FI81782B - Foerfarande foer framstaellning av nya terapeutiskt anvaendbara 1-styrensulfonyl-2-oxo-5-hydroxi-pyrrolidinderivat. - Google Patents
Foerfarande foer framstaellning av nya terapeutiskt anvaendbara 1-styrensulfonyl-2-oxo-5-hydroxi-pyrrolidinderivat. Download PDFInfo
- Publication number
- FI81782B FI81782B FI871353A FI871353A FI81782B FI 81782 B FI81782 B FI 81782B FI 871353 A FI871353 A FI 871353A FI 871353 A FI871353 A FI 871353A FI 81782 B FI81782 B FI 81782B
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- Finland
- Prior art keywords
- compound
- oxo
- formula
- compounds
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- FSXXIZVBPWNJGV-UHFFFAOYSA-N 5-hydroxy-1-(2-phenylethenylsulfonyl)pyrrolidin-2-one Chemical class OC1CCC(=O)N1S(=O)(=O)C=CC1=CC=CC=C1 FSXXIZVBPWNJGV-UHFFFAOYSA-N 0.000 title claims description 3
- 230000001225 therapeutic effect Effects 0.000 title abstract 3
- 239000002253 acid Substances 0.000 title 1
- 238000007669 thermal treatment Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 60
- 238000000034 method Methods 0.000 claims abstract description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 7
- 238000002360 preparation method Methods 0.000 claims description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 18
- -1 alkyl radical Chemical class 0.000 abstract description 6
- 150000005840 aryl radicals Chemical class 0.000 abstract 1
- 206010003549 asthenia Diseases 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 36
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 27
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 22
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 18
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 18
- 239000000243 solution Substances 0.000 description 17
- 241001465754 Metazoa Species 0.000 description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 229910052799 carbon Inorganic materials 0.000 description 9
- 239000000741 silica gel Substances 0.000 description 9
- 229910002027 silica gel Inorganic materials 0.000 description 9
- 239000002904 solvent Substances 0.000 description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- OAMZXMDZZWGPMH-UHFFFAOYSA-N ethyl acetate;toluene Chemical compound CCOC(C)=O.CC1=CC=CC=C1 OAMZXMDZZWGPMH-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 4
- ABAUZPSEXCYJLX-UHFFFAOYSA-N 2-(4-methoxyphenyl)ethenesulfonyl chloride Chemical compound COC1=CC=C(C=CS(Cl)(=O)=O)C=C1 ABAUZPSEXCYJLX-UHFFFAOYSA-N 0.000 description 3
- ONWRSBMOCIQLRK-UHFFFAOYSA-N 2-phenylethenesulfonyl chloride Chemical compound ClS(=O)(=O)C=CC1=CC=CC=C1 ONWRSBMOCIQLRK-UHFFFAOYSA-N 0.000 description 3
- ZXRWQRYMEYRQKX-UHFFFAOYSA-N 5-ethoxypyrrolidin-2-one Chemical compound CCOC1CCC(=O)N1 ZXRWQRYMEYRQKX-UHFFFAOYSA-N 0.000 description 3
- QAKFPYIAROCGIF-UHFFFAOYSA-N 5-propan-2-yloxypyrrolidin-2-one Chemical compound CC(C)OC1CCC(=O)N1 QAKFPYIAROCGIF-UHFFFAOYSA-N 0.000 description 3
- QPBUKZHFIMVDBV-UHFFFAOYSA-N 5-propoxypyrrolidin-2-one Chemical compound CCCOC1CCC(=O)N1 QPBUKZHFIMVDBV-UHFFFAOYSA-N 0.000 description 3
- 208000000044 Amnesia Diseases 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 208000026139 Memory disease Diseases 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 230000006399 behavior Effects 0.000 description 3
- 239000003480 eluent Substances 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 230000006984 memory degeneration Effects 0.000 description 3
- 208000023060 memory loss Diseases 0.000 description 3
