 Methyl (4-{(E)-[(4-iodophenyl)imino]methyl}phenoxy)acetate (7.0 g, 17.7 mmol), was placed in a dry 250 ml 3-necked flask under inert atmosphere and dissolved in 100 ml dry DCM. Et 3 N (5.5 ml, 39.5 mmol) and 2-chloro-1-methylpyridinium iodide (4.2g, 16.4 mmol) were added. {[(2R)-2-{[tert-Butyl(dimethyl)silyloxy}-2-(4-fluorophenyl)ethyl]thio} acetic acid ( 5.4 g, 15.7 mmol) was dissolved in 50 ml dry DCM and slowly added to the above 10 solution over 7-8 h. The mixture was stirred over night and diluted with 50 ml DCM. HCI (1 M, 100 ml) was added followed by NaHCO 3 (5%) until pH was 8-9 of the aqueous. The organic phase was washed with 0.3 M KHS0 4 , brine until neutral pH, dried with MgSO 4 and concentrated. The solid was dissolved in EtOAc: heptane (4:1) and filtered on a short SiO 2 column using a gradient from 1/4 to 1/1 of EtOAc/heptane as eluent. Concentration yielded 15 10.65 g. The mixture was purified by preparative HPLC on a C8 column (500x50 mm) using a gradient from 20-100% MeCN in 0.1 M ammonium acetate as eluent. The product fraction was concentrated to yield 7.13 g of the trans diastereomeric mixture. M/z: 720.2 (M-1). The diastereomeric mixture was separated by HPLC on a Chiralpak IA column (4.6x250mm) using heptane/THF (80/20) as mobile phase. The second eluting diastereomer was collected 20 and the solution concentrated to yield the title compound. 'H-NMR (400 MHz, MeOD) 5: 0.13 (s, 3H), 0.02 (s, 3H), 0.85 (s, 911), 3.00 (ddd, 2H), 3.81 (s, 311), 4.02 (d, 1H), 4.76 (s, 2H), 4.84-4.90 (m, 1H), 4.94 (dd, 1H), 6.97-7.06 (m, 4H), 7.09 (d, 2H), 7.30-7.40 (m, 4H), 7.61 (d, 2H). 25 Method 7 Methyl {4-[(2R,3R)-3-{[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4 fluorophenyl)ethy]thio}--(4-{3-[(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4 30 oxoazetidin-2-yl]phenoxy}acetate Methyl {4-[(2R,3R)-3-{[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4 fluorophenyl)ethyl]thio}-1-(4-iodophenyl)-4-oxoazetidin-2-yl]phenoxy} acetate (500 mg, 0.69 WO 2007/126358 PCT/SE2007/000400 - 60 mmol) and N-prop-2-yn-1-ylmethanesulfonamide ( 150 mg, 1.13 mmol) were mixed in 15 ml water and 4 ml MeCN. K 2 C0 3 (220 mg, 1.59 mmol), Pd(PPh 3
)
4 (40 mg, 5 mol%) and Cul (13 mg, 10 mol%) were added. The solution was stirred at 50'C for 2 h and at ambient temperature over night. EtOAc (20 ml) and 2 M HCI (1 ml) were added. The mixture was 5 stirred for 5 min and the phases were separated. The aqueous phase was extracted with EtOAc. The combined organic phases were washed with 2% NaHCO 3 , brine (2x), dried with MgSO 4 and concentrated to yield the title compound. M/z: 725.3 (M-1). 