GB1594368A - Prostaglandin derivatives - Google Patents
Prostaglandin derivatives Download PDFInfo
- Publication number
- GB1594368A GB1594368A GB50921/77A GB5092177A GB1594368A GB 1594368 A GB1594368 A GB 1594368A GB 50921/77 A GB50921/77 A GB 50921/77A GB 5092177 A GB5092177 A GB 5092177A GB 1594368 A GB1594368 A GB 1594368A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxy
- group
- methyl
- trans
- octenyl
- 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.)
- Expired
Links
- 150000003180 prostaglandins Chemical class 0.000 title claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 46
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 40
- 238000000034 method Methods 0.000 claims description 24
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 23
- KPSZWAJWFMFMFF-UHFFFAOYSA-N delta-Hexylen-alpha-carbonsaeure Natural products CC=CCCCC(O)=O KPSZWAJWFMFMFF-UHFFFAOYSA-N 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 11
- 125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 claims description 10
- 229910052731 fluorine Chemical group 0.000 claims description 7
- 125000001153 fluoro group Chemical group F* 0.000 claims description 7
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 125000004185 ester group Chemical group 0.000 claims description 6
- 125000004043 oxo group Chemical group O=* 0.000 claims description 6
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 230000007062 hydrolysis Effects 0.000 claims description 2
- 238000006460 hydrolysis reaction Methods 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims description 2
- 239000000825 pharmaceutical preparation Substances 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- -1 methoxy - 5,6 - dihydro - 2H - pyranyl ether Chemical compound 0.000 description 30
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 25
- 239000000203 mixture Substances 0.000 description 19
- 239000002904 solvent Substances 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 16
- 239000002253 acid Substances 0.000 description 15
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 12
- 125000003118 aryl group Chemical group 0.000 description 8
- 239000003960 organic solvent Substances 0.000 description 8
- 230000032050 esterification Effects 0.000 description 7
- 238000005886 esterification reaction Methods 0.000 description 7
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 239000003638 chemical reducing agent Substances 0.000 description 6
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 6
- 235000019341 magnesium sulphate Nutrition 0.000 description 6
- 150000004714 phosphonium salts Chemical class 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 125000001033 ether group Chemical group 0.000 description 5
- 239000007800 oxidant agent Substances 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- QHMQWEPBXSHHLH-UHFFFAOYSA-N sulfur tetrafluoride Chemical compound FS(F)(F)F QHMQWEPBXSHHLH-UHFFFAOYSA-N 0.000 description 5
- BSLQOMDPHRTERI-UHFFFAOYSA-N 1-diethoxyphosphoryl-3-(trifluoromethyl)heptan-2-one Chemical compound CCCCC(C(F)(F)F)C(=O)CP(=O)(OCC)OCC BSLQOMDPHRTERI-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- 241000700159 Rattus Species 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 150000008065 acid anhydrides Chemical class 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000004440 column chromatography Methods 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- 230000002140 halogenating effect Effects 0.000 description 4
- MNWFXJYAOYHMED-UHFFFAOYSA-N hexane carboxylic acid Natural products CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 4
- 238000005984 hydrogenation reaction Methods 0.000 description 4
- CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 4
- 239000012429 reaction media Substances 0.000 description 4
- 239000000741 silica gel Substances 0.000 description 4
- 229910002027 silica gel Inorganic materials 0.000 description 4
- WRIKHQLVHPKCJU-UHFFFAOYSA-N sodium bis(trimethylsilyl)amide Chemical compound C[Si](C)(C)N([Na])[Si](C)(C)C WRIKHQLVHPKCJU-UHFFFAOYSA-N 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- 239000001117 sulphuric acid Substances 0.000 description 4
- 235000011149 sulphuric acid Nutrition 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003377 acid catalyst Substances 0.000 description 3
- 238000005903 acid hydrolysis reaction Methods 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 230000036772 blood pressure Effects 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 231100000252 nontoxic Toxicity 0.000 description 3
- 230000003000 nontoxic effect Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 3
- 125000006239 protecting group Chemical group 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- FLZPTLSRDKJVLE-UHFFFAOYSA-N 1,2-dimethoxyethane-1,2-diol Chemical compound COC(O)C(O)OC FLZPTLSRDKJVLE-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- KCGNALBCJLJETQ-UHFFFAOYSA-N 1-bromo-3-(trifluoromethyl)heptan-2-one Chemical compound CCCCC(C(F)(F)F)C(=O)CBr KCGNALBCJLJETQ-UHFFFAOYSA-N 0.000 description 2
- BNPZSCCCDNKDPT-UHFFFAOYSA-N 2-(trifluoromethyl)hexanoic acid Chemical compound CCCCC(C(O)=O)C(F)(F)F BNPZSCCCDNKDPT-UHFFFAOYSA-N 0.000 description 2
- WMJLBTMSFOBPTE-UHFFFAOYSA-N 2-(trifluoromethyl)hexanoyl chloride Chemical compound CCCCC(C(Cl)=O)C(F)(F)F WMJLBTMSFOBPTE-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 208000025865 Ulcer Diseases 0.000 description 2
- 238000007239 Wittig reaction Methods 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000001350 alkyl halides Chemical class 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- 230000000026 anti-ulcerogenic effect Effects 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 229940117975 chromium trioxide Drugs 0.000 description 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N chromium trioxide Inorganic materials O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 2
- GAMDZJFZMJECOS-UHFFFAOYSA-N chromium(6+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Cr+6] GAMDZJFZMJECOS-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- RBLGLDWTCZMLRW-UHFFFAOYSA-K dicalcium;phosphate;dihydrate Chemical compound O.O.[Ca+2].[Ca+2].[O-]P([O-])([O-])=O RBLGLDWTCZMLRW-UHFFFAOYSA-K 0.000 description 2
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 2
- SIPUZPBQZHNSDW-UHFFFAOYSA-N diisobutylaluminium hydride Substances CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 2
- 239000003937 drug carrier Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000006266 etherification reaction Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 150000004678 hydrides Chemical class 0.000 description 2
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 2
- 229960000905 indomethacin Drugs 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 235000019359 magnesium stearate Nutrition 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000035935 pregnancy Effects 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- 210000002784 stomach Anatomy 0.000 description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- 230000036269 ulceration Effects 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- ICLYJLBTOGPLMC-KVVVOXFISA-N (z)-octadec-9-enoate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCC\C=C/CCCCCCCC(O)=O ICLYJLBTOGPLMC-KVVVOXFISA-N 0.000 description 1
