FI87769B - Foerfarande foer framstaellning av farmakologiskt vaerdefull fenoxiaettiksyra - Google Patents
Foerfarande foer framstaellning av farmakologiskt vaerdefull fenoxiaettiksyra Download PDFInfo
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- FI87769B FI87769B FI873413A FI873413A FI87769B FI 87769 B FI87769 B FI 87769B FI 873413 A FI873413 A FI 873413A FI 873413 A FI873413 A FI 873413A FI 87769 B FI87769 B FI 87769B
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- mixture
- compound
- ethyl acetate
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- 230000000144 pharmacologic effect Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 26
- 150000003839 salts Chemical class 0.000 claims abstract description 19
- 238000002360 preparation method Methods 0.000 claims abstract description 18
- LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical compound OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 claims abstract description 17
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 14
- 125000005843 halogen group Chemical group 0.000 claims abstract description 13
- 125000001424 substituent group Chemical group 0.000 claims abstract description 10
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 7
- -1 phenol compound Chemical class 0.000 claims description 56
- 125000003277 amino group Chemical group 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 125000004953 trihalomethyl group Chemical group 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- UKRZQNFRBNAPMT-UHFFFAOYSA-N 2-[4-[2-[(4-chlorophenyl)sulfonylamino]propyl]phenoxy]acetic acid Chemical compound C=1C=C(Cl)C=CC=1S(=O)(=O)NC(C)CC1=CC=C(OCC(O)=O)C=C1 UKRZQNFRBNAPMT-UHFFFAOYSA-N 0.000 claims description 2
- 150000001242 acetic acid derivatives Chemical class 0.000 claims description 2
- 229940092714 benzenesulfonic acid Drugs 0.000 claims description 2
- QHCNLJSNVJYSQR-UHFFFAOYSA-N 2-[4-[3-amino-2-(4-chlorophenyl)sulfonylpropyl]phenoxy]acetic acid Chemical compound ClC1=CC=C(C=C1)S(=O)(=O)C(CC1=CC=C(OCC(=O)O)C=C1)CN QHCNLJSNVJYSQR-UHFFFAOYSA-N 0.000 claims 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract description 21
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 14
- 208000007536 Thrombosis Diseases 0.000 abstract description 5
- 238000011282 treatment Methods 0.000 abstract description 4
- 239000003814 drug Substances 0.000 abstract description 3
- 238000011321 prophylaxis Methods 0.000 abstract description 3
- 208000005189 Embolism Diseases 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 154
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 123
- 239000000203 mixture Substances 0.000 description 100
- 150000001875 compounds Chemical class 0.000 description 95
- 239000000243 solution Substances 0.000 description 74
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 64
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 56
- 235000019439 ethyl acetate Nutrition 0.000 description 52
- 239000002904 solvent Substances 0.000 description 48
- 239000003921 oil Substances 0.000 description 45
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 39
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 38
- 238000006243 chemical reaction Methods 0.000 description 38
- 239000000047 product Substances 0.000 description 35
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 34
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 33
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 33