1 H-NMR (400 MHz, DMSO-d 6 ) 5: -0.18 (s, 3H), -0.04 (s, 3H), 0.77 (s, 9H), 2.85-3.02 (m, 5H), 3.69 (s, 3H), 3.80 (dd, 1H), 4.01 (d, 2H), 4.29 (d, 1H), 4.79 (s, 2H), 4.91 (dd, 1H), 5.11 (d, 1H), 6.95 (d, 2H), 10 7.09-7.18 (m, 2H), 7.18-7.25 (d, 2H), 7.32-7.42 (m, 6H). Method 8 15 {4-[(2R,3R)-3-{[(2R)-2-{[tert-butyl(dimethyl)silylloxy}-2-(4-fluorophenyl)ethy~lthio}-1-(4 {3-[(methylsulfonyl)amino]prop-1-yn-1-yllphenyl)-4-oxoazetidin-2-yllphenoxylacetic acid 20 Methyl {4-[(2R,3R)-3-{[(2R)-2-{[tert-butyl(dimethyl)silyl]oxy}-2-(4 fluorophenyl)ethyl]thio}-1-(4-{3-[(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4 oxoazetidin-2-yl]phenoxy} acetate (530mg, 0.73 mmol) was dissolved in 15 ml MeCN. Water (0.2 ml), Et 3 N (1.0 ml, 7.2 mmol) and LiC1 (630 mg, 14.9 mmol) were added and the mixture 25 was stirred at 35'C over night. The mixture was filtered and concentrated. The residue was extracted between EtOAc and 0.3 M KHSO 4 . The aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine (2x) and concentrated. The brown residue was purified by preparative HPLC on a C8 column (150x30 mm) using a gradient from 20-60% MeCN in 0.1 M ammonium acetate as eluent. The title compound was obtained 30 in 170 mg (33%) as a slightly brownish solid. M/z: 711.2 (M-1). 'H-NMR (400 MHz, DMSO-d 6 ) 8: -0.18 (s, 3H), -0.04 (s, 3H), 0.78 (s, 9H), 2.93 (ddd, 2H), 2.98 (s, 3H), 4.01 (d, 2H), 4.29 (d, 1H), 4.67 (s, 2H), 4.88-4.94 (m, 1H), 5.11 (d, 1H), 6.93 (d, 2H), 7.09-7.18 (m, 2H), 7.21 (d, 2H), 7.32-7.42 (m, 6H), 7.58 (t, 1H), 12.97 (brs, 1H).
WO 2007/126358 PCT/SE2007/000400 -61 Method 9 Glycyl-3-methyl-D-valine trifluoroacetate 5 To a 30 C solution of N-(tert-butoxycarbonyl)glycine (0.450 g, 2.569 mmol) and N methylmorpholine (1.30 g, 12.84 mmol) in CH 2 Cl 2 (50 ml) was added TBTU (0.99 g, 3.08 mmol). After 1.5 h, D-tert-leucine (0.303 g, 2.31 mmol) was added. After 30 minutes, the reaction was quenched by the addition of water (1 ml). The mixture was concentrated and the residue was purified through preparative HPLC using an eluent of 0-40% CH 3 CN in 0.1M 10 NH 4 OAc buffer. Pure fractions were collected and concentrated. To the residue were added
CH
2 Cl 2 (10 ml) and TFA (3 ml). Full conversion to the corresponding aminoacid was obtained after 30 minutes. The reaction mixture was concentrated to give the desired compound. 1 H NMR [(CD 3
)
2 SO), 400 MHz] &:0.94 (s, 9H), 3.60-3.67 (m, 2H), 4.16 (d, 1H), 7.90-8.00 (m, 3H), 8.47 (d, 1H). 15 It will be appreciated by those skilled in the art that the examples may be modified within the realms of the invention, why the invention is not limited to particular embodiments. 20 Absorption Absorption of the compounds of formula (I) was tested in a Caco-2 cells model 25 (Gastroenterology 1989, 96, 736): Compound (I) Caco value (10~ 6 cm/sec) N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethylthio} -1- 0.02 (4-{3-[(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2 yl]phenoxy}acetyl)glycyl-D-valine WO 2007/126358 PCTISE2007OOO400 -62 N-(1{4-[(2R,3R)-3- { [(2R)-2-(4-fluorophenyl)-2-hydroxyethyIlio I-1-- 0.04

