WO2010097672A1 - Process for the preparation of prostaglandin derivatives - Google Patents
Process for the preparation of prostaglandin derivatives Download PDFInfo
- Publication number
- WO2010097672A1 WO2010097672A1 PCT/IB2010/000315 IB2010000315W WO2010097672A1 WO 2010097672 A1 WO2010097672 A1 WO 2010097672A1 IB 2010000315 W IB2010000315 W IB 2010000315W WO 2010097672 A1 WO2010097672 A1 WO 2010097672A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compound
- formula
- give
- group
- preparation
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title claims abstract description 44
- 238000000034 method Methods 0.000 title claims abstract description 23
- 150000003180 prostaglandins Chemical class 0.000 title claims abstract description 16
- 150000001875 compounds Chemical class 0.000 claims abstract description 113
- 229960002470 bimatoprost Drugs 0.000 claims abstract description 14
- AQOKCDNYWBIDND-FTOWTWDKSA-N bimatoprost Chemical compound CCNC(=O)CCC\C=C/C[C@H]1[C@@H](O)C[C@@H](O)[C@@H]1\C=C\[C@@H](O)CCC1=CC=CC=C1 AQOKCDNYWBIDND-FTOWTWDKSA-N 0.000 claims abstract description 14
- MKPLKVHSHYCHOC-AHTXBMBWSA-N travoprost Chemical compound CC(C)OC(=O)CCC\C=C/C[C@H]1[C@@H](O)C[C@@H](O)[C@@H]1\C=C\[C@@H](O)COC1=CC=CC(C(F)(F)F)=C1 MKPLKVHSHYCHOC-AHTXBMBWSA-N 0.000 claims abstract description 14
- 229960001160 latanoprost Drugs 0.000 claims abstract description 13
- GGXICVAJURFBLW-CEYXHVGTSA-N latanoprost Chemical compound CC(C)OC(=O)CCC\C=C/C[C@H]1[C@@H](O)C[C@@H](O)[C@@H]1CC[C@@H](O)CCC1=CC=CC=C1 GGXICVAJURFBLW-CEYXHVGTSA-N 0.000 claims abstract description 13
- 229960002368 travoprost Drugs 0.000 claims abstract description 13
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 9
- 125000004043 oxo group Chemical group O=* 0.000 claims abstract 5
- 238000006243 chemical reaction Methods 0.000 claims description 32
- 239000002904 solvent Substances 0.000 claims description 24
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 14
- 125000006239 protecting group Chemical group 0.000 claims description 10
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
- 239000011591 potassium Substances 0.000 claims description 6
- 229910052700 potassium Inorganic materials 0.000 claims description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 5
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 125000001072 heteroaryl group Chemical group 0.000 claims description 3
- 150000004678 hydrides Chemical class 0.000 claims description 3
- RTLMATDNIKWIIO-UHFFFAOYSA-N 2-n,2-n,6-n,6-n-tetrakis(2-chloroethyl)-4,8-di(piperidin-1-yl)pyrimido[5,4-d]pyrimidine-2,6-diamine Chemical group C=12N=C(N(CCCl)CCCl)N=C(N3CCCCC3)C2=NC(N(CCCl)CCCl)=NC=1N1CCCCC1 RTLMATDNIKWIIO-UHFFFAOYSA-N 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims 3
- 150000001340 alkali metals Chemical class 0.000 claims 3
- 239000002585 base Substances 0.000 claims 2
- 239000000543 intermediate Substances 0.000 abstract description 7
- 150000003169 prostaglandin F2α derivatives Chemical class 0.000 abstract description 3
- 239000000243 solution Substances 0.000 description 57
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 50
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 40
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 36
- 239000000047 product Substances 0.000 description 30
- 238000003756 stirring Methods 0.000 description 27
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 24
- 239000012074 organic phase Substances 0.000 description 21
- 239000012071 phase Substances 0.000 description 21
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 20
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- 239000008346 aqueous phase Substances 0.000 description 18
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 18
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 16
- 235000019341 magnesium sulphate Nutrition 0.000 description 16
- 238000004440 column chromatography Methods 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 239000003921 oil Substances 0.000 description 13
