CA2307889A1 - Cyclic phosphonate ester inhibitors of microsomal triglyceride transfer protein and method - Google Patents
Cyclic phosphonate ester inhibitors of microsomal triglyceride transfer protein and method Download PDFInfo
- Publication number
- CA2307889A1 CA2307889A1 CA002307889A CA2307889A CA2307889A1 CA 2307889 A1 CA2307889 A1 CA 2307889A1 CA 002307889 A CA002307889 A CA 002307889A CA 2307889 A CA2307889 A CA 2307889A CA 2307889 A1 CA2307889 A1 CA 2307889A1
- Authority
- CA
- Canada
- Prior art keywords
- aryl
- alkyl
- amino
- oxo
- trifluoroethyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- -1 Cyclic phosphonate ester Chemical class 0.000 title claims abstract description 94
- 238000000034 method Methods 0.000 title claims description 21
- 239000003112 inhibitor Substances 0.000 title abstract description 9
- 102100031545 Microsomal triglyceride transfer protein large subunit Human genes 0.000 title description 37
- 108010038232 microsomal triglyceride transfer protein Proteins 0.000 title description 37
- 150000001875 compounds Chemical class 0.000 claims abstract description 109
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims abstract description 14
- 150000003626 triacylglycerols Chemical class 0.000 claims abstract description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 119
- 125000003118 aryl group Chemical group 0.000 claims description 117
- 125000001072 heteroaryl group Chemical group 0.000 claims description 66
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 50
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 48
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 47
- 125000003342 alkenyl group Chemical group 0.000 claims description 44
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 37
- 125000003545 alkoxy group Chemical group 0.000 claims description 34
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 34
- 125000001424 substituent group Chemical group 0.000 claims description 34
- 125000004104 aryloxy group Chemical group 0.000 claims description 33
- 229910052739 hydrogen Inorganic materials 0.000 claims description 33
- 125000000304 alkynyl group Chemical group 0.000 claims description 30
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 29
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 29
- 125000001188 haloalkyl group Chemical group 0.000 claims description 27
- 239000001257 hydrogen Substances 0.000 claims description 27
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 26
- 125000004414 alkyl thio group Chemical group 0.000 claims description 25
- 229910052760 oxygen Inorganic materials 0.000 claims description 25
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 24
- 125000005843 halogen group Chemical group 0.000 claims description 22
- 125000002947 alkylene group Chemical group 0.000 claims description 20
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 19
- 150000001204 N-oxides Chemical class 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 229910052717 sulfur Inorganic materials 0.000 claims description 16
- 235000010290 biphenyl Nutrition 0.000 claims description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 14
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 14
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 14
- 125000005368 heteroarylthio group Chemical group 0.000 claims description 14
- 150000002632 lipids Chemical class 0.000 claims description 14
- 239000001301 oxygen Substances 0.000 claims description 14
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 13
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims description 13
- 125000005110 aryl thio group Chemical group 0.000 claims description 13
- 125000004450 alkenylene group Chemical group 0.000 claims description 12
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 12
- 229910052736 halogen Inorganic materials 0.000 claims description 12
- 150000002367 halogens Chemical class 0.000 claims description 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 12
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 11
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims description 11
- 201000001320 Atherosclerosis Diseases 0.000 claims description 10
- 125000003282 alkyl amino group Chemical group 0.000 claims description 10
- 125000004658 aryl carbonyl amino group Chemical group 0.000 claims description 10
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims description 10
- 125000005842 heteroatom Chemical group 0.000 claims description 10
- 125000004043 oxo group Chemical group O=* 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 10
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 9
- 125000004419 alkynylene group Chemical group 0.000 claims description 9
- 125000001769 aryl amino group Chemical group 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 9
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 8
- 125000005135 aryl sulfinyl group Chemical group 0.000 claims description 8
- 125000004657 aryl sulfonyl amino group Chemical group 0.000 claims description 8
- 125000005241 heteroarylamino group Chemical group 0.000 claims description 8
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 8
- 239000011593 sulfur Substances 0.000 claims description 8
- 125000005018 aryl alkenyl group Chemical group 0.000 claims description 7
- 125000005114 heteroarylalkoxy group Chemical group 0.000 claims description 7
- 125000000623 heterocyclic group Chemical group 0.000 claims description 7
- 230000002401 inhibitory effect Effects 0.000 claims description 7
- 125000005592 polycycloalkyl group Chemical group 0.000 claims description 7
- 208000031226 Hyperlipidaemia Diseases 0.000 claims description 6
- 125000005015 aryl alkynyl group Chemical group 0.000 claims description 6
- 229910052731 fluorine Inorganic materials 0.000 claims description 6
- 125000004447 heteroarylalkenyl group Chemical group 0.000 claims description 6
- 125000005150 heteroarylsulfinyl group Chemical group 0.000 claims description 6
- 125000005143 heteroarylsulfonyl group Chemical group 0.000 claims description 6
- 208000008589 Obesity Diseases 0.000 claims description 5
- 206010033645 Pancreatitis Diseases 0.000 claims description 5
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 5
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 5
- 125000005100 aryl amino carbonyl group Chemical group 0.000 claims description 5
- 125000005129 aryl carbonyl group Chemical group 0.000 claims description 5
- 125000005160 aryl oxy alkyl group Chemical group 0.000 claims description 5
- 125000005164 aryl thioalkyl group Chemical group 0.000 claims description 5
- 125000004429 atom Chemical group 0.000 claims description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims description 5
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 5
- 125000005647 linker group Chemical group 0.000 claims description 5
- 235000020824 obesity Nutrition 0.000 claims description 5
- 125000005089 alkenylaminocarbonyl group Chemical group 0.000 claims description 4
- 125000005095 alkynylaminocarbonyl group Chemical group 0.000 claims description 4
- 125000001691 aryl alkyl amino group Chemical group 0.000 claims description 4
- 125000005199 aryl carbonyloxy group Chemical group 0.000 claims description 4
- 125000004350 aryl cycloalkyl group Chemical group 0.000 claims description 4
- 239000004305 biphenyl Chemical group 0.000 claims description 4
- 235000012000 cholesterol Nutrition 0.000 claims description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000005223 heteroarylcarbonyl group Chemical group 0.000 claims description 4
- 125000005224 heteroarylcarbonylamino group Chemical group 0.000 claims description 4
- 125000005419 heteroarylsulfonylamino group Chemical group 0.000 claims description 4
- 201000001421 hyperglycemia Diseases 0.000 claims description 4
- 210000002966 serum Anatomy 0.000 claims description 4
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 3
- 208000035150 Hypercholesterolemia Diseases 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 3
- 150000001345 alkine derivatives Chemical class 0.000 claims description 3
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- 125000002837 carbocyclic group Chemical group 0.000 claims description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 3
- 201000005577 familial hyperlipidemia Diseases 0.000 claims description 3
- 208000020346 hyperlipoproteinemia Diseases 0.000 claims description 3
- 208000006575 hypertriglyceridemia Diseases 0.000 claims description 3
- 150000002576 ketones Chemical class 0.000 claims description 3
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 claims description 3
- COLOHWPRNRVWPI-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound [CH2]C(F)(F)F COLOHWPRNRVWPI-UHFFFAOYSA-N 0.000 claims description 2
- 101100495918 Arabidopsis thaliana CHR23 gene Proteins 0.000 claims description 2
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 2
- 125000000033 alkoxyamino group Chemical group 0.000 claims description 2
- 125000004992 haloalkylamino group Chemical group 0.000 claims description 2
- 125000002883 imidazolyl group Chemical group 0.000 claims 3
- 125000004076 pyridyl group Chemical group 0.000 claims 3
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical group C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
- 125000003396 thiol group Chemical class [H]S* 0.000 claims 2
- 125000001589 carboacyl group Chemical group 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 111
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 87
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 70
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 56
- 239000000243 solution Substances 0.000 description 52
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 51
- 238000006243 chemical reaction Methods 0.000 description 48
- 235000019439 ethyl acetate Nutrition 0.000 description 40
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 36
- 229910052786 argon Inorganic materials 0.000 description 36
- 239000007787 solid Substances 0.000 description 30
- 239000011541 reaction mixture Substances 0.000 description 24
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 22
- 239000003921 oil Substances 0.000 description 19
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 18
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- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000007257 deesterification reaction Methods 0.000 description 1
- 230000007850 degeneration Effects 0.000 description 1
- 230000003412 degenerative effect Effects 0.000 description 1
- 239000003398 denaturant Substances 0.000 description 1
- 238000010511 deprotection reaction Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 235000020805 dietary restrictions Nutrition 0.000 description 1
- 235000015872 dietary supplement Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 210000001842 enterocyte Anatomy 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- KGAWPIXNSIYQPC-UHFFFAOYSA-N ethyl piperidine-2-carboxylate;hydrochloride Chemical compound Cl.CCOC(=O)C1CCCCN1 KGAWPIXNSIYQPC-UHFFFAOYSA-N 0.000 description 1
- 238000004992 fast atom bombardment mass spectroscopy Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
- 230000009395 genetic defect Effects 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 210000002216 heart Anatomy 0.000 description 1
- 230000002440 hepatic effect Effects 0.000 description 1
- 206010073071 hepatocellular carcinoma Diseases 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000007327 hydrogenolysis reaction Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000012133 immunoprecipitate Substances 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 239000007972 injectable composition Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910001416 lithium ion Inorganic materials 0.000 description 1
- UBJFKNSINUCEAL-UHFFFAOYSA-N lithium;2-methylpropane Chemical compound [Li+].C[C-](C)C UBJFKNSINUCEAL-UHFFFAOYSA-N 0.000 description 1
- 210000001853 liver microsome Anatomy 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
- 238000006140 methanolysis reaction Methods 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- QAFJIJWLEBLXHH-UHFFFAOYSA-N methyl 2-fluorobenzoate Chemical compound COC(=O)C1=CC=CC=C1F QAFJIJWLEBLXHH-UHFFFAOYSA-N 0.000 description 1
- 210000001589 microsome Anatomy 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 230000035772 mutation Effects 0.000 description 1
- SDXHXQHPTCVQKW-UHFFFAOYSA-N n-(1,3-dihydroxypropan-2-yl)-2-[4-(trifluoromethyl)phenyl]benzamide Chemical compound OCC(CO)NC(=O)C1=CC=CC=C1C1=CC=C(C(F)(F)F)C=C1 SDXHXQHPTCVQKW-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- HEGSGKPQLMEBJL-RKQHYHRCSA-N octyl beta-D-glucopyranoside Chemical compound CCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HEGSGKPQLMEBJL-RKQHYHRCSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006186 oral dosage form Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- 208000033808 peripheral neuropathy Diseases 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- RLZZZVKAURTHCP-UHFFFAOYSA-N phenanthrene-3,4-diol Chemical compound C1=CC=C2C3=C(O)C(O)=CC=C3C=CC2=C1 RLZZZVKAURTHCP-UHFFFAOYSA-N 0.000 description 1
- DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 description 1
- 125000005538 phosphinite group Chemical group 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 210000002381 plasma Anatomy 0.000 description 1
- 238000002264 polyacrylamide gel electrophoresis Methods 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000651 prodrug Substances 0.000 description 1
- 229940002612 prodrug Drugs 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052705 radium Inorganic materials 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000006884 silylation reaction Methods 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 1
- BAZAXWOYCMUHIX-UHFFFAOYSA-M sodium perchlorate Chemical compound [Na+].[O-]Cl(=O)(=O)=O BAZAXWOYCMUHIX-UHFFFAOYSA-M 0.000 description 1
- 229910001488 sodium perchlorate Inorganic materials 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 125000004385 trihaloalkyl group Chemical group 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- CSRZQMIRAZTJOY-UHFFFAOYSA-N trimethylsilyl iodide Substances C[Si](C)(C)I CSRZQMIRAZTJOY-UHFFFAOYSA-N 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 241000701447 unidentified baculovirus Species 0.000 description 1
- 239000002691 unilamellar liposome Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 235000019168 vitamin K Nutrition 0.000 description 1
- 239000011712 vitamin K Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/657163—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom
- C07F9/657181—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom the ring phosphorus atom and, at least, one ring oxygen atom being part of a (thio)phosphonic acid derivative
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P3/04—Anorexiants; Antiobesity agents
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- Health & Medical Sciences (AREA)
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- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Child & Adolescent Psychology (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Novel cyclic phosphonate ester inhibitors of MTP are provided which have structure (I) wherein R2, L2, A, B, L1, R1 and R5a are as set out herein. These compounds are useful in lowering serum cholesterol and triglycerides.
Description
CYCLIC PHOSPHONATE ESTER INHIBITORS OF
MICROSOMAL T.~GLYCERIDE TRANSFER PROTEIN AND METHOD
Field of the Invention This invention relates to novel cyclic phosphonate esters which inhibit microsomal triglyceride transfer protein, and to methods for decreasing serum lipids and treating atherosclerosis employing such compounds.
Bac)~,around of the invention The microsomal triglyceride transfer protein (MTP) catalyzes the transport of triglyceride (TG), cholesteryl ester (CE), and phosphatidylcholine (PC) between small unilamellar vesicles (SW). Wetterau & Zilversmit, Chem.
Phys. Lipids ~$, 205-22 (1985). When transfer rates are expressed as the percent of the donor lipid transferred per time, MTP expresses a distinct preference for neutral lipid transport (TG and CE), relative to phospholipid transport.
The protein from bovine liver has been isolated and characterized. Wetterau & Zilversmit, Chem. Phys. Limas _3$, 205-22 (1985). Polyacrylamide gel electrophoresis analysis of the purified protein suggests that the transfer protein is a complex of two subunits of apparent molecular weights 58,000 and 88,000, since a single band was present when purified MTP was electrophoresed under nondenaturing condition, while two bands of apparent molecular weights 58,000 and 88,000 were identified when electrophoresis was performed in the presence of sodium dodecyl sulfate (SDS).
These two polypeptides are hereinafter referred to as 58 kDa and 88 kDa, respectively, or the 58 kDa and the 88 kDa component of MTP, respectively, or the low molecular weight subunit and the high molecular weight subunit of MTP, respectively.
Characterization of the 58,000 molecular weight component of bovine MTP indicates that it is the previously characterized multifunctional protein, protein disulfide isomerase (PDI). Wetterau et a ., J. Biol. Chem.
9800-7 (1990). The presence of PDI in the transfer protein is supported by evidence showing that (1) the amino terminal 25 amino acids of the bovine 58,000 kDa component of MTP is identical to that of bovine PDI, and (2) disulfide isomerase activity was expressed by bovine MTP
following the dissociation of the 58 kDa - 88 kDa protein complex. In addition, antibodies raised against bovine PDI, a protein which by itself has no TG transfer activity, were able to immunoprecipitate bovine TG transfer activity from a solution containing purified bovine MTP.
PDI normally plays a role in the folding and assembly of newly synthesized disulfide bonded proteins within the lumen of the endoplasmic reticulum. Bulleid &
Freedman, Nature ,3~5, 649-51 (1988). It catalyzes the proper pairing of cysteine residues into disulfide bonds, thus catalyzing the proper folding of disulfide bonded proteins. In addition, PDI has been reported to be identical to the beta subunit of human prolyl 4-hydroxylase. Koivu et~, J. Biol. Chem. 2 (1987). The role of PDI in the bovine transfer protein is not clear. It does appear to be an essential component of the transfer protein as dissociation of PDI from the 88 kDa component of bovine MTP by either low concentrations of a denaturant (guanidine HC1), a chaotropic agent (sodium perchlorate), or a nondenaturing detergent (octyl glucoside) results in a loss of transfer activity.
Wetterau etal., Biochemistry ,~(~, 9728-35 (1991). Isolated bovine PDI has no apparent lipid transfer activity, suggesting that either the 88 kDa polypeptide is the transfer protein or that it confers transfer activity to the protein complex.
The tissue and subcellular distribution of MTP
activity in rats has been investigated. Wetterau &
Zilversmit, Biochem. Bionhys. Acta 87~, 610-7 (1986).
Lipid transfer activity was found in liver and intestine.
Little or no transfer activity was found in plasma, brain, heart, or kidney. Within the liver, MTP was a soluble protein located within the lumen of the microsomal fraction. Approximately equal concentrations were found in-the smooth and rough microsomes.
Abetalipoproteinemia is an autosomal recessive disease characterized by a virtual absence of plasma lipoproteins which contain apolipoprotein B (apoB). Kane &
Havel in The Metabolic Basis of Inherited Diseasg, Sixth edition, 1139-64 (1989). Plasma TG levels may be as low as a few mg/dL, and they fail to rise after fat ingestion.
Plasma cholesterol levels are often only 20-45 mg/dL.
These abnormalities are the result of a genetic defect in the assembly and/or secretion of very low density lipoproteins (VLDL) in the liver and chylomicrons in the intestine. The molecular basis for this defect has not been previously determined. In subjects examined, triglyceride, phospholipid, and cholesterol synthesis appear normal. At autopsy, subjects are free of atherosclerosis. Schaefer et al., Clin. Chem. ~, B9-12 (1988). A link between the apoB gene and abetalipoproteinemia has been excluded in several families.
Talmud et al., ~T. Clin. Invest. ~, 1803-6 (1988) and Huang et a ., ,Am. J. Hum. Gent. 4~C, 1141-8 (2990).
Subjects with abetalipoproteinemia are afflicted with numerous maladies. Kane & Havel, vide supra Subjects have fat malabsorption and TG accumulation in their enterocytes and hepatocytes. Due to the absence of TG-rich plasma lipoproteins, there is a defect in the transport of fat-soluble vitamins such as vitamin E. This results in acanthocytosis of erythrocytes, spinocerebellar ataxia with degeneration of the fasciculus cuneatus and gracilis, peripheral neuropathy, degenerative pigmentary retinopathy, and ceroid myopathy. Treatment of abetalipoproteinemic subjects includes dietary restriction of fat intake and dietary supplementation with vitamins A, E and K .
,~ vit , MTP catalyzes the transport of lipid molecules between phospholipid membranes. Presumably, it plays a similar role in vivo, and thus plays some role in lipid metabolism. The subcellular (lumen of the microsomal_-fraction) and tissue distribution (liver and intestine) of MTP have led to speculation that it plays a role in the assembly of plasma lipoproteins, as these are the sites of plasma lipoprotein assembly. Wetterau & Zilversmit, Bioc~em. Biqphvs. Acta 87~, 610-7 (1986). The ability of MTP to catalyze the transport of TG between membranes is consistent with this hypothesis, and suggests that MTP may catalyze the transport of TG from its site of synthesis in the endoplasmic reticulum (ER) membrane to nascent lipoprotein particles within the lumen of the ER.
Olofsson and colleagues have studied lipoprotein assembly in HepG2 cells. Bostrom et ., J. Biol. Chem.
~, 4434-42 (1988). Their results suggest small precursor lipoproteins become larger with time. This would be consistent with the addition or transfer of lipid molecules to nascent lipoproteins as they are assembled. MTP may play a role in this process. In support of this hypothesis, Howell and Palade, J. Cell Biol. ~?, 833-45 (1982), isolated nascent lipoproteins from the hepatic Golgi fraction of rat liver. There was a spectrum of sizes of particles present with varying lipid and protein compositions. Particles of high density lipoprotein (HDL) density, yet containing apoB, were found. Higgins and Hutson, ~T. Lipid Res. ,~5, 1295-1305 (1984), reported lipoproteins isolated from Golgi were consistently larger than those from the endoplasmic reticulum, again suggesting the assembly of lipoproteins is a progressive event.
However, there is no direct evidence in the prior art demonstrating that MTP plays a role in lipid metabolism or the assembly of plasma lipoprotein.
Recent reports (Science, Vol. 258, page 999, 1992;
D. Sharp et al, Nature, Vol. 365, page 65, 1993) demonstrate that the defect causing abetalipoproteinemia is in the MTP gene, and as a result, the MTP protein.
Individuals with abetalipoproteinemia have no MTP activity, as a result of mutations in the MTP gene, some of which have been characterized. These results indicate that MTP
is required for the synthesis of apoB containing lipoproteins, such as VLDL, the precursor to LDL. It therefore follows that inhibitors of MTP would inhibit the synthesis of VLDL and LDL, thereby lowering VLDL levels, LDL levels, cholesterol levels, and triglyceride levels in animals and man.
Canadian Patent Application No. 2,091,102 published March 2, 1994 (corresponding to U.S. application Serial No.
117,362, filed September 3, 1993 (file DC2lb)) which is incorporated herein by reference), reports MTP inhibitors which also block the production of apoB containing lipoproteins in a human hepatic cell line (HepG2 cells).
This provides further support for the proposal that an MTP
inhibitor would lower apoB containing lipoprotein and lipid levels irk vivo. This Canadian patent application discloses a method for identifying the MTP inhibitors (\
N N
/
which has the name 2-[1-(3,3-diphenylpropyl)-4-piperidinyl]-2, 3-dihydro-3-oxo-1~i-isoindole hydrochloride and O
\ ~N \
/ ,, J OCH3 which has the name 1-[3-(6-fluoro-1-tetralanyl)-methyl]-4-O-methoxyphenyl piperazine.
EP 0643057A1 published March 15, 1995, discloses MTP
inhibitors of the structure I
or II
O
R3. I- / _N~N_ R~
X ' RS
R N ~N R' or III
o . _ J.
Y
where X is : CHIie, -cH- C8 Or -C= c- :
I I
R9 Ri0 R9 Ri0 R8, R9 and R1~ are independently hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl, or cycloalkylalkyl;
Y is -(cHZ)~; or -iC-O
where m is 2 or 3;
R1 is alkyl, alkenyl, alkynyl, aryl, heteroaryl, arylalkyl (wherein alkyl has at least 2 carbons), diarylalkyl, arylalkenyl, diarylalkenyl, arylalkynyl, diarylalkynyl, diarylalkylaryl, heteroazylalkyl (wherein alkyl has at least 2 carbons), cycloalkyl, or cycloalkylalkyl (wherein alkyl has at least 2 carbons); all of the aforementioned R1 groups being optionally substituted through available carbon atoms with l, 2, or 3 groups selected from halo, haloalkyl, alkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl, fluorenyl, heteroarylalkyl, hydroxy or oxo; or R1 is a group of the structure Rts '~~ _ , tt Z
R~2 R~3 ~~ Rta Rll is a bond, alkylene, alkenylene or alkynylene of up to 6 carbon atoms, arylene (for example ) ~ , or mixed arylene-alkylene (for example ~- ( CH1 ) a. ) where n is 1 to 6;
R12 is hydrogen, alkyl, alkenyl, aryl, heteroaryl, haloalkyl, arylalkyl, arylalkenyl, cycloalkyl, aryloxy, alkoxy, arylalkoxy, heteroarylalkyl or cycloalkylalkyl;
Z is a bond, O, S, N-alkyl, N-aryl, or alkylene or alkenylene of from 1 to 5 carbon atoms;
R13~ R14~ R15~ ~d R16 are independently hydrogen, alkyl, halo, haloalkyl, aryl, cycloalkyl, cycloheteroalkyl, alkenyl, alkynyl, hydroxy, alkoxy, nitro, amino, thio, alkylsulfonyl, arylsulfonyl, alkylthio, arylthio, carboxy, aminocarbonyl, alkylcarbonyloxy, alkylcarbonylamino, arylalkyl, heteroaryl, heteroarylalkyl, or aryloxy;
or R1 is Ri7 (C8Z)D~
Ri8 wherein p is 1 to 8 and R1~ and R18 are each independently H, alkyl, alkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl or cycloalkylalkyl, at least one of R1~ and R18 being other than H;
or Rl is Ri9 RZi wherein R19 is aryl or heteroaryl;
R2~ is aryl or heteroaryl;
R21 is H, alkyl, aryl, alkylaryl, arylalkyl, S ~aryloxy, arylalkoxy, heteroaryl, heteroarylalkyl, heteroarylalkoxy, cycloalkyl, cycloalkylalkyl or cycloalkylalkoxy;
R2, R3, R4 are independently hydrogen, halo, alkyl, haloalkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, hydroxy or haloalkyl;
R5 is alkyl of at least 2 carbons, alkenyl, alkynyl;
aryl, heteroaryl, arylalkyl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl, polycycloalkyl, polycycloalkylalkyl, 1S cycloalkenyl, cycloalkenylalkyl, polycycloalkenyl, polycycloalkenylalkyl, heteroarylcarbonyl, all of the R5 and R6 substituents being optionally substituted through available carbon atoms with 1, 2, or 3 groups selected from hydrogen, halo, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl, aryl, heteroaryl, arylalkyl, arylcycloalkyl, arylalkynyl, aryloxy, aryloxyalkyl, arylalkoxy, arylazo, heteroaryloxo, heteroarylalkyl, heteroarylalkenyl, heteroaryloxy, hydroxy, 2S vitro, cyano, amino, substituted amino (wherein the amino includes 1 or 2 substituents which are alkyl, or aryl or any of the other aryl compounds mentioned in the definitions), thiol, alkylthio, arylthio, heteroarylthio, arylthioalkyl, alkylcarbonyl, arylcarbonyl, arylaminocarbonyl, alkoxycarbonyl, aminocarbonyl, alkynylaminocarbonyl, alkylaminocarbonyl, alkenylaminocarbonyl, alkylcarbonyloxy, arylcarbonyloxy, alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfinylalkyl, arylsulfonyl, alkylsulfonyl, 3S arylsulfonylamino; with the proviso that when RS is CH3, R6 _ g _ is not H; and where R5 is phenyl, the phenyl preferably includes an ortho hydrophobic substituent such as alkyl, haloalkyl, aryl, aryloxy or arylalkyl;
R6 is hydrogen or C1-C4 alkyl or C1-C4 alkenyl;
S R~ is alkyl, aryl or arylalkyl wherein alkyl or the alkyl portion is optionally substituted with oxo; and including pharmaceutically acceptable salts and anions thereof or esters thereof.
In the formula I compounds, where X is CH2 and R2 , R3 and R4 are each H, R1 will be other than 3,3-diphenylpropyl.
In the formula ITI compounds, where one of R2, R3 and R4 is 6-fluoro, and the others are H, R~ will be other than 4-O-methoxyphenyl.
U.S. Application Serial No. 472,067, filed June 6, 1995 (file DC2le) discloses compounds of the structure o N~N_ R~
X ' or or or R2 O R~
R3. I_ ,\
X ' R5, o fJ-~N- R~
R~
Rs, D N
Rs J
or o ~3. I. w ~N.~ _ / i Y.N J
O O
where O is - C- or - s- ;
O
X is: CHRs, -C- ~ -CH- CH- or O Rs Rto R9 Rt°
R8, R9 and R1~ are independently hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl, or cycloalkylalkyl;
x 3s -(C8Z)m- or -c-wherein m is 2 or 3;
R1 is alkyl, alkenyl, alkynyl, aryl, heteroaryl, arylalkyl wherein alkyl has at least 2 carbons, diarylalkyl, arylalkenyl, diarylalkenyl, arylalkynyl, diarylalkynyl, diarylalkylaryl, heteroarylalkyl wherein alkyl has at least 2 carbons, cycloalkyl, or cycloalkylalkyl wherein alkyl has at least 2 carbons, all optionally substituted through available carbon atoms with l, 2, 3 or 4 groups selected from halo, haloalkyl, alkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl;
fluorenyl, heteroarylalkyl, hydroxy or oxo;
or R1 is a fluorenyl-type group of the structure ~~/Rts ~,--.,/Rts t~ Rts i i , i tt -Rtt-Zt _ Rtt_ t 'Z or Z
or Z
Rt2 ~ ~ Rt~Z2 ~ ~ Rt2 Z2 Het R13 V~ R14 Rt3 v ' Rt4 13 Rt4 WO 99/2156a PCT/US98/21750 is Ris Het 1 or Ri~Z Z
Het 2 Or R1 is an indenyl-type group of the structure R14 13\ 14 R \n/ R
11_ 1 - R Z or , R11- Z1 \ / or 12 2 / Rl6a / 16a R - ZRisa (CH2~ R12- Z2 R
Rl5a E
(a - 2,3 or 4) Het ~ He!