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 32
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 26
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 23
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 21
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 20
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 20
- 239000007858 starting material Substances 0.000 description 20
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 19
- 239000010410 layer Substances 0.000 description 18
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 16
- 229910000027 potassium carbonate Inorganic materials 0.000 description 16
- 125000004432 carbon atom Chemical group C* 0.000 description 15
- 238000001704 evaporation Methods 0.000 description 15
- 230000008020 evaporation Effects 0.000 description 15
- 239000000284 extract Substances 0.000 description 14
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 13
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- 230000000694 effects Effects 0.000 description 12
- 238000005481 NMR spectroscopy Methods 0.000 description 11
- 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 10
- ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 description 10
- 239000011780 sodium chloride Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 241000699670 Mus sp. Species 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000013078 crystal Substances 0.000 description 9
- 229920006395 saturated elastomer Polymers 0.000 description 9
- 159000000000 sodium salts Chemical class 0.000 description 9
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 8
- 235000017557 sodium bicarbonate Nutrition 0.000 description 8
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 7
- 230000000702 anti-platelet effect Effects 0.000 description 7
- 239000003146 anticoagulant agent Substances 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 7
- 239000000706 filtrate Substances 0.000 description 7
- YDCHPLOFQATIDS-UHFFFAOYSA-N methyl 2-bromoacetate Chemical compound COC(=O)CBr YDCHPLOFQATIDS-UHFFFAOYSA-N 0.000 description 7
- 238000010898 silica gel chromatography Methods 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- CSKNSYBAZOQPLR-UHFFFAOYSA-N benzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 238000004440 column chromatography Methods 0.000 description 6
- 125000006239 protecting group Chemical group 0.000 description 6
- 238000001953 recrystallisation Methods 0.000 description 6
- 102000008186 Collagen Human genes 0.000 description 5
- 108010035532 Collagen Proteins 0.000 description 5
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 229940114079 arachidonic acid Drugs 0.000 description 5
- 235000021342 arachidonic acid Nutrition 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 239000002026 chloroform extract Substances 0.000 description 5
- 229920001436 collagen Polymers 0.000 description 5
- 239000012230 colorless oil Substances 0.000 description 5
- 230000003287 optical effect Effects 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 239000000741 silica gel Substances 0.000 description 5
- 229910002027 silica gel Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 4
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 4
- 150000008041 alkali metal carbonates Chemical class 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 4