权利要求:
Claims (17)
[1] 1. A compound of formula (I): 0 RI R6 0 OH O N N N ~ OH R3 S H 0 R2 R5 N 0 N- -S R4 5 0 (I) wherein: R 1 is hydrogen, CI 6 alkyl, C 3 - 6 cycloalkyl or aryl; 10 R2 and Rare independently hydrogen, a branched or unbranched Ci- 6 alkyl, C 3 - 6 cycloalkyl or aryl; wherein said C1. 6 alkyl may be optionally substituted by one or more hydroxy, amino, guanidino, cyano, carbamoyl, carboxy, CI 6 alkoxy, aryl C1. 6 alkoxy,(C-C 4 ) 3 Si, N (C1. 6 alkyl)amino, NN-(CI 6 alkyl) 2 amino, C1. 6 alkylS(O)a,, C 3 . 6 cycloalkyl, aryl or aryl C1- 6 alkylS(O)a, wherein a is 0-2; and wherein any aryl group may be optionally substituted by one 15 or two substituents selected from halo, hydroxy, C1. 6 alkyl, CI. 6 alkoxy, or cyano; R 3 is hydrogen, alkyl, halo, C1. 6 alkoxy or C 1 - 6 alkylS-; R 4 is methyl or aryl; R 6 is hydrogen, C 1 . 6 alkyl, or arylC1. 6 alkyl; wherein R and R 2 may form a ring with 2-7 carbon atoms and wherein R 6 and R 2 may form a 20 ring with 3-6 carbon atoms; n=0 or 1; or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. 25 WO 2007/126358 PCT/SE2007/000400 - 64
[2] 2. A compound of formula (12): 5 0 R1 R6 0 OH O N OH 0 H R2 R5 R3 .. N 0 Hf11 NS- R4 (12) wherein: 10 R' is hydrogen, CI 6 alkyl, C3- 6 cycloalkyl or aryl; R 2 and R5 are independently hydrogen, a branched or unbranched C 1 . 6 alkyl, hydroxy, amino, guanidino, cyano, carbamoyl, carboxy, C1. 6 alkoxy, aryl CI 6 alkoxy,(C 1 -C 4
[3] ) 3 Si, N (CI- 6 alkyl)amino, NN-(C1.6alkyl) 2 amino, CI 6 alkylS(O)a,, C3- 6 cycloalkyl, aryl or aryl C 1 . 6 15 alkylS(O)a, wherein a is 0-2; and wherein any aryl group may be optionally substituted by one or two substituents selected from halo, hydroxy, C 1 - 6 alkyl, C1. 6 alkoxy, or cyano; R 3 is hydrogen, alkyl, halo, C1. 6 alkoxy or C1. 6 alkylS-; R4 is methyl or aryl; R 6 is hydrogen, C 1 . 6 alkyl, or arylC 1 . 6 alkyl; 20 wherein R5 and R2 may form a ring with 2-7 carbon atoms and wherein R 6 and R2 may form a ring with 3-6 carbon atoms; n= 0 or 1 or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof. 25 3. A compound according to claim 1 or 2, wherein: R' is hydrogen. WO 2007/126358 PCT/SE2007/000400 - 65
[4] 4. A compound according to any of the preceding claims, wherein: R 2 and R 5 are hydrogen or a branched or unbranched C1. 6 alkyl, C3- 6 cycloalkyl or aryl; wherein said C1. 6 alkyl may be optionally substituted by one or more hydroxyl or amino. 5
[5] 5. A compound according to any of the preceding claims, wherein: R 3 is halo.
[6] 6. A compound according to any of the preceding claims, wherein: 10 R 3 is fluorine.
[7] 7. A compound according to any of the preceding claims, wherein: R 6 is hydrogen. 15
[8] 8. A compound according to claim 1 or 2 wherein; R 1 is hydrogen; R 2 and R 5 are hydrogen or a branched or unbranched C1.. 6 alkyl, C 3 . 6 cycloalkyl or aryl; wherein said CI- 6 alkyl may be optionally substituted by one or more hydroxyl or amino R 3 is halo and; 20 and R 6 is hydrogen.
[9] 9. One or more compounds chosen from: 25 N-({4-[(2R,3R)-3-{[( 2 R)- 2 -( 4 -fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2-yl]phenoxy}acetyl)glycyl-3 cyclohexyl-D-alanine; N-({ 4-[(2R,3R)-3-{[( 2 R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio }-1-(4- { 3 30 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2-yl]phenoxy}acetyl)glycyl D-valine; WO 2007/126358 PCT/SE2007/000400 -66 N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)amino]prop-1-yn-1-yl phenyl)-4-oxoazetidin-2-yl]phenoxy}acetyl)glycyl- 3 5 methyl-D-valine; N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{ 3 [(methylsulfonyl)aminolprop-1-yn-1-yl}phenyl)-4-oxoazetidin-2-yllphenoxy}acetyl)glycyl D-lysine; 10 N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2 yl]phenoxy}acetyl)glycylglycine; and 15 N-({4-[(2R,3R)-3-{[(2R)-2-(4-fluorophenyl)-2-hydroxyethyl]thio}-1-(4-{3 [(methylsulfonyl)amino]prop-1-yn-1-yl}phenyl)-4-oxoazetidin-2-yl]phenoxy}acetyl)glycine.
[10] 10. A method of treating or preventing hyperlipidemic conditions comprising the 20 administration of an effective amount of a compound according to any one of claims 1 to 9 to a mammal in need thereof.