_ R11_ Z1 or _ Rii_ Zi ;
R12_ Z2 ~ Rl6a R12_ Z2 / Rl6a Risa (CH2)a G ~ Rlsa Z1 and Z2 are the same or different and are independently a bond, O, S, H
- NH- C- ~ - C- or - C- , O ~ ~0~2 ~ O alkyl O ~ O OH
with the proviso that with respect to ~, at least one of Z1 and Z2 will be other than a bond; R11 is a bond, alkylene, alkenylene or alkynylene of up to 10 carbon~atoms; azylene or mixed arylene-alkylene; R12 is hydrogen, alkyl, alkenyl, aryl, haloalkyl, trihaloalkyl, trihaloalkylalkyl, heteroaryl, heteroarylalkyl, arylalkyl, arylalkenyl, cyclo-alkyl, aryloxy, alkoxy, arylalkoxy or cycloalkylalkyl, with the provisos that (1) when R12 is H, aryloxy, alkoxy or arylalkoxy, -NH-C- , -N-C-. -C-then Z2 is o attryt o ~ o or a bond and -(2) when Z2 is a bond, R12 cannot be heteroaryl or heteroarylalkyl;
Z is bond, 0, S, N-alkyl, N-aryl, or alkylene or alkenylene from 1 to 5 carbon atoms; R13, R14~ R15~ ~d R16 are independently hydrogen, alkyl, halo, haloalkyl, aryl, cycloalkyl, cycloheteroalkyl, alkenyl, alkynyl, hydroxy, alkoxy, nitro, amino, thio, alkylsulfonyl, arylsulfonyl, alkylthio, arylthio, aminocarbonyl, alkylcarbonyloxy, arylcarbonylamino, alkylcarbonylamino, arylalkyl, heteroazyl, heteroarylalkyl or aryloxy;
Rl5a ~d Rl6a are independently hydrogen, alkyl, halo, haloalkyl, aryl, cycloalkyl, cycloheteroalkyl, alkenyl, alkynyl, alkoxy, alkylsulfonyl, arylsulfonyl, alkylthio, arylthio, aminocarbonyl, alkylcarbonyloxy, arylcarbonylamino, alkylcarbonylamino, arylalkyl, heteroaryl, heteroarylalkyl, or axyloxy;
or R1 is a group of the structure -(CHZ)D-<
wherein p is 1 to 8 and R1~ and R18 are each independently H, alkyl, alkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl or cycloalkylalkyl at least one of R1~ and R18 being other than H;
or R1 is a graup of the structure R2o - Rts R2~
wherein R19 is aryl or heteroaryl;
R2~ is aryl or heteroaryl;
R21 is H, alkyl, aryl, alkylaryl, arylalkyl, aryloxy, arylalkoxy, heteroaryl, heteroarylalkyl, heteroarylalkoxy, cycloalkyl, cycloalkylalkyl or cycloalkylalkoxy;
R2, R3, R4 are independently hydrogen, halo, alkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, _ arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, hydroxy or haloalkyl;
R5 is independently alkyl, alkenyl, alkynyl, aryl, alkoxy, aryloxy, arylalkoxy, heteroaryl, arylalkyl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl, polycycloalkyl, polycycloalkylalkyl, cycloalkenyl, cycloheteroalkyl, heteroaryloxy, cycloalkenylalkyl, polycycloalkenyl, polycycloalkenylalkyl, heteroarylcarbonyl, amino, alkylamino, arylamino, heteroarylamino, cycloalkyloxy, cycloalkylamino, all optionally substituted through available carbon atoms with 1, 2, 3 or 4 groups selected from hydrogen, halo, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, cycloheteroalkyl, cyclohetero-alkylalkyl, aryl, heteroaryl, arylalkyl, arylcycloalkyl, arylalkenyl, arylalkynyl, aryloxy, aryloxyalkyl, arylalkoxy, arylazo, heteroaryloxo, heteroarylalkyl, heteroarylalkenyl, heteroaryloxy, hydroxy, nitro, cyano, amino, substituted amino, thiol, alkylthio, arylthio, heteroarylthio, arylthioalkyl, alkylcarbonyl, arylcarbonyl, arylaminocarbonyl, alkoxycarbonyl, aminocarbonyl, alkynylaminocarbonyl, alkylaminocarbonyl, alkenylaminocarbonyl, alkylcarbonyloxy, axylcarbonyloxy, alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfinylalkyl, arylsulfonyl, alkylsulfonyl, arylsulfonylamino, heteroarylcarbonylamino, heteroarylsulfinyl, heteroarylthio, heteroarylsulfonyl, alkylsulfinyl;
R6 is hydrogen or C1-C4 alkyl or C1-C4 alkenyl; all optionally substituted with 2, 2, 3 or 4 groups which may independently be any of the substituents listed in the definition of RS set out above;
R~ is alkyl, aryl or arylalkyl wherein alkyl by itself or as part of arylalkyl is optionally substituted o with oxo f ~ f ~ f Het Het 1 and Het 2 are the same or different and are independently selected from heteroaryl containing 5- or 6-ring members; and O
N-oxides thereof; and pharmaceutically acceptable salts thereof; with the provisos that where in the first fornnula X is CH2, and R2, R3 and R4 are each H, then R1 will be other than 3,3-diphenylpropyl, and in the fifth formula, where one of R2, R3 and R~ is 6-fluoro, and the others are H, R7 will be other than 4-(2-methoxyphenyl).
U.S. Provisional application 60/017,224 filed May 5, 1996, discloses a compound which has the structure o ~o)Q oa 3 ~ 1 2 ~~ 1 R2 ~ L1 RsiWA $iWRl R wLz-$~BiLwRl rya a~ ~Ra Rx or or I ~ is including pharmaceutically acceptable salts thereof, N-oxides thereof, wherein q is 0, 1 or 2;
A is ( 1 ) a bond;
( 2 ) -O- ; or -N-(3) R
where R5 is H or lower alkyl, or R5 together with R2 forms a carbocyclic or heterocyclic ring system containing 4 to 8 members in the ring;
B is a fluorenyl-type group of the structure .~' w l w R~ Re, R3 4, R
or Het I /~ or R3, X ~ Ra R9' X ~ Ra R3 Ra, Het 1 Het 2 Or Ra, X Ra B is an indenyl-type group of the structure R3, R3 3.
~,~/ R
or S R3b ~ ~ or 3 (CH~
R ~~ Rab S
(a = 2,3 or 4) Raa R3, R3 R3~ Het Het ) f ;
or R3b R3b S Ras (CHy)a Raa RX is H, alkyl or aryl;
R1 is alkyl, alkenyl, alkynyl, alkoxyl, (alkyl or aryl)3Si (where each alkyl or aryl group is independent), cycloalkyl, cycloalkenyl, substituted alkylamino, substituted arylalkylamino, aryl, arylalkyl, arylamino, aryloxy, heteroaryl, heteroarylamino, heteroaryloxy, arylsulfonylamino, heteroarylsulfonylamino, arylthio, arylsulfinyl, arylsulfonyl, alkylthio, alkylsulfinyl, alkylsulfonyl, heteroarylthio, heteroarylsulfinyl, hetero-arylsulfonyl, -PO(R13) (R14) , (where R13 and R14 are independently alkyl, aryl, alkoxy, aryloxy, heteroaryl, WO 99/215b4 PCT/US98/21750 heteroarylalkyl, heteroaryloxy, heteroarylalkoxy, cycloheteroalkyl, cycloheteroalkylalkyl, cycloheteroalkoxy~
or cycloheteroalkylalkoxy); aminocarbonyl (where the amino may optionally be substituted with one or two aryl, alkyl or heteroaryl groups); cyano, 1,1-(alkoxy or aryloxy)2alkyl (where the two aryl or alkyl substituents can be independently defined, or linked to one another to form a ring connected to L1 (or L2 in the case of R2) at the 2-position); 1,3-dioxane or 1,3-dioxolane connected to L1 (or L2 in the case of R2) at the 4-position; the Rl group may optionally be substituted with 1, 2, 3 or 4 substituents, which can be any of the R3 or R1 groups or alkylcarbonylamino, cycloalkylcarbonylamino, arylcarbonylamino, heteroarylcarbonylamino, alkoxycarbonylamino, aryloxycarbonylamino, heteroaryloxylcarbonylamino, uriedo (where the uriedo nitrogens may optionally be substituted with alkyl, aryl or heteroaryl), heterocyclylcarbonylamino (where the heterocycle is connected to the carbonyl group via a nitrogen or carbon atom), alkylsulfonylamino, arylsulfonylamino, heteroarylsulfonylamino, R2o O
R2~
N-J
R~
inhere d i s : CHR23 ~ - ~c- -CS - c$- or -c= ~ -~ ' gsa gas RaaRSs R23~ R24 ~d R25 are independently hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, heteroaryl, heteroazylalkyl, cycloalkyl, or cycloalkylalkyl;
R20~ R21~ R22 are independently hydrogen, halo, alkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, hydroxy or haloalkyl; and these substituents may either be directly attached to Rl, or attached via an alkylene at an open position;
R2 is independently any of the groups set out for R1, H, polyhaloalkyl, or cycloheteroalkyl, and may be optionally substituted with one to four of any of the groups defined for R3 or substituents defined for R1;
L1 is a linking group containing from 1 to 10 carbons in a linear chain including alkylene, alkenylene or alkynylene, which may contain, within the linking chain any of the following: one or two alkenes, one or two alkynes, an oxygen, an amino group, an oxo group, and may be substituted with one to five alkyl or halo groups;
L2 may be the same or different from L1 and may independently be any of the L1 groups set out above or a singe bond;
R3, R3', R4 and R4' may be the same or different and are independently selected from H, halogen, CF3, haloalkyl, hydroxy, alkoxy, alkyl, aryl, alkenyl, aikenyloxy, alkynyl, alkynyloxy, alkanoyl, vitro, amino, thiol, alkylthio, alkylsulfinyl, alkylsulfonyl, carboxy, alkoxycarbonyl, aminocarbonyl, alkylcarbonyloxy, alkylcarbonylamino, cycloheteroalkyl, cycloheteroalkylalkyl, cyano, Ar-, Ar-alkyl, ArO, Ar-amino, Ar-thio, Ar-sulfinyl, Ar-sulfonyl, Ar-carbonyl, Ar-carbonyloxy or Ar-carbonylamino, wherein Ar is aryl or heteroaryl and Ar may optionally include l, 2 or 3 additional rings fused to Ar;
R3a and R3b are the same or different and are independently any of the R3 groups except hydroxy, vitro, amino or thio;
f ~ f ~ f lief Het t and Het 2 are the same or different and independently represent a 5 or 6 membered heteroaryl ring which contains 1, 2, 3 or 4 heteroatoms in the ring which are independently N, S or O;
and including N-oxides;
X is a bond, or is one of the following groups:
) -s- _ I
(o)n.
) _o-(3) -(4) iC\
R~ R8 (5) -C C~
R9 \RioR9'/~10~
(s) -~ i-R9~ Rio"
or wherein ~c\
R9 Rio Y is O, N-R6 or S;
n' is 0, 1 or 2;
R6 is H, lower alkyl, aryl, -C(O)-R11 or -C (O) -O-R11;
R~ and R8 are the same or different and are independently H, alkyl, aryl, halogen, -O-R12, or R~ and R8 together can be oxygen to form a ketone;
R9, R1~, R9' and Rl~' are the same or different and are independently H, lower alkyl, aryl or -O-R11 R9~ and Rlo" are the same or different and are independently H, lower alkyl, aryl, halogen or -O-R11;
Rll is alky or aryl;
R12 is H, alkyl or aryl;
with the following provisos for compound of the structure LZ ~ Li Rai wA $i ~Ri (a) when R1 is unsubstituted alkyl or unsubstituted arylalkyl, L1 cannot contain amino; _ (b) when Rz is alkyl, L1 cannot contain amino and oxo in adjacent positions (to form an amido group);
(c) when RZL2A- is H2N-, R1L1 cannot contain amino;
(d) when R1 is cyano, L1 must have more than 2 carbons;
(e) R1L1 must contain at least 3 carbons;
with respect to compounds of formulas I, IA and IB, where R1 is cycloheteroalkyl, R1 is exclusive of 1-piperidinyl, 1-pyrrolidinyl, 1-azetidinyl or 1-(2-oxo-pyrrolidinyl);
with respect to the sulfur containing compounds and alcohols, R2L2 cannot have an O or N atom directly attached to S=(0}q or CRX(OH), and for IA, R2L2 cannot be H.
Sum~arv of the Invention In accordance with the present invention, novel compounds are provided which are inhibitors of MTP and have the structure Ra R2/!v Li \O
O
O
R H[~i RSa including pharmaceutically acceptable salts thereof, and stereoisomers and diasteromers thereof wherein A is (1) a bond;
(2) -O- ; or -- N-R ;
where R5 is H or lower alkyl or R5 together with R2 forms a 30 carbocyclic or heterocyclic ring system containing 4 to 8 members in the ring.
A~ B~
B is a fluorenyl-type group of the structure:
R3 / R4. RS / R4.
or Het R3. X ~ R4 R3' X ~ R4 R3 R4.
or Het'1 Het2 (the above B is also referred to as a fluorenyl-type ring or moiety); or R~ X R4 B is an indenyl-type group of the structure R3.
R3 3~ 3 or ~'w.'~'/ R R R3.
Z ~ R3b ~ ~ or He_l se (cH~ J or R I~~ R3b R9b (a = 2,3 or 4) Raa S Raa ~~H~a R3.
Het f (the above B is also referred to as R3b an indenyl-type ring or moiety);
R~
Ra and Rb may be the same or different and can be hydrogen, alkyl, aryl, arylalkyl or heteroaryl (linked to the ring via a carbon atom);
Rsa is H, lower alkyl or aryl;
R1 is independently alkyl, alkenyl, alkynyl, aryl, alkoxy, aryloxy, arylalkoxy, heteroaryl, heteroarylalkoxy, arylalkyl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl, polycycloalkyl, polycycloalkylalkyl, cycloalkenyl, cycloheteroalkyl, heteroaryloxy, cycloalkenylalkyl, polycycloalkenyl, polycycloalkenylalkyl, heteroarylcarbonyl, amino, alkylamino, arylamino, heteroarylamino, cycloalkyloxy, cycloalkylamino, all optionally substituted through available carbon atoms with 1, 2, 3 or 4 groups selected from hydrogen, halo, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl, aryl, heteroaryl, arylalkyl, arylcycloalkyl, arylalkenyl, arylalkynyl, aryloxy, aryloxyalkyl, arylalkoxy, arylazo, heteroaryloxo, heteroarylalkyl, heteroarylalkenyl, heteroaryloxy, hydroxy, nitro, cyano, amino, substituted amino, thiol, alkylthio, arylthio, heteroarylthio, arylthioalkyl, alkylcarbonyl, arylcarbonyl, arylaminocarbonyl, alkoxycarbonyl, aminocarbonyl, alkynylaminocarbonyl, alkylaminocarbonyl, alkenyl-aminocarbonyl, alkylcarbonyloxy, arylcarbonyloxy, alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfinylalkyl, arylsulfonyl, alkylsulfonyl, azylsulfonylamino, heteroarylcarbonylamino, hetero-arylsulfinyl, heteroarylthio, heteroarylsulfonyl, alkylsulfinyl; or R1 and R5a can be joined to form a ring of the structure R2o O
R2~- I_ \ N
a J
R~
cohere a is : c»23, - c- -ca._ cg- or -c= c_ :
I I
0 ~ Ra4 Rzs Rz~ Ras R23, R24 and R25 are independently hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl, or cycloalkylalkyl;
R2o~ R21~ R22 are independently hydrogen, halo, alkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, hydroxy or haloalkyl; and these preferred substituents may either be directly attached to Rl, or attached via an alkylene chain at an open position.
R2 is hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, alkoxyl, (alkyl or aryl)3Si (where each alkyl or aryl group is independent), cycloalkyl, cycloalkenyl, substituted alkylamino, substituted arylalkylamino, aryl, arylalkyl, arylamino, aryloxy, heteroaryl, heteroarylamino, heteroaryloxy, arylsulfonylamino, heteroarylsulfonylamino, arylthio, arylsulfinyl, arylsulfonyl, alkylthio, alkylsulfinyl, alkylsulfonyl, heteroarylthio, heteroarylsulfinyl, heteroarylsulfonyl, cycloheteroalkyl, cycloheteroalkylalkyl, -PO(R13)(R14), (where R13 and R14 are independently alkyl, aryl, alkoxy, aryloxy, heteroaryl, heteroarylalkyl, heteroaryloxy, heteroarylalkoxy, cycloheteroalkyl, cycloheteroalkylalkyl, cycloheteroalkoxy, or cycloheteroalkoxyalkyl); or cyano, 1,1-(alkoxyl or aryloxy)Zalkyl (where the two aryl or alkyl substituents can be independently defined.
The R2 group may optionally have from one to four substituents, which include any of the R1 substituents, and any of the preferred R2 substituents set out below.
Preferred R2 group when L2 and A are each a single bond include the following: haloalkylamino,(where halo includes CF3), alkylamino, cycloalkylamino, arylamino, heteroarylamino, alkoxyamino, aryloxyamino, heteroaryloxyamino, heterocyclylamino (where the heterocycle is connected to the carbonyl group via a nitrogen or carbon atom).
L1 is a linking group containing from 1 to 10 carbons in a linear chain (including alkylene, alkenylene or alkynylene), which may contain, within the linking chain any of the following: one or two alkenes, one or two alkynes, an oxygen, an amino group optionally substituted with alkyl or aryl, an oxo group; and may be substituted with one to five alkyl or halo groups (preferably F). _ L2 may be the same or different from L1 and may independently be any of the L1 groups set out above or a S single bond.
R3, R3', R4 and R4' may be the same or different and are independently selected from H, halogen, CF3, haloalkyl, hydroxy, alkoxy, alkyl, aryl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, alkanoyl, nitro, amino, thiol, alkylthio, alkylsulfinyl, alkylsulfonyl, carboxy, alkoxycarbonyl, aminocarbonyl, alkylcarbonyloxy, alkylcarbonylamino, cycloheteroalkyl, cycloheteroalkylalkyl, cyano, Ar, Ar-alkyl, ArO, Ar-amino, Ar-thio, Ar-sulfinyl, Ar-sulfonyl, Ar-carbonyl, Ar-carbonyloxy or Ar-carbonylamino, wherein Ar is aryl or heteroaryl and Ar may optionally include 1, 2 or 3 additional rings fused to Ar;
R3a and R3b are the same or different and are independently any of the R3 groups;
f ~ f ~ f Het Het t and Het 2 ' are the same or different and independently represent a 5 or 6 membered heteroaryl ring which may contain 1, 2, 3 or 4 heteroatoms in the ring which are independently N, S or 0; and including N-oxides.
X (in the fluorenyl type ring) is a bond, or is one of the following groups:
(i) -s-I
(O)a~
(2) _p_ (3) - I-(4) R~ R8 WO 99/215b4 PCT/US98/21750 (5) -C ~' _ g9 'giogg~~~0~ _ (s) ~ i--g9~ gio~
MICROSOMAL T.~GLYCERIDE TRANSFER PROTEIN AND METHOD
Field of the Invention This invention relates to novel cyclic phosphonate esters which inhibit microsomal triglyceride transfer protein, and to methods for decreasing serum lipids and treating atherosclerosis employing such compounds.
Bac)~,around of the invention The microsomal triglyceride transfer protein (MTP) catalyzes the transport of triglyceride (TG), cholesteryl ester (CE), and phosphatidylcholine (PC) between small unilamellar vesicles (SW). Wetterau & Zilversmit, Chem.
Phys. Lipids ~$, 205-22 (1985). When transfer rates are expressed as the percent of the donor lipid transferred per time, MTP expresses a distinct preference for neutral lipid transport (TG and CE), relative to phospholipid transport.
The protein from bovine liver has been isolated and characterized. Wetterau & Zilversmit, Chem. Phys. Limas _3$, 205-22 (1985). Polyacrylamide gel electrophoresis analysis of the purified protein suggests that the transfer protein is a complex of two subunits of apparent molecular weights 58,000 and 88,000, since a single band was present when purified MTP was electrophoresed under nondenaturing condition, while two bands of apparent molecular weights 58,000 and 88,000 were identified when electrophoresis was performed in the presence of sodium dodecyl sulfate (SDS).
These two polypeptides are hereinafter referred to as 58 kDa and 88 kDa, respectively, or the 58 kDa and the 88 kDa component of MTP, respectively, or the low molecular weight subunit and the high molecular weight subunit of MTP, respectively.
Characterization of the 58,000 molecular weight component of bovine MTP indicates that it is the previously characterized multifunctional protein, protein disulfide isomerase (PDI). Wetterau et a ., J. Biol. Chem.
9800-7 (1990). The presence of PDI in the transfer protein is supported by evidence showing that (1) the amino terminal 25 amino acids of the bovine 58,000 kDa component of MTP is identical to that of bovine PDI, and (2) disulfide isomerase activity was expressed by bovine MTP
following the dissociation of the 58 kDa - 88 kDa protein complex. In addition, antibodies raised against bovine PDI, a protein which by itself has no TG transfer activity, were able to immunoprecipitate bovine TG transfer activity from a solution containing purified bovine MTP.
PDI normally plays a role in the folding and assembly of newly synthesized disulfide bonded proteins within the lumen of the endoplasmic reticulum. Bulleid &
Freedman, Nature ,3~5, 649-51 (1988). It catalyzes the proper pairing of cysteine residues into disulfide bonds, thus catalyzing the proper folding of disulfide bonded proteins. In addition, PDI has been reported to be identical to the beta subunit of human prolyl 4-hydroxylase. Koivu et~, J. Biol. Chem. 2 (1987). The role of PDI in the bovine transfer protein is not clear. It does appear to be an essential component of the transfer protein as dissociation of PDI from the 88 kDa component of bovine MTP by either low concentrations of a denaturant (guanidine HC1), a chaotropic agent (sodium perchlorate), or a nondenaturing detergent (octyl glucoside) results in a loss of transfer activity.
Wetterau etal., Biochemistry ,~(~, 9728-35 (1991). Isolated bovine PDI has no apparent lipid transfer activity, suggesting that either the 88 kDa polypeptide is the transfer protein or that it confers transfer activity to the protein complex.
The tissue and subcellular distribution of MTP
activity in rats has been investigated. Wetterau &
Zilversmit, Biochem. Bionhys. Acta 87~, 610-7 (1986).
Lipid transfer activity was found in liver and intestine.
Little or no transfer activity was found in plasma, brain, heart, or kidney. Within the liver, MTP was a soluble protein located within the lumen of the microsomal fraction. Approximately equal concentrations were found in-the smooth and rough microsomes.
Abetalipoproteinemia is an autosomal recessive disease characterized by a virtual absence of plasma lipoproteins which contain apolipoprotein B (apoB). Kane &
Havel in The Metabolic Basis of Inherited Diseasg, Sixth edition, 1139-64 (1989). Plasma TG levels may be as low as a few mg/dL, and they fail to rise after fat ingestion.
Plasma cholesterol levels are often only 20-45 mg/dL.
These abnormalities are the result of a genetic defect in the assembly and/or secretion of very low density lipoproteins (VLDL) in the liver and chylomicrons in the intestine. The molecular basis for this defect has not been previously determined. In subjects examined, triglyceride, phospholipid, and cholesterol synthesis appear normal. At autopsy, subjects are free of atherosclerosis. Schaefer et al., Clin. Chem. ~, B9-12 (1988). A link between the apoB gene and abetalipoproteinemia has been excluded in several families.
Talmud et al., ~T. Clin. Invest. ~, 1803-6 (1988) and Huang et a ., ,Am. J. Hum. Gent. 4~C, 1141-8 (2990).
Subjects with abetalipoproteinemia are afflicted with numerous maladies. Kane & Havel, vide supra Subjects have fat malabsorption and TG accumulation in their enterocytes and hepatocytes. Due to the absence of TG-rich plasma lipoproteins, there is a defect in the transport of fat-soluble vitamins such as vitamin E. This results in acanthocytosis of erythrocytes, spinocerebellar ataxia with degeneration of the fasciculus cuneatus and gracilis, peripheral neuropathy, degenerative pigmentary retinopathy, and ceroid myopathy. Treatment of abetalipoproteinemic subjects includes dietary restriction of fat intake and dietary supplementation with vitamins A, E and K .
,~ vit , MTP catalyzes the transport of lipid molecules between phospholipid membranes. Presumably, it plays a similar role in vivo, and thus plays some role in lipid metabolism. The subcellular (lumen of the microsomal_-fraction) and tissue distribution (liver and intestine) of MTP have led to speculation that it plays a role in the assembly of plasma lipoproteins, as these are the sites of plasma lipoprotein assembly. Wetterau & Zilversmit, Bioc~em. Biqphvs. Acta 87~, 610-7 (1986). The ability of MTP to catalyze the transport of TG between membranes is consistent with this hypothesis, and suggests that MTP may catalyze the transport of TG from its site of synthesis in the endoplasmic reticulum (ER) membrane to nascent lipoprotein particles within the lumen of the ER.
Olofsson and colleagues have studied lipoprotein assembly in HepG2 cells. Bostrom et ., J. Biol. Chem.
~, 4434-42 (1988). Their results suggest small precursor lipoproteins become larger with time. This would be consistent with the addition or transfer of lipid molecules to nascent lipoproteins as they are assembled. MTP may play a role in this process. In support of this hypothesis, Howell and Palade, J. Cell Biol. ~?, 833-45 (1982), isolated nascent lipoproteins from the hepatic Golgi fraction of rat liver. There was a spectrum of sizes of particles present with varying lipid and protein compositions. Particles of high density lipoprotein (HDL) density, yet containing apoB, were found. Higgins and Hutson, ~T. Lipid Res. ,~5, 1295-1305 (1984), reported lipoproteins isolated from Golgi were consistently larger than those from the endoplasmic reticulum, again suggesting the assembly of lipoproteins is a progressive event.
However, there is no direct evidence in the prior art demonstrating that MTP plays a role in lipid metabolism or the assembly of plasma lipoprotein.
Recent reports (Science, Vol. 258, page 999, 1992;
D. Sharp et al, Nature, Vol. 365, page 65, 1993) demonstrate that the defect causing abetalipoproteinemia is in the MTP gene, and as a result, the MTP protein.
Individuals with abetalipoproteinemia have no MTP activity, as a result of mutations in the MTP gene, some of which have been characterized. These results indicate that MTP
is required for the synthesis of apoB containing lipoproteins, such as VLDL, the precursor to LDL. It therefore follows that inhibitors of MTP would inhibit the synthesis of VLDL and LDL, thereby lowering VLDL levels, LDL levels, cholesterol levels, and triglyceride levels in animals and man.
Canadian Patent Application No. 2,091,102 published March 2, 1994 (corresponding to U.S. application Serial No.
117,362, filed September 3, 1993 (file DC2lb)) which is incorporated herein by reference), reports MTP inhibitors which also block the production of apoB containing lipoproteins in a human hepatic cell line (HepG2 cells).
This provides further support for the proposal that an MTP
inhibitor would lower apoB containing lipoprotein and lipid levels irk vivo. This Canadian patent application discloses a method for identifying the MTP inhibitors (\
N N
/
which has the name 2-[1-(3,3-diphenylpropyl)-4-piperidinyl]-2, 3-dihydro-3-oxo-1~i-isoindole hydrochloride and O
\ ~N \
/ ,, J OCH3 which has the name 1-[3-(6-fluoro-1-tetralanyl)-methyl]-4-O-methoxyphenyl piperazine.
EP 0643057A1 published March 15, 1995, discloses MTP
inhibitors of the structure I
or II
O
R3. I- / _N~N_ R~
X ' RS
R N ~N R' or III
o . _ J.
Y
where X is : CHIie, -cH- C8 Or -C= c- :
I I
R9 Ri0 R9 Ri0 R8, R9 and R1~ are independently hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl, or cycloalkylalkyl;
Y is -(cHZ)~; or -iC-O
where m is 2 or 3;
R1 is alkyl, alkenyl, alkynyl, aryl, heteroaryl, arylalkyl (wherein alkyl has at least 2 carbons), diarylalkyl, arylalkenyl, diarylalkenyl, arylalkynyl, diarylalkynyl, diarylalkylaryl, heteroazylalkyl (wherein alkyl has at least 2 carbons), cycloalkyl, or cycloalkylalkyl (wherein alkyl has at least 2 carbons); all of the aforementioned R1 groups being optionally substituted through available carbon atoms with l, 2, or 3 groups selected from halo, haloalkyl, alkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl, fluorenyl, heteroarylalkyl, hydroxy or oxo; or R1 is a group of the structure Rts '~~ _ , tt Z
R~2 R~3 ~~ Rta Rll is a bond, alkylene, alkenylene or alkynylene of up to 6 carbon atoms, arylene (for example ) ~ , or mixed arylene-alkylene (for example ~- ( CH1 ) a. ) where n is 1 to 6;
R12 is hydrogen, alkyl, alkenyl, aryl, heteroaryl, haloalkyl, arylalkyl, arylalkenyl, cycloalkyl, aryloxy, alkoxy, arylalkoxy, heteroarylalkyl or cycloalkylalkyl;
Z is a bond, O, S, N-alkyl, N-aryl, or alkylene or alkenylene of from 1 to 5 carbon atoms;
R13~ R14~ R15~ ~d R16 are independently hydrogen, alkyl, halo, haloalkyl, aryl, cycloalkyl, cycloheteroalkyl, alkenyl, alkynyl, hydroxy, alkoxy, nitro, amino, thio, alkylsulfonyl, arylsulfonyl, alkylthio, arylthio, carboxy, aminocarbonyl, alkylcarbonyloxy, alkylcarbonylamino, arylalkyl, heteroaryl, heteroarylalkyl, or aryloxy;
or R1 is Ri7 (C8Z)D~
Ri8 wherein p is 1 to 8 and R1~ and R18 are each independently H, alkyl, alkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl or cycloalkylalkyl, at least one of R1~ and R18 being other than H;
or Rl is Ri9 RZi wherein R19 is aryl or heteroaryl;
R2~ is aryl or heteroaryl;
R21 is H, alkyl, aryl, alkylaryl, arylalkyl, S ~aryloxy, arylalkoxy, heteroaryl, heteroarylalkyl, heteroarylalkoxy, cycloalkyl, cycloalkylalkyl or cycloalkylalkoxy;
R2, R3, R4 are independently hydrogen, halo, alkyl, haloalkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, hydroxy or haloalkyl;
R5 is alkyl of at least 2 carbons, alkenyl, alkynyl;
aryl, heteroaryl, arylalkyl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl, polycycloalkyl, polycycloalkylalkyl, 1S cycloalkenyl, cycloalkenylalkyl, polycycloalkenyl, polycycloalkenylalkyl, heteroarylcarbonyl, all of the R5 and R6 substituents being optionally substituted through available carbon atoms with 1, 2, or 3 groups selected from hydrogen, halo, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl, aryl, heteroaryl, arylalkyl, arylcycloalkyl, arylalkynyl, aryloxy, aryloxyalkyl, arylalkoxy, arylazo, heteroaryloxo, heteroarylalkyl, heteroarylalkenyl, heteroaryloxy, hydroxy, 2S vitro, cyano, amino, substituted amino (wherein the amino includes 1 or 2 substituents which are alkyl, or aryl or any of the other aryl compounds mentioned in the definitions), thiol, alkylthio, arylthio, heteroarylthio, arylthioalkyl, alkylcarbonyl, arylcarbonyl, arylaminocarbonyl, alkoxycarbonyl, aminocarbonyl, alkynylaminocarbonyl, alkylaminocarbonyl, alkenylaminocarbonyl, alkylcarbonyloxy, arylcarbonyloxy, alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfinylalkyl, arylsulfonyl, alkylsulfonyl, 3S arylsulfonylamino; with the proviso that when RS is CH3, R6 _ g _ is not H; and where R5 is phenyl, the phenyl preferably includes an ortho hydrophobic substituent such as alkyl, haloalkyl, aryl, aryloxy or arylalkyl;
R6 is hydrogen or C1-C4 alkyl or C1-C4 alkenyl;
S R~ is alkyl, aryl or arylalkyl wherein alkyl or the alkyl portion is optionally substituted with oxo; and including pharmaceutically acceptable salts and anions thereof or esters thereof.