- LJCZNYWLQZZIOS-UHFFFAOYSA-N 2,2,2-trichlorethoxycarbonyl chloride Chemical compound ClC(=O)OCC(Cl)(Cl)Cl LJCZNYWLQZZIOS-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
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- CPVNCBJFUQQXSU-UHFFFAOYSA-O 4-carboxybutyl(triphenyl)phosphanium Chemical compound C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CCCCC(=O)O)C1=CC=CC=C1 CPVNCBJFUQQXSU-UHFFFAOYSA-O 0.000 description 1
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- 125000005530 alkylenedioxy group Chemical group 0.000 description 1
- 125000000746 allylic group Chemical group 0.000 description 1
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- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
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- 125000004104 aryloxy group Chemical group 0.000 description 1
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- AZWXAPCAJCYGIA-UHFFFAOYSA-N bis(2-methylpropyl)alumane Chemical compound CC(C)C[AlH]CC(C)C AZWXAPCAJCYGIA-UHFFFAOYSA-N 0.000 description 1
- VHAXQSFPTJUMLT-UHFFFAOYSA-N bis(3-methylbutan-2-yl)boron Chemical compound CC(C)C(C)[B]C(C)C(C)C VHAXQSFPTJUMLT-UHFFFAOYSA-N 0.000 description 1
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- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229960001342 dinoprost Drugs 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical group C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000012374 esterification agent Substances 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- XTUTXYBGTIFZFQ-UHFFFAOYSA-N ethyl 2,2-difluorohexanoate Chemical compound CCCCC(F)(F)C(=O)OCC XTUTXYBGTIFZFQ-UHFFFAOYSA-N 0.000 description 1
- WPRNRQBWGNUKIJ-UHFFFAOYSA-N ethyl 2-(trifluoromethyl)hexanoate Chemical compound CCCCC(C(F)(F)F)C(=O)OCC WPRNRQBWGNUKIJ-UHFFFAOYSA-N 0.000 description 1
- PNPBANMQNQUHNB-UHFFFAOYSA-N ethyl 2-methyl-2-(trifluoromethyl)hexanoate Chemical compound CCCCC(C)(C(F)(F)F)C(=O)OCC PNPBANMQNQUHNB-UHFFFAOYSA-N 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 235000010855 food raising agent Nutrition 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
- PKHMTIRCAFTBDS-UHFFFAOYSA-N hexanoyl hexanoate Chemical compound CCCCCC(=O)OC(=O)CCCCC PKHMTIRCAFTBDS-UHFFFAOYSA-N 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 125000002346 iodo group Chemical group I* 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 230000004130 lipolysis Effects 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- NSPJNIDYTSSIIY-UHFFFAOYSA-N methoxy(methoxymethoxy)methane Chemical compound COCOCOC NSPJNIDYTSSIIY-UHFFFAOYSA-N 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PXGPLTODNUVGFL-YNNPMVKQSA-N prostaglandin F2alpha Chemical compound CCCCC[C@H](O)\C=C\[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(O)=O PXGPLTODNUVGFL-YNNPMVKQSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 210000002460 smooth muscle Anatomy 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 208000010110 spontaneous platelet aggregation Diseases 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 229940117013 triethanolamine oleate Drugs 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
- C07D307/935—Not further condensed cyclopenta [b] furans or hydrogenated cyclopenta [b] furans
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/15—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing halogen
- C07C53/19—Acids containing three or more carbon atoms
- C07C53/21—Acids containing three or more carbon atoms containing fluorine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/38—Acyl halides
- C07C53/46—Acyl halides containing halogen outside the carbonyl halide group
- C07C53/50—Acyl halides containing halogen outside the carbonyl halide group of acids containing three or more carbon atoms
-
- 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/141—Esters of phosphorous acids
- C07F9/143—Esters of phosphorous acids with unsaturated acyclic alcohols
-
- 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
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- Chemical & Material Sciences (AREA)
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Description
(54) PROSTAGLANDIN DERIVATIVES
(71) We, F. HOFFMANN-LA ROCHE & CO.,
AKTIENGESELLSCHAFT, a Swiss Company of 124-184 Grenzacherstrasse,
Basle, Switzerland, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement:- The present invention relates to prostaglandin derivatives. More particularly, the invention is concerned with prostaglandin derivatives, a process for the manufacture thereof and pharmaceutical and veterinary preparations containing same.
The prostaglandin derivatives provided by the present invention are compounds of the general formula
wherein R represents a hydrogen atom or a lower alkyl group, R1 represents a
hydrogen atom or a lower alkyl group, R2 represents a hydroxy group and
R3 represents a hydrogen atom or R2 and R3 together represent an oxo
group, R4 represents a hydrogen or fluorine atom or a lower alkyl group,
R4 represents a trifluoromethyl group or, when R4 represents a fluorine
atom, R4 may also represent a fluorine atom and X represents the -CH=CH- or -C112-CH2- group, and enantiomers and racemates thereof, the double bond of the substituted octenyl side chain having trans configuration, and the optional double bond in X having cis or trans configuration.
A particular aspect of the present invention is concerned with those prostaglandin derivatives defined earlier in which R1 represents a lower alkyl group. In a preferred aspect of this invention, R represents a hydrogen atom.
According to the process provided by the present invention, the prostaglandin derivatives aforesaid (i.e. the compounds of formula I and enantiomers and racemates thereof) are manufactured by hydrolysing the group denoted by R6 in a compound of the general formula
wherein R, R1, R2, R3, R4, R4, X and the double bond or bonds have the
significance given earlier and R6 represents a hydroxy group protected by
a hydrolysable ether or ester group.
chain and branched-chain alkyl groups containing from 1 to 7 carbon atoms such as
methyl, ethyl and propyl. preferably methyl. The term "lower alkoxy"
comprehends groups containing from 1 to 7 carbon atoms such as methoxy and ethoxy.
The term "lower alkanoic acid" comprehends an alkanoic acid containing from I
to 7 carbon atoms such as formic acid and acetic acid. The term "halogen" or
"halo" comprehends fluorine, chlorine, bromine and iodine or fluoro, chloro,
bromo and iodo. respectively, unless otherwise stated.
In the process provided by this invention, all compounds containing one or more asymmetric carbon atoms can be produced as racemic mixtures. These racemic mixtures which are obtained can be resolved according to well-known methods, whereupon subsequent products may be obtained as the corresponding optically pure enantiomers.