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 208000010110 spontaneous platelet aggregation Diseases 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- XTNWJMVJVSGKLR-UHFFFAOYSA-N 2-[4-[2-(benzenesulfonamido)ethyl]phenoxy]acetic acid Chemical compound C1=CC(OCC(=O)O)=CC=C1CCNS(=O)(=O)C1=CC=CC=C1 XTNWJMVJVSGKLR-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 3
- 230000000740 bleeding effect Effects 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000002024 ethyl acetate extract Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 238000000338 in vitro Methods 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 230000003389 potentiating effect Effects 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
- 229910052727 yttrium Inorganic materials 0.000 description 3
- JISYSNUFDJQBKV-UHFFFAOYSA-N 1-(3-methoxy-4-phenylmethoxyphenyl)propan-2-amine Chemical compound COC1=CC(CC(C)N)=CC=C1OCC1=CC=CC=C1 JISYSNUFDJQBKV-UHFFFAOYSA-N 0.000 description 2
- BGBASCKIEQPJAW-UHFFFAOYSA-N 2-(2-fluoro-4-methoxyphenyl)propan-1-amine;hydrochloride Chemical compound Cl.COC1=CC=C(C(C)CN)C(F)=C1 BGBASCKIEQPJAW-UHFFFAOYSA-N 0.000 description 2
- ZCHZSZLUOLHRLG-UHFFFAOYSA-N 2-[4-[1-[(4-fluorophenyl)sulfonylamino]propan-2-yl]phenoxy]acetic acid Chemical compound C=1C=C(OCC(O)=O)C=CC=1C(C)CNS(=O)(=O)C1=CC=C(F)C=C1 ZCHZSZLUOLHRLG-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
- 241000961787 Josa Species 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 206010035664 Pneumonia Diseases 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- HSDAJNMJOMSNEV-UHFFFAOYSA-N benzyl chloroformate Chemical compound ClC(=O)OCC1=CC=CC=C1 HSDAJNMJOMSNEV-UHFFFAOYSA-N 0.000 description 2
- OCCSKVHYUZXXBF-UHFFFAOYSA-N benzyl n-[2-(4-hydroxyphenyl)propyl]carbamate Chemical compound C=1C=C(O)C=CC=1C(C)CNC(=O)OCC1=CC=CC=C1 OCCSKVHYUZXXBF-UHFFFAOYSA-N 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine hydrate Chemical compound O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- LDHQCZJRKDOVOX-IHWYPQMZSA-N isocrotonic acid Chemical compound C\C=C/C(O)=O LDHQCZJRKDOVOX-IHWYPQMZSA-N 0.000 description 2
- 239000012280 lithium aluminium hydride Substances 0.000 description 2
- 210000004072 lung Anatomy 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- CEFULRUFLNIOMV-UHFFFAOYSA-N n-[2-oxo-2-(4-phenylmethoxyphenyl)ethyl]benzenesulfonamide Chemical compound C=1C=C(OCC=2C=CC=CC=2)C=CC=1C(=O)CNS(=O)(=O)C1=CC=CC=C1 CEFULRUFLNIOMV-UHFFFAOYSA-N 0.000 description 2
- 150000007530 organic bases Chemical class 0.000 description 2
- 238000007911 parenteral administration Methods 0.000 description 2
- 239000000825 pharmaceutical preparation Substances 0.000 description 2
- SSOLNOMRVKKSON-UHFFFAOYSA-N proguanil Chemical compound CC(C)\N=C(/N)N=C(N)NC1=CC=C(Cl)C=C1 SSOLNOMRVKKSON-UHFFFAOYSA-N 0.000 description 2
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 230000002792 vascular Effects 0.000 description 2
- LJCJRRKKAKAKRV-UHFFFAOYSA-N (2-amino-2-methylpropyl) 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical group CC(C)(N)COC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 LJCJRRKKAKAKRV-UHFFFAOYSA-N 0.000 description 1
- NEGYEDYHPHMHGK-MRVPVSSYSA-N (2r)-1-(4-methoxyphenyl)propan-2-amine Chemical compound COC1=CC=C(C[C@@H](C)N)C=C1 NEGYEDYHPHMHGK-MRVPVSSYSA-N 0.000 description 1
- NEGYEDYHPHMHGK-QMMMGPOBSA-N (2s)-1-(4-methoxyphenyl)propan-2-amine Chemical compound COC1=CC=C(C[C@H](C)N)C=C1 NEGYEDYHPHMHGK-QMMMGPOBSA-N 0.000 description 1
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