In the formula I compounds, where X is CH2 and R2 , R3 and R4 are each H, R1 will be other than 3,3-diphenylpropyl.
In the formula ITI compounds, where one of R2, R3 and R4 is 6-fluoro, and the others are H, R~ will be other than 4-O-methoxyphenyl.
U.S. Application Serial No. 472,067, filed June 6, 1995 (file DC2le) discloses compounds of the structure o N~N_ R~
X ' or or or R2 O R~
R3. I_ ,\
X ' R5, o fJ-~N- R~
R~
Rs, D N
Rs J
or o ~3. I. w ~N.~ _ / i Y.N J
O O
where O is - C- or - s- ;
O
X is: CHRs, -C- ~ -CH- CH- or O Rs Rto R9 Rt°
R8, R9 and R1~ are independently hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl, or cycloalkylalkyl;
x 3s -(C8Z)m- or -c-wherein m is 2 or 3;
R1 is alkyl, alkenyl, alkynyl, aryl, heteroaryl, arylalkyl wherein alkyl has at least 2 carbons, diarylalkyl, arylalkenyl, diarylalkenyl, arylalkynyl, diarylalkynyl, diarylalkylaryl, heteroarylalkyl wherein alkyl has at least 2 carbons, cycloalkyl, or cycloalkylalkyl wherein alkyl has at least 2 carbons, all optionally substituted through available carbon atoms with l, 2, 3 or 4 groups selected from halo, haloalkyl, alkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl;
fluorenyl, heteroarylalkyl, hydroxy or oxo;
or R1 is a fluorenyl-type group of the structure ~~/Rts ~,--.,/Rts t~ Rts i i , i tt -Rtt-Zt _ Rtt_ t 'Z or Z
or Z
Rt2 ~ ~ Rt~Z2 ~ ~ Rt2 Z2 Het R13 V~ R14 Rt3 v ' Rt4 13 Rt4 WO 99/2156a PCT/US98/21750 is Ris Het 1 or Ri~Z Z
Het 2 Or R1 is an indenyl-type group of the structure R14 13\ 14 R \n/ R
11_ 1 - R Z or , R11- Z1 \ / or 12 2 / Rl6a / 16a R - ZRisa (CH2~ R12- Z2 R
Rl5a E
(a - 2,3 or 4) Het ~ He!
_ R11_ Z1 or _ Rii_ Zi ;
R12_ Z2 ~ Rl6a R12_ Z2 / Rl6a Risa (CH2)a G ~ Rlsa Z1 and Z2 are the same or different and are independently a bond, O, S, H
- NH- C- ~ - C- or - C- , O ~ ~0~2 ~ O alkyl O ~ O OH
with the proviso that with respect to ~, at least one of Z1 and Z2 will be other than a bond; R11 is a bond, alkylene, alkenylene or alkynylene of up to 10 carbon~atoms; azylene or mixed arylene-alkylene; R12 is hydrogen, alkyl, alkenyl, aryl, haloalkyl, trihaloalkyl, trihaloalkylalkyl, heteroaryl, heteroarylalkyl, arylalkyl, arylalkenyl, cyclo-alkyl, aryloxy, alkoxy, arylalkoxy or cycloalkylalkyl, with the provisos that (1) when R12 is H, aryloxy, alkoxy or arylalkoxy, -NH-C- , -N-C-. -C-then Z2 is o attryt o ~ o or a bond and -(2) when Z2 is a bond, R12 cannot be heteroaryl or heteroarylalkyl;
Z is bond, 0, S, N-alkyl, N-aryl, or alkylene or alkenylene from 1 to 5 carbon atoms; R13, R14~ R15~ ~d R16 are independently hydrogen, alkyl, halo, haloalkyl, aryl, cycloalkyl, cycloheteroalkyl, alkenyl, alkynyl, hydroxy, alkoxy, nitro, amino, thio, alkylsulfonyl, arylsulfonyl, alkylthio, arylthio, aminocarbonyl, alkylcarbonyloxy, arylcarbonylamino, alkylcarbonylamino, arylalkyl, heteroazyl, heteroarylalkyl or aryloxy;
Rl5a ~d Rl6a are independently hydrogen, alkyl, halo, haloalkyl, aryl, cycloalkyl, cycloheteroalkyl, alkenyl, alkynyl, alkoxy, alkylsulfonyl, arylsulfonyl, alkylthio, arylthio, aminocarbonyl, alkylcarbonyloxy, arylcarbonylamino, alkylcarbonylamino, arylalkyl, heteroaryl, heteroarylalkyl, or axyloxy;
or R1 is a group of the structure -(CHZ)D-<
wherein p is 1 to 8 and R1~ and R18 are each independently H, alkyl, alkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl or cycloalkylalkyl at least one of R1~ and R18 being other than H;
or R1 is a graup of the structure R2o - Rts R2~
wherein R19 is aryl or heteroaryl;
R2~ is aryl or heteroaryl;
R21 is H, alkyl, aryl, alkylaryl, arylalkyl, aryloxy, arylalkoxy, heteroaryl, heteroarylalkyl, heteroarylalkoxy, cycloalkyl, cycloalkylalkyl or cycloalkylalkoxy;
R2, R3, R4 are independently hydrogen, halo, alkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, _ arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, hydroxy or haloalkyl;
R5 is independently alkyl, alkenyl, alkynyl, aryl, alkoxy, aryloxy, arylalkoxy, heteroaryl, arylalkyl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl, polycycloalkyl, polycycloalkylalkyl, cycloalkenyl, cycloheteroalkyl, heteroaryloxy, cycloalkenylalkyl, polycycloalkenyl, polycycloalkenylalkyl, heteroarylcarbonyl, amino, alkylamino, arylamino, heteroarylamino, cycloalkyloxy, cycloalkylamino, all optionally substituted through available carbon atoms with 1, 2, 3 or 4 groups selected from hydrogen, halo, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, cycloheteroalkyl, cyclohetero-alkylalkyl, aryl, heteroaryl, arylalkyl, arylcycloalkyl, arylalkenyl, arylalkynyl, aryloxy, aryloxyalkyl, arylalkoxy, arylazo, heteroaryloxo, heteroarylalkyl, heteroarylalkenyl, heteroaryloxy, hydroxy, nitro, cyano, amino, substituted amino, thiol, alkylthio, arylthio, heteroarylthio, arylthioalkyl, alkylcarbonyl, arylcarbonyl, arylaminocarbonyl, alkoxycarbonyl, aminocarbonyl, alkynylaminocarbonyl, alkylaminocarbonyl, alkenylaminocarbonyl, alkylcarbonyloxy, axylcarbonyloxy, alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfinylalkyl, arylsulfonyl, alkylsulfonyl, arylsulfonylamino, heteroarylcarbonylamino, heteroarylsulfinyl, heteroarylthio, heteroarylsulfonyl, alkylsulfinyl;
R6 is hydrogen or C1-C4 alkyl or C1-C4 alkenyl; all optionally substituted with 2, 2, 3 or 4 groups which may independently be any of the substituents listed in the definition of RS set out above;
R~ is alkyl, aryl or arylalkyl wherein alkyl by itself or as part of arylalkyl is optionally substituted o with oxo f ~ f ~ f Het Het 1 and Het 2 are the same or different and are independently selected from heteroaryl containing 5- or 6-ring members; and O
N-oxides thereof; and pharmaceutically acceptable salts thereof; with the provisos that where in the first fornnula X is CH2, and R2, R3 and R4 are each H, then R1 will be other than 3,3-diphenylpropyl, and in the fifth formula, where one of R2, R3 and R~ is 6-fluoro, and the others are H, R7 will be other than 4-(2-methoxyphenyl).
U.S. Provisional application 60/017,224 filed May 5, 1996, discloses a compound which has the structure o ~o)Q oa 3 ~ 1 2 ~~ 1 R2 ~ L1 RsiWA $iWRl R wLz-$~BiLwRl rya a~ ~Ra Rx or or I ~ is including pharmaceutically acceptable salts thereof, N-oxides thereof, wherein q is 0, 1 or 2;
A is ( 1 ) a bond;
( 2 ) -O- ; or -N-(3) R
where R5 is H or lower alkyl, or R5 together with R2 forms a carbocyclic or heterocyclic ring system containing 4 to 8 members in the ring;
B is a fluorenyl-type group of the structure .~' w l w R~ Re, R3 4, R
or Het I /~ or R3, X ~ Ra R9' X ~ Ra R3 Ra, Het 1 Het 2 Or Ra, X Ra B is an indenyl-type group of the structure R3, R3 3.
~,~/ R
or S R3b ~ ~ or 3 (CH~
R ~~ Rab S
(a = 2,3 or 4) Raa R3, R3 R3~ Het Het ) f ;
or R3b R3b S Ras (CHy)a Raa RX is H, alkyl or aryl;
R1 is alkyl, alkenyl, alkynyl, alkoxyl, (alkyl or aryl)3Si (where each alkyl or aryl group is independent), cycloalkyl, cycloalkenyl, substituted alkylamino, substituted arylalkylamino, aryl, arylalkyl, arylamino, aryloxy, heteroaryl, heteroarylamino, heteroaryloxy, arylsulfonylamino, heteroarylsulfonylamino, arylthio, arylsulfinyl, arylsulfonyl, alkylthio, alkylsulfinyl, alkylsulfonyl, heteroarylthio, heteroarylsulfinyl, hetero-arylsulfonyl, -PO(R13) (R14) , (where R13 and R14 are independently alkyl, aryl, alkoxy, aryloxy, heteroaryl, WO 99/215b4 PCT/US98/21750 heteroarylalkyl, heteroaryloxy, heteroarylalkoxy, cycloheteroalkyl, cycloheteroalkylalkyl, cycloheteroalkoxy~
or cycloheteroalkylalkoxy); aminocarbonyl (where the amino may optionally be substituted with one or two aryl, alkyl or heteroaryl groups); cyano, 1,1-(alkoxy or aryloxy)2alkyl (where the two aryl or alkyl substituents can be independently defined, or linked to one another to form a ring connected to L1 (or L2 in the case of R2) at the 2-position); 1,3-dioxane or 1,3-dioxolane connected to L1 (or L2 in the case of R2) at the 4-position; the Rl group may optionally be substituted with 1, 2, 3 or 4 substituents, which can be any of the R3 or R1 groups or alkylcarbonylamino, cycloalkylcarbonylamino, arylcarbonylamino, heteroarylcarbonylamino, alkoxycarbonylamino, aryloxycarbonylamino, heteroaryloxylcarbonylamino, uriedo (where the uriedo nitrogens may optionally be substituted with alkyl, aryl or heteroaryl), heterocyclylcarbonylamino (where the heterocycle is connected to the carbonyl group via a nitrogen or carbon atom), alkylsulfonylamino, arylsulfonylamino, heteroarylsulfonylamino, R2o O
R2~
N-J
R~
inhere d i s : CHR23 ~ - ~c- -CS - c$- or -c= ~ -~ ' gsa gas RaaRSs R23~ R24 ~d R25 are independently hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, heteroaryl, heteroazylalkyl, cycloalkyl, or cycloalkylalkyl;
R20~ R21~ R22 are independently hydrogen, halo, alkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, hydroxy or haloalkyl; and these substituents may either be directly attached to Rl, or attached via an alkylene at an open position;
R2 is independently any of the groups set out for R1, H, polyhaloalkyl, or cycloheteroalkyl, and may be optionally substituted with one to four of any of the groups defined for R3 or substituents defined for R1;
L1 is a linking group containing from 1 to 10 carbons in a linear chain including alkylene, alkenylene or alkynylene, which may contain, within the linking chain any of the following: one or two alkenes, one or two alkynes, an oxygen, an amino group, an oxo group, and may be substituted with one to five alkyl or halo groups;
L2 may be the same or different from L1 and may independently be any of the L1 groups set out above or a singe bond;
R3, R3', R4 and R4' may be the same or different and are independently selected from H, halogen, CF3, haloalkyl, hydroxy, alkoxy, alkyl, aryl, alkenyl, aikenyloxy, alkynyl, alkynyloxy, alkanoyl, vitro, amino, thiol, alkylthio, alkylsulfinyl, alkylsulfonyl, carboxy, alkoxycarbonyl, aminocarbonyl, alkylcarbonyloxy, alkylcarbonylamino, cycloheteroalkyl, cycloheteroalkylalkyl, cyano, Ar-, Ar-alkyl, ArO, Ar-amino, Ar-thio, Ar-sulfinyl, Ar-sulfonyl, Ar-carbonyl, Ar-carbonyloxy or Ar-carbonylamino, wherein Ar is aryl or heteroaryl and Ar may optionally include l, 2 or 3 additional rings fused to Ar;
R3a and R3b are the same or different and are independently any of the R3 groups except hydroxy, vitro, amino or thio;
f ~ f ~ f lief Het t and Het 2 are the same or different and independently represent a 5 or 6 membered heteroaryl ring which contains 1, 2, 3 or 4 heteroatoms in the ring which are independently N, S or O;
and including N-oxides;
X is a bond, or is one of the following groups:
) -s- _ I
(o)n.
) _o-(3) -(4) iC\
R~ R8 (5) -C C~
R9 \RioR9'/~10~
(s) -~ i-R9~ Rio"
or wherein ~c\
R9 Rio Y is O, N-R6 or S;
n' is 0, 1 or 2;
R6 is H, lower alkyl, aryl, -C(O)-R11 or -C (O) -O-R11;
R~ and R8 are the same or different and are independently H, alkyl, aryl, halogen, -O-R12, or R~ and R8 together can be oxygen to form a ketone;
R9, R1~, R9' and Rl~' are the same or different and are independently H, lower alkyl, aryl or -O-R11 R9~ and Rlo" are the same or different and are independently H, lower alkyl, aryl, halogen or -O-R11;
Rll is alky or aryl;
R12 is H, alkyl or aryl;
with the following provisos for compound of the structure LZ ~ Li Rai wA $i ~Ri (a) when R1 is unsubstituted alkyl or unsubstituted arylalkyl, L1 cannot contain amino; _ (b) when Rz is alkyl, L1 cannot contain amino and oxo in adjacent positions (to form an amido group);
(c) when RZL2A- is H2N-, R1L1 cannot contain amino;
(d) when R1 is cyano, L1 must have more than 2 carbons;
(e) R1L1 must contain at least 3 carbons;
with respect to compounds of formulas I, IA and IB, where R1 is cycloheteroalkyl, R1 is exclusive of 1-piperidinyl, 1-pyrrolidinyl, 1-azetidinyl or 1-(2-oxo-pyrrolidinyl);
with respect to the sulfur containing compounds and alcohols, R2L2 cannot have an O or N atom directly attached to S=(0}q or CRX(OH), and for IA, R2L2 cannot be H.
Sum~arv of the Invention In accordance with the present invention, novel compounds are provided which are inhibitors of MTP and have the structure Ra R2/!v Li \O
O
O
R H[~i RSa including pharmaceutically acceptable salts thereof, and stereoisomers and diasteromers thereof wherein A is (1) a bond;
(2) -O- ; or -- N-R ;
where R5 is H or lower alkyl or R5 together with R2 forms a 30 carbocyclic or heterocyclic ring system containing 4 to 8 members in the ring.
A~ B~
B is a fluorenyl-type group of the structure:
R3 / R4. RS / R4.
or Het R3. X ~ R4 R3' X ~ R4 R3 R4.
or Het'1 Het2 (the above B is also referred to as a fluorenyl-type ring or moiety); or R~ X R4 B is an indenyl-type group of the structure R3.
R3 3~ 3 or ~'w.'~'/ R R R3.
Z ~ R3b ~ ~ or He_l se (cH~ J or R I~~ R3b R9b (a = 2,3 or 4) Raa S Raa ~~H~a R3.
Het f (the above B is also referred to as R3b an indenyl-type ring or moiety);
R~
Ra and Rb may be the same or different and can be hydrogen, alkyl, aryl, arylalkyl or heteroaryl (linked to the ring via a carbon atom);
Rsa is H, lower alkyl or aryl;
R1 is independently alkyl, alkenyl, alkynyl, aryl, alkoxy, aryloxy, arylalkoxy, heteroaryl, heteroarylalkoxy, arylalkyl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl, polycycloalkyl, polycycloalkylalkyl, cycloalkenyl, cycloheteroalkyl, heteroaryloxy, cycloalkenylalkyl, polycycloalkenyl, polycycloalkenylalkyl, heteroarylcarbonyl, amino, alkylamino, arylamino, heteroarylamino, cycloalkyloxy, cycloalkylamino, all optionally substituted through available carbon atoms with 1, 2, 3 or 4 groups selected from hydrogen, halo, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl, aryl, heteroaryl, arylalkyl, arylcycloalkyl, arylalkenyl, arylalkynyl, aryloxy, aryloxyalkyl, arylalkoxy, arylazo, heteroaryloxo, heteroarylalkyl, heteroarylalkenyl, heteroaryloxy, hydroxy, nitro, cyano, amino, substituted amino, thiol, alkylthio, arylthio, heteroarylthio, arylthioalkyl, alkylcarbonyl, arylcarbonyl, arylaminocarbonyl, alkoxycarbonyl, aminocarbonyl, alkynylaminocarbonyl, alkylaminocarbonyl, alkenyl-aminocarbonyl, alkylcarbonyloxy, arylcarbonyloxy, alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfinylalkyl, arylsulfonyl, alkylsulfonyl, azylsulfonylamino, heteroarylcarbonylamino, hetero-arylsulfinyl, heteroarylthio, heteroarylsulfonyl, alkylsulfinyl; or R1 and R5a can be joined to form a ring of the structure R2o O
R2~- I_ \ N
a J
R~
cohere a is : c»23, - c- -ca._ cg- or -c= c_ :
I I
0 ~ Ra4 Rzs Rz~ Ras R23, R24 and R25 are independently hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl, or cycloalkylalkyl;
R2o~ R21~ R22 are independently hydrogen, halo, alkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, hydroxy or haloalkyl; and these preferred substituents may either be directly attached to Rl, or attached via an alkylene chain at an open position.
R2 is hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, alkoxyl, (alkyl or aryl)3Si (where each alkyl or aryl group is independent), cycloalkyl, cycloalkenyl, substituted alkylamino, substituted arylalkylamino, aryl, arylalkyl, arylamino, aryloxy, heteroaryl, heteroarylamino, heteroaryloxy, arylsulfonylamino, heteroarylsulfonylamino, arylthio, arylsulfinyl, arylsulfonyl, alkylthio, alkylsulfinyl, alkylsulfonyl, heteroarylthio, heteroarylsulfinyl, heteroarylsulfonyl, cycloheteroalkyl, cycloheteroalkylalkyl, -PO(R13)(R14), (where R13 and R14 are independently alkyl, aryl, alkoxy, aryloxy, heteroaryl, heteroarylalkyl, heteroaryloxy, heteroarylalkoxy, cycloheteroalkyl, cycloheteroalkylalkyl, cycloheteroalkoxy, or cycloheteroalkoxyalkyl); or cyano, 1,1-(alkoxyl or aryloxy)Zalkyl (where the two aryl or alkyl substituents can be independently defined.
The R2 group may optionally have from one to four substituents, which include any of the R1 substituents, and any of the preferred R2 substituents set out below.
Preferred R2 group when L2 and A are each a single bond include the following: haloalkylamino,(where halo includes CF3), alkylamino, cycloalkylamino, arylamino, heteroarylamino, alkoxyamino, aryloxyamino, heteroaryloxyamino, heterocyclylamino (where the heterocycle is connected to the carbonyl group via a nitrogen or carbon atom).
L1 is a linking group containing from 1 to 10 carbons in a linear chain (including alkylene, alkenylene or alkynylene), which may contain, within the linking chain any of the following: one or two alkenes, one or two alkynes, an oxygen, an amino group optionally substituted with alkyl or aryl, an oxo group; and may be substituted with one to five alkyl or halo groups (preferably F). _ L2 may be the same or different from L1 and may independently be any of the L1 groups set out above or a S single bond.
R3, R3', R4 and R4' may be the same or different and are independently selected from H, halogen, CF3, haloalkyl, hydroxy, alkoxy, alkyl, aryl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, alkanoyl, nitro, amino, thiol, alkylthio, alkylsulfinyl, alkylsulfonyl, carboxy, alkoxycarbonyl, aminocarbonyl, alkylcarbonyloxy, alkylcarbonylamino, cycloheteroalkyl, cycloheteroalkylalkyl, cyano, Ar, Ar-alkyl, ArO, Ar-amino, Ar-thio, Ar-sulfinyl, Ar-sulfonyl, Ar-carbonyl, Ar-carbonyloxy or Ar-carbonylamino, wherein Ar is aryl or heteroaryl and Ar may optionally include 1, 2 or 3 additional rings fused to Ar;
R3a and R3b are the same or different and are independently any of the R3 groups;
f ~ f ~ f Het Het t and Het 2 ' are the same or different and independently represent a 5 or 6 membered heteroaryl ring which may contain 1, 2, 3 or 4 heteroatoms in the ring which are independently N, S or 0; and including N-oxides.
X (in the fluorenyl type ring) is a bond, or is one of the following groups:
(i) -s-I
(O)a~
(2) _p_ (3) - I-(4) R~ R8 WO 99/215b4 PCT/US98/21750 (5) -C ~' _ g9 'giogg~~~0~ _ (s) ~ i--g9~ gio~
(7) ~C' Y-g9 gio wherein Y is 0, N-R6 or S;
n' is 0, 1 or 2;
R6 is H, lower alkyl, aryl, -C(O)-R11 or -C ( O ) -O-R11;
R7 and R8 are the same or different and axe independently H, alkyl, aryl, halogen, -O-R12, or R7 and R8 together can be oxygen to form a ketone;
R9, R1~, R9' and R1~' are the same or different and are independently H, lower alkyl, aryl or -O-R11;
R9" and Rlfl" are the same or different and are independently H, lower alkyl, aryl, halogen or R11 is alley or aryl;
R12 is H, alkyl or aryl;
with the proviso that when A is a (1) bond, R2L2 cannot be hydrogen.
The pharmaceutically acceptable salts of the compounds of formula I include alkali metal salts such as lithium, sodium or potassium, alkaline earth metal salts such as calcium or magnesium, as well as zinc or aluminum and other cations such as ammonium, choline, diethanolamine, ethylenediamine, t-butyl-amine, t-octylamine, dehydroabietylamine, as well as pharmaceutically acceptable anions such as chloride, bromide, iodide, tartrate, acetate, methanesulfonate, maleate, succinate, glutarate, and salts of naturally occurring amino acids such as arginine, lysine, alanine and the like, and prodrug esters thereof.
In addition, in accordance with the present invention, a method for preventing, inhibiting or treating_ atherosclerosis, pancreatitis, hyperglycemia or obesity is provided, wherein a compound of formula I, IA or IB as defined hereinbefore is administered in an amount which decreases the activity of microsomal triglyceride transfer protein.
Furthermore, in accordance with the present invention, a method is provided for lowering serum lipid levels, cholesterol and/or triglycerides, or inhibiting and/or treating hyperlipemia, hyperlipidemia, hyperlipoproteinemia, hypercholesterolemia, atherosclerosis, hyperglycemia, pancreatitis, obesity, hypertriglyceridemia, Type II diabetes (NIDDM) wherein a compound of formula I as defined hereinbefore is administered in an amount which decreases the activity of microsomal triglyceride transfer protein.
filed Description of the Invention The following definitions apply to the terms as used throughout this specification, unless othezwise limited in specific instances.
The term "MTP" refers to a polypeptide or protein complex that (1) if obtained from an organism (e. g., cows, humans, tec.), can be isolated from the microsomal fraction of homogenized tissue; and (2) stimulates the transport of triglycerides, cholesterol esters, or phospholipids from synthetic phospholipid vesicles, membranes or lipoproteins to synthetic vesicles, membranes, or lipoproteins and which is distinct from the cholesterol ester transfer protein [Drayna et , Naturg ~, 632-634 (1987)] which may have similar catalytic properties.
The phrase "stabilizing" atherosclerosis as used in the present application refers to slowing down the development of and/or inhibiting the formation of new atherosclerotic lesions.
The phrase "causing the regression of"
atherosclerosis as used in the present application refers to reducing and/or eliminating atherosclerotic lesions.
Unless otherwise indicated, the term "lower alkyl", "alkyl" or "alk" as employed herein alone or as part of another group includes both straight and branched chain hydrocarbons, containing 1 to 40 carbons, preferably 1 to 20 carbons, more preferably 1 to 12 carbons, in the normal chain,such as methyl, ethyl, propyl, isopropyl, butyl, t-butyl, isobutyl, pentyl, hexyl, isohexyl, heptyl, 4,4-dimethylpentyl, octyl, 2,2,4-trimethylpentyl, nonyl, decyl, undecyl, dodecyl, the various branched chain isomers thereof, and the like as well as such groups including 1 to 4 substituents which may be any of the R3 groups, or the R1 substituents set out herein.
Unless othervuise indicated, the term "cycloalkyl" as employed herein alone or as part of another group includes saturated or partially unsaturated (containing 1 or 2 double bonds) cyclic hydrocarbon groups containing 1 to 3 rings, including monocyclicalkyl, bicyclicalkyl and tricyclicalkyl, containing a total of 3 to 20 carbons forming the rings, preferably 4 to 12 carbons, forming the ring and which may be fused to 1 aromatic ring as described for aryl, which include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclodecyl and cyclododecyl, cyclohexenyl, any of which groups may be optionally substituted with 1 to 4 substituents which may be any of the R3 groups, or the R1 substituents set out herein.
The term "cycloalkenyl" as employed herein alone or as part of another group refers to cyclic hydrocarbons containing 5 to 20 carbons, preferably 6 to 12 carbons and 1 or 2 double bonds. Exemplary cycloalkenyl groups include cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl, cyclohexadienyl, and cycloheptadienyl, which may be optionally substituted as defined for cycloalkyl.
The term "polycycloalkyl" as employed herein alone or as part of another group refers to a bridged multicyclic group containing 5 to 20 carbons and containing 0 to 3 bridges, preferably 6 to 12 carbons and 1 or 2 bridges.
Exemplary polycycloalkyl groups include [3.3.0]-bicyclooctanyl, adamantanyl, [2.2.1]-bicycloheptanyl, [2.2.2]-bicyclooctanyl and the like and may be optionally substituted as defined for cycloalkyl.
The term "polycycloalkenyl" as employed herein alone or as part of another group refers to a bridged multicyclic group containing 5 to 20 carbons and containing 0 to 3 bridges and containing 1 or 2 double bonds, preferably 6 to 12 carbons and 1 or 2 bridges. Exemplary polycycloalkyl groups include [3.3.0]-bicyclooctenyl, [2.2.1]-bicycloheptenyl, [2.2.2]-bicyclooctenyl and the like and may be optionally substituted as defined for cycloalkyl.
The term "aryl" as employed herein alone or as part of another group refers to monocyclic and bicyclic aromatic groups containing 6 to 10 carbons in the ring portion (such as phenyl or naphthyl) and may optionally include one to three additional rings fused to Ar (such as aryl, cycloalkyl, heteroaryl or cycloheteroalkyl rings) and may be optionally substituted through available carbon atoms with 1, 2, or 3 groups selected from hydrogen, halo, haloalkyl, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyl, trifluoromethyl, trifluoromethoxy, alkynyl, cyclo-alkylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl, aryl, heteroaryl, arylalkyl, aryloxy, aryloxyalkyl, arylalkoxy, arylthio, arylazo, heteroarylalkyl, heteroarylalkenyl, heteroarylheteroaryl, heteroaryloxy, hydroxy, vitro, cyano, amino, substituted amino wherein the amino includes 1 or 2 substituents (which are alkyl, aryl or any of the other aryl compounds mentioned in the definitions), thiol, alkylthio, arylthio, heteroarylthio, arylthioalkyl, alkoxyarylthio, alkylcarbonyl, arylcarbonyl, alkyl-aminocarbonyl, arylaminocarbonyl, alkoxycarbonyl, aminocarbonyl, alkylcarbonyloxy, arylcarbonyloxy, alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfinylalkyl, arylsulfonylamino or arylsulfon-aminocarbonyl or any of the R3 groups, or the R1 substituents set out herein.
The term "aralkyl", "aryl-alkyl" or "aryllower alkyl" as used herein alone or as part of another group refers to alkyl groups as discussed above having an aryl substituent, such as benzyl or phenethyl, or naphthylpropyl, or an aryl as defined above. .
The term "lower alkoxy", "alkoxy", "aryloxy" or "aralkoxy" as employed herein alone or as part of another group includes any of the above alkyl, aralkyl or aryl groups linked to an oxygen atom.
The term "amino" as employed herein alone or as part of another group may optionally be substituted with one or two substituents such as alkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl and/or cycloalkyl.