In the formulae given in this Specification, a thickened tapered line indicates a substituent which has the p-orientation (above the plane of the molecule), a brushed line ( Ililíl,l) indicates a substituent which has the aorientation (below the plane of the molecule) and a wavy lines 3 indicates a substituent which has either the a- or p-orientation or a mixture thereof. If will be appreciated that the formulae given in this Specification are set forth for convenience and are to be construed as including other forms (i.e. enantiomers and racemates) and are not to be construed as being limited to the particular form shown.
The term "aryl" used in this Specification signifies a mononuclear aromatic hydrocarbon group (e.g. phenyl and tolyl), which can be unsubstituted or which can carry one or more substituents selected from lower alkylenedioxy, halogen, nitro, lower alkyl or lower alkoxy, or a polynuclear aryl group (e.g. naphthyl, anthryl, phenanthryl and azulyl), which can carry one or more of the aforementioned substituents. The preferred aryl groups are the substituted and unsubstituted mononuclear aryl groups, particularly phenyl. The term "aryl-(lower alkyl)" comprehends groups in which the aryl and lower alkyl moieties are as defined earlier, particularly benzyl.
The term "hydrolysable ester or ether group" used in this Specification designates any ester or ether group which can be hydrolysed to give the hydroxy group. Examples of such ester groups are those in which the acyl moiety is derived from a lower alkenoic acid, an aryl-(lower alkanoic) acid, phosphoric acid, carbonic acid or a lower alkanedicarboxylic acid. Among the acids which can be used to form such ester groups are the acid anhydrides and the acid halides, preferably acid chlorides or acid bromides, with the lower alkanoic acid anhydrides (e.g. acetic anhydride and caproic anhydride), the aryl-(lower alkanoic) acid anhydrides, lower alkanedicarboxylic acid anhydrides (e.g. succinic anhydride) and chloroformates (e.g. trichloroethylchloroformate) being preferred. A suitable ether providing a protecting group is, for example, the tetrahydropyranyl ether or 4 methoxy - 5,6 - dihydro - 2H - pyranyl ether. Other suitable ethers are the arylmethyl ethers such as the benzyl, benzhydryl and trityl ethers, the a-(lower alkoxy)-(lower alkyl) ethers such as the methoxymethyl ether, the allylic ether and the trialkylsilyl ethers such as the trimethylsilyl ether and the dimethyl tert.butylsilyl ether.
The removal of the aforementioned protecting groups can be carried out in a conventional manner and liberates the free hydroxy group. If the hydroxy group is protected by a hydrolysable ether group, any conventional ether hydrolysis technique can be used, preferably treatment with an aqueous inorganic acid.
Hydrolysable ester groups can be removed by treatment with a base in an aqueous medium in a conventional manner. Among the preferred bases there may be mentioned aqueous sodium hydroxide. Such treatment will also convert a lower alkoxycarbonyl group denoted by R1 and/or the -COOR group into a carboxy group.
A carboxy group present (R=H) can be converted into a lower alkoxycarbonyl group by conventional esterification techniques. As the esterification agent there is used, for example, diazomethane or a lower alkanol or a reactive derivative thereof
(e.g. a lower alkyl halide). Any conventional conditions can be adopted for this
esterification.
The starting materials of formula II can be prepared according to the following
Formula Scheme in which R1, R4, R4 and R6 and the double bond or bonds have
the significance given earlier.
Formula Scheme
Having regard to the foregoing Formula Scheme, a compound of formula Ill is converted into a compound of formula IV by reaction with a phosphonium salt of the general formula
wherein R4 and R4 have the significance given earlier, R, R and R5. each represent an aryl or di(lower alkylamino) group and Y'O represents a halogen anion, or with a phosphonate of the general formula
wherein R4 and R4 have the significance given earlier and R7 and R71 each
represent an aryl, aryloxy or lower alkoxy group.
The reaction of a compound of formula III with a phosphonium salt of formula
IX to give a compound of formula IV is carried out by means of a Wittig reaction.
Any of the conditions which are conventional in Wittig reactions can be used in carrying out this reaction.
The reaction of a compound of formula III with a phosphonate of formula X to give a compound of formula IV is carried out by means of a Horner reaction. Any of the conditions which are conventional in Horner-type reactions can be used in carrying out this reaction.
A compound of formula V can be obtained by treating a compound of formula
IV with a reducing agent. In carrying out this reduction, any conventional reducing agent which will selectively reduce a carbonyl group to a hydroxy group can be used. Preferred reducing agents are the hydrides, particularly the aluminium hydrides such as the alkali metal aluminium hydrides, and the borohydrides such as the alkali metal borohydrides, with zinc borohydride being quite particularly preferred.
In carrying out this reduction, temperature and pressure are not critical, and the reduction can be carried out at room temperature and atmospheric pressure or at elevated or reduced temperatures and pressures. Generally, it is preferred to carry out this reduction at a temperature of from -30 C to the reflux temperature of the reduction mixture. This reduction can be carried out in the presence of an inert organic solvent. Any conventional inert organic solvent such as the conventional inert organic solvents mentioned hereinbefore or water can be used. Among the preferred solvents are methanol, dimethoxyethyleneglycol and ethers such as tetrahydrofuran, diethyl ether and dioxane.
A compound of formula V may be separated into its two isomers by conventional methods to produce one isomer of the general formula
and the other isomer of the general formula
wherein R1, R4 and R4 have the significance given earlier.
Any conventional separation method such as column chromatography, vapour
phase chromatography etc can be used to carry out this separation. Either of the
aforementioned isomers can be used in the subsequent step. The configuration of
the hydroxy group on the octenyl side-chain will be carried through the subsequent
steps so that the hydroxy group on the octenyl side-chain in the prostaglandin
derivatives provided by this invention will have the same configuration as in the
compound of formula VA and VB, respectively.
A compound of formula V, VA or VB can be converted into a compound of
formula VI by esterifying or etherifying the free hydroxy group with a hydrolysable
ether or ester protecting group. This esterification or etherification can be carried
out according to conventional esterification or etherification procedures. Among
the preferred hydrolysable ester groups are the lower alkanoyl groups, especially
acetyl. Among the preferred hydrolysable ether groups are 2-tetrahydropyranyl
groups.
A compound of formula VI in which R1 represents a lower alkoxycarbonyl group and R6 represents a hydroxy group protected by a hydrolysable ether group can be subjected to alkaline hydrolysis (e.g. with aqueous sodium hydroxide solution) to yield a compound of formul Vl in which R, represents a carboxy group without removing the protecting group present on the hydroxy group.