[11] 11. A method of treating or preventing atherosclerosis comprising the administration of an effective amount of a compound according to any one of claims 1 to 9 to a mammal in need 25 thereof.
[12] 12. A method for treating or preventing Alzheimers' disease comprising the administration of an effective amount of a compound according to any one of claims 1 to 9 to a mammal in need thereof. 30
[13] 13. A method for treating or preventing cholesterol associated tumors comprising the administration of an effective amount of a compound according to any one of claims 1 to 9 to a mammal in need thereof. WO 2007/126358 PCT/SE2007/000400 -67
[14] 14. A pharmaceutical formulation comprising a compound according to any one of claims 1 to 9 in admixture with pharmaceutically acceptable adjuvants, diluents and/or carriers. 5
[15] 15. A combination of a compound according to formula (I) or (12) with a PPAR alpha and/or gamma agonist.
[16] 16. A combination of a compound according to formula (I) or (12) with an HMG Co-A reductase inhibitor. 10
[17] 17. A process for preparing a compound of formula (I) or a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug thereof which process (wherein variable groups are, unless otherwise specified, as defined in formula (I)) comprises of: 15 Process 1) reacting a compound of formula (II): OH OH R3 N 0 O N // sr~o R4 (II) with a compound of formula (III): R 6 0 R 1 0 L N N OH 20 0 R 2 R 5 (III) wherein L is a displaceable group; WO 2007/126358 PCT/SE2007/000400 - 68 Process 2) reacting an acid of formula (IV): 0 OH OH R3 N 0 N /0 R4 (IV) or an activated derivative thereof; with an amine of formula (V): R6 R' 0 H 2 N OH 5 0 R 2 R 5 (V) Process 3): reacting an acid of formula (VI): 0 Ri OH o OH R3 O N 0 0 H N, // S-o R4 (VI) 10 or an activated derivative thereof, with an amine of formula (VII): WO 2007/126358 PCT/SE2007/000400 - 69 R 6 HN OH R 2 R 5 (VII) Process 4): reducing a compound of formula (VIII): R 6 0 R0 O O N N OH 3 S H O R 2 R 5 0 N"> R4 5 (VIII) Process 5): reacting a compound of formula (IX): R6 O R 1 O O N OH Hly HS 0 R 2 R 5 N 0 0 R4 (IX) with a compound of formula (X): OH 3 L 10 MX WO 2007/126358 PCT/SE2007/000400 -70 wherein L is a displaceable group; Process 6): reacting a compound of formula (XI): R6 0 R1 0 OJ N OH L OH L N R2 R 5 N 0 N - I : : : . 0 0 R4 (XI) 5 wherein L is a displaceable group; with a compound of formula (XII): OH 3 SH (XII) Process 7): De-esterifying a compound of formula (XIII) 0 R 1 R 6 0 OH 0 OR 3R 0 R 2 R 5 N O~ S=O R4 10 (XIII) wherein the group C(O)OR is an ester group; and thereafter if necessary or desirable: i) converting a compound of the formula (I) into another compound of the formula (I); ii) removing any protecting groups; 15 iii) forming a pharmaceutically acceptable salt, solvate, solvate of such a salt or a prodrug; or WO 2007/126358 PCT/SE2007/000400 -71 iv) separating two or more enantiomers.

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同族专利:

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公开号 | 公开日

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UY30310A1|2008-11-28|

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KR20080110926A|2008-12-19|

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AR060623A1|2008-07-02|

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AU2007243998B2|2011-05-19|

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US20090069285A1|2009-03-12|

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EP2013165A1|2009-01-14|

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法律状态:
2011-09-29| MK25| Application lapsed reg. 22.2i(2) - failure to pay acceptance fee|

优先权:

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申请号 | 申请日 | 专利标题

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US79546106P| true| 2006-04-27|2006-04-27||

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US60/795,461||2006-04-27||

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PCT/SE2007/000400|WO2007126358A1|2006-04-27|2007-04-25|Diphenylazetidinone derivates possessing cholesterol absor tion inhibitor activit.|

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