The term "lower alkylthio", alkylthio", "arylthio"
or "aralkylthio" as employed herein alone or as part of 2S another group includes any of the above alkyl, aralkyl or aryl groups linked to a sulfur atom.
The term "lower alkylamino", "alkylamino", "arylamino", or "arylalkylamino" as employed herein alone or as part of another group includes any of the above alkyl, aryl or arylalkyl groups linked to a nitrogen atom.
The term "acyl" as employed herein by itself or part of another group, as defined herein, refers to an organic radical linked to a carbon 1 y group; examples of acyl groups include alkanoyl, alkenoyl, aroyl, aralkanoyl, heteroaroyl, cycloalkanoyl, and the like.
The term "alkanoyl" as used herein alone or as part of another group refers to alkyl linked to a carbonyl group.
Unless otherwise indicated, the term "lower alkenyl"
or "alkenyl" as used herein by itself or as part of another group refers to straight or branched chain radicals of 2 to 20 carbons, preferably 3 to 12 carbons, and more preferably 1 to 8 carbons in the normal chain, which include one to six double bonds in the normal chain, such as vinyl, 2-propenyl, 3-butenyl, 2-butenyl, 4-pentenyl, 3-pentenyl, 2-hexenyl, 3-hexenyl, 2-heptenyl, 3-heptenyl, 4-heptenyl, 3-octenyl, 3-nonenyl, 4-decenyl, 3-undecenyl, 4-dodecenyl, 4,8,12-tetradecatrienyl, and the like, and which may be optionally substituted with 1 to 4 substituents, namely, halogen, haloalkyl, alkyl, alkoxy, alkex~yl, alkynyl, aryl, arylalkyl, cycloalkyl, amino, hydroxy, heteroaryl, cycloheteroalkyl, alkanoylamino, alkylamido, arylcarbonylamino, vitro, cyano, thiol, alkylthio or any of the R3 groups, or the R1 substituents set out herein.
Unless otherwise indicated, the term "lower alkynyl"
or "alkynyl" as used herein by itself or as part of another group refers to straight or branched chain radicals of 2 to 20 carbons, preferably 2 to 12 carbons and more preferably 2 to 8 carbons in the normal chain, which include one triple bond in the normal chain, such as 2-propynyl, 3-butynyl, 2-butynyl, 4-pentynyl, 3-pentynyl, 2-hexynyl, 3-hexynyl, 2-heptynyl, 3-heptynyl, 4-heptynyl, 3-octynyl, 3-nonynyl, 4-decynyl,3-undecynyl, 4-dodecynyl and the like, and which may be optionally substituted with 1 to 4 substituents, namely, halogen, haloalkyl, alkyl, alkoxy, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, amino, heteroaryl, cycloheteroalkyl, hydroxy, alkanoylamino, alkylamido, arylcarbonylamino, vitro, cyano, thiol, and/or alkylthio, or any of the R3 groups, or the R1 substituents set out herein.
The term "alkylene" as employed herein alone or as part of another group refers to alkyl groups as defined above having single bonds for attachment to other groups at two different carbon atoms and may optionally be substituted as defined above for "alkyl".
The teams "alkenylene" and "alkynylene" as employed herein alone or as part of another group refer to alkenyl groups as defined above and alkynyl groups as defined above, respectively, having single bonds for attachment at two different carbon atoms.
Suitable alkylene, alkenylene or alkynylene groups or (CH2)m, (CH2)n or (CH2)p (which may include alkylene, alkenylene or alkynylene groups) as defined herein, may optionally include 1, 2, or 3 substituents which include any of the R3 groups, or the R1 substituents set out herein.
Examples of alkylene, alkenylene and alkynylene include -CH=~H-CHZ- ! -CgaCg~Cg- ! -C-C-CHZ- !
-- CH2 C- CHZ CHy CHZ C--.
O O
~3 '_ CgZC = CC82 - ~ - Ca Cg - CHZ , '-~~s)s- ! -(CHZ)s- ! -(CHz)a- !
~3 -- (C$2 ) 2- ~ - CHZCBa- ! - CHgCH- ! '- Cg2CgCgZ~ !
~3 C8Z- ! -_ ~ CH~C$Z- ! - CH ~ CHZ- !
~3 C2H5 l ~3 ~3 F
-Cg2-C_CHa- f -(C8a)~ ~ --(CH~)a-C-CHI- , ~3 Cl ~3 ~3 -c$a-~-Via- ~ -(~a)a- i'H- ~ -cHa-cH- i- s - csa - ca - cH - cHa , - cHa - ~H- cHa - ~ H- , ~3 ~3 CHg CHg OCHg - CH- CHaCHa- y- CH _ CHaCHa- ~ -~ CHaOCBa-- OCHaCHa- ~ ~ CHaN8C8a- ~ -- NBCHaCHa-ICH3 -' -- CHaC$a_.
(CHa)3-CFa- ~ -cga-N-cga-The term "halogen" or "halo" as used herein alone or as part of another group refers to chlorine, bromine, fluorine, and iodine as well as CF3, with chlorine or fluorine being preferred.
The term ~metal ion" refers to alkali metal ions such as sodium, potassium or lithium and alkaline earth metal ions such as magnesium and calcium, as well as zinc and aluminum.
The term "heterocyclyl" as used herein refers to "cycloheteroalkyl" groups and "heteroaryl" groups as def fined herein .
The term "cycloheteroalkyl" as used herein alone or as part of another group refers to a 5-, 6- or 7-membered saturated or partially unsaturated ring which includes 1 to 2 hetero atoms such as nitrogen, oxygen and/or sulfur, linked through a carbon atom or a heteroatom, where possible, optionally via the linker (CHZ)p (which is defined above), such as O\ N~O S' O
N~ O ~ N
' ' J ' O
N ~/ O
s and the like. The above groups may include 1 to 4 substituents such as alkyl, halo, oxo and/or any of of the R3 groups, or the R1 substituents set out herein. In addition, any of the above rings can be fused to a cycloalkyl, aryl, heteroaryl or cycloheteroalkyl ring.
The term "cycloheteroalkoxy" as used herein alone or as part of another group refers to a 4-, 5-, 6- or 7-membered saturated or partially saturated ring which includes at least one oxygen atom in the ring and at least 1 or 2 other hetero atoms in the ring such as nitrogen, oxygen and/or sulfur, linked through a carbon or heteroatom, where possible, optionally via the linker (CH2)p, such as o~ N s.~ o~N~.
, N O "'i~ O , V ' p N ~ N ~/
O/ ~ O~ ~ N V
and the like. The above groups may include 1 to 4 substituents such as alkyl, halo, oxo and/or any of of the R3 groups, or the R1 substituents set out herein. In addition, any of the above rings can be fused to a cycloalkyl, aryl, heteroaryl or cycloheteroalkyl ring.
The term "heteroaryl" as used herein alone or as part of another group refers to a 5- or 6- membered aromatic ring which includes 1, 2, 3 or 4 hetero atoms such as nitrogen, oxygen or sulfur,and such rings fused to an aryl, cycloalkyl, heteroaryl or cycloheteroalkyl ring (e. g.
benzothiophenyl, indolyl), and includes possible N-oxides, such as N~ S 0 ~ ~ / ~ ~ / s N~~ N
I
U
N
~N N N~ N
N~/O N~/S
~N,H N~N ~ N ~ ' i5 N._ N ~O
% ~ / ~ / ~ ~ ~ ~!~
<>>~ >>~> ~ ~ 'U
N ~ I
and the like.
Ar may be either aryl or heteroaryl as defined above.
f ~ f ~ f Het Het t and Het 2 ' are the same or different, as defined hereinbefore, and are attached to the central ring of the indenyl or fluorenyl type group at adjacent positions (that is, ortho or 1,2-positions). Examples of such groups include O
/ I '~ / I '~ , I '~ ~ '~ _ Nr~~ N~~ .~ ~ I
O
O i I , I ~ I '~ I
/I
I ' y ~.r' .r~' ft' "
p' ~ '~ .r'~ ' N~ ~~ 1 / a ~ O
N' s~
N 't, a N ~ ~ N, / ~/
N
/i'~ ~ /w~,~
N ' I u,~
wherein a is selected from O, S, and NR7a;
R7a is H, lower alkyl, aryl, -C (O) R7b, -C (O) OR7b%
R7b is alkyl or aryl.
5 The heteroazyl groups including the above groups may optionally include 1 to 4 substituents such as any of the R3 groups, or the R1 substituents set out herein. In addition, any of the above rings can be fused to a cycloalkyl, aryl, heteroaryl or cycloheteroalkyl ring.
The term cycloheteroalkylalkyl" as used herein alone or as part of another group refers to cycloheteroalkyl groups as defined above linked through a C atom or heteroatom to a (CH2)p chain.
The term "heteroarylalkyl" or "heteroaryl-alkenyl"
as used herein alone or as part of another group refers to a heteroaryl group as defined above linked through a C atom or heteroatom to a -(CH2)p- chain, alkylene or alkenylene as defined above.
The term "polyhaloalkyl" as used herein refers to an "alkyl" group as defined above which includes from 2 to 9, preferably from 2 to 5, halo substituents, such as F or C1, preferably F, such as CF3CH2, CF3 or CF3CF2CH2.
Preferred are compounds of formula I wherein A is NH, B is Ra Rs X
X is a bond, oxygen or sulfur; R3 and R4 are independently H or F.
Preferred R2 groups are alkyl, polyfluoroalkyl (such as 1,1,1-trifluoroethyl), alkenyl, aryl, heteroaryl or heteroarylalkyl, such as 2-pyridylmethyl (preferably substituted with one of the preferred R2 substituents above).
It is preferred that Ll contains 2 to 7 atoms in the linear chain and L2 is a bond or lower alkylene.
The preferred L2 group is alkylene such as CH2 or a bond.
The preferred A group is -NH-.
Preferred R1 groups are as set out in the preferred compounds shown in the following Table.
More preferred are compounds of the invention which have the following structures wherein R1C0, n and the geometry are as indicated below.
COHHCHzCFs O
\ ~CH2)n P~~ -O
/ ~ ~ '~ NHCOR~
Preferred Structures of Cyclic Phosphonates R1 CO = n geometry R' CO = n geometry CsH
I / ~ traps H CO ~ traps / CO
\I
\ /
( / 1 cis / CO ~ traps / ~o \
\
~ N 1 traps / I CO 1 traps / CO
\I
I\
C
/ 2 traps ~ 1 traps / co / co \I \I
I \ -1 traps 2 cis ~ N
/ CO / CO
\ I \ I
O
/ OC- 1 traps \I
The compounds of formula I may be prepared by the exemplary processes described in the following reaction schemes. Exemplary reagents and procedures for these reactions appear hereinafter and in the working Examples.
Methods for preparing starting materials useful in preparing cyclophosphonates in accordance with the present invention, are shown in the folowing reaction schemes.
Scheme 1.
Acylatioa Ra OH (carbodiimide coupliaQ) Ra O8 RICOaH, R1N=C=NRZ, BOBt lA. NS NCORl Rb R5a Rb R5a OB OH
Ra O8 ACylBtion Ra OCOR1 Ra OH
3 R1COC1, 3 EtgN 1 Solvolysis 18. pg NCOR Me08, NaH NCORl b R5a R5a ~ R5a R OH Rb OCORl Rb OH
Ra OH Silylation Ra OSi(CH3)3 1. Acylatioa Ra OH
I(~g)gSiIZNH (R1COC1, Et3N) 1C. pg ~5a ~S8 ~ 2. Msthaaolysis) NCOR
Rb R Rb R5a (M~OH, HCl) R5a OH OSi(C8g)g Rb O$
As seen in Scheme lA, serinol derivative (~) can be acylated via carbodiimide coupling directly to 3_.
Alternatively, as seen in Scheme 1B, ~ can be acylated with acid chlorides to tri-acylated ,~,. Subsequent solvolysis provides diols 3_. As seen in Scheme 1C, the diols 3_ could also be prepared from bis-O-trimethylsilylated amine ~, acylation with acid chlorides and subsequent methanolysis to provide ~.
It will be appreciated that in the reactions to follow, unless otherwise indicated, the moiety "B° in the starting materials, intermediates and final products is set out as I / x I /
for purposes of illustration only.
It will be appreciated that the "B" moiety in the starting materials, intermediates and final products in all reactions set forth herein, unless indicated to the contrary, may be any of the fluorenyl-type groups l w Ra. ./. ~ Ra, Ra. Re, R3 ~' ~ ( = R° ~ R3 Het ~ /~ R4 Or X~ X
R3.
R4.
Het 1 Het X as well as any of indenyl-type groups R3.
R3 3.
or ~~~ R' S R3b ~ ~ or a (CH~
R SC ~~ _.
(a - 2,3 or 4) Rsa R3.
R3 R3.
Het Het ~ f .
I or R3b ~ R3b Rsa (CH~a R3a The above B moieties (including all fluorenyl-type groups and all indenyl-type groups) are collectively referred to as "fluorenyl-type" moieties. The use of the first fluorenyl-type group (as set out in the previous paragraph) in the Reaction Schemes is for purposes of illustration only; any of the 3 fluorenyl groups or 4 indenyl groups as set out above may be employed in any of the Reaction Schemes set out herein in place of \
I / X I / .
The compounds of formula I of the invention may be prepared as shown in Reaction Scheme 2.
Schenne 2 1. TMSBr 2. C1COCOC1 \ ~ \ Ra O8 / / O
O ILl-.._ p~0alkyl 3' NCORl, amiae base R5a A Oalkyl Rb OH
LsRz \ ~\ ~\ ~\
+ /
/ / O Ra O L1 II Ra O L1 ~~ O A O O
b 1 LZR2 Rb NCORi LZRZ R 8 RS° R
H R5a 7-Cis Io 7-trees Ip As seen in Scheme 2, dialkyl phosphonate ester Im is treated with bromotrimethylsilane and then is treated with oxalyl chloride and dimethylformamide (employing conventional procedures) to give a diphosphinyl dichloride intermediate which (without purification) is reacted with diol ~, (which may be chiral or achiral) (as formed in Scheme lA, 1B or 1C) and an amine base such as triethylamine to give a mixture of the 7-traps and 7-cis isomers (Io and Ip, respectively) of the invention. The 7-trans and 7-cis isomers may be separated by conventional chromatographic techniques.
Scheme 3 Preparation of Other Acyl Derivatives From 7-trans Compounds ~ i ~ _i o II Ra O~L~ p~ O
LZR2 Rb NCORl.
H R5s (where R1' is as I°~ arylmsthyloxy or (7-traas) heteroarylmathyloxy) Hydrogeaolysis 1. 8a, Pd-C/EtOH
2. RICOaH, R1N=C=NRZ, HOBt Io' Io ~ O
II Ra O Ll- P~
O
Z Rb NCORl g RSa Io 7-traa8 As seen in Scheme 3, the 7-traps isomer Io' (R1'=OCH2C6H5) (and the corresponding 7-cis isomer) may be made to undergo hydrogenolysis to form an amine intermediate which can be reacted with R1COZH to prepare other aryl derivatives in accordance with the invention.
The starting material Im may be prepared according to the following Reaction Schemes 4 and 4A.
Reaction Scheme 4 X
X , 1 ) base 2) Hal-L~-Y
O L~-Y
O Y=Hal A or O-PG ~ Ih (Y=Hal) L2R2 XIVa (Y=OPG) Y=OPG
\ X ~ \ Deprotection F- (for example, i i n-Bu4NF) O \Li-OH
A
L2R2 =g Halide Formation X
~ , \L~-Hal A
L2R2 Ih where PG is as oxygea protoctiag group, such as t-Bu(C83)ZSi or t8u(Ph)gSi-X
Arbuzov I ~ I ~ ~ Oalkyl Reaction O
Ih ~ L1~ Oalkyl Excess (AlkylO)2P(OG1~) im -20°C to 180°C L2R2 (Q~ is alkyl, triorganosiiyl (such as trimethylsilyl or t-butyldimethyisilyl), H, the latter in the presence of base such as butyilithium, sodium hydride, or sodium bis-(trimethylsilylamide) Reaction Scheme 4A
(A~ternative Mgthod fQr Makina Ih) 1 ) base /
2) Ha1-L~-Y ~
~r o _Lm x 3)C1COCOCU DMF N-R5 0 08 4) (R21-2)RSNH izRs II Ih Protected alcohol XIVa can be converted into a wide variety of functional groups through the intermediary of a halide Ih. For example, the alcohol Ig can be converted to the halide Ih of the invention by either activation through the sulfonate ester (tosyl chloride, or mesyl chloride) and iodide displacement (NaI or KI in acetone or 2-butanone), or by reaction with triphenylphosphine, I2 and imidazole.
The halide Ih can undergo an Arbuzov reaction to form phosphonates, phosphinates and phosphine oxides of the invention Im. The Arbuzov reaction can be accomplished with phosphites, phosphinites, and phosphonites (for example, (alkyl0)3P or (alkyl0)2POSi(alkyl)3 or (alkyl0)2POH, the latter being in the presence of a base such as butyllithium, sodium hydride or sodium bis(trimethylsilylamide)) at temperatures within the range from about -20°C to about 180°C.
The starting material VIIIA for compound Im may be prepared as shown in Reaction Scheme 5.
Reaction Scheme 5 (Amides) Preparation of Compounds of Formula I where A is - N
O
COOH R L ~ ~ C
1) amide formation R5 e.g. 1) acid chloride formation ~ , ~ , 2) (R2L2)RSNH ~X' v vi=~
A= -N-~5 R
As seen in Scheme 5, the amide VIIIA may be formed by treating II with thionyl chloride or oxalyl chloride in an inert organic solvent such as dichloromethane (optionally in the presence of dimethylformamide (DID')) to form the acid chloride IIA
o CI- C
x xxar Acid chloride IIA, without separation from the reaction mixture, is treated with amine (R2L2)R5NH at a reduced temperature within the range from about -40°C to about room temperature, to form the amide VIIIA.
Amide VIIIA may be converted to compounds of formula I employing the procedure set out in Reaction Scheme 4/4A.
In carrying out the above reaction to form amide VIIIA, the amine will be employed in a molar ratio to acid chloride IIA within the range from about 4:1, to about 1:1, optionally in the presence of a tertiary amine base or other acid scavenger.
Alternative formation of amide VIIIA from acid II
and (R2L2)R5NH can be carried out via standard literature procedures.
Ruction Scheme 6 !Class Esters) Preparation of Esters VIIIA (A - -0-) O
H02 H 1) Acid, R2L20H or RZL~-O-C H
2) (COCI)2, R2L20H
3) DCC, HOST, DMAP, R2L20H
esterification As seen in Reaction Scheme 6, ester compounds of formula VIIIB wherein A = oxygen can be prepared by an acid catalyzed esterification of acid II employing an acid such as H2S04 or p-toluene-sulfonic acid in the presence of an alcohol such as ally! alcohol, ethanol or methanol.
Alternatively, activation of the acid II to the acid chloride (with oxaly chloride or thionyl chloride) followed by treatment with an alcohol optionally in the presence of a tertiary amine base or other acid scavenger, gives compounds of formula VIIIB.
Various additional methods of activation include mixed anhydride formation ((CF3C00)2 or i-BuOCOCl) or formation of the acylimidazole (carbonyldiimidazole) or with DCC and HOBT in the presence of DMAP (4-dimethyl-aminopyridine). These activated intermediates readily form esters upon treatment with alcohols.
Ruction Scheme 7 (Amides from Isoc3ranates ) Preparation of Amides VIIIC (A is NH) O
RzL2HN ~~
\ \
1) base / X I / 2) R2L2NC0 [ / I
X
iy v===c Compounds of formula VIIIC
where A is -NH- (amides) can be prepared by the methods shown in Reaction Scheme 7 from known compound IV.
Treatment of compound IV with base, such as n-BuLi, followed by reacting the anion with an isocyanate gives compound VIIIC.
Scheme 8 Alt~~at~ Scheme for ~om~ound Im2 \ X I \ ~ \ X ~ \
/ / Deesterification ~O OAlkyl O OTMS
t u/ > O 1 u/
O-~L -P TMSBr or TMSI L '-p A \OAlkyl (Optional tertiary ~A \OTMS
R2L2 amine base) R2L2 Im Disilyl Ester Intermediate Phosphonate Ester Formation (COCI)2, DMF, CH2CI2 to or ip Compounds Im may be modified by the various transformations set out in Reaction Scheme 8.
The compounds of the invention may be employed in preventing, stabilizing or causing regression of atherosclerosis in a man~nalian species by administering a therapeutically effective amount of a compound to decrease the activity of MTP.
WO 99/21564 PCT/US9$/21750 The compounds of the invention can be tested for MTP
inhibitory activity employing the procedures set out in _ U.S. application Serial No. 117,362 filed September 3, 1993, employing MTP isolated from one of the following sources:
(1) bovine liver microsomes, (2) HepG2 cells (human hepatoma cells) or (3) recombinant human MTP expressed in baculovirus.
The compounds of the invention may also be employed in lowering serum lipid levels, such as cholesterol or triglyceride (TG) levels, in a mammalian species, by administering a therapeutically effective amount of a compound to decrease the activity of MTP.
The compounds of the invention may be employed in the treatment of various other conditions or diseases using agents which decrease activity of MTP. For example, compounds of the invention decrease the amount or activity of MTP and therefore decrease serum cholesterol and TG
levels, and TG, fatty acid and cholesterol absorption and thus are useful in treating hypercholesterolemia, hypertriglyceridemia, hyperlipemia, hyperlipoproteinemia, hyperlipidemia, pancreatitis, hyperglycemia, atherosclerosis, non-insulin dependent diabetes (Type II
diabetes) and obesity.
The compounds of the present invention are agents that decrease the activity of MTP and can be administered to various mammalian species, such as monkeys, dogs, cats, rats, humans, e~., in need of such treatment. These agents can be administered systemically, such as orally or parenterally.
The agents that decrease the activity or amount of MTP can be incorporated in a conventional systemic dosage form, such as a tablet, capsule, elixir or injectable formulation. The above dosage forms will also include the necessary physiologically acceptable carrier material, excipient, lubricant, buffer, antibacterial, bulking agent (such as mannitol), anti-oxidants (ascorbic acid or sodium bisulfate) or the like. Oral dosage forms are preferred, although parenteral forms are quite satisfactory as well.
The dose administered must be carefully adjusted according to the age, weight, and condition of the patient, as well as the route of administration, dosage form and regimen, and the desired result. In general, the dosage forms described above may be administered in amounts of from about 5 to about 500 mg per day in single or divided doses of one to four times daily.
The following Examples represent preferred embodiments of the invention. All temperatures are in °C
unless indicated otherwise.
NOTE: The phrase "flash chromatography" refers to chromatography performed on EM Industries Silica Gel 60 (catalog #9385-9), 230-400 mesh under 10-20 psi of nitrogen pressure.
~ple 1 (E)-9-[4-[2-Oxo-5-([[4'-(trifluoromethyl)[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide, N-oxide.
N~ CF3 CF3 ~~O C /
I\
traps isomer Example 2 (Z)-9-[4-[2-Oxo-5-[[[4'-(trifluoromethyl)[1,1'-biphenylJ-2-yl]carbonylJaminoJ-1,3,2-dioxaphosphorinan-2-ylJbutylJ-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide, N-oxide.
O
/ N/~ CF3 CF3 H I\
\ _ w--.~ o /
O'P~O
\/ O ~ _. . \
A.
cis isomer OH OH
H \I
O /
\I
To a stirred solution of 1.33 g (5.00 mmol) of 4'-trifluorophenyl-2-benzoic acid (Aldrich Chemical Co.), 0.455 g (5.00 mmol) of serinol (Aldrich Chemical Co.), 0.750 g (5.0 mmol) of HOBt and 0.5 mL (3.6 mmol) of triethylamine in 10 mL of dichloromethane at room temperature under argon, was added 1.0 g (5.25 mmol) of EDCI, portionwise, over 3 min. After 16 h, the reaction mixture was diluted with ethyl acetate, washed once with saturated sodium bicarbonate solution, once with brine and once with 10~ citric acid solution, dried (MgS04) and evaporated. Purification by flash chromatography on silica gel (5 x 15 cm column, ethyl acetate) provided title compound as a white solid, mp 146-148°C, 1.23 g, 72~ yield.
B.
CONHCHzCFa P03Et2 B(1) .
O
-OH
Br To a solution of 9-fluorenecarboxylic acid (Aldrich) (50 g, 240 mmol) in THF (1200 mL) at 0°C was added dropwise a solution of n-butyllithium (2.5M, 221 mL, 530 mmol) in THF. The yellow reaction was stirred at O~C for 1 h, then 1,4-dibromobutane (31.3 mL, 260 mmol) was added dropwise over 30 min. The reaction was stirred at O~C for 30 min, then the reaction was warmed to RT fox 30 h. The reaction was extracted with water (3 x 750 mL). The combined aqueous layers were extracted with ethyl ether (800 mL).
The aqueous layer was made acidic with HC1 solution (1N, 500 mL), then extracted with dichloromethane (3 x 750 mL).
The combined organic layers were dried over MgSO~.
Evaporation gave title compound (71 g, 85~) as a white solid.
B(2) .
Hn CF3 Br To a solution of Part B(1) acid (60 g, 173 mmol) and DMF (100 11.L) in CH2C12 (600 mL) under argon at 0'C was added oxalyl chloride (104 mL, 2. OM in CH2C12, 208 nunol) dropwise. The reaction was stirred at 0'C for 10 min, then-warmed to RT and stirred for 1.5 h. The reaction was concentrated in vacuo to give the crude acid chloride as a yellow oil. To a suspension of 2,2,2-trifluoroethylamine hydrochloride (25.9 g, 191 mmol) in CH2C12 (500 mL) at O~C
under argon was added triethylamine (73 mL, 521 mmol) followed by dropwise addition of a solution of the crude acid chloride in CH2C12 (15 mL). The reaction was stirred at 0'C for 1 h, diluted with CH2C12 (500 mL), and washed with water (2 x 300 mL), 1N HC1 (2 x 300 mL), saturated NaHC03 (2 x 300 mL), and brine (2 x 300 mL), then dried over MgS04. Evaporation gave 80 g of a oil which was purified by flash chromatography on silica gel (2.5 kg).
The crude product was loaded in a mixture of CH2C12 and hexane, and eluted with a step gradient of 10~ EtOAc/hexane (4L) to 15~ EtOAc/hexane (2L) to 20~ EtOAc/hexane (4L).
Pure fractions were combined and evaporated to give title compound (52.5 g, 71~) as a white solid (mp 88-92'C).
B(3) .
cOtyHGH2Cfa P09Et2 A solution of 2.13 g (5.00 mmol) of Part B(2) compound in 3.5 mL of triethylphosphite under argon was heated to 110°C for 16 h and then to 180°C for 4 h. The reaction was cooled and then the volatiles were distilled off at 100°C at 1 Torr. The residue was purified by flash chromatography (5x15 cm column, EtOAc) to give title compound (1.92 g, 79~) as a waxy yellow solid (mp 87-89°C).
mp : 87-89°C
MS (FAB) m/e 484 (M+H).
Anal. Cald'd for C24H2gN04PF3+0.13 mol H20:
C, 59.33; H, 6.07; N, 2.88; P, 6.37; F, 11.73 _ Found: C, 59.09; H, 5.98; N, 2.95; P, 6.51; F, 11.92.
C. (E)-9-[4-[2-Oxo-5-[([4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide, N-oxide (Exam~~le 1 ) D. (Z)-9-[4-[2-Oxo-5-[((4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide, N-oxide (Example 2) To a stirred solution of 500 mg (1.03 mmol) of Part B compound in 10 mL of dichloromethane at room temperature under argon was added 0.45 mL (3.4 mmol) of bromotrimethylsilane. After 1 h, the reaction mixture was evaporated to provide a thick oil. The oil was dissolved in 5 mL of dichloromethane at room temperature under argon and treated with 0.26 mL (3.0 mmol) of oxalyl chloride and 100 N,L of DMF. After 2 h, the reaction mixture was evaporated and redissolved in 10 mL of dichloromethane. To this solution at room temperature under argon, was added 340 mg (1.0 mmol) of Part A compound and 0.5 mL (3.6 mmol) of triethylamine. After 14 h, the reaction was diluted with ethyl acetate and washed once with 10~ citric acid solution, dried (MgSO,) and evaporated. Purification by flash chromatography on silica gel (5 x 15 cm column, 1 L
85:15 ethyl acetate/hexanes, then ethyl acetate) provided two fractions.
The less polar fraction was designated Part C
(Example 1) compound, white solid, mp 105-107°C, 205 mg, 27~ yield.
MICROANALYSIS Calculated for C37 H33 FsN20sP + 0.55 H20:
C, 60.01; H, 4.64; N, 3.78; F, 15.39; P, 4.18 _ Found: C, 60.00; H, 4.48; N, 3.64; F, 15.10; P, 3.75.
MS (electrospray, + ions) m/e 731.
The more polar fraction was designated Part D
(Example 2) compound, white solid, mp 102-104°C, 130 mg, 17~.
1H NMR, i3C NMR, IR and mass spectrometry were consistent for the indicated compound.
IO
MICROANALYSIS Calculated for C37 Hs3 F6N205P + 064 H20:
C, 59.88; H, 4.66; N, 3.77; F, 15.36; P, 4.17 Found: C, 59.88; H, 4.44; N, 3.75; F, 15.08; P, 4.14.
MS (electrospray, + ions) m/e 731.
Examble 3 traps-9-[4-[5-(Benzoytamino)-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide.