A compound of formula VI is converted into a compound of formula VII by treatment with a reducing agent. In carrying out this reduction, any conventional reducing agent which will selectively reduce a carbonyl group to a hydroxy group can be used. Preferred reducing agents are the hydrides, particularly the aluminium hydrides such as the alkali metal aluminium hydride, and the borohydrides such as alkali metal borohydrides, with diisobutylaluminium hydride being particularly preferred. Also, this reduction can be carried out using a di(branched-chain lower alkyl)borane such as bis(3-methyl-2-butyl)borane. In carrying out this reduction, temperature and pressure are not critical and the reduction can be carried out at room temperature and atmospheric pressure or at elevated or reduced temperatures and pressures. Generally, it is preferred to carry out this reduction at a temperature of from -70"C to room temperature (300 C). This reduction can be carried out in the presence of an inert organic solvent. Any conventional inert organic solvents can be used in carrying out this reduction. Among the preferred solvents are dimethoxyethyleneglycol and ethers such as tetrahydrofuran, diethyl ether and dioxane.
A compound of formula IIA is obtained from a compound of formula VII by reaction with 9 phosphonium salt of the general formula
wherein R5, Rso, R51 and YO have the significance given earlier.
It has been found that a compound of formula VII will react with a phosphonium salt of formula XI to produce a compound of formula IIA having a predominantly cis double-bond in the 5-position of the acid chain in a solvent medium containing hexamethylphosphoramide using sodium bistrimethylsilylamide as a base. If solvents other than hexamethylphosphoramide or bases other than sodium bistrimethylsilylamide are used, the compound of formula IIA may result in poorer yields. However, conventional inert organic solvents may be mixed with the hexamethylphosphoramide to form the solvent medium. If other solvents are used, these solvents can be conventional inert organic solvents. On the other hand, the solvent system can contain only the hexamethylphosphoramide. Therefore, this reaction is carried out using hexamethylphosphoramide as the solvent and sodium bistrimethylsilylamide as the base. In carrying out this reaction, temperature and pressure are not critical and this reaction can be carried out at room temperature and pressure. However, if desired, higher or lower temperatures can be used. Generally, it is preferred to carry out this reaction at a temperature of from 0 C to 500 C.
A compound of formula IIA can be converted into a compound of the general formula
wherein R1, R4, R4 and R6 have the significance given earlier, by treatment with an oxidising agent. Any conventional oxidising agent which will convert a hydroxy group into an oxo group can be used in carrying out this oxidation. Among the preferred oxidising agents are chromate oxidising agents such as chromium trioxide. Any of the conditions which are conventional in using these oxidising agents can be used to carry out the present oxidation.
A compound of formula IIA or IIB can be converted into a compound of formula II in which X represents the -CH2-CH2- group by hydrogenation. Any conventional hydrogenation method such as catalytic hydrogenation can be used to carry out this hydrogenation. Among the preferred hydrogenation methods is the use of hydrogen in the presence of a noble metal catalyst such as platinum of palladium under conventional conditions.
The carboxy group in a compound of formula II, IIA or IIB can be converted into a lower alkoxycarbonyl group by esterification with diazomethane or a reactive derivative of a lower alkanol such as a lower alkyl halide. Any conventional esterification conditions can be used in carrying out this esterification.
The phosphonium salts of formula IX and the phosphonates of formula X can be obtained from a compound of the general formula
wherein R4 and R4 have the significance given earlier and R8 represents a lower
alkyl group, via the following intermediates:
wherein R4 and R4 have the significance given earlier and X represents a halogen
atom.
A compound of formula VIII is converted into a compound of formula XII by acid hydrolysis. Any conventional method of acid hydrolysis can be used.
Generally, this acid hydrolysis is carried out at a temperature from 200C to 1200C in the presence of an aqueous mineral acid such as sulphuric acid.
A compound of formula XII is converted into a compound of formula XIII by treatment with a halogenating agent. Any conventional halogenating agent can be used. Among the preferred halogenating agents there may be mentioned oxalyl chloride, thionyl chloride and phosphorus pentachloride. Any of the conditions which are conventional in using these halogenating agents can be used in carrying out this halogenation.
A compound of formula XIII can be converted into a compound of formula
XIV by reaction with diazomethane under conditions which are conventional in reacting an acid halide with diazomethane.
A compound of formula XIV is converted into a compound of formula XV by treatment with a gaseous hydrohalide acid such as gaseous hydrogen bromide under conditions which are conventional for converting a diazo compound into a halide.
A compound of formula XV is converted into a phosphonate of formula X by reaction with a tri(lower alkyl)phosphite under conventional conditions.
A compound of formula XV can be converted into a phosphonium salt of formula IX by reaction with a tri[aryl or di(lower alkyl)aminolphosphine under conventional conditions.
A compound of formula VIII hereinbefore in which R4 represents a
trifluoromethyl group can be prepared from a compound of the general formula
wherein R4 and R8 have the significance given earlier, by reaction with sulphur tetrafluoride. The sulphur tetrafluoride is reacted with a compound of formula XVI in a closed container at a temperature of from 20"C to 85"C. Generally, from 1 to 4 mol of sulphur tetrafluoride are present per mol of the compound of formula XVI. Amounts of sulphur tetrafluoride greater than 4 mol per mol of the compound of formula XVI may, however, be used. If desired, acid catalysts and/or a solvent may be present in the reaction medium. Any conventional inert organic solvent, preferably a halogenated hydrocarbon such as methylene chloride, may, if desired, be present in the reaction medium. If desired, any conventional acid catalyst such as hydrofluoric acid, boron trifluoride etc can be added to the reaction medium. On the other hand, no solvent and/or acid catalyst need be added to the reaction medium.
The prostaglandin derivatives provided by the present invention have the ability to modify the activity of the alimentary and reproductive smooth muscles, to block mucous and enzyme secretions by the stomach, to stimulate the synthesis of adrenal corticoids and to modify blood pressure and lipolysis.
Furthermore, they are active in inducing labour during pregnancy in femals and for therapeutically terminating pregnancy. The present prostaglandin derivatives in which R2 and R3 together represent an oxo group are useful in that they lower blood pressure and inhibit blood platelet aggregation. The present prostaglandin derivatives in which R2 and R3 together represent an oxo group are especially valuable as anti-ulcerogenic agents. The present prostaglandin derivatives in which
R2 represents a hydroxy group and R3 represents a hydrogen atom are active as blood pressure raising agents in the same manner as prostaglandin F2.