- PIRRWUMTIBFCCW-UHFFFAOYSA-N 1-(2-fluoro-4-methoxyphenyl)ethanone Chemical compound COC1=CC=C(C(C)=O)C(F)=C1 PIRRWUMTIBFCCW-UHFFFAOYSA-N 0.000 description 1
- QILWOKAXHOAFOF-UHFFFAOYSA-N 1-(3-chloro-4-methoxyphenyl)ethanone Chemical compound COC1=CC=C(C(C)=O)C=C1Cl QILWOKAXHOAFOF-UHFFFAOYSA-N 0.000 description 1
- HTWBCLIOMBETGN-UHFFFAOYSA-N 1-(4-methoxy-3-methylphenyl)propan-2-amine Chemical compound COC1=CC=C(CC(C)N)C=C1C HTWBCLIOMBETGN-UHFFFAOYSA-N 0.000 description 1
- OKQDJBQNHXBFJH-UHFFFAOYSA-N 1-(4-methoxyphenyl)butan-2-amine Chemical compound CCC(N)CC1=CC=C(OC)C=C1 OKQDJBQNHXBFJH-UHFFFAOYSA-N 0.000 description 1
- WZZBNLYBHUDSHF-DHLKQENFSA-N 1-[(3s,4s)-4-[8-(2-chloro-4-pyrimidin-2-yloxyphenyl)-7-fluoro-2-methylimidazo[4,5-c]quinolin-1-yl]-3-fluoropiperidin-1-yl]-2-hydroxyethanone Chemical compound CC1=NC2=CN=C3C=C(F)C(C=4C(=CC(OC=5N=CC=CN=5)=CC=4)Cl)=CC3=C2N1[C@H]1CCN(C(=O)CO)C[C@@H]1F WZZBNLYBHUDSHF-DHLKQENFSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- PVJZBZSCGJAWNG-UHFFFAOYSA-N 2,4,6-trimethylbenzenesulfonyl chloride Chemical compound CC1=CC(C)=C(S(Cl)(=O)=O)C(C)=C1 PVJZBZSCGJAWNG-UHFFFAOYSA-N 0.000 description 1
- BXCOSWRSIISQSL-UHFFFAOYSA-N 2,5-dichlorobenzenesulfonyl chloride Chemical compound ClC1=CC=C(Cl)C(S(Cl)(=O)=O)=C1 BXCOSWRSIISQSL-UHFFFAOYSA-N 0.000 description 1
- FGIPEFFHGNAIHV-UHFFFAOYSA-N 2-(2-fluoro-4-methoxyphenyl)propanenitrile Chemical compound COC1=CC=C(C(C)C#N)C(F)=C1 FGIPEFFHGNAIHV-UHFFFAOYSA-N 0.000 description 1
- CPNUQMILFGVACN-UHFFFAOYSA-N 2-(3-chloro-4-methoxyphenyl)propan-1-amine;hydrobromide Chemical compound Br.COC1=CC=C(C(C)CN)C=C1Cl CPNUQMILFGVACN-UHFFFAOYSA-N 0.000 description 1
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- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
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- DQIYXNXRGUELMM-UHFFFAOYSA-N methyl 2-[4-(2-aminopropyl)phenoxy]acetate;hydrochloride Chemical compound Cl.COC(=O)COC1=CC=C(CC(C)N)C=C1 DQIYXNXRGUELMM-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
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- SNGXTIRMXIOEPV-UHFFFAOYSA-N n-[1-(4-hydroxyphenyl)butan-2-yl]benzenesulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)NC(CC)CC1=CC=C(O)C=C1 SNGXTIRMXIOEPV-UHFFFAOYSA-N 0.000 description 1
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- HCLSMLLWRNENQV-UHFFFAOYSA-N n-[2-(4-hydroxyphenyl)propyl]acetamide Chemical compound CC(=O)NCC(C)C1=CC=C(O)C=C1 HCLSMLLWRNENQV-UHFFFAOYSA-N 0.000 description 1
- HUYWGXORTHXVKM-UHFFFAOYSA-N n-[2-(4-hydroxyphenyl)propyl]benzenesulfonamide Chemical compound C=1C=C(O)C=CC=1C(C)CNS(=O)(=O)C1=CC=CC=C1 HUYWGXORTHXVKM-UHFFFAOYSA-N 0.000 description 1
- LCXIAGKCOYANPX-UHFFFAOYSA-N n-[2-(4-methoxyphenyl)propyl]acetamide Chemical compound COC1=CC=C(C(C)CNC(C)=O)C=C1 LCXIAGKCOYANPX-UHFFFAOYSA-N 0.000 description 1
- HVNPMTXMZVZCOU-UHFFFAOYSA-N n-[2-hydroxy-2-(4-phenylmethoxyphenyl)propyl]benzenesulfonamide Chemical compound C=1C=C(OCC=2C=CC=CC=2)C=CC=1C(O)(C)CNS(=O)(=O)C1=CC=CC=C1 HVNPMTXMZVZCOU-UHFFFAOYSA-N 0.000 description 1
- QKIWHADSHFVRFN-UHFFFAOYSA-N n-propan-2-ylbenzenesulfonamide Chemical compound CC(C)NS(=O)(=O)C1=CC=CC=C1 QKIWHADSHFVRFN-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
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- 229940124531 pharmaceutical excipient Drugs 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- XTUSEBKMEQERQV-UHFFFAOYSA-N propan-2-ol;hydrate Chemical compound O.CC(C)O XTUSEBKMEQERQV-UHFFFAOYSA-N 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 230000006340 racemization Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 125000005650 substituted phenylene group Chemical group 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