- 230000015572 biosynthetic process Effects 0.000 description 11
- 239000012047 saturated solution Substances 0.000 description 11
- 239000007787 solid Substances 0.000 description 11
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 10
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 10
- 239000012300 argon atmosphere Substances 0.000 description 10
- 230000003068 static effect Effects 0.000 description 10
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 238000007792 addition Methods 0.000 description 8
- 0 *[C@@](CCc1ccccc1)C=C[C@@](C1C2)[C@@](*)C[C@@]1OC2O Chemical compound *[C@@](CCc1ccccc1)C=C[C@@](C1C2)[C@@](*)C[C@@]1OC2O 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 125000000468 ketone group Chemical group 0.000 description 6
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 150000001299 aldehydes Chemical class 0.000 description 5
- 235000019270 ammonium chloride Nutrition 0.000 description 5
- 238000004040 coloring Methods 0.000 description 5
- 238000010791 quenching Methods 0.000 description 5
- 235000017557 sodium bicarbonate Nutrition 0.000 description 5
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- ILMRJRBKQSSXGY-UHFFFAOYSA-N tert-butyl(dimethyl)silicon Chemical compound C[Si](C)C(C)(C)C ILMRJRBKQSSXGY-UHFFFAOYSA-N 0.000 description 5
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- -1 acetic acid Chemical class 0.000 description 4
- OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000008363 phosphate buffer Substances 0.000 description 4
- PXGPLTODNUVGFL-BRIYLRKRSA-N (E,Z)-(1R,2R,3R,5S)-7-(3,5-Dihydroxy-2-((3S)-(3-hydroxy-1-octenyl))cyclopentyl)-5-heptenoic acid Chemical class CCCCC[C@H](O)C=C[C@H]1[C@H](O)C[C@H](O)[C@@H]1CC=CCCCC(O)=O PXGPLTODNUVGFL-BRIYLRKRSA-N 0.000 description 3
- MLOSJPZSZWUDSK-UHFFFAOYSA-N 4-carboxybutyl(triphenyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CCCCC(=O)O)C1=CC=CC=C1 MLOSJPZSZWUDSK-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- FIWILGQIZHDAQG-UHFFFAOYSA-N NC1=C(C(=O)NCC2=CC=C(C=C2)OCC(F)(F)F)C=C(C(=N1)N)N1N=C(N=C1)C1(CC1)C(F)(F)F Chemical compound NC1=C(C(=O)NCC2=CC=C(C=C2)OCC(F)(F)F)C=C(C(=N1)N)N1N=C(N=C1)C1(CC1)C(F)(F)F FIWILGQIZHDAQG-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 235000011089 carbon dioxide Nutrition 0.000 description 3
- 150000002596 lactones Chemical class 0.000 description 3
- 238000003760 magnetic stirring Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229940094443 oxytocics prostaglandins Drugs 0.000 description 3
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical class [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 3
- 229910000104 sodium hydride Inorganic materials 0.000 description 3
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 3
- BCNZYOJHNLTNEZ-UHFFFAOYSA-N tert-butyldimethylsilyl chloride Chemical compound CC(C)(C)[Si](C)(C)Cl BCNZYOJHNLTNEZ-UHFFFAOYSA-N 0.000 description 3
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 3
- OBTZDIRUQWFRFZ-UHFFFAOYSA-N 2-(5-methylfuran-2-yl)-n-(4-methylphenyl)quinoline-4-carboxamide Chemical compound O1C(C)=CC=C1C1=CC(C(=O)NC=2C=CC(C)=CC=2)=C(C=CC=C2)C2=N1 OBTZDIRUQWFRFZ-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- 108010084311 Novozyme 435 Proteins 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 150000004292 cyclic ethers Chemical class 0.000 description 2
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- AGJSNMGHAVDLRQ-IWFBPKFRSA-N methyl (2s)-2-[[(2s)-2-[[(2s)-2-[[(2r)-2-amino-3-sulfanylpropanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxy-2,3-dimethylphenyl)propanoyl]amino]-4-methylsulfanylbutanoate Chemical compound SC[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(=O)N[C@@H](CCSC)C(=O)OC)CC1=CC=C(O)C(C)=C1C AGJSNMGHAVDLRQ-IWFBPKFRSA-N 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- FMCAFXHLMUOIGG-JTJHWIPRSA-N (2s)-2-[[(2r)-2-[[(2s)-2-[[(2r)-2-formamido-3-sulfanylpropanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxy-2,5-dimethylphenyl)propanoyl]amino]-4-methylsulfanylbutanoic acid Chemical compound O=CN[C@@H](CS)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(=O)N[C@@H](CCSC)C(O)=O)CC1=CC(C)=C(O)C=C1C FMCAFXHLMUOIGG-JTJHWIPRSA-N 0.000 description 1