The aforementioned anti-ulcerogenic effect is evidenced by the fact that the EDso of a derivative such as 7 - [3a - methyl - 5 - oxo - 2p - (3a - hydroxy - 4 trifluoromethyl - 4 - methyl - 1 - trans - octenyl) - Ia - cyclopentyll - cis - 5 heptenoic acid is 0.47 i.p. and 0.0001 p.o. when administered to rats in the following test:
Rats were fasted for 16 hours prior to the subcutaneous administration of indomethacin at a dosage of 100 mg/kg. Simultaneously with the indomethacin administration, the prostaglandin derivatives to be tested were administered intraperitoneally at three dosage levels and orally at six dosage levels. These dosages of the prostaglandin derivatives were repeated every 30 minutes for 6 hours (12 dosages). After 6 hours, the rats were killed and the stomachs were examined for ulceration or haemorrhage. Protection from incidence of ulceration was used to determine activity. 5 rats were used per dosage level and ED50 values were calculated.
The prostaglandin derivatives provided by the present invention can be used in the pharmaceutical and veterinary fields in a variety of pharmaceutical or veterinary preparations which can take the form of tablets, pills, powders, capsules, injectables, solutions, suppositories, emulsions, dispersions, feed pre-mixes and other suitable forms. The pharmaceutical or veterinary preparations conveniently contain a prostaglandin derivative provided by this invention in admixture with a non-toxic pharmaceutical organic carrier or a non-toxic pharmaceutical inorganic carrier. Typical pharmaceutically acceptable carriers are, for example, water, gelatin, lactose, starches, magnesium stearate, talc, vegetable oils, polyalkyleneglycols, petroleum jelly and other conventionally used pharmaceutically acceptable carriers. The pharmaceutical preparations may also contain non-toxic auxiliary substances such as emulsifying agents, preserving agents and wetting agents; for example, sorbitan monolaurate, triethanolamine oleate, polyoxyethylene sorbitan and dioctyl sodium sulphosuccinate.
The following Examples illustrate the process provided by the present invention:
Example I
To a mixture of 6 g of chromium trioxide and 9.5 g of pyridine in 150 ml of methylene chloride were added at OOC 4.5 g of 7 - [3a - methyl - 5a - hydroxy 2p - [3zr - (2 - tetrahydropyranyloxy) - 4 - trifluoromethyl - 1 - trans - octenyli - Ia - cyclopentyl] - cis - 5 - heptenoic acid dissolved in 50 ml of methylene chloride. The mixture was stirred for 1 hour at room temperature and filtered through a bed of Celite (registered Trade Mark). The Celite was washed with methylene chloride and the combined methylene chloride solutions were washed with dilute hydrochloric acid to remove any remaining pyridine. The methylene chloride was then removed under reduced pressure and the residue was treated with 5Q ml of acetic acid/water (3:1 parts by volume) at 35"C for 15 hours. The solvents were then removed under a high vacuum and the residue was purified by column chromatography to give the product, 7 - [3a - methyl - 5 - oxo - 2p - (3a hydroxy - 4 - trifluoromethyl - I - trans - octenyl) - la - cyclophentyl] - cis - 5 heptenoic acid.
The starting material was prepared as follows:
To a 4 litre stainless steel bomb were added 237 g (1.26 mol) of 2carboethoxyhexanoic acid, 260 ml of methylene chloride and 19 ml of 48% hydrofluoric acid. The bomb was sealed with an assembly consisting of a rupture disc (14001600 psi) and a needle valve. It was then cooled in a dry ice/acetone bath for 30 minutes and evacuated to less than 10 mm Hg pressure. While maintaining the bomb in the cooling bath, 600 g (5.56 mol) of sulphur tetrafluoride were condensed into the bomb from an attached lecture bottle. The needle valve closed and the bomb was removed from the cooling bath and allowed to remain at room temperature with only occasional agitation for 13 days. After this period, the bomb was vented and the residual materials were taken up in 2.2 litres of pentane and dried over sodium fluoride/magnesium sulphate. Distillation of the filtered pentane solution gave 117g (44%) of ethyl 2 - tnfluoromethylhexanoate of boiling point 690-760C/20 mm Hg.
10.05 g of ethyl 2 - trifluoromethylhexanoate were mixed with 50 ml of
concentrated sulphuric acid and warmed to 750C for 20 hours. After cooling, the
acid was poured into excess ice. The resulting mixture was saturated with sodium
chloride and extracted with three 100 ml portions of diethyl ether. The combined ether extracts were dried over magnesium sulphate and evaporated to give a residual oil which yielded 7.50 g of 2 - trifluoromethylhexanoic acid upon
distillation; boiling point 80"--85"C/2.8 mm Hg.
2.3 g of 2 - trifluoromethylhexanoic acid were added dropwise to 10 g of oxalyl
chloride and the mixture was heated to reflux for 2 hours. Distillation of the mixture after this time yielded 2.27 g (90 /O) of 2 - trifluoromethylhexanoyl chloride of boiling point 670-700C/43 mm Hg.
2.27 g of 2 - trifluoromethylhexanoyl chloride were added dropwise to an excess of ethereal diazomethane solution at OOC. After I hour, the excess diazomethane was removed with a stream of nitrogen. The ether solution at OOC was then treated with an excess of hydrogen bromide gas. After 15 minutes, the solution was washed with three 10 ml portions of saturated sodium chloride solution, dried over magnesium sulphate and evaporated to cdnstant weight in a vacuum to give 2.56 g (88%) of 3 - trifluoromethyl - 1 - bromoheptan - 2 - one which was not further purified.
A mixture of 2.50 g of 3 - trifluoromethyl - 1 - bromoheptan - 2 - one and 5.1 g of triethyl phosphite was heated to 1000C and continuously flushed with a slow stream of nitrogen. After 6 hours, the mixture was distilled to give 2.60 g of a mixture of diethyl (3 - trifluoromethyl - 2 - oxoheptyl)phosphonate and diethyl 2 (3 - trifluoromethylhept - 1 - enyl) - phosphate. The diethyl(3 - trifluoromethyl 2 - oxoheptyl)phosphonate was isolated from this mixture.
To a suspension of 0.7 g of sodium hydride in 150 ml of diglyme were added 6 g of diethyl (3 - trifluoromethyl - 2 - oxoheptyl)phosphonate. After stirring for 1.5 hour, 5 g of 3,3ap,4,5,6,6aQ - hexahydro - 4p - formyl - 5a - methyl - 2 - oxo 2H - cyclopenta[b]furan dissolved in 30 ml of glyme were added dropwise at OOC.