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- VULIHENHKGDFAB-UHFFFAOYSA-N Pterolactam Chemical compound COC1CCC(=O)N1 VULIHENHKGDFAB-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- OQNGCCWBHLEQFN-UHFFFAOYSA-N chloroform;hexane Chemical compound ClC(Cl)Cl.CCCCCC OQNGCCWBHLEQFN-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000008034 disappearance Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 239000000825 pharmaceutical preparation Substances 0.000 description 2
- 230000000144 pharmacologic effect Effects 0.000 description 2
- 239000012047 saturated solution Substances 0.000 description 2
- 229910000033 sodium borohydride Inorganic materials 0.000 description 2
- 239000012279 sodium borohydride Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 229960002317 succinimide Drugs 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- ONWRSBMOCIQLRK-VOTSOKGWSA-N (e)-2-phenylethenesulfonyl chloride Chemical compound ClS(=O)(=O)\C=C\C1=CC=CC=C1 ONWRSBMOCIQLRK-VOTSOKGWSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- XNSAJUNQAHRZLI-UHFFFAOYSA-N 1-(2-phenylethenylsulfonyl)-5-propan-2-yloxypyrrolidin-2-one Chemical compound CC(C)OC1CCC(=O)N1S(=O)(=O)C=CC1=CC=CC=C1 XNSAJUNQAHRZLI-UHFFFAOYSA-N 0.000 description 1
- PUJCFQUNEIBKJP-UHFFFAOYSA-N 1-[2-(4-nitrophenyl)ethenylsulfonyl]-5-propan-2-yloxypyrrolidin-2-one Chemical compound CC(C)OC1CCC(=O)N1S(=O)(=O)C=CC1=CC=C([N+]([O-])=O)C=C1 PUJCFQUNEIBKJP-UHFFFAOYSA-N 0.000 description 1
- PCZYYQQIBHXXNF-UHFFFAOYSA-N 1-[2-(4-phenylphenyl)ethenylsulfonyl]-5-propan-2-yloxypyrrolidin-2-one Chemical compound CC(C)OC1CCC(=O)N1S(=O)(=O)C=CC1=CC=C(C=2C=CC=CC=2)C=C1 PCZYYQQIBHXXNF-UHFFFAOYSA-N 0.000 description 1
- UAJRSHJHFRVGMG-UHFFFAOYSA-N 1-ethenyl-4-methoxybenzene Chemical compound COC1=CC=C(C=C)C=C1 UAJRSHJHFRVGMG-UHFFFAOYSA-N 0.000 description 1
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 description 1
- OWLOBIFPHPJEEU-UHFFFAOYSA-N 1-propan-2-yloxypyrrolidin-2-one Chemical compound CC(C)ON1CCCC1=O OWLOBIFPHPJEEU-UHFFFAOYSA-N 0.000 description 1
- TVTJUIAKQFIXCE-HUKYDQBMSA-N 2-amino-9-[(2R,3S,4S,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-prop-2-ynyl-1H-purine-6,8-dione Chemical compound NC=1NC(C=2N(C(N(C=2N=1)[C@@H]1O[C@@H]([C@H]([C@H]1O)F)CO)=O)CC#C)=O TVTJUIAKQFIXCE-HUKYDQBMSA-N 0.000 description 1
- RXXCIBALSKQCAE-UHFFFAOYSA-N 3-methylbutoxymethylbenzene Chemical compound CC(C)CCOCC1=CC=CC=C1 RXXCIBALSKQCAE-UHFFFAOYSA-N 0.000 description 1
- RWURZOCIKRPZCG-UHFFFAOYSA-N 5-ethoxy-1-(2-phenylethenylsulfonyl)pyrrolidin-2-one Chemical compound CCOC1CCC(=O)N1S(=O)(=O)C=CC1=CC=CC=C1 RWURZOCIKRPZCG-UHFFFAOYSA-N 0.000 description 1
- CMDRHQMJVGPJMF-UHFFFAOYSA-N 5-ethoxy-1-[2-(4-methoxyphenyl)ethenylsulfonyl]pyrrolidin-2-one Chemical compound CCOC1CCC(=O)N1S(=O)(=O)C=CC1=CC=C(OC)C=C1 CMDRHQMJVGPJMF-UHFFFAOYSA-N 0.000 description 1
- ZBKXCRFTMISRHG-UHFFFAOYSA-N 5-ethoxy-1-[2-(4-nitrophenyl)ethenylsulfonyl]pyrrolidin-2-one Chemical compound CCOC1CCC(=O)N1S(=O)(=O)C=CC1=CC=C([N+]([O-])=O)C=C1 ZBKXCRFTMISRHG-UHFFFAOYSA-N 0.000 description 1
- QICXYPJUWXPHHT-UHFFFAOYSA-N 5-ethoxy-1-[2-(4-phenylphenyl)ethenylsulfonyl]pyrrolidin-2-one Chemical compound CCOC1CCC(=O)N1S(=O)(=O)C=CC1=CC=C(C=2C=CC=CC=2)C=C1 QICXYPJUWXPHHT-UHFFFAOYSA-N 0.000 description 1
- WJEIAQBMQDKBKH-UHFFFAOYSA-N 5-ethoxy-1-[2-[3-(trifluoromethyl)phenyl]ethenylsulfonyl]pyrrolidin-2-one Chemical compound CCOC1CCC(=O)N1S(=O)(=O)C=CC1=CC=CC(C(F)(F)F)=C1 WJEIAQBMQDKBKH-UHFFFAOYSA-N 0.000 description 1
- LQVYBXZZJPHTDB-UHFFFAOYSA-N 5-methoxy-1-(2-phenylethenylsulfonyl)pyrrolidin-2-one Chemical compound COC1CCC(=O)N1S(=O)(=O)C=CC1=CC=CC=C1 LQVYBXZZJPHTDB-UHFFFAOYSA-N 0.000 description 1
- AJVZDYLDLSCTOJ-UHFFFAOYSA-N 5-pentoxypyrrolidin-2-one Chemical compound CCCCCOC1CCC(=O)N1 AJVZDYLDLSCTOJ-UHFFFAOYSA-N 0.000 description 1