- FMCAFXHLMUOIGG-IWFBPKFRSA-N (2s)-2-[[(2s)-2-[[(2s)-2-[[(2r)-2-formamido-3-sulfanylpropanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxy-2,5-dimethylphenyl)propanoyl]amino]-4-methylsulfanylbutanoic acid Chemical compound O=CN[C@@H](CS)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(=O)N[C@@H](CCSC)C(O)=O)CC1=CC(C)=C(O)C=C1C FMCAFXHLMUOIGG-IWFBPKFRSA-N 0.000 description 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- MBGWNNJXMYHKQO-UHFFFAOYSA-N 1-dimethoxyphosphoryl-3-[3-(trifluoromethyl)phenoxy]propan-2-one Chemical compound COP(=O)(OC)CC(=O)COC1=CC=CC(C(F)(F)F)=C1 MBGWNNJXMYHKQO-UHFFFAOYSA-N 0.000 description 1
- ONYIBVIIOCEBIV-UHFFFAOYSA-N 1-dimethoxyphosphoryl-4-phenylbutan-2-one Chemical compound COP(=O)(OC)CC(=O)CCC1=CC=CC=C1 ONYIBVIIOCEBIV-UHFFFAOYSA-N 0.000 description 1
- JWUJQDFVADABEY-UHFFFAOYSA-N 2-methyltetrahydrofuran Chemical compound CC1CCCO1 JWUJQDFVADABEY-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- 208000010412 Glaucoma Diseases 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical class C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 1
- 229930194542 Keto Chemical group 0.000 description 1
- RCIZQFNBJUSVHP-WTDVLVBFSA-N O[C@@H](COc1cccc(C(F)(F)F)c1)/C=C/[C@H](C(C1)[C@H](C2)OC1O)[C@@H]2O Chemical compound O[C@@H](COc1cccc(C(F)(F)F)c1)/C=C/[C@H](C(C1)[C@H](C2)OC1O)[C@@H]2O RCIZQFNBJUSVHP-WTDVLVBFSA-N 0.000 description 1
- 102000004005 Prostaglandin-endoperoxide synthases Human genes 0.000 description 1
- 108090000459 Prostaglandin-endoperoxide synthases Proteins 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 229940114079 arachidonic acid Drugs 0.000 description 1
- 235000021342 arachidonic acid Nutrition 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 238000011914 asymmetric synthesis Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 229910000085 borane Inorganic materials 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- AGJSNMGHAVDLRQ-HUUJSLGLSA-N methyl (2s)-2-[[(2r)-2-[[(2s)-2-[[(2r)-2-amino-3-sulfanylpropanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxy-2,3-dimethylphenyl)propanoyl]amino]-4-methylsulfanylbutanoate Chemical compound SC[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(=O)N[C@@H](CCSC)C(=O)OC)CC1=CC=C(O)C(C)=C1C AGJSNMGHAVDLRQ-HUUJSLGLSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C405/00—Compounds containing a five-membered ring having two side-chains in ortho position to each other, and having oxygen atoms directly attached to the ring in ortho position to one of the side-chains, one side-chain containing, not directly attached to the ring, a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, and the other side-chain having oxygen atoms attached in gamma-position to the ring, e.g. prostaglandins ; Analogues or derivatives thereof
Definitions
- the present invention concerns a new process for the preparation of prostaglandin derivatives, in particular prostaglandin F 2a derivatives, for example bimatoprost, latanoprost and travoprost.
- the invention also concerns the new intermediates of said process and their use in the preparation of prostaglandin derivatives.
- Prostaglandins are a class of endogenous molecules derived from arachidonic acid by action of prostaglandin synthetase and have various biological activities.
- prostaglandins are formed of a ring and two side chains, said ring and chains being replaceable (usually by hydroxy or keto groups) and optionally being partly unsaturated.
- the compounds bimatoprost, latanoprost and travoprost are analogues of prostaglandin F 2a and are used in therapy in the treatment of glaucoma, in particular to reduce high endo-ocular pressure.
- the derivatives of the prostaglandins like those mentioned above are usually prepared according to a synthesis method which starts from Corey aldehyde ([3 ⁇ R(3 ⁇ ,4 ⁇ ,5 ⁇ ,6 ⁇ )]-(-)-5-(hydroxy)hexahydro-2-oxo-2H-cyclopenta[b]furan-4- carboxaldehyde), hydroxy-protected, to which the two side chains are attached.