After stirring for 3 hours at room temperature, 500 ml of diethyl ether were added
and the mixture was washed with water. The organic layer was then dried over
magnesium sulphate and the solvent was removed under reduced pressure. The
residue was then washed through 75 g of silica gel to give 3,3ap,4,5,6,6ap - hexahydro - 4fi- (3 - oxo- 4- trifluoromethyl - I - trans - octenyl) - 5a - methyl - 2 - oxo - 2H - cylcopenta[b]furan.
To a solution of 4.5 g of 3,3ap,4,5,6,6ap - hexahydro - 4p - (3 - oxo - 4 trifluoromethyl - 1 - trans - octenyl) - 5a - methyl - 2 - oxo - 2H cyclopentatbituran in 100 ml of diglyme was added an excess of zinc borohydriffe in
50 ml of glyme and the resulting solution was stirred for 3 hours. The solution was cooled to 0 C and treated with 200 ml of water, 400 ml of diethyl ether and 10 ml of 0.5-N aqueous sulphuric acid. The ether was separated and dried over magnesium
sulphate, and the solvent was removed under reduced pressure to give
3,3a ,4,5,6,6a - hexahydro - 4p (3 hydroxy - 4 - trifluoromethyl - I - trans
octenyl) - Sa methyl - 2 oxo - 2H - cyclopenta[b]furan. Column
chromatography on silica gel using diethyl ether/hexane (70:30 parts by volume) then afforded first 3,3a ,4,5,6,6a - hexahydro - 4p - (3a - hydroxy - 4 triiiuoromethyl - I - trans - octenl)- Sa - methyl - 2 - oxo 2H
cyclopentalb]furan and then 3,3ap,4,5,6,6ap - hexahydro - 4p - (3p - hydroxy 4 - trifluoromethyl - 1 - trans - octenyl) - 5- - methyl - 2 - oxo - 2H
cyclopenta!bjfuran.
A solution of 5 g of 3,3a ,4,5,6,6a - hexahydro - 4p - (3cr - hydroxy - 4 trifluoromethyl - I - trans - octenyl) - 5a - methyl - 2 - oxo - 2H cyclopenta[b]furan, 12 g of dihydropyran and 25 mg of p-toluenesulphonic acid in 200 ml of methylene choride was stirred at 25"C for 3 hours. The solution was washed with saturated sodium bicarbonate solution, the methylene chloride solution was dried over a magnesium sulphate and the volatile components were evaporated under reduced pressure to give 6.4 g of 3,3a ,4,5,6,6a - hexahydro 4p - [3a - (2 - tetrahydropyranyloxy) - 4 - trifluoromethyl - 1 - trans - octenyl] 5a - methyl - 2 - oxo - 2H - cyclopenta[b]furan.
To a solution of 3,3ap,4,5,6,6ap- hexahydro - 4p- [3cr- (2 tetrahydropyranyloxy) - 4 - trifluoromethyl - I - trans - octenyl) - 5a - methyl 2 - oxo - 2H - cyclopenta[b]furan in 150 ml of toluene was added dropwise at -78"C I equivalent of diisobutyl aluminium hydride in the same solvent. The mixture was stirred at this temperature for 2 hours, after which time 20 ml of methanol were slowly added and the mixture was stirred for 2 hours at room temperature. Th washed with ethyl acetate and the solvents were then removed under reduced pressure. The residue was then washed through a column of silica gel to give 3,3ass,4,5,6,6ass - hexahydro - 4p - [3a - (2 - tetrahydropyranyloxy) - 4 trifluoromethyl - 1 - trans - octenyll - 5a - methyl - 211 - cyclopenta[b]furan - 2 - ol.
3.6 g of 3,3ass,4,5,6,6ass - hexahydro - 4ss - [3a - (2 - tetrahydropyranyloxy) 4 - trifluoromethyl - I - trans - octenyl] - Sa - methyl - 211 - cyclopenta[b]furan - 2 - owl in 150 ml of hexamethylphosphoric acid triamide were reacted with 2.2 equivalents of Wittig reagent generated by the reaction of 7.0 g (0.0384 mol) of sodium bistrimethylsilylamide with 8.4 g (0.19 mol) of 4 carboxybutyltriphenylphosphonium bromide. After stirring for 30 minutes, the mixture was acidified to pH 6.5 with dilute sulphuric acid and the hexamethylphosphoramide was removed under a high vacuum. The mixture was then extracted several times with ether and the ether solution was dried over sodium sulphate. The solvent was then removed under reduced pressure and the residue was chromatographed on silica gel to give 3.5 g of 7 - [3a - methyl hydroxy - 2ss - [3a - (2 - tetrahydropyranyloxy) - 4 - trifluoromethyl - I - trans octenyl] - la - cyclopentyl] - cis - 5 - heptenoic acid.
Example 2
According to the procedure described in Example 1, 7 - [3a - methyl - Sa hydroxy -3P[3a - (2 - tetrahydropyranyloxy) - 4 - trifluoromethyl - 4 - methyl 1 - trans - octenyl] - Ia - cyclopentyl] - cis - 5 - heptanoic acid was converted into 7 - [3a - methyl - 5 - oxo - 2P - 3a - hydroxy - 4 - trifluoromethyl - 4 methyl - 1 - trans - octenyl) - la - cyclopentyl] - cis - 5 - heptanoic acid.
The starting material was prepared according to the procedure described in
Example 1 via the following intermediates:
Ethyl 2 - trifluoromethyl - 2 - methylhexanoate, diethyl (3 - trifluoromethyl - 2 - oxoheptyl)phosphonate,
3,3ass,4,5,6,6ass - hexahydro - 4ss - (3 - oxo - 4 - methyl - 4 trifluoromethyl - 1 - trans - octenyl) - 5a - methyl - 2 - oxo - 211 - cyclopenta[b]furan,
3,3ass,4,5,6,6ass - hexahydro - 43a - hydroxy - 4 - trifluoromethyl - 4 methyl - 1 - trans - octenyl) - 5a - methyl - 2 - oxo - 2H - cyclopenta[b]furan,
3,3ap,4,5,6,6ap - hexahydro - 4p - [3a - (2 - tetrahydropyranyloxy) - 4 - trifluorometh I - 4 - methyl - I - trans - octenyl] - 5a - methyl - 2 - oxo - 2H cyclopentalbl uran, and
3,3ass,4,5,6,6ass - hexahydro - 4ss - [3a - (2 - tetrahydropyranyloxy) - 4 trifluoromethyl - 4 - methyl - I - trans - octenyl] - 5a - methyl - 211 - cyclopenta[b]furan - 2 - ol.
