NO821725L - Fremgangsmaate for fremstilling av heterocykliske amidoxim-derivater. - Google Patents
Fremgangsmaate for fremstilling av heterocykliske amidoxim-derivater.Info
- Publication number
- NO821725L NO821725L NO821725A NO821725A NO821725L NO 821725 L NO821725 L NO 821725L NO 821725 A NO821725 A NO 821725A NO 821725 A NO821725 A NO 821725A NO 821725 L NO821725 L NO 821725L
- Authority
- NO
- Norway
- Prior art keywords
- oxo
- dihydro
- methyl
- derivatives
- heterocyclic
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 4
- 238000002360 preparation method Methods 0.000 title claims description 3
- -1 1-oxo-1H-isoquinolin-2-yl 2- oxo-2H- quinolin-1-yl Chemical group 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 9
- 150000002825 nitriles Chemical class 0.000 claims description 7
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 claims description 6
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims description 4
- 229910000104 sodium hydride Inorganic materials 0.000 claims description 4
- 239000012312 sodium hydride Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 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 2
- 239000002253 acid Substances 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000007912 intraperitoneal administration Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- DNXIKVLOVZVMQF-UHFFFAOYSA-N (3beta,16beta,17alpha,18beta,20alpha)-17-hydroxy-11-methoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]-yohimban-16-carboxylic acid, methyl ester Natural products C1C2CN3CCC(C4=CC=C(OC)C=C4N4)=C4C3CC2C(C(=O)OC)C(O)C1OC(=O)C1=CC(OC)=C(OC)C(OC)=C1 DNXIKVLOVZVMQF-UHFFFAOYSA-N 0.000 description 2
- 206010015995 Eyelid ptosis Diseases 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- LCQMZZCPPSWADO-UHFFFAOYSA-N Reserpilin Natural products COC(=O)C1COCC2CN3CCc4c([nH]c5cc(OC)c(OC)cc45)C3CC12 LCQMZZCPPSWADO-UHFFFAOYSA-N 0.000 description 2
- QEVHRUUCFGRFIF-SFWBKIHZSA-N Reserpine Natural products O=C(OC)[C@@H]1[C@H](OC)[C@H](OC(=O)c2cc(OC)c(OC)c(OC)c2)C[C@H]2[C@@H]1C[C@H]1N(C2)CCc2c3c([nH]c12)cc(OC)cc3 QEVHRUUCFGRFIF-SFWBKIHZSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 208000035475 disorder Diseases 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 201000003004 ptosis Diseases 0.000 description 2
- BJOIZNZVOZKDIG-MDEJGZGSSA-N reserpine Chemical compound O([C@H]1[C@@H]([C@H]([C@H]2C[C@@H]3C4=C([C]5C=CC(OC)=CC5=N4)CCN3C[C@H]2C1)C(=O)OC)OC)C(=O)C1=CC(OC)=C(OC)C(OC)=C1 BJOIZNZVOZKDIG-MDEJGZGSSA-N 0.000 description 2
- 229960003147 reserpine Drugs 0.000 description 2
- MDMGHDFNKNZPAU-UHFFFAOYSA-N roserpine Natural products C1C2CN3CCC(C4=CC=C(OC)C=C4N4)=C4C3CC2C(OC(C)=O)C(OC)C1OC(=O)C1=CC(OC)=C(OC)C(OC)=C1 MDMGHDFNKNZPAU-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- JNAYPRPPXRWGQO-UHFFFAOYSA-N 2-chloropropanenitrile Chemical compound CC(Cl)C#N JNAYPRPPXRWGQO-UHFFFAOYSA-N 0.000 description 1
- 208000020401 Depressive disease Diseases 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 241000699666 Mus <mouse, genus> Species 0.000 description 1
- 230000007059 acute toxicity Effects 0.000 description 1
- 231100000403 acute toxicity Toxicity 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 230000001430 anti-depressive effect Effects 0.000 description 1
- 239000000935 antidepressant agent Substances 0.000 description 1
- 229940005513 antidepressants Drugs 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000008298 dragée Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- LBAQSKZHMLAFHH-UHFFFAOYSA-N ethoxyethane;hydron;chloride Chemical compound Cl.CCOCC LBAQSKZHMLAFHH-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 125000000593 indol-1-yl group Chemical group [H]C1=C([H])C([H])=C2N([*])C([H])=C([H])C2=C1[H] 0.000 description 1