- the protection of the hydroxy group is generally obtained via the formation of esters, using for example benzoic acid or its derivatives or aliphatic carboxylic acids such as acetic acid, or with THP (tetrahydropyranyl).
- the protection by means of the protective groups indicated above has considerable drawbacks, for example the difficulty of final release, not facilitating the subsequent asymmetric synthesis steps or, in the case of the THP, the introduction of a further chiral centre which entails the formation of diastereoisomers, significantly complicating the NMR spectra and the chromatographic profile.
- the invention concerns a process for the preparation of prostaglandin derivatives which comprises: a) reacting the ([3 ⁇ R(3 ⁇ ,4 ⁇ ,5 ⁇ ,6 ⁇ )]-(-)-5-(fert- butyldimethylsilyl)hexahydro-2-oxo-2H-cyclopenta[b]furan-4- carboxaldehyde) of formula (I)
- R represents a benzyl group or a phenoxy group
- the phenyl can be optionally substituted by a group selected from halogens, hydroxy derivatives, alkyls, aryls, heteroaryls and trifluoromethyl, in the presence of a base and an appropriate solvent, to give the compound of formula (III)
- hydroxy derivatives indicates a hydroxy or structurally correlated groups of formula O-X, where X is an alkyl or an aryl; a preferred hydroxy derivative is OH.
- alkyls indicates linear or branched alkyls, saturated or unsaturated, Cl-ClO, preferably C1-C4.
- aryls includes for example the phenyl group, phenyls substituted, preferably with the trifluoroniethyl or fluorine group.
- heteroaryls includes for example imidazoles, indols, pyridines, furans and thiophenes, optionally substituted.
- halogen refers to an atom of bromine, chlorine, fluorine or iodine, the fluorine being preferred.
- R represents a benzyl group.
- R represents a phenoxy group substituted with a trifluoromethyl group, advantageously R is a 3- trifluoromethyl phenoxy.
- the base used in the reaction step (a) is a strong base, such as a hydride or an alcoholate of alkaline metals, preferably hydride, for example sodium hydride.
- the solvent used in step (a) is advantageously an inert solvent, for example an ether, such as dimethoxyethane or a cyclic ether, like tetrahydrofuran or 2-methyl tetrahydrofuran, the latter cyclic ethers being preferred.
- an ether such as dimethoxyethane or a cyclic ether, like tetrahydrofuran or 2-methyl tetrahydrofuran, the latter cyclic ethers being preferred.
- the reactions of the steps (a) and (b) are preferably carried out in an inert atmosphere, for example under argon or nitrogen.
- Asymmetric reduction agent here indicates a reducing agent able to reduce the ketone group of the side chain to a hydroxy group, approaching the re face of the carbonylic system.
- Said reducing agent is advantageously DIP-Cl (diisopinocamphenylchlorine borane) .
- steps (a) and (b) above are carried out at low temperatures, for example between -30° and +10°C, advantageously between -30°C and 0°C. Details of more advantageous reaction conditions are provided in the experimental section of the present invention.
- the compound of formula (FV) represents a key new intermediate in the synthesis of prostaglandin derivatives, especially prostaglandin F 2 ⁇ derivatives.
- R is a non-substituted benzyl group or a phenoxy group substituted with a trifluoromethyl group, advantageously the 3- trifluoromethylphenoxy group, are particularly preferred compounds.
- the invention concerns use of the compound of formula (IV) as an intermediate for the synthesis of prostaglandin derivatives, for example of prostaglandin F 2 ⁇ such as bimatoprost, latanoprost and travoprost.
- the invention concerns a process for preparation of the bimatoprost which comprises:
- Ph 3 P CH(CH) 3 COOM where M is an alkaline metal, preferably potassium, to give the compound of formula (VII)
- AIk is the residue of an inferior alkyl, preferably a C1-C4 alkyl, for example methyl; (h) forming the amide of the compound (VIII) to give the compound (IX)
- the invention concerns a process for preparation of the latanoprost which comprises:
- Ph 3 P CH(CH) 3 COO M where M is an alkaline metal, preferably potassium, to give the compound of formula (XIV)
- the process for the preparation of the latanoprost is performed according to the following Scheme (III) Latanoprost
- the invention concerns a process for preparation of the travoprost which comprises:
- Ph 3 P CH(CH) 3 COOM where M is an alkaline metal, preferably potassium, to give the compound of formula (XIX)
- the invention also concerns the compounds bimatoprost, latanoprost and travoprost obtained with the process of the invention.