Example 3
A solution of 200 mg of 7 - [3a - methyl - 5a - hydroxy - 2ss - [3(r - (2 tetrahydropyranyloxy) - 4 - trifluoromethyl - I - trans - octenyl] - Ia - cyclopentyl] - cis - 5 - heptenoic acid in 5 ml of acetic acid/water (3:1 parts by volume) was kept at 350C for 15 hours. The solvent was then removed under high vacuum and the residue was purified by column chromatography to give the product, 7 - [3a - methyl - 5a - hydroxy - 2ss - (3a - hydroxy - 4 trifluoromethyl - 1 - trans - octenyl) - 1α - cyclopentyl] - cis - 5 - heptenoic acid.
Example 4
According to the procedure described in Example 3, 7 - [3a - methyl - 5a hydroxy - 2p - [3a - (2 - tetrahydropyranyloxy) - 4 - trifluoromethyl - 4- methyl - I - trans - octenyl] - la - cyclopentyl] - cis - 5 - heptenoic acid was converted into 7 - [3a - methyl - 5a - hydroxy - 2p - (3a - hydroxy - 4 trifluoromethyl - 4 - methyl - I - trans - octenyl) - la - cyclqpentyl1 - cis - 5 heptenoic acid.
Example 5
According to the procedure described in Example 1, 7 - [5cr - hydroxy - 2ss [3ct - (2 - tetrahydropyranyloxy) - 4 - trifluoromethyl - i - trans - octenyl] - I a cyclopentyl] - cis - 5 - heptenoic acid was converted into 7 - [5 - oxo - 2p - (3a hydroxy -4 - trifluoromethyl - 1 - trans - octenyl) - la - cyclopentyll - cis - 5 heptanoic acid.
Example 6
According to the procedure described in Example 1, 7 - [5ct - hydroxy - 2P [3a - (2 - tetrahydropyranyloxy) - 4 - trifluoromethyl - 4 - methyl - I - trans octenyl] - Ia - cyclopentyl] - cis - 5 - heptenoic acid was converted into 7 - [5 oxo - 2,B - (3a - hydroxy - 4 - trifluoromethyl - 4 - methyl - I trans - octenyl) Ia - cyclopentyl] - cis - 5 - heptenoic acid.
Example 7
According to the procedure described in Example 3, 7 - ISa - hydroxy 2A-- [3a - (2 - tetrahydropyranyloxy) - 4 - trifluoromethyl - 1- trans - octenyli - 1- cyclopentyl] - cis - 5 - heptenoic acid was converted into 7 - [5a - hydroxy - 2p (3sr - hydroxy - 4 - trifluoromethyl - I - trans - octenyl) - la - cyclopentyl] cis - 5 - heptenoic acid.
Example 8
According to the procedure described in Example 3, 7 - [5a - hydroxy - 2p - [3a - (2 - tetrahydropyranyloxy) - 4 - trifluoromethyl - 4 - methyl - I - trans octenyl] - la - cyclopentyl] - cis - 5 - heptenoic acid was converted into 7 [5a - hydroxy - 2,B(3a - hydroxy - 4 - trifluoromethyl - 4 - methyl - I - trans octenyl) - la - cyclopentyl] - cis - 5 - heptenoic acid.
Example 9
Nat. (5Z, 13E) - I l(R) - methyl - 16,16 - difluoro - 15(R) - (tetrahydro 211 - 2 - pyranyloxy) - 9(S) - hydroxyprosta - 5,13 - dienoic acid was warmed at 40"C with a mixture of acetic acid/water/tetrahydrofuran (55:30:15) to yield nat.
(5Z, 13E) - Il(R) - methyl - 16,16 - difluoro - 9(S),15(R) - dihydroxyprosta 5,13 - dienoic acid, a light yellow viscous oil. The mass spectrum is in agreement with the structure indicated.
The starting material was prepared via the following intermediates:
Ethyl 2,2 - difluorohexanoate,
dimethyl (2 - oxo - 3,4 - difluoroheptyl)phosphate,
3,3a(R),4,5,6,6a(S) - hexahydro - 4(R) - (4,4 - difluoro - 3 - oxo - I - trans octenyl) - 5(R) - methyl - 2H - cyclopenta[b]furan - 2 - one,
3,3a(R),4,5,6,6a(S)-hexahydro - 4(R) - (4,4 - difluoro - 3(R) - hydroxy - I trans - octenyl) - 5(R) - methyl - 2H - cyclopenta[b]furan - 2 - one 3,3a(R),4,5,6,6a(S) - hexahydro - 4R - [4,4 - difluoro - 3(R) - (tetrahydro 211 - 2 - pyranyloxy) - I - trans - octenyl] - 5(R) - methyl - 2(H)- cyclopenta[b]furan - 2 - one, and
3,3a(R),4,5,6,6a(R) - hexahydro - 4(R) - [4,4 - difluoro - 3(R) - (tetrahydro 2H - 2 - pyranyloxy) - I - trans - octenyl] - 5(R),- methyl - 2(H) cyclopenta[b]furan - 2 - ol.
Example 10
In an analogous manner to that described in Example 1, nat. (5Z, 13E) 11(R) - methyl - 16,16 - difluoro - 15(R) - (tetrahydro - 2H - 2 - pyranyloxy) - 9(S) - hydroxyprosta - 5,13 - dienoic acid was converted into (5Z, 13E) - 11(R) methyl - 16.16 - difluoro - 15(R) - hydroxy - 9 - oxoprosta - 5,13 - dienoic acid, a light yellow viscous oil; [a]25D=67.76 (in chloroform).
The following example illustrates a typical preparation containing one of the prostaglandin derivatives provided by the present invention:
Example A
A tablet containing the following ingredients was prepared:
Ingredient Per tablet 7-[3α-Methyl-5-oxo-2ss-(3α-hydroxy-4-
trifluoromethyl- 1 -trans-octenyl)- l a- cyclopentyl]-cis-5-heptenoic acid 25 mg
Dicalcium phosphate dihydrate, unmilled 175 mg
Corn starch 24 mg
Magnesium stearate I mg
Total weight 225 mg
Claims (15)
- WHAT WE CLAIM IS:1. Compounds of the general formulawherein R represents a hydrogen atom or a lower alkyl group, R1 represents a hydrogen atom or a lower alkyl group, R2 represents a hydroxy group and R3 represents a hydrogen atom or R and R3 together represents an oxo group, R4 represents a hydrogen or fluorine atom or a lower alkyl group, R4 represents a trifluoromethyl group or, when R4 represents a fluorine atom R4 may also represent a fluorine atom and X represents the -CH=CH- or -CH2-CH2- group, and enantiomers and racemates thereof, the double bond of the substituted octenyl side chain having trans configuration and the optional double bond in X having cis or trans configuration.