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- 239000003826 tablet Substances 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- CFOAUYCPAUGDFF-UHFFFAOYSA-N tosmic Chemical compound CC1=CC=C(S(=O)(=O)C[N+]#[C-])C=C1 CFOAUYCPAUGDFF-UHFFFAOYSA-N 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- GGUBFICZYGKNTD-UHFFFAOYSA-N triethyl phosphonoacetate Chemical compound CCOC(=O)CP(=O)(OCC)OCC GGUBFICZYGKNTD-UHFFFAOYSA-N 0.000 description 1
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
- 229940038773 trisodium citrate Drugs 0.000 description 1
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- 229910052725 zinc Inorganic materials 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/03—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C311/06—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by carboxyl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Claims (2)
1. Förfarande för framställning av farmakologiskt värdefull fenoxiättiksyra med formeln (I) R1 R2 r5so,nh -cc -U a \S-ocH->conRfi (i) 1» ιΛ=/ där ringen A är en fenylengrupp eller fenylengrupp med 1-2 substituenter av följande: lägre alkylgrupp, lägre alkoxigrupp och halogenatom; antingen en eller tvä av grupperna R^, R2, R3 och R^ är en lägre alkylgrupp och de övriga grupperna avser väteatomer; R3 är en fenylgrupp eller fenylgrupp med 1-3 substituenter av följande: lägre alkylgrupp, halogenatom, lägre alkoxigrupp, trihalogenmetylgrupp och nitrogrupp; och R6 är väte eller en lägre alkylgrupp, eller dess sait, kännetecknat därav, att a) en fenolförening med formeln (II) R1 R2 R5S02NH - C - C -M A 'S—OH (II) h där ringen A, , R2, R3, R^ och R3 avser det samma som ovan, eller dess sait, kondenseras med ett ättiksyraderivat med formeln (III) X1CH2COOR61 (III) där χΐ är en reaktiv grupp och -COOR3^· är en karboxylgrupp eller skyddad karboxylgrupp, eller b) ett fenyloxiättiksyraderivat med formeln (IV) 58 87769 R1 R2 YC - C ~U A V— OCHoCOOR61 (IV) A* där Y är en aminogrupp, skyddad aminogrupp eller reaktiva grupp, och ringen A, R^, R2, R^, R* och -COOR®^ avser det sanvna som ovan, eller dess salt, kondenseras med en bensensul-fonsyraförening med formeln (V) R1 2 3S02Z (V) där Z är en hydroxigrupp eller reaktiva grupp, da Y är en aminogrupp eller skyddad aminogrupp, eller Z är en aminogrupp, dä Y är en reaktiva grupp, och R^ avser det samma som ovan, och vid behov omvandlas produkten ytterligare till sitt sait.
2. Förfarande enligt patentkravet 1, kännetecknat därav, att 4-(2-(4-klorfenyl)sulfonylaminopropyl)fenoxiättik-syra eller dess sait framställs . Förfarande enligt patentkravet 1, kännetecknat 2 därav, att (-)-4-(2-(4-klorfenyl)sulfonyl-aminopropy1)fenoxi- 3 ättiksyraa eller dess sait framställs.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18469386 | 1986-08-06 | ||
| JP18469386 | 1986-08-06 | ||
| JP2685887 | 1987-02-06 | ||
| JP2685887 | 1987-02-06 |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| FI873413A0 FI873413A0 (fi) | 1987-08-06 |
| FI873413A FI873413A (fi) | 1988-02-07 |
| FI87769B true FI87769B (fi) | 1992-11-13 |
| FI87769C FI87769C (sv) | 1993-02-25 |
Family
ID=26364708
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI873413A FI87769C (sv) | 1986-08-06 | 1987-08-06 | Förfarande för framställning av farmakologiskt värdefull fenoxiättiksy ra |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4866196A (sv) |