- the (-)-DIP-Cl (50-65% in weight in heptane, 55 ml, 0.14 moles, 6 eq) is added under stirring to a solution, of III (10 g, 0.024 moles) in tetrahydrofuran (110 mL), in a static argon atmosphere at a temperature of -30°C; the colourless transparent solution becomes clear pale yellow and over time this colouring disappears.
- the (-)-DIP-Cl (50-65% in weight in heptane, 1.22 ml, 3.17 moles, 6 eq) is added under stirring to a solution of III (265 mg, 0.529 mmoles) in tetrahydrofuran (5 mL), in a static argon atmosphere at a temperature of -30°C; the colourless transparent solution becomes clear pale yellow and over time this colouring disappears.
- DIBAL-H (1 M in hexane, 4.12 ml, 4.12 mmoles, 1.15 eq) is slowly added to a solution of lactone V (1.9 g, 3.58 mmoles) in dichloromethane (60 mL) cooled to -30°C in a static argon atmosphere. After the additions have been made, the reaction is complete after 30 min.
- a saturated solution of Rochelle salts 80 mL is added, again at -30°C, and the solution is diluted with dichloromethane; after a few minutes the dry ice and acetone bath is removed and the solution is left under vigorous stirring until the two phases can be clearly distinguished (approximately 90 minutes).
- the potassium tert-butylate (4.5 g, 32.2 mmoles, 9 eq) is added at room temperature in small portions to a suspension of (4- carboxybutyl)triphenylphosphonium bromide (9 g, 16.1 mmoles, 4.5 eq) in tetrahydrofuran (45 mL) in a static argon atmosphere; during the addition the solution heats up and takes on an orange colouring which increasingly verges on bright red.
- the solution is left under stirring for 30 minutes at room temperature and is then cooled to 0 0 C, after which the lactol VI is added 'via cannula' (1.9 g, 3.57 mmoles) dissolved in tetrahydrofuran (20 mL); the solution turns paler, after 15 minutes the ice and water bath is removed and the solution is left under stirring at room temperature. After three hours the reaction is complete and is quenched by adding a saturated solution of ammonium chloride (100 mL) and acetic acid (1.9 mL, 1.05 eq with respect to the potassium tert-butylate).
- Ethyl amine (70% in water, 60 mL) is added at room temperature to a solution of the compound VIII (1.25 g, 0.002 moles) in tetrahydrofuran (12 mL), the reaction is performed at this temperature under magnetic stirring and is complete after approximately 52 hours.
- the products are purified by means of column chromatography (hexane-AcOEt 8:2 v/v). The compound IX is obtained with a yield of 90%.
- Triethylamine (4.3 mL, 0.031 moles, 10 eq) and palladium catalyst 10% on carbon (130 mg, 10% in weight with respect to 3) are added to a solution of IV in tetrahydrofuran (50 mL), three vacuum-hydrogen cycles are performed and the solution is then left under vigorous stirring in a hydrogen atmosphere at atmospheric pressure at room temperature. After one hour the reaction is complete. The catalyst is filtered and the solvent is removed at reduced pressure. The product is purified by means of column chromatography (hexane- AcOEt 8:2 v/v). The pure product is obtained as a colourless oil with a yield.of 93%.
- the potassium tert-butylate (4 g, 35.5 mmoles, 9 eq) is added at room temperature in small portions to a suspension of (4- carboxybutyl)triphenylphosphonium bromide (8 g, 17.7 mmoles, 4.5 eq) in tetrahydrofuran (45 mL) in a static argon atmosphere; during the addition the solution heats up and takes on an orange colouring which increasingly verges on bright red.
- the solution is left for 30 minutes under stirring at room temperature and is then cooled to 0°C, after which the lactol XIII is added 'via cannula' (2 g, 3.94 mmoles) dissolved in tetrahydrofuran (20 mL); the solution turns paler, after 15 minutes the ice and water bath is removed and the solution is left under stirring at room temperature.
- the enzyme Lipase Novozym 435 (500 mg) is added to a solution of XV (1 g, 2.56 mmoles) in isopropyl alcohol (10 mL). The solution is kept at 30°C under magnetic stirring (never above 200 rpm). The reaction is complete after 18 hours. The enzyme is simply filtered and recovered, and the solvent is removed at reduced pressure. The product is purified by means of column chromatography (pure AcOEt) to give the pure product in the form of a pale yellow oil with a yield of 92%.