O
H
O
/ Oy,, '~- N
HH /
traps isomer A. N-(1,3-Dibenzoxyloxy-2-propyl)benzamide OCOCsHS
H
O OCOCsNs To a stirred slurry of 1.82 g (20.0 mmol) of serinol and 9.2 mL (66 mmol} of triethylamine in 20 mL of dichloromethane at -5°C under argon, was added dropwise, 7.0 mL (61 mmol) of benzoyl chloride (Aldrich) over 30 min.
After 2 h, the reaction was diluted with ethyl acetate and washed three times with 1 ~ hydrochloric acid, once with brine, twice with saturated sodium bicarbonate solution, dried (MgSO,) and evaporated. The resulting white solid was recrystallized from ethyl acetate/hexane to provide title compound, mp 96-98°C, 5.62 g, 70~ yield.
B. N-(1,3-Dihy~lroxv-2-propyl)benza~ide OH
H
O OH
To a stirred solution of 160 mg (4.0 mmol) of 60~
sodium hydride in 50 mL of methanol at room temperature under argon, was added 4.03 g (10.0 mmol) of Part A
compound. The slurry was heated to reflux where a clear solution forms. After 3 h, the reaction was cooled and 1.5 mL of 4 I~ hydrogen chloride in dioxane was added.
Evaporation and re-evaporation from methanol onto silica gel (5 g) and purification by flash chromatography on silica gel (5 x 15 cm column, 3:47 methanol/ethyl acetate) gave title compound as white solid, 1.22 g, 62~ yield.
C. trans-9-[4-[5-(Benzoylamino)-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamid.e To a stirred solution of 699 mg (1.45 mmol) of Example 1 Part B compound in 5 mL of dichloromethane at room temperature under argon was added 0.63 mL (4.8 mmol) of bromotrimethylsilane. After 1 h, the reaction mixture was evaporated to provide a thick oil. The oil was dissolved in 3 mL of dichloromethane at room temperature under argon and treated with 0.26 mL (3.0 mmol) of oxalyl chloride and 50 N,L of DMF. After 2 h, the reaction mixture was evaporated and redissolved in 3 mL of dichloromethane.
To this solution at room temperature under argon, was added 283 mg (1.45 mmol) of Example 3 Part B compound and 0.6 mL_ (4.3 mmol) of triethylamine. After 2 h, the reaction was diluted with ethyl acetate and washed once with 10~ citric acid solution, dried (MgSOq) and evaporated. Purification by flash chromatography on silica gel (5 x 15 cm column, ethyl acetate) provided title compound, white solid, mp 166-168°C, 245 mg, 29~ yield.
MICROANALYSIS Calculated for C3oH3oF3N205P + 0.5 H20:
C, 60.50; H, 5.25; N, 4.70; F, 9.57 Found: C, 60.47; H, 5.01; N, 4.62; F, 9.30.
MS (electrospray, + ions) m/e 587.
~ lie 4 traps-9-[5-[2-Oxo-5-[[[4'-(trifluoromethyl)[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide.
_ O CF3 / N/~ CF3 H I \
\ V~ ~,~0 O /
/ O~N I \
traps isomer ~ In a 5 cis-9-[5-[2-Oxo-5-{[[4'-(trifluoromethyl)[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide.
O
/ N/~ CF3 CF3 I\
\ /
O ~' O O
/ O~ \
N I
cis isomer A. 2-Amino-1,3-bis(trimethylsilyloxy)propane ost(cH3b _ ~ NH2 OSi(CH3b A stirred solution of 1.84 g (20.0 mmol) of serinol in 4.25 mL (20.1 mmol) of hexamethyldisilazane containing 1 drop of bromotrimethylsilane was heated to 180°C under argon. After 16 h, the reaction mixture was partially cooled and distilled at 0.6 Torr, collecting the fraction with by 44-47°C to give title compound as a colorless liquid, 4.05 g, 86~.
B. N-[(1,3-Dihydroxy)-2-propyl]-2-(4-tri-fluoromethylphenyl)benzamide OH OH
H
O /
CFa A solution of 4'-trifluoromethyl-2-biphenylcarbonyl chloride [prepared from 4.40 g (16.5 mmol) of the corresponding carboxylic acid] in 10 mL of THF was added dropwise to a solution of 3.88 g (16.5 mmol) of Part A
compound and 2.40 mL (17.2 mmol) of triethylamine in 20 mL
of THF at 0°C over 10 min. The resulting slurry was stirred for 1 h, diluted with ether, filtered and the filtrate evaporated. The residual oil was dissolved in 50 mL of methanol and treated with 0.5 mL of 4 N_t hydrogen chloride in dioxane. After stirring at room temperature for 1 h, the reaction mass was evaporated and the white solid recrystallized from ethyl acetate/hexane to give title compound, mp 146-148°C, 5.08 g, 91~k yield.
C.
CONHCHzCF3 _ w _ ~ ~ ~ P03Eiz C(1) .
O
OH
Br To a solution of 9-fluorenecarboxylic acid (Aldrich) (10 g, 48 mmol) in THF (250 mL) at 0°C was added dropwise a solution of n-butyllithium (2.5M, 42.2 mL, 106 mmol) in THF. The yellow reaction was stirred at 0°C for 1 h, then 1,5-dibromobutane (16.8 mL, 124 mmol) was added dropwise over 30 min. The reaction was stirred at 0°C for 30 min, then the reaction was warmed to RT for 30 h. The reaction was extracted with water (3 x 150 mL). The combined aqueous layers were extracted with ethyl ether (160 mL). The aqueous layer was made acidic with HC1 solution (1N, 100 mL), then extracted with dichloromethane (3 x 150 mL). The combined organic layers were dried over MgS04. Evaporation gave title compound as a white solid.
C(2) .
Br To a solution of all of Part C(1) acid and DMF (20 u.L) in CHZC12 (120 mL) under argon at 0'C was added oxalyl chloride (24 mL, 2.0 M in CH2C12, 48 mmol) dropwise. The reaction was stirred at 0'C for 10 min, then warmed to RT
and stirred for 1.5 h. The reaction was concentrated in vacuo to give the crude acid chloride as a yellow oil. To a suspension of 2,2,2-trifluoroethylamine hydrochloride (6.51 g, 48 mmol) in CHZC12 (125 mL) at 0°C under argon was added triethylamine (16 mL, 115 mmol) followed by dropwise addition of a solution of the crude acid chloride in CH2C12 (15 mL). The reaction was stirred at 0'C for 1 h, diluted with CH2C12 (120 mL), and washed with water (2 x 100 mL), 1N HC1 (2 x 100 mL), saturated NaHC03 (2 x 100 mL), and brine (2 x 100 mL), then dried over MgS04. Evaporation gave 17.6 g of an oil which was purified by flash chromatography on silica gel (500 g). The crude product was loaded in a mixture of CHZC12 and hexane, and eluted with a step gradient of 10~ EtOAc/hexane (4L) to 15~
EtOAc/hexane (2L) to 20~ EtOAc/hexane (4L). Pure fractions were combined and evaporated to give title compound (14.7 g, 72~) as a white solid ( m.p. 92-96°C).
C(3) .
Ht~--~ O ~-CHa O ~~ ~CH3 O
A solution of 2.69 g (6.11 mmol) of Part C(2) compound in 15 mL of freshly distilled triethylphos-phite under argon was heated to 180°C for 16 h. The reaction was cooled and then the volatiles were distilled off at 100°C
at 1 Torr. The residue was triturated in ether to give title compound (2.25 g, 74~) as a white solid (mp 141-143°C) .
D. traps-9-[5-[2-Oxo-5-[[[4'-(trifluoro-methyl)[l,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide SExamDle 4) E. cis-9-(5-[2-Oxo-5-([[4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide ~ .xa le 5 ) To a stirred solution of 1.68 g (3.42 mmol) of Part C compound in 10 mL of dichloromethane at room temperature under argon was added 1.35 mL (10.0 mmol) of bromotrimethylsilane. After 14 h, the reaction mixture was evaporated to provide a thick oil. The oil was dissolved in 10 mL of dichloromethane at room temperature under argon and treated with 0.91 mL (10.5 mmol) of oxalyl chloride and 50 ~1.L of DMF. After 2 h, the reaction mixture was evaporated and redissolved in 10 mL of dichloromethane. To this solution at room temperature under argon, was added 1.09 g (3.2 mmol) of Part B compound and 1.0 mL (7.0 mmol) of triethylamine. After 1 h, the reaction was diluted with ethyl acetate and washed once with 10~ citric acid solution, dried (MgSO,) and evaporated. Purification by flash chromatography on silica gel (5 x 20 cm column, 2 L
85:15 ethyl acetate/hexanes, then 2 L 3:97 methanol/ethyl acetate) provided two fractions.
The less polar fraction was designated Part D (Example 4) compound, white solid, mp 165-167°C, 805 mg, 34~ yield.
MICROANALYSIS Calculated for C38H35F6N205P + 0.38 H20:
C, 60.73; H, 4.80; N, 3.73; F, 15.17; P, 4.12 Found: C, 60.73; H, 4.70; N, 3.60; F, 15.33; P, 3.88.
MS (electrospray, + ions) m/e 745.
The more polar fraction was designated Part E
(Example 5), compound, white foam, mp 110-114°C, 650 mg, 27~.
MICROANALYSIS Calculated for C3gH35F6N205P + 0.38 H20:
C, 60.73; H, 4.80; N, 3.73; P, 4.12 Found: C, 60.74; H, 4.78; N, 3.55; P, 3.84.
MS (electrospray, + ions) m/e 745.
~xa~le 6 trans-[2-Oxo-2-[4-[9-[[(2,2,2-trifluoroethyl)amino]carbonyl]-9H-fluoren-9-yl]butyl]-1,3,2-dioxaphosphorinan-5-yl]carbamic acid, phenylmethyl ester.
O
N/.. CF3 H
i o N
HH /
traps isomer A. N-Benzyloxycarbonyl-1,3-dihydroxy-2-aminopropane OH
H
O~ OH
O
To a stirred slurry of 1.00 g (4.24 mmol) of Example 5 Part A compound and 0.65 mL (4.7 mmol) of triethylamine in 10 mL of THF at 0°C under argon, was added dropwise, 0.6 mL (4.2 mmol) of benzyloxy carbonyl chloride (Aldrich) over 10 min. The reaction was allowed to warm to room temperature and stirred for 14 h. The reaction mixture was diluted with ether and filtered. The filtrate was evaporated, the residue dissolved in 25 mL of methanol to which 2 drops of 4 ~ hydrogen chloride in dioxane was added and the solution heated to 40°C for 30 min. Evaporation and trituration with hexane/ether gave title compound as a white solid, mp 104-106°C, 880 mg, 92~ yield.
MS (electrospray, + ions) m/z 226.
B. traps-[2-Oxo-2-[4-[9-[[(2,2,2-trifluoro-ethyl)amino]carbonyl]-9H-fluoren-9-yl]butyl]-1,3,2-dioxaphosphorinan-5-yl]carbamic acid, phenvlmethyl ester To a stirred solution of 1.76 g (3.64 mmol) of Example 1 Part B compound in 5 mL of dichloromethane at room temperature under argon was added 1.65 mL (12.6 mmol) of bromotrimethylsilane. After 1 h, the reaction mixture was evaporated to provide a thick oil. The oil was dissolved in 20 mL of dichloromethane at room temperature under argon and treated with 1.2 mL (13.8 mmol) of oxalyl chloride and 100 ~t.L of DMF. After 2 h, the reaction mixture was evaporated and redissolved in 5 mL of dichloro-methane. To this solution at room temperature under argon, was added 820 mg (3.64 mmol) of Part A compound and 1.1 mL
(7.9 mmol) of triethylamine. After 2 h, the reaction was diluted with ethyl acetate and washed once with 10~ citric acid solution, dried (MgSO,) and evaporated. Purification by flash chromatography on silica gel (5 x 25 cm column, 85:15 ethyl acetate/hexane) provided title compound, white solid, mp 160-163°C, 535 mg, 23~ yield.
MS (electrospray, + ions) m/e 617.
~~'~.1 1~
traps-1-(Phenylmethyl)-N-[2-[4-[9-[[(2,2,2-trifluoroethyl)amino)carbonylJ-9H-fluoren-9-yl]butyl]-1,3,2-dioxaphosphorinan-5-yl]-2-piperidinecarboxamide, -hydrochloride.
O
/ ~ CFa /
H ~O O \
V-- ~.
/ O I H
H
traps isomer A. N-Benzylpipecolic acid hydrochloride ~HCI
A mixture of ethyl pipecolinate hydrochloride (10 g, 52 mmol), benzylbromide (7 mL, 57 mmol) and potassium carbonate (15 g, 114 mmol) in DNIF' (80 mL) was stirred at room temperature overnight. The solvent was removed in v cuo. The residue was partitioned between dichloromethane (100 mL) and water (50 mL). The aqueous layer was extracted with dichloromethane (2 x 100 mL), dried over Na2S04, then evaporated to give a yellow oil. The crude product was chromatographed (500 g silica gel) eluting with a stepgradient of 8~-15~ ethyl acetate in hexane. Pure fractions were combined to give title compound (12.3 g, 96~) as a colorless oil.
B. traps-1-(Phenylmethyl)-N-[2-[4-[9-[[(2,2,2-trifluoroethyl)amino]carbonyl]-9H-fluoren-9-yl]butyl]-1,3,2-dioxaphosphorinan-5-vll-2-uineridinecarboxamide. hvdrochloride An argon-purged slurry of 51.1 mg (0.829 mmol) of Example 6 compound and 100 mg of 10~ palladium-on-charcoal in 5 mL of ethanol at room temperature was partially evacuated and subjected to hydrogenation from a filled balloon. After 16 h, the reaction mixture was purged with argon and filtered through a 0.45 ~ nylon filter.
Evaporation and then re-evaporation from dichloromethane -gave a white foam. This material was dissolved in 10 mL of dichloromethane and stirred under argon at room temperature while 212 mg (0.83 mmol, HC1 salt) of Part A compound, 125 mg (0.83 mmol) of HOBt, 175 mg (0.92 mmol) of EDCI and 175 ~tL (1.26 mmol) of triethylamine were added. After 6 h, the reaction mixture was quenched with saturated sodium bicarbonate solution and extracted twice with ethyl acetate. The organic extracts were combined, dried (MgS04) and evaporated. Purification by flash chromatography on silica gel (5 x 20 cm column, ethyl acetate) provided the free base of title compound. This material was dissolved in dichloromethane, treated with 0.3 mL of 4 ~! hydrogen chloride in dioxane and evaporated to provide title compound as a white solid, mp 125-128°C, 365 mg, 61~ yield.
MICROANALYSIS Calculated for C36HaiF3NsOsP+HCl+1 dioxane+0.33 H20:
C, 59.01; H, 6.27; N, 5.16; C1, 4.35; F, 7.00 Found: C, 59.00; H, 6.25; N, 5.11; C1, 4.14; F, 6.96.
MS (electrospray, + ions) m/e 684.
E~c~mple 8 traps-9-[4-[2-Oxo-5-[[2-(2-pyridinyl)benzoyl]amino]-7 ,3,2-dioxaphosphorinan 2-yi]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide, hydrochloride.
O
i\
\ ~'~--\ ~~~° o / ~ N \
H
traps isomer WO 99/21564 PC"1'/US98/21750 A. 2-(2-Pyridyl)benzoic acid O ~N
HO
A(1). 2-Methyl -1-(2-pyridyl)benzene I ~1 iN
/ I
To a degassed solution of 2-bromopyridine (1.9 mL, 20 mmol) in ethylene glycol dimethyl ether (60 mL) under argon, tetrakis(triphenylphosphane) palladium (o) (700 mg, 0.6 mmol) was added. After stirring for 10 min, 2-methylphenyl boronic acid (2.9 g, 22 mmol) was added, followed by sodium bicarbonate solution (5.04 g, 60 mmol in 60 mL water). The mixture was heated to reflux (-- 85°C) and stirred overnight. After cooling to room temperature, the solvent was evaporated, the residue was partitioned between water and ether, and the aqueous layer was extracted twice with ether. The combined organic layers were dried (Na2S04), and the solvent was evaporated to give a black oil. This oil was distilled at cl Torr at ~95°C to give title compound (2.75 g, 82~ yield) as a clear oil.
A(2) .
I ~1 ~N
COOH
A solution of Part A(1) compound (850 mg, 5.0 mmol) and potassium permanganate (1.9 g, 12.0 mmol) in water (25 mL) was heated to reflux and stirred for 1 hour. The hot reaction mixture was filtered, and the filtrate was evaporated to dryness. The solid residue was dissolved in_-water (5 mL) and acidified with acetic acid to pH 4-5. The resulting precipitate was isolated by filtration and rinsed with water to give a white solid (800 mg) which was recrystallized from hot ethanol (12 mL) to give title compound as a white solid (453 mg, 45~ yield).
B. traps-9-[4-[2-Oxo-5-[[2-(2-pyridinyl)-benzoyl]amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluor dye-9-carboxamide, hydrochloride An argon-purged slurry of 505 mg (0.82 mmol) of Example 6 compound and 100 mg of 10~ palladium-on-charcoal in 10 mL of methanol at room temperature was partially evacuated and subjected to hydrogenation from a filled balloon. After 4 h, the reaction mixture was purged with argon and filtered through a 0.45 ].~, nylon filter.
Evaporation and then re-evaporation from toluene gave a white foam. This material was dissolved in 10 mL of dichloromethane and stirred under argon at room temperature while 169 mg (0.83 mmol) of Part A compound, 162 mg (0.85 mmol) of EDCI and 60 N.L (0.43 mmol) of triethylamine were added. After 16 h, the reaction mixture was quenched with saturated sodium bicarbonate solution and extracted twice with ethyl acetate. The organic extracts were combined, dried (Na2S04) and evaporated. Purification by flash chromatography on silica gel (5 x 15 cm column, 1:24 methanol/ethyl acetate) provided the free base of the title compound. This material was dissolved in dichloromethane, treated with 0.3 mL of 4 ~! hydrogen chloride in dioxane and evaporated to provide title compound as a white solid, mp 132-136°C, 524 mg, 81~ yield.
MICROANALYSIS Calculated for C35H33F3N305P + HCl + dioxane +
0.25 H20: _-C, 59.09; H, 5.40; N, 5.30; C1, 4.47; F, 7.19;
P, 3 . 91 Found: C, 59.12; H, 5.28; N, 5.24; Cl, 4.48; F, 7.37;
P, 4.08.
MS (electrospray, + ions) m/e 664.
Example 9 traps-9-[4-[5-[[2-(2-Benzothiazolyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide.
/ N CFa H
~N
~, S
P O
O
H
traps isomer A.
H
O
S
Part A compound is a commercial compound supplied by Maybridge Chemical Company.
B. traps-9-[4-[5-[[2-(2-Benzothiazolyl) benzoyl]amino]-2-oxo-1,3,2-dioxaphos-phorinan-2-yl]butyl]-N-(2,2,2-trifluoro-e~~y~,-9H-fluorene-9-carboxamide An argon-purged slurry of 371 mg (0.60 mmol) of Example 6 compound and 90 mg of 10~ palladium-on-charcoal in 10 mL of methanol at room temperature was partially evacuated and subjected to hydrogenation from a filled balloon. After 4 h, the reaction mixture was purged with argon and filtered through a 0.45 ~. nylon filter.
Evaporation and then re-evaporation from toluene gave a white foam. This material was dissolved in 5 mL of dichloromethane and stirred under argon at room temperature_-while 153 mg (0.60 mmol) of Part A compound, 114 mg (0.60 mmol) of EDCI and 42 ~,L (0.3 mmol) of triethylamine were added. After 16 h, the reaction mixture was quenched with saturated sodium bicarbonate solution and extracted twice with ethyl acetate. The organic extracts were combined, dried (Na2S04) and evaporated. Purification by flash chromatography on silica gel (5 x 15 cm column, 1:3 hexanes/ethyl acetate) provided title compound as a white solid, mp 117-118°C, 269 mg, 62~ yield.
MICROANALYSIS Calculated for C37H33F3N305PS:
C, 61.75; H, 4.62; N, 5.84; F, 7.92; S, 4.45;
P, 4.30 Found: C, 62.02; H, 4.97; N, 5.55; F, 7.64; S, 4.06;
P, 4.42.
MS (electrospray, + ions) m/e 720.
Example 10 traps-9-[4-[5-[[2-(4-Morpholinyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-triouoroethyl)-9H-fluorene-9-carboxamide.
O
/ _ N CF3 O
H
\ ~ ~P, O N
J oJ' H
traps isomer A. 2-(1-Morpholino)benzoic acid C~~
O N
HO
A(1). Methyl 2-(1-morpholino)benzoate A solution of methyl 2-fluorobenzoate (15.4 g, 100 mmol) in morpholine (44 mL, 500 mmol) was heated at 50°C
for 30 min, and then warmed to 100°C and stirred for 2 h, then cooled to 50°C and stirred overnight. The reaction was then heated to reflex for 2.5 h. The excess morphol.ine was evaporated. The remainder was dissolved in ethyl acetate and washed successively with H20 (50 mL), saturated NaHC03 solution (2 x 50 mL), H20 (3 x 50 mL) and brine (50 mL). Drying (MgS04) and evaporation gave a yellow oil.
The crude product was dissolved in dichloromethane/ethyl acetate/hexane (4:1:4) and chromatographed (400 g silica gel) eluting with a step gradient of 20~ to 35~ ethyl acetate in hexane. Pure fractions were combined and evaporated to give title compound (10.5 g, 48~) as an oil which crystallized on standing to a white solid.
A(2). 2-(1-Morpholino)benzoic acid O CN
HO
Sodium hydroxide (10 g, 250 mmol) was dissolved in water (75 mL) and added to a solution of Part A(1) compound (10.4 g, 47.1 mmol) in methanol (75 mL). The reaction was stirred at RT for 1 h and the solvent was evaporated. The white residue was dissolved in H20 (100 mL) and adjusted to pH 1.5 with 1N HC1. The aqueous layer was extracted with chloroform (3 x 250 mL). The combined organic layers were - s7 -WO 99/21564 PCT/US9$/21750 dried (Na2S04) and evaporated to give title compound (9.76 g, 85~) as a white solid (m. p. 156-157°C).
B. traps-9-[4-[5-[[2-(4-Morpholinyl)-benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-f luo~"rene-9 -carboxamide An argon-purged slurry of 359 mg (0.582 mmol) of Example 6 compound and 100 mg of 10~ palladium-on-charcoal in 15 mL of methanol at room temperature was partially evacuated and subjected to hydrogenation from a filled balloon. After 16 h, the reaction mixture was purged with argon and filtered through a 0.45 ).~, nylon filter.
Evaporation and then re-evaporation from toluene gave a white foam. This material was dissolved in 5 mL of dichloromethane and stirred under argon at room temperature while 121 mg (0.584 mmol) of Part A compound, 88 mg (0.59 mmol) of HOBt, 122 mg (0.64 mmol) of EDCI and 41 N,L (0.3 mmol) of triethylamine were added. After 6 h, the reaction mixture was quenched with saturated sodium bicarbonate solution and extracted twice with ethyl acetate. The organic extracts were combined, dried (Na2S04) and evaporated. Purification by flash chromatography on silica gel (5 x 20 cm column, ethyl acetate) provided title compound as a white solid, mp 108-111°C, 265 mg, 66~ yield.
MICROANALYSIS Calculated for C34H37F3N306P+0.15 H20+0.23 EtOAc:
C, 60.38; H, 5.68; N, 6.05; F, 8.21 Found: C, 60.37; H, 5.54; N, 5.93; F, 7.91.
MS (electrospray, + ions) m/e 695.
dole 11 traps-9-[4-[5-[[2-(2-Benzoxazolyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide. -O
I / N~ CFA
H
~N
\ ~~ O O
P. O
/ O~ N '"
H
A. 2-(2-Bromophenyl)benzoxazole Br O
To a stirred slurry of 5.46 g (50.0 mmol) of 2-aminophenol (Aldrich) and 10.05 g (50.0 mmol) of 2-bromobenzoic acid in 100 mL of xylenes under argon at room temperature was added 6.10 g (100 mmol) of boric acid.
Using a Dean-Stark trap, the reaction was heated to refiux for 48 h. A total of 3.2 mL of water was separated. The reaction mixture was cooled, diluted with ethyl acetate and filtered. The filtrate was washed once with 3 ~i hydrochloric acid, once with water and three times with saturated sodium bicarbonate solution. The organic phase was dried (MgSO,) and evaporated. Purification by flash chromatography on silica gel (5x20 cm column, 2:1 dichloromethane/hexane) gave title compound as a light yellow solid, 5.90 g, 43~.
B. 2-(2-Benzoxazolyl)benzoic acid To a stirred solution of 700 mg (2.55 mmol) of Part A compound in 10 mL of THF under argon at -78°C was added a solution of t-butyllithium (3.3 mL, 1.7 A~, 5.6 mmol) in pentane over the course of 30 min. The reaction mixture was stirred for 1 h and then a dry stream of carbon dioxide gas was passed through the solution for lh. The reaction was allowed to warm to room temperature in situ. After 16 h, the mixture was diluted with ether and washed once with 50 mL of 10~ sodium hydroxide solution. The aqueous phase was adjusted to pH 3.5 using solid citric acid. The resulting solid was filtered, washed with water and air-dried to give 610 mg of title compound as a pink solid, mp >250°C, 100.
C. trans-9-[4-[5-[[2-(Benzoxazolyl)benzoyl]-amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide To a stirred solution of 117 mg (0.24 mmol) of Example 6 compound under argon at room temperature in 3 mL
of dichloromethane was added 72 mg (0.30 mmol) of Part B
compound, 45 mg (0.3 mmol) of HOBt, 65 mg (0.30 mmol) of EDCI and 20 ElL (0.15 mmol) of triethylamine. After 16 h, the reaction mixture was quenched with saturated sodium bicarbonate solution and extracted twice with ethyl acetate. The organic extracts were combined, dried (Na2S04) and evaporated. Purification by flash chromatography on silica gel (2.5 x 15 cm column, 1:3 hexanes/ethyl acetate) provided title compound as a white solid, mp 104-107°C, 38 mg, 20~ yield.
WO 99/21564 PCTlUS98/21750 MICROANALYSIS Calculated for C37H3gF3N306P+2 . 3 H20+0 . 5 EtOAc :
C, 59.36; H, 5.31; N,5.32; F, 7.22; P, 3.92 _ Found: C, 59.32; H, 5.24; N,5.43; F, 7.45; P, 4.20.
MS (electrospray, + ions) m/e 704.
Following are examples of additional compounds of the invention which may be prepared employing procedures described hereinbefore and in Examples 1 to 11. Although the following compounds are shown in the form of cis-isomers, in accordance with the invention, the corresponding trans-isomers are covered as well.
Fs I i I i I
HN
F3C-~ O O,p~, O
F I ~ I ~ F F3 i ~ O I
HN
F3C-~ O~P\' O
O O~N w H
O
R2~LsA~B.LsP~
O~NCOR~
R5a I\ I\ I
/ / I\
HN /
F3~ O~P~- O
o ~~ I \
O
/
I \ I \ F3 / / I\
HN O /
F3G-J O\~p~, O O°TH~2 -H I \
I \ ~ \ I
/ / I\
HN ~ O / CI
F3CrJ O
O O~H I W
WO 99/Z1564 PCT/US98/21'750 \ \
I/ I/ I\
HN /
F3C~ O~P\ O
O O~~ I \
\ ~. N
I/ I/ ~ I\
HN /
F3G- J O~P\~ O
O O~.H I \
/
I \ I ~.. F3 / / I\
HN ~ O /
FsG-/ O F F U P\' p H I/
\ \
i/ I/ /I
HN " ~ O O
F G-~ O
O ~Pp-~H I \
I ~ I ~ -/ /
HN ' ~ O H2SPh F3C~ O ~ Pp~-N
H I/
I ~ I ~ F3 / /
I
HN O /
F3G-J O c~-~
O~ p~N ( w ~' I ~
/ /
F3G-~ O ~ P~ p~
O _ H I /
I
/ /
H /
O~p~ O
O O~N
N H I /
I ~ I ~
/ /
HN O
F3C~ O
O
/
I ~ I ~ F3 / /
HN ~ O /
F GJ O p' 3 O, O~H I W
/ /
F3Cr-~ O O P~,.
O~-N
n' is 0, 1 or 2;
R6 is H, lower alkyl, aryl, -C(O)-R11 or -C ( O ) -O-R11;
R7 and R8 are the same or different and axe independently H, alkyl, aryl, halogen, -O-R12, or R7 and R8 together can be oxygen to form a ketone;
R9, R1~, R9' and R1~' are the same or different and are independently H, lower alkyl, aryl or -O-R11;
R9" and Rlfl" are the same or different and are independently H, lower alkyl, aryl, halogen or R11 is alley or aryl;
R12 is H, alkyl or aryl;
with the proviso that when A is a (1) bond, R2L2 cannot be hydrogen.
The pharmaceutically acceptable salts of the compounds of formula I include alkali metal salts such as lithium, sodium or potassium, alkaline earth metal salts such as calcium or magnesium, as well as zinc or aluminum and other cations such as ammonium, choline, diethanolamine, ethylenediamine, t-butyl-amine, t-octylamine, dehydroabietylamine, as well as pharmaceutically acceptable anions such as chloride, bromide, iodide, tartrate, acetate, methanesulfonate, maleate, succinate, glutarate, and salts of naturally occurring amino acids such as arginine, lysine, alanine and the like, and prodrug esters thereof.
In addition, in accordance with the present invention, a method for preventing, inhibiting or treating_ atherosclerosis, pancreatitis, hyperglycemia or obesity is provided, wherein a compound of formula I, IA or IB as defined hereinbefore is administered in an amount which decreases the activity of microsomal triglyceride transfer protein.