| EP (1) | EP0255728B1 (sv) |
| KR (1) | KR910007942B1 (sv) |
| CN (1) | CN1011780B (sv) |
| AT (1) | ATE69807T1 (sv) |
| AU (1) | AU597707B2 (sv) |
| CA (1) | CA1277675C (sv) |
| DE (1) | DE3774795D1 (sv) |
| DK (1) | DK408987A (sv) |
| ES (1) | ES2038630T3 (sv) |
| FI (1) | FI87769C (sv) |
| GR (1) | GR3003215T3 (sv) |
| HK (1) | HK42193A (sv) |
| HU (1) | HU200442B (sv) |
| IL (1) | IL83230A (sv) |
| MY (1) | MY101801A (sv) |
| NO (1) | NO166938C (sv) |
| PH (1) | PH24750A (sv) |
| PT (1) | PT85502B (sv) |
| SG (1) | SG15593G (sv) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3642105A1 (de) * | 1986-12-10 | 1988-06-16 | Bayer Ag | Substituierte aminomethyl-5,6,7,8-tetrahydronaphtyl-oxyessigsaeuren, neue zwischenprodukte, verfahren zu ihrer herstellung sowie ihre verwendung in arzneimitteln |
| GB8708233D0 (en) * | 1987-04-07 | 1987-05-13 | Smith Kline French Lab | Pharmaceutically active compounds |
| JPH068275B2 (ja) * | 1988-02-04 | 1994-02-02 | 田辺製薬株式会社 | フェノキシ酢酸誘導体 |
| JPH068274B2 (ja) * | 1988-01-19 | 1994-02-02 | 田辺製薬株式会社 | フェノキシ酢酸誘導体 |
| DE68909958D1 (de) * | 1988-01-19 | 1993-11-25 | Tanabe Seiyaku Co | Phenoxyessigsäure-Derivate, ihre Herstellung, pharmazeutische Zusammensetzungen, die sie enthalten, und deren Verwendung. |
| DE3821540A1 (de) * | 1988-06-25 | 1989-12-28 | Boehringer Mannheim Gmbh | Neue sulfonamide, verfahren zu ihrer herstellung sowie solche sulfonamide enthaltende arzneimittel |
| US5280043A (en) * | 1988-10-10 | 1994-01-18 | Smith Kline & French Laboratories Ltd. | Sulphonamido containing phenylalkanoic acids as thromboxane A2 antagonists |
| JPH02169562A (ja) * | 1988-12-22 | 1990-06-29 | Tanabe Seiyaku Co Ltd | グリシン誘導体及びその製法 |
| US5256812A (en) * | 1989-01-31 | 1993-10-26 | Hoffmann-La Roche Inc. | Carboxamides and sulfonamides |
| US5084466A (en) * | 1989-01-31 | 1992-01-28 | Hoffmann-La Roche Inc. | Novel carboxamide pyridine compounds which have useful pharmaceutical utility |
| FR2645537B1 (fr) * | 1989-04-05 | 1994-03-04 | Fabre Medicament Pierre | Nouveaux sulfonamides derives d'acides benzocycliques ou benzoheterocycliques, leur preparation et leur application en therapeutique |
| DE3942923A1 (de) * | 1989-12-23 | 1991-06-27 | Boehringer Mannheim Gmbh | Neue phenoxyalkylcarbonsaeure-amide, verfahren zu ihrer herstellung sowie diese verbindungen enthaltende arzneimittel |
| US5179105A (en) * | 1990-10-16 | 1993-01-12 | Terumo Kabushiki Kaisha | Phenoxyacetic acid compounds, method for production thereof, and pharmaceutical preparations containing same |
| DE4037174A1 (de) * | 1990-11-22 | 1992-05-27 | Boehringer Mannheim Gmbh | Neue sulfonamide, verfahren zu ihrer herstellung und arzneimittel, die diese verbindungen enthalten |
| JPH05125038A (ja) * | 1991-03-07 | 1993-05-21 | Tanabe Seiyaku Co Ltd | フエノキシアルカン酸誘導体及びその製法 |
| CA2092152A1 (en) * | 1992-03-23 | 1993-09-24 | Azuma Igarashi | Phenoxyacetic acid compounds and medical preparations containing them |
| GB9220137D0 (en) * | 1992-09-23 | 1992-11-04 | Pfizer Ltd | Therapeutic agents |
| GB9702194D0 (en) | 1997-02-04 | 1997-03-26 | Lilly Co Eli | Sulphonide derivatives |
| CN107501136B (zh) * | 2017-09-19 | 2019-05-28 | 西南大学 | 一种制备偕二芳基甲胺类化合物的方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2809377A1 (de) * | 1978-03-04 | 1979-09-13 | Boehringer Mannheim Gmbh | Phenoxyalkylcarbonsaeure-derivate, verfahren zu deren herstellung sowie diese verbindungen enthaltende arzneimittel |