- the potassium tert-butylate (321 g, 2.86 mmoles, 9 eq) is added at room temperature in small portions to a suspension of (4- carboxybutyl)triphenylphosphonium bromide (633 mg, 1.43 mmoles, 4.5 eq) in tetrahydrofuran (7 mL) in a static argon atmosphere; during the additions the solution heats up and takes on an orange colouring which increasingly verges on bright red.
- the solution is left for 30 minutes under stirring at room temperature and is then cooled to 0°C, after which the lactol XVIII is added 'via cannula' (195 mg, 0.32 mmoles) dissolved in tetrahydrofuran (5 mL); the solution turns paler, after 15 minutes the ice and water bath is removed and the solution is left under stirring at room temperature.
- the enzyme Lipase Novozym 435 (15 mg) is added to a solution of XX (30 g, 0.065 mmoles) in isopropyl alcohol (450 ⁇ L). The solution is kept at 30°C under magnetic stirring (never above 200 rpm). The reaction is complete after 18 hours. The enzyme is simply filtered and recovered, and the solvent is removed at reduced pressure. The product is purified by means of column chromatography (pure AcOEt) to give the pure product in the form of a colourless oil with a yield of 93%.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2751686A CA2751686A1 (en) | 2009-02-27 | 2010-02-18 | Process for the preparation of prostaglandin derivatives |
EP10708795A EP2401252A1 (en) | 2009-02-27 | 2010-02-18 | Process for the preparation of prostaglandin derivatives |
JP2011551540A JP2012519163A (en) | 2009-02-27 | 2010-02-18 | Method for producing prostaglandin derivative |
AU2010217347A AU2010217347A1 (en) | 2009-02-27 | 2010-02-18 | Process for the preparation of prostaglandin derivatives |
US13/203,670 US20120016136A1 (en) | 2009-02-27 | 2010-02-18 | Process for the preparation of prostaglandin derivatives |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ITMI2009A000292A IT1393112B1 (en) | 2009-02-27 | 2009-02-27 | PROCEDURE FOR THE PREPARATION OF PROSTAGLANDINE DERIVATIVES |
ITMI2009A000292 | 2009-02-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2010097672A1 true WO2010097672A1 (en) | 2010-09-02 |
Family
ID=41466820
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2010/000315 WO2010097672A1 (en) | 2009-02-27 | 2010-02-18 | Process for the preparation of prostaglandin derivatives |
Country Status (7)
Country | Link |
---|---|
US (1) | US20120016136A1 (en) |
EP (1) | EP2401252A1 (en) |
JP (1) | JP2012519163A (en) |
AU (1) | AU2010217347A1 (en) |
CA (1) | CA2751686A1 (en) |
IT (1) | IT1393112B1 (en) |
WO (1) | WO2010097672A1 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2488508A1 (en) * | 2009-10-16 | 2012-08-22 | Cayman Chemical Company, Incorporated | Process for the preparation of f-series prostaglandins |
EP2495235A1 (en) | 2011-03-04 | 2012-09-05 | Newchem S.p.A. | Process for the synthesis of prostaglandins and intermediates thereof |
WO2012146085A1 (en) * | 2011-04-29 | 2012-11-01 | 上海源力生物技术有限公司 | Intermediate for synthesizing prostaglandin medicines and preparation method therefor |
JP2012246301A (en) * | 2012-08-10 | 2012-12-13 | Cayman Chemical Co Inc | Method for preparing prostaglandins f |
EP2837621A1 (en) | 2013-08-15 | 2015-02-18 | Chirogate International Inc. | Processes for the preparation of isomer free prostaglandins |
JP2015506343A (en) * | 2011-12-21 | 2015-03-02 | キノイン・ジヨージセル・エーシユ・ベジエーセテイ・テルメーケク・ジヤーラ・ゼー・エル・テー | Preparation method of travoprost |
US9290432B2 (en) | 2012-11-30 | 2016-03-22 | CHINOIN Gyógyszer és Vegyészeti Termékek Gyára Zrt. | Process for the preparation of travoprost |
CN111018766A (en) * | 2018-10-10 | 2020-04-17 | 广州楷模生物科技有限公司 | Method for synthesizing bimatoprost |
CN112608294A (en) * | 2020-12-16 | 2021-04-06 | 西安国康瑞金制药有限公司 | Preparation method of latanoprost |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017502089A (en) | 2014-01-10 | 2017-01-19 | マニスティー パートナーズ エルエルシーManistee Partners Llc | Migraine treatment |