Furthermore, in accordance with the present invention, a method is provided for lowering serum lipid levels, cholesterol and/or triglycerides, or inhibiting and/or treating hyperlipemia, hyperlipidemia, hyperlipoproteinemia, hypercholesterolemia, atherosclerosis, hyperglycemia, pancreatitis, obesity, hypertriglyceridemia, Type II diabetes (NIDDM) wherein a compound of formula I as defined hereinbefore is administered in an amount which decreases the activity of microsomal triglyceride transfer protein.
filed Description of the Invention The following definitions apply to the terms as used throughout this specification, unless othezwise limited in specific instances.
The term "MTP" refers to a polypeptide or protein complex that (1) if obtained from an organism (e. g., cows, humans, tec.), can be isolated from the microsomal fraction of homogenized tissue; and (2) stimulates the transport of triglycerides, cholesterol esters, or phospholipids from synthetic phospholipid vesicles, membranes or lipoproteins to synthetic vesicles, membranes, or lipoproteins and which is distinct from the cholesterol ester transfer protein [Drayna et , Naturg ~, 632-634 (1987)] which may have similar catalytic properties.
The phrase "stabilizing" atherosclerosis as used in the present application refers to slowing down the development of and/or inhibiting the formation of new atherosclerotic lesions.
The phrase "causing the regression of"
atherosclerosis as used in the present application refers to reducing and/or eliminating atherosclerotic lesions.
Unless otherwise indicated, the term "lower alkyl", "alkyl" or "alk" as employed herein alone or as part of another group includes both straight and branched chain hydrocarbons, containing 1 to 40 carbons, preferably 1 to 20 carbons, more preferably 1 to 12 carbons, in the normal chain,such as methyl, ethyl, propyl, isopropyl, butyl, t-butyl, isobutyl, pentyl, hexyl, isohexyl, heptyl, 4,4-dimethylpentyl, octyl, 2,2,4-trimethylpentyl, nonyl, decyl, undecyl, dodecyl, the various branched chain isomers thereof, and the like as well as such groups including 1 to 4 substituents which may be any of the R3 groups, or the R1 substituents set out herein.
Unless othervuise indicated, the term "cycloalkyl" as employed herein alone or as part of another group includes saturated or partially unsaturated (containing 1 or 2 double bonds) cyclic hydrocarbon groups containing 1 to 3 rings, including monocyclicalkyl, bicyclicalkyl and tricyclicalkyl, containing a total of 3 to 20 carbons forming the rings, preferably 4 to 12 carbons, forming the ring and which may be fused to 1 aromatic ring as described for aryl, which include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclodecyl and cyclododecyl, cyclohexenyl, any of which groups may be optionally substituted with 1 to 4 substituents which may be any of the R3 groups, or the R1 substituents set out herein.
The term "cycloalkenyl" as employed herein alone or as part of another group refers to cyclic hydrocarbons containing 5 to 20 carbons, preferably 6 to 12 carbons and 1 or 2 double bonds. Exemplary cycloalkenyl groups include cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl, cyclohexadienyl, and cycloheptadienyl, which may be optionally substituted as defined for cycloalkyl.
The term "polycycloalkyl" as employed herein alone or as part of another group refers to a bridged multicyclic group containing 5 to 20 carbons and containing 0 to 3 bridges, preferably 6 to 12 carbons and 1 or 2 bridges.
Exemplary polycycloalkyl groups include [3.3.0]-bicyclooctanyl, adamantanyl, [2.2.1]-bicycloheptanyl, [2.2.2]-bicyclooctanyl and the like and may be optionally substituted as defined for cycloalkyl.
The term "polycycloalkenyl" as employed herein alone or as part of another group refers to a bridged multicyclic group containing 5 to 20 carbons and containing 0 to 3 bridges and containing 1 or 2 double bonds, preferably 6 to 12 carbons and 1 or 2 bridges. Exemplary polycycloalkyl groups include [3.3.0]-bicyclooctenyl, [2.2.1]-bicycloheptenyl, [2.2.2]-bicyclooctenyl and the like and may be optionally substituted as defined for cycloalkyl.
The term "aryl" as employed herein alone or as part of another group refers to monocyclic and bicyclic aromatic groups containing 6 to 10 carbons in the ring portion (such as phenyl or naphthyl) and may optionally include one to three additional rings fused to Ar (such as aryl, cycloalkyl, heteroaryl or cycloheteroalkyl rings) and may be optionally substituted through available carbon atoms with 1, 2, or 3 groups selected from hydrogen, halo, haloalkyl, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyl, trifluoromethyl, trifluoromethoxy, alkynyl, cyclo-alkylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl, aryl, heteroaryl, arylalkyl, aryloxy, aryloxyalkyl, arylalkoxy, arylthio, arylazo, heteroarylalkyl, heteroarylalkenyl, heteroarylheteroaryl, heteroaryloxy, hydroxy, vitro, cyano, amino, substituted amino wherein the amino includes 1 or 2 substituents (which are alkyl, aryl or any of the other aryl compounds mentioned in the definitions), thiol, alkylthio, arylthio, heteroarylthio, arylthioalkyl, alkoxyarylthio, alkylcarbonyl, arylcarbonyl, alkyl-aminocarbonyl, arylaminocarbonyl, alkoxycarbonyl, aminocarbonyl, alkylcarbonyloxy, arylcarbonyloxy, alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfinylalkyl, arylsulfonylamino or arylsulfon-aminocarbonyl or any of the R3 groups, or the R1 substituents set out herein.
The term "aralkyl", "aryl-alkyl" or "aryllower alkyl" as used herein alone or as part of another group refers to alkyl groups as discussed above having an aryl substituent, such as benzyl or phenethyl, or naphthylpropyl, or an aryl as defined above. .
The term "lower alkoxy", "alkoxy", "aryloxy" or "aralkoxy" as employed herein alone or as part of another group includes any of the above alkyl, aralkyl or aryl groups linked to an oxygen atom.
The term "amino" as employed herein alone or as part of another group may optionally be substituted with one or two substituents such as alkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl and/or cycloalkyl.
The term "lower alkylthio", alkylthio", "arylthio"
or "aralkylthio" as employed herein alone or as part of 2S another group includes any of the above alkyl, aralkyl or aryl groups linked to a sulfur atom.
The term "lower alkylamino", "alkylamino", "arylamino", or "arylalkylamino" as employed herein alone or as part of another group includes any of the above alkyl, aryl or arylalkyl groups linked to a nitrogen atom.
The term "acyl" as employed herein by itself or part of another group, as defined herein, refers to an organic radical linked to a carbon 1 y group; examples of acyl groups include alkanoyl, alkenoyl, aroyl, aralkanoyl, heteroaroyl, cycloalkanoyl, and the like.
The term "alkanoyl" as used herein alone or as part of another group refers to alkyl linked to a carbonyl group.
Unless otherwise indicated, the term "lower alkenyl"
or "alkenyl" as used herein by itself or as part of another group refers to straight or branched chain radicals of 2 to 20 carbons, preferably 3 to 12 carbons, and more preferably 1 to 8 carbons in the normal chain, which include one to six double bonds in the normal chain, such as vinyl, 2-propenyl, 3-butenyl, 2-butenyl, 4-pentenyl, 3-pentenyl, 2-hexenyl, 3-hexenyl, 2-heptenyl, 3-heptenyl, 4-heptenyl, 3-octenyl, 3-nonenyl, 4-decenyl, 3-undecenyl, 4-dodecenyl, 4,8,12-tetradecatrienyl, and the like, and which may be optionally substituted with 1 to 4 substituents, namely, halogen, haloalkyl, alkyl, alkoxy, alkex~yl, alkynyl, aryl, arylalkyl, cycloalkyl, amino, hydroxy, heteroaryl, cycloheteroalkyl, alkanoylamino, alkylamido, arylcarbonylamino, vitro, cyano, thiol, alkylthio or any of the R3 groups, or the R1 substituents set out herein.
Unless otherwise indicated, the term "lower alkynyl"
or "alkynyl" as used herein by itself or as part of another group refers to straight or branched chain radicals of 2 to 20 carbons, preferably 2 to 12 carbons and more preferably 2 to 8 carbons in the normal chain, which include one triple bond in the normal chain, such as 2-propynyl, 3-butynyl, 2-butynyl, 4-pentynyl, 3-pentynyl, 2-hexynyl, 3-hexynyl, 2-heptynyl, 3-heptynyl, 4-heptynyl, 3-octynyl, 3-nonynyl, 4-decynyl,3-undecynyl, 4-dodecynyl and the like, and which may be optionally substituted with 1 to 4 substituents, namely, halogen, haloalkyl, alkyl, alkoxy, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, amino, heteroaryl, cycloheteroalkyl, hydroxy, alkanoylamino, alkylamido, arylcarbonylamino, vitro, cyano, thiol, and/or alkylthio, or any of the R3 groups, or the R1 substituents set out herein.
The term "alkylene" as employed herein alone or as part of another group refers to alkyl groups as defined above having single bonds for attachment to other groups at two different carbon atoms and may optionally be substituted as defined above for "alkyl".
The teams "alkenylene" and "alkynylene" as employed herein alone or as part of another group refer to alkenyl groups as defined above and alkynyl groups as defined above, respectively, having single bonds for attachment at two different carbon atoms.
Suitable alkylene, alkenylene or alkynylene groups or (CH2)m, (CH2)n or (CH2)p (which may include alkylene, alkenylene or alkynylene groups) as defined herein, may optionally include 1, 2, or 3 substituents which include any of the R3 groups, or the R1 substituents set out herein.
Examples of alkylene, alkenylene and alkynylene include -CH=~H-CHZ- ! -CgaCg~Cg- ! -C-C-CHZ- !
-- CH2 C- CHZ CHy CHZ C--.
O O
~3 '_ CgZC = CC82 - ~ - Ca Cg - CHZ , '-~~s)s- ! -(CHZ)s- ! -(CHz)a- !
~3 -- (C$2 ) 2- ~ - CHZCBa- ! - CHgCH- ! '- Cg2CgCgZ~ !
~3 C8Z- ! -_ ~ CH~C$Z- ! - CH ~ CHZ- !
~3 C2H5 l ~3 ~3 F
-Cg2-C_CHa- f -(C8a)~ ~ --(CH~)a-C-CHI- , ~3 Cl ~3 ~3 -c$a-~-Via- ~ -(~a)a- i'H- ~ -cHa-cH- i- s - csa - ca - cH - cHa , - cHa - ~H- cHa - ~ H- , ~3 ~3 CHg CHg OCHg - CH- CHaCHa- y- CH _ CHaCHa- ~ -~ CHaOCBa-- OCHaCHa- ~ ~ CHaN8C8a- ~ -- NBCHaCHa-ICH3 -' -- CHaC$a_.
(CHa)3-CFa- ~ -cga-N-cga-The term "halogen" or "halo" as used herein alone or as part of another group refers to chlorine, bromine, fluorine, and iodine as well as CF3, with chlorine or fluorine being preferred.
The term ~metal ion" refers to alkali metal ions such as sodium, potassium or lithium and alkaline earth metal ions such as magnesium and calcium, as well as zinc and aluminum.
The term "heterocyclyl" as used herein refers to "cycloheteroalkyl" groups and "heteroaryl" groups as def fined herein .
The term "cycloheteroalkyl" as used herein alone or as part of another group refers to a 5-, 6- or 7-membered saturated or partially unsaturated ring which includes 1 to 2 hetero atoms such as nitrogen, oxygen and/or sulfur, linked through a carbon atom or a heteroatom, where possible, optionally via the linker (CHZ)p (which is defined above), such as O\ N~O S' O
N~ O ~ N
' ' J ' O
N ~/ O
s and the like. The above groups may include 1 to 4 substituents such as alkyl, halo, oxo and/or any of of the R3 groups, or the R1 substituents set out herein. In addition, any of the above rings can be fused to a cycloalkyl, aryl, heteroaryl or cycloheteroalkyl ring.
The term "cycloheteroalkoxy" as used herein alone or as part of another group refers to a 4-, 5-, 6- or 7-membered saturated or partially saturated ring which includes at least one oxygen atom in the ring and at least 1 or 2 other hetero atoms in the ring such as nitrogen, oxygen and/or sulfur, linked through a carbon or heteroatom, where possible, optionally via the linker (CH2)p, such as o~ N s.~ o~N~.
, N O "'i~ O , V ' p N ~ N ~/
O/ ~ O~ ~ N V
and the like. The above groups may include 1 to 4 substituents such as alkyl, halo, oxo and/or any of of the R3 groups, or the R1 substituents set out herein. In addition, any of the above rings can be fused to a cycloalkyl, aryl, heteroaryl or cycloheteroalkyl ring.
The term "heteroaryl" as used herein alone or as part of another group refers to a 5- or 6- membered aromatic ring which includes 1, 2, 3 or 4 hetero atoms such as nitrogen, oxygen or sulfur,and such rings fused to an aryl, cycloalkyl, heteroaryl or cycloheteroalkyl ring (e. g.
benzothiophenyl, indolyl), and includes possible N-oxides, such as N~ S 0 ~ ~ / ~ ~ / s N~~ N
I
U
N
~N N N~ N
N~/O N~/S
~N,H N~N ~ N ~ ' i5 N._ N ~O
% ~ / ~ / ~ ~ ~ ~!~
<>>~ >>~> ~ ~ 'U
N ~ I
and the like.
Ar may be either aryl or heteroaryl as defined above.
f ~ f ~ f Het Het t and Het 2 ' are the same or different, as defined hereinbefore, and are attached to the central ring of the indenyl or fluorenyl type group at adjacent positions (that is, ortho or 1,2-positions). Examples of such groups include O
/ I '~ / I '~ , I '~ ~ '~ _ Nr~~ N~~ .~ ~ I
O
O i I , I ~ I '~ I
/I
I ' y ~.r' .r~' ft' "
p' ~ '~ .r'~ ' N~ ~~ 1 / a ~ O
N' s~
N 't, a N ~ ~ N, / ~/
N
/i'~ ~ /w~,~
N ' I u,~
wherein a is selected from O, S, and NR7a;
R7a is H, lower alkyl, aryl, -C (O) R7b, -C (O) OR7b%
R7b is alkyl or aryl.
5 The heteroazyl groups including the above groups may optionally include 1 to 4 substituents such as any of the R3 groups, or the R1 substituents set out herein. In addition, any of the above rings can be fused to a cycloalkyl, aryl, heteroaryl or cycloheteroalkyl ring.
The term cycloheteroalkylalkyl" as used herein alone or as part of another group refers to cycloheteroalkyl groups as defined above linked through a C atom or heteroatom to a (CH2)p chain.
The term "heteroarylalkyl" or "heteroaryl-alkenyl"
as used herein alone or as part of another group refers to a heteroaryl group as defined above linked through a C atom or heteroatom to a -(CH2)p- chain, alkylene or alkenylene as defined above.
The term "polyhaloalkyl" as used herein refers to an "alkyl" group as defined above which includes from 2 to 9, preferably from 2 to 5, halo substituents, such as F or C1, preferably F, such as CF3CH2, CF3 or CF3CF2CH2.
Preferred are compounds of formula I wherein A is NH, B is Ra Rs X
X is a bond, oxygen or sulfur; R3 and R4 are independently H or F.
Preferred R2 groups are alkyl, polyfluoroalkyl (such as 1,1,1-trifluoroethyl), alkenyl, aryl, heteroaryl or heteroarylalkyl, such as 2-pyridylmethyl (preferably substituted with one of the preferred R2 substituents above).
It is preferred that Ll contains 2 to 7 atoms in the linear chain and L2 is a bond or lower alkylene.
The preferred L2 group is alkylene such as CH2 or a bond.
The preferred A group is -NH-.
Preferred R1 groups are as set out in the preferred compounds shown in the following Table.
More preferred are compounds of the invention which have the following structures wherein R1C0, n and the geometry are as indicated below.
COHHCHzCFs O
\ ~CH2)n P~~ -O
/ ~ ~ '~ NHCOR~
Preferred Structures of Cyclic Phosphonates R1 CO = n geometry R' CO = n geometry CsH
I / ~ traps H CO ~ traps / CO
\I
\ /
( / 1 cis / CO ~ traps / ~o \
\
~ N 1 traps / I CO 1 traps / CO
\I
I\
C
/ 2 traps ~ 1 traps / co / co \I \I
I \ -1 traps 2 cis ~ N
/ CO / CO
\ I \ I
O
/ OC- 1 traps \I
The compounds of formula I may be prepared by the exemplary processes described in the following reaction schemes. Exemplary reagents and procedures for these reactions appear hereinafter and in the working Examples.
Methods for preparing starting materials useful in preparing cyclophosphonates in accordance with the present invention, are shown in the folowing reaction schemes.
Scheme 1.
Acylatioa Ra OH (carbodiimide coupliaQ) Ra O8 RICOaH, R1N=C=NRZ, BOBt lA. NS NCORl Rb R5a Rb R5a OB OH
Ra O8 ACylBtion Ra OCOR1 Ra OH
3 R1COC1, 3 EtgN 1 Solvolysis 18. pg NCOR Me08, NaH NCORl b R5a R5a ~ R5a R OH Rb OCORl Rb OH
Ra OH Silylation Ra OSi(CH3)3 1. Acylatioa Ra OH
I(~g)gSiIZNH (R1COC1, Et3N) 1C. pg ~5a ~S8 ~ 2. Msthaaolysis) NCOR
Rb R Rb R5a (M~OH, HCl) R5a OH OSi(C8g)g Rb O$
As seen in Scheme lA, serinol derivative (~) can be acylated via carbodiimide coupling directly to 3_.
Alternatively, as seen in Scheme 1B, ~ can be acylated with acid chlorides to tri-acylated ,~,. Subsequent solvolysis provides diols 3_. As seen in Scheme 1C, the diols 3_ could also be prepared from bis-O-trimethylsilylated amine ~, acylation with acid chlorides and subsequent methanolysis to provide ~.
It will be appreciated that in the reactions to follow, unless otherwise indicated, the moiety "B° in the starting materials, intermediates and final products is set out as I / x I /
for purposes of illustration only.
It will be appreciated that the "B" moiety in the starting materials, intermediates and final products in all reactions set forth herein, unless indicated to the contrary, may be any of the fluorenyl-type groups l w Ra. ./. ~ Ra, Ra. Re, R3 ~' ~ ( = R° ~ R3 Het ~ /~ R4 Or X~ X
R3.
R4.
Het 1 Het X as well as any of indenyl-type groups R3.
R3 3.
or ~~~ R' S R3b ~ ~ or a (CH~
R SC ~~ _.
(a - 2,3 or 4) Rsa R3.
R3 R3.
Het Het ~ f .
I or R3b ~ R3b Rsa (CH~a R3a The above B moieties (including all fluorenyl-type groups and all indenyl-type groups) are collectively referred to as "fluorenyl-type" moieties. The use of the first fluorenyl-type group (as set out in the previous paragraph) in the Reaction Schemes is for purposes of illustration only; any of the 3 fluorenyl groups or 4 indenyl groups as set out above may be employed in any of the Reaction Schemes set out herein in place of \
I / X I / .
The compounds of formula I of the invention may be prepared as shown in Reaction Scheme 2.
Schenne 2 1. TMSBr 2. C1COCOC1 \ ~ \ Ra O8 / / O
O ILl-.._ p~0alkyl 3' NCORl, amiae base R5a A Oalkyl Rb OH
LsRz \ ~\ ~\ ~\
+ /
/ / O Ra O L1 II Ra O L1 ~~ O A O O
b 1 LZR2 Rb NCORi LZRZ R 8 RS° R
H R5a 7-Cis Io 7-trees Ip As seen in Scheme 2, dialkyl phosphonate ester Im is treated with bromotrimethylsilane and then is treated with oxalyl chloride and dimethylformamide (employing conventional procedures) to give a diphosphinyl dichloride intermediate which (without purification) is reacted with diol ~, (which may be chiral or achiral) (as formed in Scheme lA, 1B or 1C) and an amine base such as triethylamine to give a mixture of the 7-traps and 7-cis isomers (Io and Ip, respectively) of the invention. The 7-trans and 7-cis isomers may be separated by conventional chromatographic techniques.
Scheme 3 Preparation of Other Acyl Derivatives From 7-trans Compounds ~ i ~ _i o II Ra O~L~ p~ O
LZR2 Rb NCORl.
H R5s (where R1' is as I°~ arylmsthyloxy or (7-traas) heteroarylmathyloxy) Hydrogeaolysis 1. 8a, Pd-C/EtOH
2. RICOaH, R1N=C=NRZ, HOBt Io' Io ~ O
II Ra O Ll- P~
O
Z Rb NCORl g RSa Io 7-traa8 As seen in Scheme 3, the 7-traps isomer Io' (R1'=OCH2C6H5) (and the corresponding 7-cis isomer) may be made to undergo hydrogenolysis to form an amine intermediate which can be reacted with R1COZH to prepare other aryl derivatives in accordance with the invention.
The starting material Im may be prepared according to the following Reaction Schemes 4 and 4A.
Reaction Scheme 4 X
X , 1 ) base 2) Hal-L~-Y
O L~-Y
O Y=Hal A or O-PG ~ Ih (Y=Hal) L2R2 XIVa (Y=OPG) Y=OPG
\ X ~ \ Deprotection F- (for example, i i n-Bu4NF) O \Li-OH
A
L2R2 =g Halide Formation X
~ , \L~-Hal A
L2R2 Ih where PG is as oxygea protoctiag group, such as t-Bu(C83)ZSi or t8u(Ph)gSi-X
Arbuzov I ~ I ~ ~ Oalkyl Reaction O
Ih ~ L1~ Oalkyl Excess (AlkylO)2P(OG1~) im -20°C to 180°C L2R2 (Q~ is alkyl, triorganosiiyl (such as trimethylsilyl or t-butyldimethyisilyl), H, the latter in the presence of base such as butyilithium, sodium hydride, or sodium bis-(trimethylsilylamide) Reaction Scheme 4A
(A~ternative Mgthod fQr Makina Ih) 1 ) base /
2) Ha1-L~-Y ~
~r o _Lm x 3)C1COCOCU DMF N-R5 0 08 4) (R21-2)RSNH izRs II Ih Protected alcohol XIVa can be converted into a wide variety of functional groups through the intermediary of a halide Ih. For example, the alcohol Ig can be converted to the halide Ih of the invention by either activation through the sulfonate ester (tosyl chloride, or mesyl chloride) and iodide displacement (NaI or KI in acetone or 2-butanone), or by reaction with triphenylphosphine, I2 and imidazole.
The halide Ih can undergo an Arbuzov reaction to form phosphonates, phosphinates and phosphine oxides of the invention Im. The Arbuzov reaction can be accomplished with phosphites, phosphinites, and phosphonites (for example, (alkyl0)3P or (alkyl0)2POSi(alkyl)3 or (alkyl0)2POH, the latter being in the presence of a base such as butyllithium, sodium hydride or sodium bis(trimethylsilylamide)) at temperatures within the range from about -20°C to about 180°C.
The starting material VIIIA for compound Im may be prepared as shown in Reaction Scheme 5.
Reaction Scheme 5 (Amides) Preparation of Compounds of Formula I where A is - N
O
COOH R L ~ ~ C
1) amide formation R5 e.g. 1) acid chloride formation ~ , ~ , 2) (R2L2)RSNH ~X' v vi=~
A= -N-~5 R
As seen in Scheme 5, the amide VIIIA may be formed by treating II with thionyl chloride or oxalyl chloride in an inert organic solvent such as dichloromethane (optionally in the presence of dimethylformamide (DID')) to form the acid chloride IIA
o CI- C
x xxar Acid chloride IIA, without separation from the reaction mixture, is treated with amine (R2L2)R5NH at a reduced temperature within the range from about -40°C to about room temperature, to form the amide VIIIA.
Amide VIIIA may be converted to compounds of formula I employing the procedure set out in Reaction Scheme 4/4A.
In carrying out the above reaction to form amide VIIIA, the amine will be employed in a molar ratio to acid chloride IIA within the range from about 4:1, to about 1:1, optionally in the presence of a tertiary amine base or other acid scavenger.
Alternative formation of amide VIIIA from acid II
and (R2L2)R5NH can be carried out via standard literature procedures.
Ruction Scheme 6 !Class Esters) Preparation of Esters VIIIA (A - -0-) O
H02 H 1) Acid, R2L20H or RZL~-O-C H
2) (COCI)2, R2L20H
3) DCC, HOST, DMAP, R2L20H
esterification As seen in Reaction Scheme 6, ester compounds of formula VIIIB wherein A = oxygen can be prepared by an acid catalyzed esterification of acid II employing an acid such as H2S04 or p-toluene-sulfonic acid in the presence of an alcohol such as ally! alcohol, ethanol or methanol.
Alternatively, activation of the acid II to the acid chloride (with oxaly chloride or thionyl chloride) followed by treatment with an alcohol optionally in the presence of a tertiary amine base or other acid scavenger, gives compounds of formula VIIIB.
Various additional methods of activation include mixed anhydride formation ((CF3C00)2 or i-BuOCOCl) or formation of the acylimidazole (carbonyldiimidazole) or with DCC and HOBT in the presence of DMAP (4-dimethyl-aminopyridine). These activated intermediates readily form esters upon treatment with alcohols.
Ruction Scheme 7 (Amides from Isoc3ranates ) Preparation of Amides VIIIC (A is NH) O
RzL2HN ~~
\ \
1) base / X I / 2) R2L2NC0 [ / I
X
iy v===c Compounds of formula VIIIC
where A is -NH- (amides) can be prepared by the methods shown in Reaction Scheme 7 from known compound IV.
Treatment of compound IV with base, such as n-BuLi, followed by reacting the anion with an isocyanate gives compound VIIIC.
Scheme 8 Alt~~at~ Scheme for ~om~ound Im2 \ X I \ ~ \ X ~ \
/ / Deesterification ~O OAlkyl O OTMS
t u/ > O 1 u/
O-~L -P TMSBr or TMSI L '-p A \OAlkyl (Optional tertiary ~A \OTMS
R2L2 amine base) R2L2 Im Disilyl Ester Intermediate Phosphonate Ester Formation (COCI)2, DMF, CH2CI2 to or ip Compounds Im may be modified by the various transformations set out in Reaction Scheme 8.
The compounds of the invention may be employed in preventing, stabilizing or causing regression of atherosclerosis in a man~nalian species by administering a therapeutically effective amount of a compound to decrease the activity of MTP.
WO 99/21564 PCT/US9$/21750 The compounds of the invention can be tested for MTP
inhibitory activity employing the procedures set out in _ U.S. application Serial No. 117,362 filed September 3, 1993, employing MTP isolated from one of the following sources:
(1) bovine liver microsomes, (2) HepG2 cells (human hepatoma cells) or (3) recombinant human MTP expressed in baculovirus.
The compounds of the invention may also be employed in lowering serum lipid levels, such as cholesterol or triglyceride (TG) levels, in a mammalian species, by administering a therapeutically effective amount of a compound to decrease the activity of MTP.
The compounds of the invention may be employed in the treatment of various other conditions or diseases using agents which decrease activity of MTP. For example, compounds of the invention decrease the amount or activity of MTP and therefore decrease serum cholesterol and TG
levels, and TG, fatty acid and cholesterol absorption and thus are useful in treating hypercholesterolemia, hypertriglyceridemia, hyperlipemia, hyperlipoproteinemia, hyperlipidemia, pancreatitis, hyperglycemia, atherosclerosis, non-insulin dependent diabetes (Type II
diabetes) and obesity.
The compounds of the present invention are agents that decrease the activity of MTP and can be administered to various mammalian species, such as monkeys, dogs, cats, rats, humans, e~., in need of such treatment. These agents can be administered systemically, such as orally or parenterally.
The agents that decrease the activity or amount of MTP can be incorporated in a conventional systemic dosage form, such as a tablet, capsule, elixir or injectable formulation. The above dosage forms will also include the necessary physiologically acceptable carrier material, excipient, lubricant, buffer, antibacterial, bulking agent (such as mannitol), anti-oxidants (ascorbic acid or sodium bisulfate) or the like. Oral dosage forms are preferred, although parenteral forms are quite satisfactory as well.
The dose administered must be carefully adjusted according to the age, weight, and condition of the patient, as well as the route of administration, dosage form and regimen, and the desired result. In general, the dosage forms described above may be administered in amounts of from about 5 to about 500 mg per day in single or divided doses of one to four times daily.
The following Examples represent preferred embodiments of the invention. All temperatures are in °C
unless indicated otherwise.
NOTE: The phrase "flash chromatography" refers to chromatography performed on EM Industries Silica Gel 60 (catalog #9385-9), 230-400 mesh under 10-20 psi of nitrogen pressure.
~ple 1 (E)-9-[4-[2-Oxo-5-([[4'-(trifluoromethyl)[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide, N-oxide.
N~ CF3 CF3 ~~O C /
I\
traps isomer Example 2 (Z)-9-[4-[2-Oxo-5-[[[4'-(trifluoromethyl)[1,1'-biphenylJ-2-yl]carbonylJaminoJ-1,3,2-dioxaphosphorinan-2-ylJbutylJ-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide, N-oxide.
O
/ N/~ CF3 CF3 H I\
\ _ w--.~ o /
O'P~O
\/ O ~ _. . \
A.
cis isomer OH OH
H \I
O /
\I
To a stirred solution of 1.33 g (5.00 mmol) of 4'-trifluorophenyl-2-benzoic acid (Aldrich Chemical Co.), 0.455 g (5.00 mmol) of serinol (Aldrich Chemical Co.), 0.750 g (5.0 mmol) of HOBt and 0.5 mL (3.6 mmol) of triethylamine in 10 mL of dichloromethane at room temperature under argon, was added 1.0 g (5.25 mmol) of EDCI, portionwise, over 3 min. After 16 h, the reaction mixture was diluted with ethyl acetate, washed once with saturated sodium bicarbonate solution, once with brine and once with 10~ citric acid solution, dried (MgS04) and evaporated. Purification by flash chromatography on silica gel (5 x 15 cm column, ethyl acetate) provided title compound as a white solid, mp 146-148°C, 1.23 g, 72~ yield.