- WUSKXVFGSTYKEM-UHFFFAOYSA-N CCCCCC1CCC(=O)N1S(=O)(=O)C=CC2=CC=CC=C2 Chemical compound CCCCCC1CCC(=O)N1S(=O)(=O)C=CC2=CC=CC=C2 WUSKXVFGSTYKEM-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 240000007472 Leucaena leucocephala Species 0.000 description 1
- 235000010643 Leucaena leucocephala Nutrition 0.000 description 1
- 241000699666 Mus <mouse, genus> Species 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 230000007059 acute toxicity Effects 0.000 description 1
- 231100000403 acute toxicity Toxicity 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000036626 alertness Effects 0.000 description 1
- 229910000102 alkali metal hydride Inorganic materials 0.000 description 1
- 150000008046 alkali metal hydrides Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229940125851 compound 27 Drugs 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229940019778 diethylene glycol diethyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- ZKQFHRVKCYFVCN-UHFFFAOYSA-N ethoxyethane;hexane Chemical compound CCOCC.CCCCCC ZKQFHRVKCYFVCN-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 230000003340 mental effect Effects 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000829 suppository Substances 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
- 238000010998 test method Methods 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/46—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
- C07D207/48—Sulfur atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Claims (3)
1 I H 25 jossa Rx merkitsee samaa kuin edellä, saatetaan reagoimaan yhdisteen kanssa, jonka kaava on (III) RCH=CH-S02Hal (III) 30 jossa Hai on kloori- tai bromiatomi ja R merkitsee samaa kuin edellä. 81 7 82 14 Förfarande för framställning av terapeutiskt an-vändbara l-styrensulfonyl-2-oxo-5-hydroxi-pyrrolidinderi-5 vat med formeln (I) (I) SO·, I l CH
10 CH R 15 väri R3 är en högst 8 kolatomer innehällande alkylgrupp med rak eller förgrenad kedja och R är en fenylgrupp, vilken kan vara substituerad med en 1-5 kolatomer innehällande alkylgrupp eller med en N02-, CF3- eller fenylgrupp, kännetecknat därav, att en förening med for-20 mein (II) (II) R10^\n^%0 H 25 väri Rx har ovan angivna betydelse, omsätts med en förening med formeln (III)
30 RCH*CH-S02Hal (III) väri Hai är en klor- eller bromatom och R har ovan angivna betydelse. li
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT19916/86A IT1204494B (it) | 1986-03-28 | 1986-03-28 | Derivati della 1-stirene solfonil 2-osso 5-alcossi pirrolidina,loro procedimento di preparazione e loro applicazione come farmaci |
| IT1991686 | 1986-03-28 |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| FI871353A0 FI871353A0 (fi) | 1987-03-27 |
| FI871353A FI871353A (fi) | 1987-09-29 |
| FI81782B true FI81782B (fi) | 1990-08-31 |
| FI81782C FI81782C (sv) | 1990-12-10 |
Family
ID=11162311
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI871353A FI81782C (sv) | 1986-03-28 | 1987-03-27 | Förfarande för framställning av nya terapeutiskt användbara 1-styrensu lfonyl-2-oxo-5-hydroxi-pyrrolidinderivat |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4810722A (sv) |
| EP (1) | EP0239500B1 (sv) |
| JP (1) | JPS62270558A (sv) |
| KR (1) | KR870008840A (sv) |
| AT (1) | ATE71936T1 (sv) |
| AU (1) | AU591255B2 (sv) |
| CA (1) | CA1282072C (sv) |
| DE (1) | DE3776171D1 (sv) |
| DK (1) | DK157487A (sv) |
| ES (1) | ES2038191T3 (sv) |
| FI (1) | FI81782C (sv) |
| GR (1) | GR3003643T3 (sv) |
| HU (1) | HU198181B (sv) |
| IE (1) | IE60102B1 (sv) |
| IT (1) | IT1204494B (sv) |
| MX (1) | MX173415B (sv) |
| PT (1) | PT84475B (sv) |