CN111662318B (en) * | 2019-03-08 | 2024-02-02 | 上海医药工业研究院 | Iloprost key intermediate and preparation method thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4322557A (en) * | 1981-02-17 | 1982-03-30 | Pfizer Inc. | 1-Aryloxy-2-(S)-hydroxy-3-(triarylphosphonio)-propane derivatives as prostaglandin intermediates |
US6388128B1 (en) * | 1998-10-05 | 2002-05-14 | Alcon Manufacturing, Ltd. | Stannane synthesis of prostanoids |
US20070155973A1 (en) * | 2005-12-30 | 2007-07-05 | Everlight Usa, Inc. | Novel intermediate compound for the preparation of prostaglandin F analogue |
EP1886992A1 (en) * | 2006-08-04 | 2008-02-13 | Daiichi Fine Chemical Co., Ltd. | Method for preparing prostaglandin derivative |
-
2009
- 2009-02-27 IT ITMI2009A000292A patent/IT1393112B1/en active
-
2010
- 2010-02-18 CA CA2751686A patent/CA2751686A1/en not_active Abandoned
- 2010-02-18 AU AU2010217347A patent/AU2010217347A1/en not_active Abandoned
- 2010-02-18 EP EP10708795A patent/EP2401252A1/en not_active Withdrawn
- 2010-02-18 WO PCT/IB2010/000315 patent/WO2010097672A1/en active Application Filing
- 2010-02-18 JP JP2011551540A patent/JP2012519163A/en active Pending
- 2010-02-18 US US13/203,670 patent/US20120016136A1/en not_active Abandoned
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4322557A (en) * | 1981-02-17 | 1982-03-30 | Pfizer Inc. | 1-Aryloxy-2-(S)-hydroxy-3-(triarylphosphonio)-propane derivatives as prostaglandin intermediates |
US6388128B1 (en) * | 1998-10-05 | 2002-05-14 | Alcon Manufacturing, Ltd. | Stannane synthesis of prostanoids |
US20070155973A1 (en) * | 2005-12-30 | 2007-07-05 | Everlight Usa, Inc. | Novel intermediate compound for the preparation of prostaglandin F analogue |
EP1886992A1 (en) * | 2006-08-04 | 2008-02-13 | Daiichi Fine Chemical Co., Ltd. | Method for preparing prostaglandin derivative |
Non-Patent Citations (1)
Title |
---|
VIONNET J.-P. ET AL.: "Facile preparation of (+-)-12-epiprostaglandins from 7-oxabicyclo[2.2.1]hept-5-en-2-one via an all-cis-formyllactone related to Corey lactone", HELVETICA CHIMICA ACTA, vol. 77, 1994, pages 1781 - 1790, XP002563009 * |
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2488508A4 (en) * | 2009-10-16 | 2013-04-24 | Cayman Chemical Co Inc | Process for the preparation of f-series prostaglandins |
US8901319B2 (en) | 2009-10-16 | 2014-12-02 | Cayman Chemical Company, Incorporated | Process for the preparation of F-series prostaglandins |
EP2488508A1 (en) * | 2009-10-16 | 2012-08-22 | Cayman Chemical Company, Incorporated | Process for the preparation of f-series prostaglandins |
EP2495235A1 (en) | 2011-03-04 | 2012-09-05 | Newchem S.p.A. | Process for the synthesis of prostaglandins and intermediates thereof |
WO2012146085A1 (en) * | 2011-04-29 | 2012-11-01 | 上海源力生物技术有限公司 | Intermediate for synthesizing prostaglandin medicines and preparation method therefor |
JP2015506343A (en) * | 2011-12-21 | 2015-03-02 | キノイン・ジヨージセル・エーシユ・ベジエーセテイ・テルメーケク・ジヤーラ・ゼー・エル・テー | Preparation method of travoprost |
JP2012246301A (en) * | 2012-08-10 | 2012-12-13 | Cayman Chemical Co Inc | Method for preparing prostaglandins f |
US9290432B2 (en) | 2012-11-30 | 2016-03-22 | CHINOIN Gyógyszer és Vegyészeti Termékek Gyára Zrt. | Process for the preparation of travoprost |
TWI616433B (en) * | 2012-11-30 | 2018-03-01 | 齊諾應醫藥及化學品股份有限公司 | Novel process for the preparation of travoprost |
EP2837621A1 (en) | 2013-08-15 | 2015-02-18 | Chirogate International Inc. | Processes for the preparation of isomer free prostaglandins |
US9464028B2 (en) | 2013-08-15 | 2016-10-11 | Chirogate International Inc. | Processes and intermediates for the preparations of isomer free prostaglandins |