B.
CONHCHzCFa P03Et2 B(1) .
O
-OH
Br To a solution of 9-fluorenecarboxylic acid (Aldrich) (50 g, 240 mmol) in THF (1200 mL) at 0°C was added dropwise a solution of n-butyllithium (2.5M, 221 mL, 530 mmol) in THF. The yellow reaction was stirred at O~C for 1 h, then 1,4-dibromobutane (31.3 mL, 260 mmol) was added dropwise over 30 min. The reaction was stirred at O~C for 30 min, then the reaction was warmed to RT fox 30 h. The reaction was extracted with water (3 x 750 mL). The combined aqueous layers were extracted with ethyl ether (800 mL).
The aqueous layer was made acidic with HC1 solution (1N, 500 mL), then extracted with dichloromethane (3 x 750 mL).
The combined organic layers were dried over MgSO~.
Evaporation gave title compound (71 g, 85~) as a white solid.
B(2) .
Hn CF3 Br To a solution of Part B(1) acid (60 g, 173 mmol) and DMF (100 11.L) in CH2C12 (600 mL) under argon at 0'C was added oxalyl chloride (104 mL, 2. OM in CH2C12, 208 nunol) dropwise. The reaction was stirred at 0'C for 10 min, then-warmed to RT and stirred for 1.5 h. The reaction was concentrated in vacuo to give the crude acid chloride as a yellow oil. To a suspension of 2,2,2-trifluoroethylamine hydrochloride (25.9 g, 191 mmol) in CH2C12 (500 mL) at O~C
under argon was added triethylamine (73 mL, 521 mmol) followed by dropwise addition of a solution of the crude acid chloride in CH2C12 (15 mL). The reaction was stirred at 0'C for 1 h, diluted with CH2C12 (500 mL), and washed with water (2 x 300 mL), 1N HC1 (2 x 300 mL), saturated NaHC03 (2 x 300 mL), and brine (2 x 300 mL), then dried over MgS04. Evaporation gave 80 g of a oil which was purified by flash chromatography on silica gel (2.5 kg).
The crude product was loaded in a mixture of CH2C12 and hexane, and eluted with a step gradient of 10~ EtOAc/hexane (4L) to 15~ EtOAc/hexane (2L) to 20~ EtOAc/hexane (4L).
Pure fractions were combined and evaporated to give title compound (52.5 g, 71~) as a white solid (mp 88-92'C).
B(3) .
cOtyHGH2Cfa P09Et2 A solution of 2.13 g (5.00 mmol) of Part B(2) compound in 3.5 mL of triethylphosphite under argon was heated to 110°C for 16 h and then to 180°C for 4 h. The reaction was cooled and then the volatiles were distilled off at 100°C at 1 Torr. The residue was purified by flash chromatography (5x15 cm column, EtOAc) to give title compound (1.92 g, 79~) as a waxy yellow solid (mp 87-89°C).
mp : 87-89°C
MS (FAB) m/e 484 (M+H).
Anal. Cald'd for C24H2gN04PF3+0.13 mol H20:
C, 59.33; H, 6.07; N, 2.88; P, 6.37; F, 11.73 _ Found: C, 59.09; H, 5.98; N, 2.95; P, 6.51; F, 11.92.
C. (E)-9-[4-[2-Oxo-5-[([4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide, N-oxide (Exam~~le 1 ) D. (Z)-9-[4-[2-Oxo-5-[((4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide, N-oxide (Example 2) To a stirred solution of 500 mg (1.03 mmol) of Part B compound in 10 mL of dichloromethane at room temperature under argon was added 0.45 mL (3.4 mmol) of bromotrimethylsilane. After 1 h, the reaction mixture was evaporated to provide a thick oil. The oil was dissolved in 5 mL of dichloromethane at room temperature under argon and treated with 0.26 mL (3.0 mmol) of oxalyl chloride and 100 N,L of DMF. After 2 h, the reaction mixture was evaporated and redissolved in 10 mL of dichloromethane. To this solution at room temperature under argon, was added 340 mg (1.0 mmol) of Part A compound and 0.5 mL (3.6 mmol) of triethylamine. After 14 h, the reaction was diluted with ethyl acetate and washed once with 10~ citric acid solution, dried (MgSO,) and evaporated. Purification by flash chromatography on silica gel (5 x 15 cm column, 1 L
85:15 ethyl acetate/hexanes, then ethyl acetate) provided two fractions.
The less polar fraction was designated Part C
(Example 1) compound, white solid, mp 105-107°C, 205 mg, 27~ yield.
MICROANALYSIS Calculated for C37 H33 FsN20sP + 0.55 H20:
C, 60.01; H, 4.64; N, 3.78; F, 15.39; P, 4.18 _ Found: C, 60.00; H, 4.48; N, 3.64; F, 15.10; P, 3.75.
MS (electrospray, + ions) m/e 731.
The more polar fraction was designated Part D
(Example 2) compound, white solid, mp 102-104°C, 130 mg, 17~.
1H NMR, i3C NMR, IR and mass spectrometry were consistent for the indicated compound.
IO
MICROANALYSIS Calculated for C37 Hs3 F6N205P + 064 H20:
C, 59.88; H, 4.66; N, 3.77; F, 15.36; P, 4.17 Found: C, 59.88; H, 4.44; N, 3.75; F, 15.08; P, 4.14.
MS (electrospray, + ions) m/e 731.
Examble 3 traps-9-[4-[5-(Benzoytamino)-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide.
O
H
O
/ Oy,, '~- N
HH /
traps isomer A. N-(1,3-Dibenzoxyloxy-2-propyl)benzamide OCOCsHS
H
O OCOCsNs To a stirred slurry of 1.82 g (20.0 mmol) of serinol and 9.2 mL (66 mmol} of triethylamine in 20 mL of dichloromethane at -5°C under argon, was added dropwise, 7.0 mL (61 mmol) of benzoyl chloride (Aldrich) over 30 min.
After 2 h, the reaction was diluted with ethyl acetate and washed three times with 1 ~ hydrochloric acid, once with brine, twice with saturated sodium bicarbonate solution, dried (MgSO,) and evaporated. The resulting white solid was recrystallized from ethyl acetate/hexane to provide title compound, mp 96-98°C, 5.62 g, 70~ yield.
B. N-(1,3-Dihy~lroxv-2-propyl)benza~ide OH
H
O OH
To a stirred solution of 160 mg (4.0 mmol) of 60~
sodium hydride in 50 mL of methanol at room temperature under argon, was added 4.03 g (10.0 mmol) of Part A
compound. The slurry was heated to reflux where a clear solution forms. After 3 h, the reaction was cooled and 1.5 mL of 4 I~ hydrogen chloride in dioxane was added.
Evaporation and re-evaporation from methanol onto silica gel (5 g) and purification by flash chromatography on silica gel (5 x 15 cm column, 3:47 methanol/ethyl acetate) gave title compound as white solid, 1.22 g, 62~ yield.
C. trans-9-[4-[5-(Benzoylamino)-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamid.e To a stirred solution of 699 mg (1.45 mmol) of Example 1 Part B compound in 5 mL of dichloromethane at room temperature under argon was added 0.63 mL (4.8 mmol) of bromotrimethylsilane. After 1 h, the reaction mixture was evaporated to provide a thick oil. The oil was dissolved in 3 mL of dichloromethane at room temperature under argon and treated with 0.26 mL (3.0 mmol) of oxalyl chloride and 50 N,L of DMF. After 2 h, the reaction mixture was evaporated and redissolved in 3 mL of dichloromethane.
To this solution at room temperature under argon, was added 283 mg (1.45 mmol) of Example 3 Part B compound and 0.6 mL_ (4.3 mmol) of triethylamine. After 2 h, the reaction was diluted with ethyl acetate and washed once with 10~ citric acid solution, dried (MgSOq) and evaporated. Purification by flash chromatography on silica gel (5 x 15 cm column, ethyl acetate) provided title compound, white solid, mp 166-168°C, 245 mg, 29~ yield.
MICROANALYSIS Calculated for C3oH3oF3N205P + 0.5 H20:
C, 60.50; H, 5.25; N, 4.70; F, 9.57 Found: C, 60.47; H, 5.01; N, 4.62; F, 9.30.
MS (electrospray, + ions) m/e 587.
~ lie 4 traps-9-[5-[2-Oxo-5-[[[4'-(trifluoromethyl)[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide.
_ O CF3 / N/~ CF3 H I \
\ V~ ~,~0 O /
/ O~N I \
traps isomer ~ In a 5 cis-9-[5-[2-Oxo-5-{[[4'-(trifluoromethyl)[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide.
O
/ N/~ CF3 CF3 I\
\ /
O ~' O O
/ O~ \
N I
cis isomer A. 2-Amino-1,3-bis(trimethylsilyloxy)propane ost(cH3b _ ~ NH2 OSi(CH3b A stirred solution of 1.84 g (20.0 mmol) of serinol in 4.25 mL (20.1 mmol) of hexamethyldisilazane containing 1 drop of bromotrimethylsilane was heated to 180°C under argon. After 16 h, the reaction mixture was partially cooled and distilled at 0.6 Torr, collecting the fraction with by 44-47°C to give title compound as a colorless liquid, 4.05 g, 86~.
B. N-[(1,3-Dihydroxy)-2-propyl]-2-(4-tri-fluoromethylphenyl)benzamide OH OH
H
O /
CFa A solution of 4'-trifluoromethyl-2-biphenylcarbonyl chloride [prepared from 4.40 g (16.5 mmol) of the corresponding carboxylic acid] in 10 mL of THF was added dropwise to a solution of 3.88 g (16.5 mmol) of Part A
compound and 2.40 mL (17.2 mmol) of triethylamine in 20 mL
of THF at 0°C over 10 min. The resulting slurry was stirred for 1 h, diluted with ether, filtered and the filtrate evaporated. The residual oil was dissolved in 50 mL of methanol and treated with 0.5 mL of 4 N_t hydrogen chloride in dioxane. After stirring at room temperature for 1 h, the reaction mass was evaporated and the white solid recrystallized from ethyl acetate/hexane to give title compound, mp 146-148°C, 5.08 g, 91~k yield.
C.
CONHCHzCF3 _ w _ ~ ~ ~ P03Eiz C(1) .
O
OH
Br To a solution of 9-fluorenecarboxylic acid (Aldrich) (10 g, 48 mmol) in THF (250 mL) at 0°C was added dropwise a solution of n-butyllithium (2.5M, 42.2 mL, 106 mmol) in THF. The yellow reaction was stirred at 0°C for 1 h, then 1,5-dibromobutane (16.8 mL, 124 mmol) was added dropwise over 30 min. The reaction was stirred at 0°C for 30 min, then the reaction was warmed to RT for 30 h. The reaction was extracted with water (3 x 150 mL). The combined aqueous layers were extracted with ethyl ether (160 mL). The aqueous layer was made acidic with HC1 solution (1N, 100 mL), then extracted with dichloromethane (3 x 150 mL). The combined organic layers were dried over MgS04. Evaporation gave title compound as a white solid.
C(2) .
Br To a solution of all of Part C(1) acid and DMF (20 u.L) in CHZC12 (120 mL) under argon at 0'C was added oxalyl chloride (24 mL, 2.0 M in CH2C12, 48 mmol) dropwise. The reaction was stirred at 0'C for 10 min, then warmed to RT
and stirred for 1.5 h. The reaction was concentrated in vacuo to give the crude acid chloride as a yellow oil. To a suspension of 2,2,2-trifluoroethylamine hydrochloride (6.51 g, 48 mmol) in CHZC12 (125 mL) at 0°C under argon was added triethylamine (16 mL, 115 mmol) followed by dropwise addition of a solution of the crude acid chloride in CH2C12 (15 mL). The reaction was stirred at 0'C for 1 h, diluted with CH2C12 (120 mL), and washed with water (2 x 100 mL), 1N HC1 (2 x 100 mL), saturated NaHC03 (2 x 100 mL), and brine (2 x 100 mL), then dried over MgS04. Evaporation gave 17.6 g of an oil which was purified by flash chromatography on silica gel (500 g). The crude product was loaded in a mixture of CHZC12 and hexane, and eluted with a step gradient of 10~ EtOAc/hexane (4L) to 15~
EtOAc/hexane (2L) to 20~ EtOAc/hexane (4L). Pure fractions were combined and evaporated to give title compound (14.7 g, 72~) as a white solid ( m.p. 92-96°C).
C(3) .
Ht~--~ O ~-CHa O ~~ ~CH3 O
A solution of 2.69 g (6.11 mmol) of Part C(2) compound in 15 mL of freshly distilled triethylphos-phite under argon was heated to 180°C for 16 h. The reaction was cooled and then the volatiles were distilled off at 100°C
at 1 Torr. The residue was triturated in ether to give title compound (2.25 g, 74~) as a white solid (mp 141-143°C) .
D. traps-9-[5-[2-Oxo-5-[[[4'-(trifluoro-methyl)[l,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide SExamDle 4) E. cis-9-(5-[2-Oxo-5-([[4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide ~ .xa le 5 ) To a stirred solution of 1.68 g (3.42 mmol) of Part C compound in 10 mL of dichloromethane at room temperature under argon was added 1.35 mL (10.0 mmol) of bromotrimethylsilane. After 14 h, the reaction mixture was evaporated to provide a thick oil. The oil was dissolved in 10 mL of dichloromethane at room temperature under argon and treated with 0.91 mL (10.5 mmol) of oxalyl chloride and 50 ~1.L of DMF. After 2 h, the reaction mixture was evaporated and redissolved in 10 mL of dichloromethane. To this solution at room temperature under argon, was added 1.09 g (3.2 mmol) of Part B compound and 1.0 mL (7.0 mmol) of triethylamine. After 1 h, the reaction was diluted with ethyl acetate and washed once with 10~ citric acid solution, dried (MgSO,) and evaporated. Purification by flash chromatography on silica gel (5 x 20 cm column, 2 L
85:15 ethyl acetate/hexanes, then 2 L 3:97 methanol/ethyl acetate) provided two fractions.
The less polar fraction was designated Part D (Example 4) compound, white solid, mp 165-167°C, 805 mg, 34~ yield.
MICROANALYSIS Calculated for C38H35F6N205P + 0.38 H20:
C, 60.73; H, 4.80; N, 3.73; F, 15.17; P, 4.12 Found: C, 60.73; H, 4.70; N, 3.60; F, 15.33; P, 3.88.
MS (electrospray, + ions) m/e 745.
The more polar fraction was designated Part E
(Example 5), compound, white foam, mp 110-114°C, 650 mg, 27~.
MICROANALYSIS Calculated for C3gH35F6N205P + 0.38 H20:
C, 60.73; H, 4.80; N, 3.73; P, 4.12 Found: C, 60.74; H, 4.78; N, 3.55; P, 3.84.
MS (electrospray, + ions) m/e 745.
~xa~le 6 trans-[2-Oxo-2-[4-[9-[[(2,2,2-trifluoroethyl)amino]carbonyl]-9H-fluoren-9-yl]butyl]-1,3,2-dioxaphosphorinan-5-yl]carbamic acid, phenylmethyl ester.
O
N/.. CF3 H
i o N
HH /
traps isomer A. N-Benzyloxycarbonyl-1,3-dihydroxy-2-aminopropane OH
H
O~ OH
O
To a stirred slurry of 1.00 g (4.24 mmol) of Example 5 Part A compound and 0.65 mL (4.7 mmol) of triethylamine in 10 mL of THF at 0°C under argon, was added dropwise, 0.6 mL (4.2 mmol) of benzyloxy carbonyl chloride (Aldrich) over 10 min. The reaction was allowed to warm to room temperature and stirred for 14 h. The reaction mixture was diluted with ether and filtered. The filtrate was evaporated, the residue dissolved in 25 mL of methanol to which 2 drops of 4 ~ hydrogen chloride in dioxane was added and the solution heated to 40°C for 30 min. Evaporation and trituration with hexane/ether gave title compound as a white solid, mp 104-106°C, 880 mg, 92~ yield.
MS (electrospray, + ions) m/z 226.
B. traps-[2-Oxo-2-[4-[9-[[(2,2,2-trifluoro-ethyl)amino]carbonyl]-9H-fluoren-9-yl]butyl]-1,3,2-dioxaphosphorinan-5-yl]carbamic acid, phenvlmethyl ester To a stirred solution of 1.76 g (3.64 mmol) of Example 1 Part B compound in 5 mL of dichloromethane at room temperature under argon was added 1.65 mL (12.6 mmol) of bromotrimethylsilane. After 1 h, the reaction mixture was evaporated to provide a thick oil. The oil was dissolved in 20 mL of dichloromethane at room temperature under argon and treated with 1.2 mL (13.8 mmol) of oxalyl chloride and 100 ~t.L of DMF. After 2 h, the reaction mixture was evaporated and redissolved in 5 mL of dichloro-methane. To this solution at room temperature under argon, was added 820 mg (3.64 mmol) of Part A compound and 1.1 mL
(7.9 mmol) of triethylamine. After 2 h, the reaction was diluted with ethyl acetate and washed once with 10~ citric acid solution, dried (MgSO,) and evaporated. Purification by flash chromatography on silica gel (5 x 25 cm column, 85:15 ethyl acetate/hexane) provided title compound, white solid, mp 160-163°C, 535 mg, 23~ yield.
MS (electrospray, + ions) m/e 617.
~~'~.1 1~
traps-1-(Phenylmethyl)-N-[2-[4-[9-[[(2,2,2-trifluoroethyl)amino)carbonylJ-9H-fluoren-9-yl]butyl]-1,3,2-dioxaphosphorinan-5-yl]-2-piperidinecarboxamide, -hydrochloride.
O
/ ~ CFa /
H ~O O \
V-- ~.
/ O I H
H
traps isomer A. N-Benzylpipecolic acid hydrochloride ~HCI
A mixture of ethyl pipecolinate hydrochloride (10 g, 52 mmol), benzylbromide (7 mL, 57 mmol) and potassium carbonate (15 g, 114 mmol) in DNIF' (80 mL) was stirred at room temperature overnight. The solvent was removed in v cuo. The residue was partitioned between dichloromethane (100 mL) and water (50 mL). The aqueous layer was extracted with dichloromethane (2 x 100 mL), dried over Na2S04, then evaporated to give a yellow oil. The crude product was chromatographed (500 g silica gel) eluting with a stepgradient of 8~-15~ ethyl acetate in hexane. Pure fractions were combined to give title compound (12.3 g, 96~) as a colorless oil.
B. traps-1-(Phenylmethyl)-N-[2-[4-[9-[[(2,2,2-trifluoroethyl)amino]carbonyl]-9H-fluoren-9-yl]butyl]-1,3,2-dioxaphosphorinan-5-vll-2-uineridinecarboxamide. hvdrochloride An argon-purged slurry of 51.1 mg (0.829 mmol) of Example 6 compound and 100 mg of 10~ palladium-on-charcoal in 5 mL of ethanol at room temperature was partially evacuated and subjected to hydrogenation from a filled balloon. After 16 h, the reaction mixture was purged with argon and filtered through a 0.45 ~ nylon filter.
Evaporation and then re-evaporation from dichloromethane -gave a white foam. This material was dissolved in 10 mL of dichloromethane and stirred under argon at room temperature while 212 mg (0.83 mmol, HC1 salt) of Part A compound, 125 mg (0.83 mmol) of HOBt, 175 mg (0.92 mmol) of EDCI and 175 ~tL (1.26 mmol) of triethylamine were added. After 6 h, the reaction mixture was quenched with saturated sodium bicarbonate solution and extracted twice with ethyl acetate. The organic extracts were combined, dried (MgS04) and evaporated. Purification by flash chromatography on silica gel (5 x 20 cm column, ethyl acetate) provided the free base of title compound. This material was dissolved in dichloromethane, treated with 0.3 mL of 4 ~! hydrogen chloride in dioxane and evaporated to provide title compound as a white solid, mp 125-128°C, 365 mg, 61~ yield.
MICROANALYSIS Calculated for C36HaiF3NsOsP+HCl+1 dioxane+0.33 H20:
C, 59.01; H, 6.27; N, 5.16; C1, 4.35; F, 7.00 Found: C, 59.00; H, 6.25; N, 5.11; C1, 4.14; F, 6.96.
MS (electrospray, + ions) m/e 684.
E~c~mple 8 traps-9-[4-[2-Oxo-5-[[2-(2-pyridinyl)benzoyl]amino]-7 ,3,2-dioxaphosphorinan 2-yi]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide, hydrochloride.
O
i\
\ ~'~--\ ~~~° o / ~ N \
H
traps isomer WO 99/21564 PC"1'/US98/21750 A. 2-(2-Pyridyl)benzoic acid O ~N
HO
A(1). 2-Methyl -1-(2-pyridyl)benzene I ~1 iN
/ I
To a degassed solution of 2-bromopyridine (1.9 mL, 20 mmol) in ethylene glycol dimethyl ether (60 mL) under argon, tetrakis(triphenylphosphane) palladium (o) (700 mg, 0.6 mmol) was added. After stirring for 10 min, 2-methylphenyl boronic acid (2.9 g, 22 mmol) was added, followed by sodium bicarbonate solution (5.04 g, 60 mmol in 60 mL water). The mixture was heated to reflux (-- 85°C) and stirred overnight. After cooling to room temperature, the solvent was evaporated, the residue was partitioned between water and ether, and the aqueous layer was extracted twice with ether. The combined organic layers were dried (Na2S04), and the solvent was evaporated to give a black oil. This oil was distilled at cl Torr at ~95°C to give title compound (2.75 g, 82~ yield) as a clear oil.
A(2) .
I ~1 ~N
COOH
A solution of Part A(1) compound (850 mg, 5.0 mmol) and potassium permanganate (1.9 g, 12.0 mmol) in water (25 mL) was heated to reflux and stirred for 1 hour. The hot reaction mixture was filtered, and the filtrate was evaporated to dryness. The solid residue was dissolved in_-water (5 mL) and acidified with acetic acid to pH 4-5. The resulting precipitate was isolated by filtration and rinsed with water to give a white solid (800 mg) which was recrystallized from hot ethanol (12 mL) to give title compound as a white solid (453 mg, 45~ yield).
B. traps-9-[4-[2-Oxo-5-[[2-(2-pyridinyl)-benzoyl]amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluor dye-9-carboxamide, hydrochloride An argon-purged slurry of 505 mg (0.82 mmol) of Example 6 compound and 100 mg of 10~ palladium-on-charcoal in 10 mL of methanol at room temperature was partially evacuated and subjected to hydrogenation from a filled balloon. After 4 h, the reaction mixture was purged with argon and filtered through a 0.45 ].~, nylon filter.
Evaporation and then re-evaporation from toluene gave a white foam. This material was dissolved in 10 mL of dichloromethane and stirred under argon at room temperature while 169 mg (0.83 mmol) of Part A compound, 162 mg (0.85 mmol) of EDCI and 60 N.L (0.43 mmol) of triethylamine were added. After 16 h, the reaction mixture was quenched with saturated sodium bicarbonate solution and extracted twice with ethyl acetate. The organic extracts were combined, dried (Na2S04) and evaporated. Purification by flash chromatography on silica gel (5 x 15 cm column, 1:24 methanol/ethyl acetate) provided the free base of the title compound. This material was dissolved in dichloromethane, treated with 0.3 mL of 4 ~! hydrogen chloride in dioxane and evaporated to provide title compound as a white solid, mp 132-136°C, 524 mg, 81~ yield.
MICROANALYSIS Calculated for C35H33F3N305P + HCl + dioxane +
0.25 H20: _-C, 59.09; H, 5.40; N, 5.30; C1, 4.47; F, 7.19;
P, 3 . 91 Found: C, 59.12; H, 5.28; N, 5.24; Cl, 4.48; F, 7.37;
P, 4.08.
MS (electrospray, + ions) m/e 664.
Example 9 traps-9-[4-[5-[[2-(2-Benzothiazolyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide.
/ N CFa H
~N
~, S
P O
O
H
traps isomer A.
H
O
S
Part A compound is a commercial compound supplied by Maybridge Chemical Company.
B. traps-9-[4-[5-[[2-(2-Benzothiazolyl) benzoyl]amino]-2-oxo-1,3,2-dioxaphos-phorinan-2-yl]butyl]-N-(2,2,2-trifluoro-e~~y~,-9H-fluorene-9-carboxamide An argon-purged slurry of 371 mg (0.60 mmol) of Example 6 compound and 90 mg of 10~ palladium-on-charcoal in 10 mL of methanol at room temperature was partially evacuated and subjected to hydrogenation from a filled balloon. After 4 h, the reaction mixture was purged with argon and filtered through a 0.45 ~. nylon filter.
Evaporation and then re-evaporation from toluene gave a white foam. This material was dissolved in 5 mL of dichloromethane and stirred under argon at room temperature_-while 153 mg (0.60 mmol) of Part A compound, 114 mg (0.60 mmol) of EDCI and 42 ~,L (0.3 mmol) of triethylamine were added. After 16 h, the reaction mixture was quenched with saturated sodium bicarbonate solution and extracted twice with ethyl acetate. The organic extracts were combined, dried (Na2S04) and evaporated. Purification by flash chromatography on silica gel (5 x 15 cm column, 1:3 hexanes/ethyl acetate) provided title compound as a white solid, mp 117-118°C, 269 mg, 62~ yield.
MICROANALYSIS Calculated for C37H33F3N305PS:
C, 61.75; H, 4.62; N, 5.84; F, 7.92; S, 4.45;
P, 4.30 Found: C, 62.02; H, 4.97; N, 5.55; F, 7.64; S, 4.06;
P, 4.42.
MS (electrospray, + ions) m/e 720.
Example 10 traps-9-[4-[5-[[2-(4-Morpholinyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-triouoroethyl)-9H-fluorene-9-carboxamide.
O
/ _ N CF3 O
H
\ ~ ~P, O N
J oJ' H
traps isomer A. 2-(1-Morpholino)benzoic acid C~~
O N
HO
A(1). Methyl 2-(1-morpholino)benzoate A solution of methyl 2-fluorobenzoate (15.4 g, 100 mmol) in morpholine (44 mL, 500 mmol) was heated at 50°C
for 30 min, and then warmed to 100°C and stirred for 2 h, then cooled to 50°C and stirred overnight. The reaction was then heated to reflex for 2.5 h. The excess morphol.ine was evaporated. The remainder was dissolved in ethyl acetate and washed successively with H20 (50 mL), saturated NaHC03 solution (2 x 50 mL), H20 (3 x 50 mL) and brine (50 mL). Drying (MgS04) and evaporation gave a yellow oil.
The crude product was dissolved in dichloromethane/ethyl acetate/hexane (4:1:4) and chromatographed (400 g silica gel) eluting with a step gradient of 20~ to 35~ ethyl acetate in hexane. Pure fractions were combined and evaporated to give title compound (10.5 g, 48~) as an oil which crystallized on standing to a white solid.
A(2). 2-(1-Morpholino)benzoic acid O CN
HO
Sodium hydroxide (10 g, 250 mmol) was dissolved in water (75 mL) and added to a solution of Part A(1) compound (10.4 g, 47.1 mmol) in methanol (75 mL). The reaction was stirred at RT for 1 h and the solvent was evaporated. The white residue was dissolved in H20 (100 mL) and adjusted to pH 1.5 with 1N HC1. The aqueous layer was extracted with chloroform (3 x 250 mL). The combined organic layers were - s7 -WO 99/21564 PCT/US9$/21750 dried (Na2S04) and evaporated to give title compound (9.76 g, 85~) as a white solid (m. p. 156-157°C).
B. traps-9-[4-[5-[[2-(4-Morpholinyl)-benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-f luo~"rene-9 -carboxamide An argon-purged slurry of 359 mg (0.582 mmol) of Example 6 compound and 100 mg of 10~ palladium-on-charcoal in 15 mL of methanol at room temperature was partially evacuated and subjected to hydrogenation from a filled balloon. After 16 h, the reaction mixture was purged with argon and filtered through a 0.45 ).~, nylon filter.
Evaporation and then re-evaporation from toluene gave a white foam. This material was dissolved in 5 mL of dichloromethane and stirred under argon at room temperature while 121 mg (0.584 mmol) of Part A compound, 88 mg (0.59 mmol) of HOBt, 122 mg (0.64 mmol) of EDCI and 41 N,L (0.3 mmol) of triethylamine were added. After 6 h, the reaction mixture was quenched with saturated sodium bicarbonate solution and extracted twice with ethyl acetate. The organic extracts were combined, dried (Na2S04) and evaporated. Purification by flash chromatography on silica gel (5 x 20 cm column, ethyl acetate) provided title compound as a white solid, mp 108-111°C, 265 mg, 66~ yield.
MICROANALYSIS Calculated for C34H37F3N306P+0.15 H20+0.23 EtOAc:
C, 60.38; H, 5.68; N, 6.05; F, 8.21 Found: C, 60.37; H, 5.54; N, 5.93; F, 7.91.
MS (electrospray, + ions) m/e 695.
dole 11 traps-9-[4-[5-[[2-(2-Benzoxazolyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide. -O
I / N~ CFA
H
~N
\ ~~ O O
P. O
/ O~ N '"
H
A. 2-(2-Bromophenyl)benzoxazole Br O
To a stirred slurry of 5.46 g (50.0 mmol) of 2-aminophenol (Aldrich) and 10.05 g (50.0 mmol) of 2-bromobenzoic acid in 100 mL of xylenes under argon at room temperature was added 6.10 g (100 mmol) of boric acid.