| DE3000377A1 (de) * | 1980-01-07 | 1981-07-09 | Boehringer Mannheim Gmbh, 6800 Mannheim | Neue sulfonamide, verfahren zu deren herstellung sowie diese verbindungen enthaltende arzneimittel |
| EP0194548A3 (de) * | 1985-03-12 | 1988-08-17 | Dr. Karl Thomae GmbH | Neue Sulfonylaminoäthylverbindungen, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| DE3535167A1 (de) * | 1985-10-02 | 1987-04-09 | Boehringer Mannheim Gmbh | Neue sulfonyl-phenyl(alkyl)amine, verfahren zu ihrer herstellung sowie arzneimittel |
| DE3610643A1 (de) * | 1986-03-29 | 1987-10-01 | Boehringer Mannheim Gmbh | Neue phenoxyalkylcarbonsaeure-derivate, verfahren zu ihrer herstellung sowie diese verbindungen enthaltende arzneimittel |
-
1987
- 1987-07-17 IL IL83230A patent/IL83230A/xx not_active IP Right Cessation
- 1987-07-29 PH PH35597A patent/PH24750A/en unknown
- 1987-07-31 CA CA000543552A patent/CA1277675C/en not_active Expired - Fee Related
- 1987-08-03 MY MYPI87001198A patent/MY101801A/en unknown
- 1987-08-05 DK DK408987A patent/DK408987A/da not_active Application Discontinuation
- 1987-08-05 KR KR1019870008601A patent/KR910007942B1/ko not_active IP Right Cessation
- 1987-08-05 AU AU76596/87A patent/AU597707B2/en not_active Ceased
- 1987-08-05 HU HU873579A patent/HU200442B/hu not_active IP Right Cessation
- 1987-08-05 NO NO873272A patent/NO166938C/no unknown
- 1987-08-06 AT AT87111402T patent/ATE69807T1/de not_active IP Right Cessation
- 1987-08-06 ES ES198787111402T patent/ES2038630T3/es not_active Expired - Lifetime
- 1987-08-06 EP EP87111402A patent/EP0255728B1/en not_active Expired - Lifetime
- 1987-08-06 CN CN87105501A patent/CN1011780B/zh not_active Expired
- 1987-08-06 PT PT85502A patent/PT85502B/pt not_active IP Right Cessation
- 1987-08-06 FI FI873413A patent/FI87769C/sv not_active IP Right Cessation
- 1987-08-06 DE DE8787111402T patent/DE3774795D1/de not_active Expired - Fee Related
-
1988
- 1988-01-04 US US07/141,403 patent/US4866196A/en not_active Expired - Fee Related
-
1991
- 1991-11-28 GR GR91401688T patent/GR3003215T3/el unknown
-
1993
- 1993-02-11 SG SG155/93A patent/SG15593G/en unknown
- 1993-04-29 HK HK421/93A patent/HK42193A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0255728A3 (en) | 1989-05-10 |
| KR910007942B1 (ko) | 1991-10-04 |
| PT85502B (pt) | 1990-06-29 |
| DK408987D0 (da) | 1987-08-05 |
| KR880002819A (ko) | 1988-05-11 |
| PT85502A (en) | 1987-09-01 |
| CN1011780B (zh) | 1991-02-27 |
| FI873413A0 (fi) | 1987-08-06 |
| AU597707B2 (en) | 1990-06-07 |
| EP0255728B1 (en) | 1991-11-27 |
| DK408987A (da) | 1988-02-07 |
| ATE69807T1 (de) | 1991-12-15 |
| NO873272D0 (no) | 1987-08-05 |
| PH24750A (en) | 1990-10-01 |
| GR3003215T3 (en) | 1993-02-17 |
| NO873272L (no) | 1988-02-08 |
| CA1277675C (en) | 1990-12-11 |
| SG15593G (en) | 1993-04-16 |
| MY101801A (en) | 1992-01-31 |
| IL83230A0 (en) | 1987-12-31 |
| HU200442B (en) | 1990-06-28 |
| DE3774795D1 (de) | 1992-01-09 |
| CN87105501A (zh) | 1988-02-17 |
| EP0255728A2 (en) | 1988-02-10 |
| FI87769C (sv) | 1993-02-25 |
| HUT45230A (en) | 1988-06-28 |
| ES2038630T3 (es) | 1993-08-01 |
| FI873413A (fi) | 1988-02-07 |
| AU7659687A (en) | 1988-02-11 |
| NO166938C (no) | 1991-09-18 |
| NO166938B (no) | 1991-06-10 |
| US4866196A (en) | 1989-09-12 |
| HK42193A (en) | 1993-05-07 |
| IL83230A (en) | 1992-06-21 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed | ||
| MM | Patent lapsed |
Owner name: TANABE SEIYAKU CO., . LTD. |