| ZA (1) | ZA871804B (sv) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2873898B2 (ja) * | 1992-04-13 | 1999-03-24 | 富山化学工業株式会社 | ベンゾ［ｂ］チオフェン−５−イル誘導体もしくはその光学活性体またはそれらの塩並びにそれらの製造法 |
| ES2107376B1 (es) * | 1995-08-02 | 1998-07-01 | Uriach & Cia Sa J | Nuevos derivados de pirimidona con actividad antifungica. |
| WO1997005131A1 (en) * | 1995-08-02 | 1997-02-13 | J. Uriach & Cia. S.A. | New carboxamides with antifungal activity |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3453289A (en) * | 1966-01-21 | 1969-07-01 | American Home Prod | P-substituted-phenylsulfonyl pyrrolidine derivatives |
| US3423426A (en) * | 1966-01-25 | 1969-01-21 | Chevron Res | N-(polyhaloalkylthio) alkenylsuccinimides |
| US3686169A (en) * | 1970-07-20 | 1972-08-22 | Monsanto Co | Thiocycloamides |
| JPS5822111B2 (ja) * | 1977-10-29 | 1983-05-06 | 協和醗酵工業株式会社 | 柑橘類果実の改質剤 |
| FR2553409B1 (fr) * | 1983-10-18 | 1986-04-18 | Choay Sa | Nouveaux benzenesulfonyl-lactames, leur procede de preparation et leur application comme substance active de compositions pharmaceutiques |
| DK167393B1 (da) * | 1985-12-30 | 1993-10-25 | Roussel Uclaf | 1-sulfonyl-2-oxo-pyrrolidinderivater, deres fremstilling og farmaceutiske praeparater med indhold deraf |
-
1986
- 1986-03-28 IT IT19916/86A patent/IT1204494B/it active
-
1987
- 1987-03-12 ZA ZA871804A patent/ZA871804B/xx unknown
- 1987-03-13 PT PT84475A patent/PT84475B/pt not_active IP Right Cessation
- 1987-03-24 JP JP62068156A patent/JPS62270558A/ja active Pending
- 1987-03-26 DE DE8787400689T patent/DE3776171D1/de not_active Expired - Fee Related
- 1987-03-26 ES ES198787400689T patent/ES2038191T3/es not_active Expired - Lifetime
- 1987-03-26 US US07/030,113 patent/US4810722A/en not_active Expired - Fee Related
- 1987-03-26 AT AT87400689T patent/ATE71936T1/de not_active IP Right Cessation
- 1987-03-26 HU HU871323A patent/HU198181B/hu not_active IP Right Cessation
- 1987-03-26 EP EP87400689A patent/EP0239500B1/fr not_active Expired - Lifetime
- 1987-03-27 MX MX005785A patent/MX173415B/es unknown
- 1987-03-27 FI FI871353A patent/FI81782C/sv not_active IP Right Cessation
- 1987-03-27 IE IE79387A patent/IE60102B1/en not_active IP Right Cessation
- 1987-03-27 CA CA000533227A patent/CA1282072C/fr not_active Expired - Lifetime
- 1987-03-27 KR KR870002830A patent/KR870008840A/ko not_active Application Discontinuation
- 1987-03-27 AU AU70737/87A patent/AU591255B2/en not_active Ceased
- 1987-03-27 DK DK157487A patent/DK157487A/da not_active IP Right Cessation
-
1992
- 1992-01-23 GR GR910402205T patent/GR3003643T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HUT43816A (en) | 1987-12-28 |
| CA1282072C (fr) | 1991-03-26 |
| IT1204494B (it) | 1989-03-01 |
| EP0239500B1 (fr) | 1992-01-22 |
| DK157487D0 (da) | 1987-03-27 |
| PT84475B (pt) | 1989-11-10 |
| HU198181B (en) | 1989-08-28 |
| IE870793L (en) | 1987-09-28 |
| ATE71936T1 (de) | 1992-02-15 |
| FI871353A0 (fi) | 1987-03-27 |
| US4810722A (en) | 1989-03-07 |
| PT84475A (fr) | 1987-04-01 |
| EP0239500A3 (en) | 1988-07-27 |
| AU7073787A (en) | 1987-10-01 |
| KR870008840A (ko) | 1987-10-21 |
| ZA871804B (en) | 1988-05-25 |
| IT8619916A0 (it) | 1986-03-28 |
| FI81782C (sv) | 1990-12-10 |
| EP0239500A2 (fr) | 1987-09-30 |
| MX173415B (es) | 1994-03-03 |
| DK157487A (da) | 1987-09-29 |
| FI871353A (fi) | 1987-09-29 |
| MX5785A (es) | 1993-10-01 |
| AU591255B2 (en) | 1989-11-30 |
| GR3003643T3 (sv) | 1993-03-16 |
| JPS62270558A (ja) | 1987-11-24 |
| DE3776171D1 (de) | 1992-03-05 |
| ES2038191T3 (es) | 1993-07-16 |
| IE60102B1 (en) | 1994-06-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed | ||
| MM | Patent lapsed |
Owner name: ROUSSEL UCLAF SOCIETE ANONYME |