Using a Dean-Stark trap, the reaction was heated to refiux for 48 h. A total of 3.2 mL of water was separated. The reaction mixture was cooled, diluted with ethyl acetate and filtered. The filtrate was washed once with 3 ~i hydrochloric acid, once with water and three times with saturated sodium bicarbonate solution. The organic phase was dried (MgSO,) and evaporated. Purification by flash chromatography on silica gel (5x20 cm column, 2:1 dichloromethane/hexane) gave title compound as a light yellow solid, 5.90 g, 43~.
B. 2-(2-Benzoxazolyl)benzoic acid To a stirred solution of 700 mg (2.55 mmol) of Part A compound in 10 mL of THF under argon at -78°C was added a solution of t-butyllithium (3.3 mL, 1.7 A~, 5.6 mmol) in pentane over the course of 30 min. The reaction mixture was stirred for 1 h and then a dry stream of carbon dioxide gas was passed through the solution for lh. The reaction was allowed to warm to room temperature in situ. After 16 h, the mixture was diluted with ether and washed once with 50 mL of 10~ sodium hydroxide solution. The aqueous phase was adjusted to pH 3.5 using solid citric acid. The resulting solid was filtered, washed with water and air-dried to give 610 mg of title compound as a pink solid, mp >250°C, 100.
C. trans-9-[4-[5-[[2-(Benzoxazolyl)benzoyl]-amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide To a stirred solution of 117 mg (0.24 mmol) of Example 6 compound under argon at room temperature in 3 mL
of dichloromethane was added 72 mg (0.30 mmol) of Part B
compound, 45 mg (0.3 mmol) of HOBt, 65 mg (0.30 mmol) of EDCI and 20 ElL (0.15 mmol) of triethylamine. After 16 h, the reaction mixture was quenched with saturated sodium bicarbonate solution and extracted twice with ethyl acetate. The organic extracts were combined, dried (Na2S04) and evaporated. Purification by flash chromatography on silica gel (2.5 x 15 cm column, 1:3 hexanes/ethyl acetate) provided title compound as a white solid, mp 104-107°C, 38 mg, 20~ yield.
WO 99/21564 PCTlUS98/21750 MICROANALYSIS Calculated for C37H3gF3N306P+2 . 3 H20+0 . 5 EtOAc :
C, 59.36; H, 5.31; N,5.32; F, 7.22; P, 3.92 _ Found: C, 59.32; H, 5.24; N,5.43; F, 7.45; P, 4.20.
MS (electrospray, + ions) m/e 704.
Following are examples of additional compounds of the invention which may be prepared employing procedures described hereinbefore and in Examples 1 to 11. Although the following compounds are shown in the form of cis-isomers, in accordance with the invention, the corresponding trans-isomers are covered as well.
Fs I i I i I
HN
F3C-~ O O,p~, O
F I ~ I ~ F F3 i ~ O I
HN
F3C-~ O~P\' O
O O~N w H
O
R2~LsA~B.LsP~
O~NCOR~
R5a I\ I\ I
/ / I\
HN /
F3~ O~P~- O
o ~~ I \
O
/
I \ I \ F3 / / I\
HN O /
F3G-J O\~p~, O O°TH~2 -H I \
I \ ~ \ I
/ / I\
HN ~ O / CI
F3CrJ O
O O~H I W
WO 99/Z1564 PCT/US98/21'750 \ \
I/ I/ I\
HN /
F3C~ O~P\ O
O O~~ I \
\ ~. N
I/ I/ ~ I\
HN /
F3G- J O~P\~ O
O O~.H I \
/
I \ I ~.. F3 / / I\
HN ~ O /
FsG-/ O F F U P\' p H I/
\ \
i/ I/ /I
HN " ~ O O
F G-~ O
O ~Pp-~H I \
I ~ I ~ -/ /
HN ' ~ O H2SPh F3C~ O ~ Pp~-N
H I/
I ~ I ~ F3 / /
I
HN O /
F3G-J O c~-~
O~ p~N ( w ~' I ~
/ /
F3G-~ O ~ P~ p~
O _ H I /
I
/ /
H /
O~p~ O
O O~N
N H I /
I ~ I ~
/ /
HN O
F3C~ O
O
/
I ~ I ~ F3 / /
HN ~ O /
F GJ O p' 3 O, O~H I W
/ /
F3Cr-~ O O P~,.
O~-N
Claims
What is Claimed is:
1. A compound which has the structure including pharmaceutically acceptable salts thereof, N-oxides thereof, wherein A is (1) a bond;
(2) -O-, or (3) where R5 is H or lower alkyl, or R5 together with R2 forms a carbocyclic or heterocyclic ring system containing 4 to 8 members in the ring;
B is a fluorenyl-type group of the structure B is an indenyl-type group of the structure R a and R b may be the same or different and are hydrogen, alkyl, aryl, arylalkyl or heteroaryl linked to the ring via a carbon atom.
R5a is H, lower alkyl or aryl;
R1 is independently alkyl, alkenyl, alkynyl, aryl, alkoxy, aryloxy, arylalkoxy, heteroaryl, heteroarylalkoxy, arylalkyl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl, polycycloalkyl, polycycloalkylalkyl, cycloalkenyl, cycloheteroalkyl, heteroaryloxy, cycloalkenylalkyl, polycycloalkenyl, polycycloalkenylalkyl, heteroarylcarbonyl, amino, alkylamino, arylamino, heteroarylamino, cycloalkyloxy, cycloalkylamino, all optionally substituted through available carbon atoms with 1, 2, 3 or 4 groups selected from hydrogen, halo, alkyl, halo-alkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl, aryl, heteroaryl, arylalkyl, arylcycloalkyl, arylalkenyl, arylalkynyl, aryloxy, aryloxyalkyl, arylalkoxy, arylazo, heteroaryloxo, heteroarylalkyl, heteroarylalkenyl, heteroaryloxy, hydroxy, nitro, cyano, amino, substituted amino, thiol, alkylthio, arylthio, heteroarylthio, arylthioalkyl, alkylcarbonyl, arylcarbonyl, arylaminocarbonyl, alkoxycarbonyl, aminocarbonyl, alkynylaminocarbonyl, alkylaminocarbonyl, alkenylaminocarbonyl, alkylcarbonyloxy, arylcarbonyloxy, alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfinylalkyl, arylsulfonyl, alkylsulfonyl, arylsulfonylamino, heteroarylcarbonylamino, heteroarylsulfinyl, heteroarylthio, heteroarylsulfonyl, alkylsulfinyl; or R1 and R5a can be joined to form a ring of the structure where J is: CHR23, R23, R24 and R25 are independently hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl, or cycloalkylalkyl;
R20, R21, R22 are independently hydrogen, halo, alkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, hydroxy or haloalkyl; and these substituents may either be directly attached to R1, or attached via an alkylene at an open position;
R2 is hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, alkoxyl, (alkyl or aryl)3Si (where each alkyl or aryl group is independent), cycloalkyl, cycloalkenyl, substituted alkylamino, substituted arylalkylamino, aryl, arylalkyl, arylamino, aryloxy, heteroaryl, heteroarylamino, heteroaryloxy, arylsulfonylamino, heteroarylsulfonylamino, arylthio, arylsulfinyl, arylsulfonyl, alkylthio, alkylsulfinyl, alkylsulfonyl, heteroarylthio, heteroarylsulfinyl, heteroarylsulfonyl, cycloheteroalkyl, cycloheteroalkylalkyl, -PO(R13)(R14), (where R13 and R14 are independently alkyl, aryl, alkoxy, aryloxy, heteroaryl, heteroarylalkyl, heteroaryloxy, heteroarylalkoxy, cycloheteroalkyl, cycloheteroalkylalkyl, cycloheteroalkoxy, or cycloheteroalkylalkoxy); cyano, 1,1-(alkoxyl or aryloxy)2alkyl (where the two aryl or alkyl substituents can be independently defined), R2 may be substituted with 1, 2, 3 or 4,substituents, which can be any of substituents for R1, or haloalkylamino, alkylamino, cycloalkylamino, arylamino, heteroarylamino, alkoxyamino, aryloxyamino, heteroaryloxylamino, heterocyclylamino (where the heterocycle is connected to the carbonyl group via a nitrogen or carbon atom);
L1 is a linking group containing from 1 to 10 carbons in a linear chain including alkylene, alkenylene or alkynylene, which may contain, within the linking chain any of the following: one or two alkenes, one or two alkynes, an oxygen, an amino group, an oxo group, and may be substituted with one to five alkyl or halo groups;
L2 may be the same or different from L1 and may independently be any of the L1 groups set out above or a singe bond;
R3, R3', R4 and R4' may be the same or different and are independently selected from H, halogen, CF3, haloalkyl, hydroxy, alkoxy, alkyl, aryl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, alkanoyl, nitro, amino, thiol, alkylthio, alkylsulfinyl, alkylsulfonyl, carboxy, alkoxycarbonyl, aminocarbonyl, alkylcarbonyloxy, alkylcarbonylamino, cycloheteroalkyl, cycloheteroalkylalkyl, cyano, Ar-, Ar-alkyl, ArO, Ar-amino, Ar-thio, Ar-sulfinyl, Ar-sulfonyl, Ar-carbonyl, Ar-carbonyloxy or Ar-carbonylamino, wherein Ar is aryl or heteroaryl and Ar may optionally include 1, 2 or 3 additional rings fused to Ar;
R3a and R3b are the same or different and are independently any of the R3 groups;
are the same or different and independently represent a 5 or 6 membered heteroaryl ring which contains 1, 2, 3 or 4 heteroatoms in the ring which are independently N, S or O;
and including N-oxides;
X is a bond, or is one of the following groups:
(2) -o- ;
wherein Y is 0, N-R6 or S;
n' is 0, 1 or 2;
R6 is H, lower alkyl, aryl, -C(O)-R11 or -C(O)-O-R11;
R7 and R8 are the same or different and are independently H, alkyl, aryl, halogen, -O-R12, or R7 and R8 together can be oxygen to form a ketone;
R9, R10, R9' and R10' are the same or different and are independently H, lower alkyl, aryl or -O-R11;
R9° and R10° are the same or different and are independently H, lower alkyl, aryl, halogen or -O-R11;
R11 is alkyl or aryl;
R12 is H, alkyl or aryl;
with the proviso that when A is a (1) bond, R2L2 cannot be H.
2. The compound as defined in Claim 1 wherein A is a bond.
3. The compound as defined in Claim 1 wherein A is -O-.
4. The compound as defined in Claim 1 wherein A is 5. The compound as defined in Claim 1 wherein B is a fluorenyl-type group.
6. The compound as defined in Claim 1 wherein B is an indenyl-type group.
7. The compound as defined in Claim 1 wherein B is A is NH;
X is a bond, oxygen or sulfur;
R3 and R4 are the same or different and are H or F;
R1 is aryl, phenyl, biphenyl or cycloheteroalkyl;
R2 is aryl, phenyl, heteroaryl, imidazolyl, pyridyl, cyclohexyl, PO(R13)(R14), heteroarylthio, benzthiazole-2-thio, imidazole-2-thio, alkyl, alkenyl or 1,3-dioxan-2-yl, wherein each of the above is optionally substituted;
L1 is a chain containing 1 to 5 atoms in a linear chain;
L2 is a bond or lower alkylene.
8. The compound as defined in Claim 1 which is (E)-9-[4-[2-oxo-5-[[[4'-(trifluoromethyl)[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
(Z)-9-[4-[2-oxo-5-[[[4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[4-[5-(benzoylamino)-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[5-[2-oxo-5-[[[4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
cis-9-[5-[2-oxo-5-[[[4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-[2-oxo-2-[4-[9-[[(2,2,2-trifluoroethyl)-amino]carbonyl]9H-fluoren-9-yl]butyl]-1,3,2-dioxa-phosphorinan-5-yl]carbamic acid;
trans-1-(phenylmethyl)-N-[2-[4-[9-[[(2,2,2-trifluoroethyl)amino]carbonyl]-9H-fluoren-9-yl]-butyl]
1,3,2-dioxaphosphorinan-5-yl]-2-piperidinecarboxamide;
trans-9-[4-[2-oxo-5-[[2-(2-pyridinyl)benzoyl]-amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[4-[5-[[2-(2-benzothiazolyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[4-[5-[[2-(4-morpholinyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
traps-9-[4-[5-[[2-(2-benzoxazolyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide or an ester thereof or an N-oxide thereof, or a pharmaceutically acceptable salt thereof.
9. The compound as defined in Claim 1 having the structure 11. The compound as defined in Claim 1 having the name (E)-9-[4-[2-oxo-5-[[[4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxa-phosphorinan-2-yl]butyl)-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[4-(5-(benzoylamino)-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoro-ethyl)-9H-fluorene-9-carboxamide;
trans-9-[5-[2-oxo-5-[[[4'-(trifluoromethyl)-[1,1'-biphenyl)-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-[2-oxo-2-[4-[9-[[(2,2,2-trifluoroethyl)-amino]carbonyl]9H-fluoren-9-yl]butyl]-1,3,2-dioxa-phosphorinan-5-yl]carbamic acid;
trans-1-(phenylmethyl)-N-[2-[4-[9-[[(2,2,2-trifluoroethyl)amino]carbonyl]-9H-fluoren-9-yl]butyl]-1,3,2-dioxaphosphorinan-5-yl]-2-piperidinecarboxamide;
trans-9-[4-[2-oxo-5-[[2-(2-pyridinyl)benzoyl]-amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[4-[5-[[2-(2-benzothiazolyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[4-[5-[[2-(4-morpholinyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
traps-9-[4-[5-[[2-(2-benzoxazolyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide; or an N-oxide thereof, or pharmaceutically acceptable salts thereof or esters thereof.
12. The compound as defined in Claim 1 wherein A is NH and R2L2 is CF3CH2.
13. A method for preventing, inhibiting or treating atherosclerosis, pancreatitis, hyperglycemia or obesity in a mammalian species, which comprises administering to a patient in need of treatment a therapeutically effective amount of a compound as defined in Claim 1.
14. A method of lowering serum lipid levels, cholesterol and/or triglycerides, or inhibiting and/or treating hyperlipemia, hyperlipidemia, hyperlipoproteinemia, hypercholesterolemia and/or hypertriglyceridemia, and/or preventing, inhibiting or treating atherosclerosis, pancreatitis or obesity in a mammalian species, which comprises administering to a patient in need of treatment a therapeutically effective amount of a compound as defined in Claim 1.
15. The method as defined in Claim 14 where B is A is NH;
X is a bond, oxygen or sulfur;
R3 and R4 are the same or different and are H or F;
R1 is aryl, phenyl, biphenyl or cycloheteroalkyl;
R2 is aryl, phenyl, heteroaryl, imidazolyl, pyridyl, cyclohexyl, PO(R13)(R14), heteroarylthio, benzthiazole-2-thio, imidazole-2-thio, alkyl or alkenyl, 1,3-dioxan-2-yl, wherein each of the above is optionally substituted;
L1 is a chain containing 1 to 5 atoms in a linear chain;
L2 is a bond or lower alkylene.
16. The method as defined in Claim 13 where B is X is a bond, oxygen or sulfur;
R3 and R4 are the same or different and are H or F;
R2 is aryl, phenyl, heteroaryl, imidazolyl, pyridyl, cyclohexyl, PO(R13)(R14), heteroarylthio, benzthiazole-2-thio, imidazole-2-thio, alkyl or alkenyl, 1,3-dioxan-2-yl, wherein each of the above is optionally substituted;
R1 is phenyl, biphenyl or piperidine;
L1 is a chain containing 1 to 5 atoms in a linear chain;
L2 is a bond or lower alkylene.
1. A compound which has the structure including pharmaceutically acceptable salts thereof, N-oxides thereof, wherein A is (1) a bond;
(2) -O-, or (3) where R5 is H or lower alkyl, or R5 together with R2 forms a carbocyclic or heterocyclic ring system containing 4 to 8 members in the ring;
B is a fluorenyl-type group of the structure B is an indenyl-type group of the structure R a and R b may be the same or different and are hydrogen, alkyl, aryl, arylalkyl or heteroaryl linked to the ring via a carbon atom.
R5a is H, lower alkyl or aryl;
R1 is independently alkyl, alkenyl, alkynyl, aryl, alkoxy, aryloxy, arylalkoxy, heteroaryl, heteroarylalkoxy, arylalkyl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl, polycycloalkyl, polycycloalkylalkyl, cycloalkenyl, cycloheteroalkyl, heteroaryloxy, cycloalkenylalkyl, polycycloalkenyl, polycycloalkenylalkyl, heteroarylcarbonyl, amino, alkylamino, arylamino, heteroarylamino, cycloalkyloxy, cycloalkylamino, all optionally substituted through available carbon atoms with 1, 2, 3 or 4 groups selected from hydrogen, halo, alkyl, halo-alkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl, aryl, heteroaryl, arylalkyl, arylcycloalkyl, arylalkenyl, arylalkynyl, aryloxy, aryloxyalkyl, arylalkoxy, arylazo, heteroaryloxo, heteroarylalkyl, heteroarylalkenyl, heteroaryloxy, hydroxy, nitro, cyano, amino, substituted amino, thiol, alkylthio, arylthio, heteroarylthio, arylthioalkyl, alkylcarbonyl, arylcarbonyl, arylaminocarbonyl, alkoxycarbonyl, aminocarbonyl, alkynylaminocarbonyl, alkylaminocarbonyl, alkenylaminocarbonyl, alkylcarbonyloxy, arylcarbonyloxy, alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfinylalkyl, arylsulfonyl, alkylsulfonyl, arylsulfonylamino, heteroarylcarbonylamino, heteroarylsulfinyl, heteroarylthio, heteroarylsulfonyl, alkylsulfinyl; or R1 and R5a can be joined to form a ring of the structure where J is: CHR23, R23, R24 and R25 are independently hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl, or cycloalkylalkyl;
R20, R21, R22 are independently hydrogen, halo, alkyl, alkenyl, alkoxy, aryloxy, aryl, arylalkyl, alkylmercapto, arylmercapto, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, hydroxy or haloalkyl; and these substituents may either be directly attached to R1, or attached via an alkylene at an open position;
R2 is hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, alkoxyl, (alkyl or aryl)3Si (where each alkyl or aryl group is independent), cycloalkyl, cycloalkenyl, substituted alkylamino, substituted arylalkylamino, aryl, arylalkyl, arylamino, aryloxy, heteroaryl, heteroarylamino, heteroaryloxy, arylsulfonylamino, heteroarylsulfonylamino, arylthio, arylsulfinyl, arylsulfonyl, alkylthio, alkylsulfinyl, alkylsulfonyl, heteroarylthio, heteroarylsulfinyl, heteroarylsulfonyl, cycloheteroalkyl, cycloheteroalkylalkyl, -PO(R13)(R14), (where R13 and R14 are independently alkyl, aryl, alkoxy, aryloxy, heteroaryl, heteroarylalkyl, heteroaryloxy, heteroarylalkoxy, cycloheteroalkyl, cycloheteroalkylalkyl, cycloheteroalkoxy, or cycloheteroalkylalkoxy); cyano, 1,1-(alkoxyl or aryloxy)2alkyl (where the two aryl or alkyl substituents can be independently defined), R2 may be substituted with 1, 2, 3 or 4,substituents, which can be any of substituents for R1, or haloalkylamino, alkylamino, cycloalkylamino, arylamino, heteroarylamino, alkoxyamino, aryloxyamino, heteroaryloxylamino, heterocyclylamino (where the heterocycle is connected to the carbonyl group via a nitrogen or carbon atom);
L1 is a linking group containing from 1 to 10 carbons in a linear chain including alkylene, alkenylene or alkynylene, which may contain, within the linking chain any of the following: one or two alkenes, one or two alkynes, an oxygen, an amino group, an oxo group, and may be substituted with one to five alkyl or halo groups;
L2 may be the same or different from L1 and may independently be any of the L1 groups set out above or a singe bond;
R3, R3', R4 and R4' may be the same or different and are independently selected from H, halogen, CF3, haloalkyl, hydroxy, alkoxy, alkyl, aryl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, alkanoyl, nitro, amino, thiol, alkylthio, alkylsulfinyl, alkylsulfonyl, carboxy, alkoxycarbonyl, aminocarbonyl, alkylcarbonyloxy, alkylcarbonylamino, cycloheteroalkyl, cycloheteroalkylalkyl, cyano, Ar-, Ar-alkyl, ArO, Ar-amino, Ar-thio, Ar-sulfinyl, Ar-sulfonyl, Ar-carbonyl, Ar-carbonyloxy or Ar-carbonylamino, wherein Ar is aryl or heteroaryl and Ar may optionally include 1, 2 or 3 additional rings fused to Ar;
R3a and R3b are the same or different and are independently any of the R3 groups;
are the same or different and independently represent a 5 or 6 membered heteroaryl ring which contains 1, 2, 3 or 4 heteroatoms in the ring which are independently N, S or O;
and including N-oxides;
X is a bond, or is one of the following groups:
(2) -o- ;
wherein Y is 0, N-R6 or S;
n' is 0, 1 or 2;
R6 is H, lower alkyl, aryl, -C(O)-R11 or -C(O)-O-R11;
R7 and R8 are the same or different and are independently H, alkyl, aryl, halogen, -O-R12, or R7 and R8 together can be oxygen to form a ketone;
R9, R10, R9' and R10' are the same or different and are independently H, lower alkyl, aryl or -O-R11;
R9° and R10° are the same or different and are independently H, lower alkyl, aryl, halogen or -O-R11;
R11 is alkyl or aryl;
R12 is H, alkyl or aryl;
with the proviso that when A is a (1) bond, R2L2 cannot be H.
2. The compound as defined in Claim 1 wherein A is a bond.
3. The compound as defined in Claim 1 wherein A is -O-.
4. The compound as defined in Claim 1 wherein A is 5. The compound as defined in Claim 1 wherein B is a fluorenyl-type group.
6. The compound as defined in Claim 1 wherein B is an indenyl-type group.
7. The compound as defined in Claim 1 wherein B is A is NH;
X is a bond, oxygen or sulfur;
R3 and R4 are the same or different and are H or F;
R1 is aryl, phenyl, biphenyl or cycloheteroalkyl;
R2 is aryl, phenyl, heteroaryl, imidazolyl, pyridyl, cyclohexyl, PO(R13)(R14), heteroarylthio, benzthiazole-2-thio, imidazole-2-thio, alkyl, alkenyl or 1,3-dioxan-2-yl, wherein each of the above is optionally substituted;
L1 is a chain containing 1 to 5 atoms in a linear chain;
L2 is a bond or lower alkylene.
8. The compound as defined in Claim 1 which is (E)-9-[4-[2-oxo-5-[[[4'-(trifluoromethyl)[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
(Z)-9-[4-[2-oxo-5-[[[4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[4-[5-(benzoylamino)-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[5-[2-oxo-5-[[[4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
cis-9-[5-[2-oxo-5-[[[4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-[2-oxo-2-[4-[9-[[(2,2,2-trifluoroethyl)-amino]carbonyl]9H-fluoren-9-yl]butyl]-1,3,2-dioxa-phosphorinan-5-yl]carbamic acid;
trans-1-(phenylmethyl)-N-[2-[4-[9-[[(2,2,2-trifluoroethyl)amino]carbonyl]-9H-fluoren-9-yl]-butyl]
1,3,2-dioxaphosphorinan-5-yl]-2-piperidinecarboxamide;
trans-9-[4-[2-oxo-5-[[2-(2-pyridinyl)benzoyl]-amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[4-[5-[[2-(2-benzothiazolyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[4-[5-[[2-(4-morpholinyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
traps-9-[4-[5-[[2-(2-benzoxazolyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide or an ester thereof or an N-oxide thereof, or a pharmaceutically acceptable salt thereof.
9. The compound as defined in Claim 1 having the structure 11. The compound as defined in Claim 1 having the name (E)-9-[4-[2-oxo-5-[[[4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl]carbonyl]amino]-1,3,2-dioxa-phosphorinan-2-yl]butyl)-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[4-(5-(benzoylamino)-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoro-ethyl)-9H-fluorene-9-carboxamide;
trans-9-[5-[2-oxo-5-[[[4'-(trifluoromethyl)-[1,1'-biphenyl)-2-yl]carbonyl]amino]-1,3,2-dioxaphosphorinan-2-yl]pentyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-[2-oxo-2-[4-[9-[[(2,2,2-trifluoroethyl)-amino]carbonyl]9H-fluoren-9-yl]butyl]-1,3,2-dioxa-phosphorinan-5-yl]carbamic acid;
trans-1-(phenylmethyl)-N-[2-[4-[9-[[(2,2,2-trifluoroethyl)amino]carbonyl]-9H-fluoren-9-yl]butyl]-1,3,2-dioxaphosphorinan-5-yl]-2-piperidinecarboxamide;
trans-9-[4-[2-oxo-5-[[2-(2-pyridinyl)benzoyl]-amino]-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[4-[5-[[2-(2-benzothiazolyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
trans-9-[4-[5-[[2-(4-morpholinyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide;
traps-9-[4-[5-[[2-(2-benzoxazolyl)benzoyl]amino]-2-oxo-1,3,2-dioxaphosphorinan-2-yl]butyl]-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide; or an N-oxide thereof, or pharmaceutically acceptable salts thereof or esters thereof.
12. The compound as defined in Claim 1 wherein A is NH and R2L2 is CF3CH2.
13. A method for preventing, inhibiting or treating atherosclerosis, pancreatitis, hyperglycemia or obesity in a mammalian species, which comprises administering to a patient in need of treatment a therapeutically effective amount of a compound as defined in Claim 1.
14. A method of lowering serum lipid levels, cholesterol and/or triglycerides, or inhibiting and/or treating hyperlipemia, hyperlipidemia, hyperlipoproteinemia, hypercholesterolemia and/or hypertriglyceridemia, and/or preventing, inhibiting or treating atherosclerosis, pancreatitis or obesity in a mammalian species, which comprises administering to a patient in need of treatment a therapeutically effective amount of a compound as defined in Claim 1.
15. The method as defined in Claim 14 where B is A is NH;
X is a bond, oxygen or sulfur;
R3 and R4 are the same or different and are H or F;
R1 is aryl, phenyl, biphenyl or cycloheteroalkyl;
R2 is aryl, phenyl, heteroaryl, imidazolyl, pyridyl, cyclohexyl, PO(R13)(R14), heteroarylthio, benzthiazole-2-thio, imidazole-2-thio, alkyl or alkenyl, 1,3-dioxan-2-yl, wherein each of the above is optionally substituted;
L1 is a chain containing 1 to 5 atoms in a linear chain;
L2 is a bond or lower alkylene.
16. The method as defined in Claim 13 where B is X is a bond, oxygen or sulfur;
R3 and R4 are the same or different and are H or F;
R2 is aryl, phenyl, heteroaryl, imidazolyl, pyridyl, cyclohexyl, PO(R13)(R14), heteroarylthio, benzthiazole-2-thio, imidazole-2-thio, alkyl or alkenyl, 1,3-dioxan-2-yl, wherein each of the above is optionally substituted;
R1 is phenyl, biphenyl or piperidine;
L1 is a chain containing 1 to 5 atoms in a linear chain;
L2 is a bond or lower alkylene.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US6334797P | 1997-10-28 | 1997-10-28 | |
US60/063,347 | 1997-10-28 | ||
PCT/US1998/021750 WO1999021564A1 (en) | 1997-10-28 | 1998-10-14 | Cyclic phosphonate ester inhibitors of microsomal triglyceride transfer protein and method |
Publications (1)
Publication Number | Publication Date |
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CA2307889A1 true CA2307889A1 (en) | 1999-05-06 |
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CA002307889A Abandoned CA2307889A1 (en) | 1997-10-28 | 1998-10-14 | Cyclic phosphonate ester inhibitors of microsomal triglyceride transfer protein and method |
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EP (1) | EP1039915A4 (en) |
JP (1) | JP2001521001A (en) |
AU (1) | AU753520B2 (en) |
CA (1) | CA2307889A1 (en) |
WO (1) | WO1999021564A1 (en) |
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FR2562543B1 (en) * | 1984-04-10 | 1987-09-25 | Elf Aquitaine | NOVEL CYCLIC PHOSPHONITES, THEIR PREPARATION AND APPLICATIONS |
CA2236684A1 (en) * | 1996-01-16 | 1997-07-24 | William A. Slusarchyk | Conformationally restricted aromatic inhibitors of microsomal triglyceride transfer protein and method |
US5760246A (en) * | 1996-12-17 | 1998-06-02 | Biller; Scott A. | Conformationally restricted aromatic inhibitors of microsomal triglyceride transfer protein and method |
-
1998
- 1998-10-14 AU AU10876/99A patent/AU753520B2/en not_active Ceased
- 1998-10-14 WO PCT/US1998/021750 patent/WO1999021564A1/en not_active Application Discontinuation
- 1998-10-14 CA CA002307889A patent/CA2307889A1/en not_active Abandoned
- 1998-10-14 EP EP98953531A patent/EP1039915A4/en not_active Withdrawn
- 1998-10-14 JP JP2000517722A patent/JP2001521001A/en active Pending
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WO1999021564A1 (en) | 1999-05-06 |
EP1039915A4 (en) | 2001-02-14 |
EP1039915A1 (en) | 2000-10-04 |
AU1087699A (en) | 1999-05-17 |
AU753520B2 (en) | 2002-10-17 |
JP2001521001A (en) | 2001-11-06 |
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