- 2. Prostaglandin derivatives as set forth in claim 1, wherein Rl represents a lower alkyl group.
- 3. Prostaglandin derivatives as set forth in claim I or claim 2, wherein R represents a hydrogen atom.
- 4. 7 - [3a - Methyl - 5 - oxo - 2p - (3a - hydroxy - 4 - trifluoromethyl - I trans - octenyl) - Ia - cyclopentyl] - cis - 5 - heptenoic acid.
- 5. 7 - [3a - Methyl - 5a - hydroxy - 2p - (3an hydroxy - 4trifluoromethyl - I - trans - octenyl) - Ia - cyclopentyl] - cis - 5 - heptenoic acid.
- 6. 7 - [3a - Methyl - 5 - oxo - 2p - (3a - hydroxy - 4 - trifluoromethyl - 4 methyl - 1 - trans - octenyl) - la - cyclopentyl] - cis - 5 - heptenoic acid.
- 7. 7 - [3cr - Methyl - 5cr - hydroxy - 2p - (3a - hydroxy - 4- trifluoromethyl - 4 - methyl - 1 - trans - octenyl) - 1a - cyclopentyl] - cis - 5 heptenoic acid.
- 8. 7 - ISa - Hydroxy - 2p - (3a - hydroxy - 4 - trifluoromethyl - I - trans octenyl) - la - cyclopentyl] - cis - 5 - heptenoic acid.
- 9. 7 - [5a - Hydroxy - 2ss - (3a - hydroxy - 4 - trifluoromethyl -4 - methyl - I - trans - octenyl) - Ia - cyclopentyl] - cis - 5 - heptenoic acid.
- 10. A process for the manufacture of the prostaglandin derivatives set forth in claim 1, which process comprises hydrolysing the group denoted by R6 in a compound of the general formulawherein R, R1, R2, R3, R4, R4, X and the double bond or bonds have the significance given in claim I and R6 represents a hydroxy group protected by a hydrolysable ether or ester group, into a hydroxy group, and, if desired, esterifying a carboxy group to form a lower alkoxycarbonyl group or converting a lower alkoxycarbonyl group into a carboxy group by basic hydrolysis.
- II. A process according to claim 10, wherein Rl represents a lower alkyl group.
- 12. A process according to claim 10 or claim 11, wherein R represents a hydrogen atom.
- 13. A process for the manufacture of the prostaglandin derivatives set forth in claim 1, substantially as hereinbefore described with reference to any one of Examples I to 10.
- 14. A prostaglandin derivative as set forth in claim 1, when manufactured by the process claimed in any one of claims 10 to 13 inclusive or by an obvious chemical equivalent thereof.
- 15. A pharmaceutical preparation or veterinary preparation containing a prostaglandin derivative as set forth in any one of claims 1 to 9 inclusive or 14 in association with a compatible carrier.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US05/745,257 US4112225A (en) | 1974-06-18 | 1976-12-08 | 16-CF3 prostaglandins |
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GB1594368A true GB1594368A (en) | 1981-07-30 |
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GB50921/77A Expired GB1594368A (en) | 1976-12-08 | 1977-12-07 | Prostaglandin derivatives |
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AU (1) | AU3118577A (en) |
BE (1) | BE861562A (en) |
DE (1) | DE2754063A1 (en) |
DK (1) | DK545177A (en) |
FR (1) | FR2373527A1 (en) |
GB (1) | GB1594368A (en) |
IE (1) | IE46103B1 (en) |
IL (1) | IL53505A0 (en) |
IT (1) | IT1089402B (en) |
LU (1) | LU78644A1 (en) |
NL (1) | NL7713542A (en) |
NZ (1) | NZ185836A (en) |
SE (1) | SE7713899L (en) |
ZA (1) | ZA777142B (en) |
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ZA764727B (en) * | 1975-09-02 | 1977-07-27 | Upjohn Co | Prostanoic acid derivatives |
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1977
- 1977-12-01 IL IL53505A patent/IL53505A0/en unknown
- 1977-12-01 ZA ZA00777142A patent/ZA777142B/en unknown
- 1977-12-02 AU AU31185/77A patent/AU3118577A/en active Pending
- 1977-12-02 NZ NZ185836A patent/NZ185836A/en unknown
- 1977-12-02 IE IE2455/77A patent/IE46103B1/en unknown
- 1977-12-05 DE DE19772754063 patent/DE2754063A1/en not_active Withdrawn
- 1977-12-06 LU LU7778644A patent/LU78644A1/xx unknown
- 1977-12-06 IT IT30499/77A patent/IT1089402B/en active
- 1977-12-06 FR FR7736746A patent/FR2373527A1/en active Granted
- 1977-12-07 JP JP14619577A patent/JPS5371040A/en active Pending
- 1977-12-07 GB GB50921/77A patent/GB1594368A/en not_active Expired
- 1977-12-07 NL NL7713542A patent/NL7713542A/en not_active Application Discontinuation
- 1977-12-07 SE SE7713899A patent/SE7713899L/en unknown
- 1977-12-07 DK DK545177A patent/DK545177A/en not_active Application Discontinuation
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IL53505A0 (en) | 1978-03-10 |
FR2373527B1 (en) | 1981-01-09 |
IE46103L (en) | 1978-06-08 |
NL7713542A (en) | 1978-06-12 |
NZ185836A (en) | 1979-03-28 |
DE2754063A1 (en) | 1978-09-07 |
DK545177A (en) | 1978-06-09 |
BE861562A (en) | 1978-06-07 |
SE7713899L (en) | 1978-06-09 |
ZA777142B (en) | 1978-09-27 |
IE46103B1 (en) | 1983-02-23 |
IT1089402B (en) | 1985-06-18 |
FR2373527A1 (en) | 1978-07-07 |
JPS5371040A (en) | 1978-06-24 |
LU78644A1 (en) | 1979-02-02 |
AU3118577A (en) | 1979-06-07 |
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Date | Code | Title | Description |
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PS | Patent sealed [section 19, patents act 1949] | ||
PCNP | Patent ceased through non-payment of renewal fee |