US9540311B2 (en) | 2013-08-15 | 2017-01-10 | Chirogate International Inc. | Processes and intermediates for the preparations of isomer free prostaglandins |
US9828356B2 (en) | 2013-08-15 | 2017-11-28 | Chirogate International Inc. | Processes and intermediates for the preparations of isomer free prostaglandis |
US9890135B1 (en) | 2013-08-15 | 2018-02-13 | Chirogate International Inc. | Processes and intermediates for the preparations of isomer free prostaglandins |
US9994543B2 (en) | 2013-08-15 | 2018-06-12 | Chirogate International Inc. | Processes and intermediates for the preparations of isomer free prostaglandins |
CN111018766A (en) * | 2018-10-10 | 2020-04-17 | 广州楷模生物科技有限公司 | Method for synthesizing bimatoprost |
CN111018766B (en) * | 2018-10-10 | 2022-04-19 | 广州楷石医药有限公司 | Method for synthesizing bimatoprost |
CN112608294A (en) * | 2020-12-16 | 2021-04-06 | 西安国康瑞金制药有限公司 | Preparation method of latanoprost |
CN112608294B (en) * | 2020-12-16 | 2021-10-26 | 西安国康瑞金制药有限公司 | Preparation method of latanoprost |
Also Published As
Publication number | Publication date |
---|---|
CA2751686A1 (en) | 2010-09-02 |
ITMI20090292A1 (en) | 2010-08-28 |
AU2010217347A1 (en) | 2011-10-13 |
JP2012519163A (en) | 2012-08-23 |
IT1393112B1 (en) | 2012-04-11 |
US20120016136A1 (en) | 2012-01-19 |
EP2401252A1 (en) | 2012-01-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2401252A1 (en) | Process for the preparation of prostaglandin derivatives | |
US7157590B2 (en) | Process for the preparation of 17-phenyl-18,19,20-thinor-pgf 2a and its derivatives | |
EP1385819A1 (en) | Process for preparing prostaglandin derivatives and stereospecific starting material thereof | |
US20030149294A1 (en) | Process for the preparation of latanoprost | |
US4978775A (en) | Process for producing bicyclo[3.3.0]octanes | |
KR101787159B1 (en) | Processes for preparation of lubiprostone | |
EP0156611B1 (en) | Intermediates for the preparation of prostaglandin analogues | |
GB2030144A (en) | Keto-bicyclooctanes | |
JPH0141142B2 (en) | ||
IE54901B1 (en) | 9-substituted carbacyclins | |
US6015922A (en) | N-alkyl-N-alkoxycarboxamides and methods of use in prostaglandin synthesis | |
EP0234158A1 (en) | (2-Chloro-3-oxo-1-alkenyl)bicyclo (3.3.0.) octene derivative and process for preparing the same | |
EP0532218B1 (en) | Process for production of prostaglandin intermediates | |
US6066751A (en) | Process for making epoxide intermediates | |
HU190996B (en) | Process for preparing prostaglandin e down 1 compounds | |
HU193032B (en) | Process for preparing bicylic ketones | |
US4169199A (en) | Precursors for prostaglandin analogue and process for preparing the same | |
EP0247202B1 (en) | Isocarbacyclin derivatives and process for their preparation | |
US4212984A (en) | Prostaglandin precursors | |
JP2664841B2 (en) | Process for producing 6,7-disubstituted-2-hydroxy-3-methylenebicyclo [3.3.0] octanes | |
KR19990067376A (en) | Preparation of 3-phenyl-1-methylenedioxyphenyl-indan-2-carboxylic acid derivative | |
JPH0141146B2 (en) | ||
JPH0141147B2 (en) | ||
HU202240B (en) | Process for producing optically active carbacycline intermediates | |
JPH05271148A (en) | Production of optically active alpha-hydrocarboxylic acid |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10708795 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2751686 Country of ref document: CA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2011551540 Country of ref document: JP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2010217347 Country of ref document: AU |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2010708795 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 13203670 Country of ref document: US |
|
ENP | Entry into the national phase |
Ref document number: 2010217347 Country of ref document: AU Date of ref document: 20100218 Kind code of ref document: A |