- 239000007928 intraperitoneal injection Substances 0.000 description 1
- VDBNYAPERZTOOF-UHFFFAOYSA-N isoquinolin-1(2H)-one Chemical compound C1=CC=C2C(=O)NC=CC2=C1 VDBNYAPERZTOOF-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical group 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/46—Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/20—Oxygen atoms
- C07D215/22—Oxygen atoms attached in position 2 or 4
- C07D215/227—Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
- C07D217/24—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
- C07D235/26—Oxygen atoms
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Neurosurgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Neurology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Psychiatry (AREA)
- Pharmacology & Pharmacy (AREA)
- Biomedical Technology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Quinoline Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8110428A FR2506767A1 (fr) | 1981-05-26 | 1981-05-26 | Derives heterocycliques d'amidoximes, leur preparation et leur application en therapeutique |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO821725L true NO821725L (no) | 1982-11-29 |
Family
ID=9258896
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO821725A NO821725L (no) | 1981-05-26 | 1982-05-25 | Fremgangsmaate for fremstilling av heterocykliske amidoxim-derivater. |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US4438121A (es) |
| EP (1) | EP0067094B1 (es) |
| JP (1) | JPS57206663A (es) |
| AR (1) | AR230047A1 (es) |
| AT (1) | ATE15894T1 (es) |
| AU (1) | AU550769B2 (es) |
| CA (1) | CA1185603A (es) |
| DE (1) | DE3266640D1 (es) |
| DK (1) | DK234182A (es) |
| ES (1) | ES8304086A1 (es) |
| FI (1) | FI821857A0 (es) |
| FR (1) | FR2506767A1 (es) |
| GR (1) | GR76445B (es) |
| HU (1) | HU186515B (es) |
| IL (1) | IL65876A (es) |
| NO (1) | NO821725L (es) |
| NZ (1) | NZ200729A (es) |
| PT (1) | PT74952B (es) |
| ZA (1) | ZA823628B (es) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2506767A1 (fr) * | 1981-05-26 | 1982-12-03 | Synthelabo | Derives heterocycliques d'amidoximes, leur preparation et leur application en therapeutique |
| FR2564461B1 (fr) * | 1984-05-15 | 1986-09-19 | Synthelabo | Derives d'isoquinoleine, leur preparation et leurs applications |
| TW200643015A (en) * | 2005-03-11 | 2006-12-16 | Akzo Nobel Nv | 2-(4-oxo-4H-quinazolin-3-yl)acetamide derivatives |
| RU2009113612A (ru) * | 2006-09-11 | 2010-10-20 | Н.В. Органон (Nl) | Ацетамидные производные хиназолинона и изохинолинона |
| JP5271909B2 (ja) * | 2006-09-11 | 2013-08-21 | エム・エス・ディー・オス・ベー・フェー | ２−（１−オキソ−１ｈ−イソキノリン−２−イル）アセトアミド誘導体 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2425288A (en) * | 1945-01-08 | 1947-08-05 | Commercial Solvents Corp | Plasticized butadiene polymer compositions containing phthalimidoalkyl alkanoates |
| US3291799A (en) | 1964-09-21 | 1966-12-13 | Hoffmann La Roche | Isoquinoline carboxamidine |
| DE1670497C3 (de) | 1967-06-06 | 1973-12-20 | Chinoin Gyogyszer- Es Vegyeszeti Termekek Gyara Rt, Budapest | Isochinohnderivate und Verfahren zu deren Herstellung |
| US3635974A (en) * | 1968-12-20 | 1972-01-18 | Boehringer Sohn Ingelheim | Alpha-phenyl-2-aminomethyl-benzylalcohols and salts thereof |
| US3686184A (en) | 1969-04-21 | 1972-08-22 | Sterling Drug Inc | 3,4-dihydro-2(1h)-isoquinolinecarboxamidoximes |
| US3795735A (en) * | 1969-12-08 | 1974-03-05 | American Cyanamid Co | Antimicrobial nitroimidazolyl-1,2,4-oxadiazoles |
| US3658832A (en) * | 1969-12-08 | 1972-04-25 | American Cyanamid Co | Novel antimicrobial nitroimidazolyl-1 2 4-oxadiazoles |
| US3654299A (en) * | 1969-12-08 | 1972-04-04 | American Cyanamid Co | Nitroimidazolyl antimicrobial agents |
| FR2150590A1 (en) * | 1971-08-27 | 1973-04-13 | Ferlux | N (2-phenyl-3-pyridayon-4-yl)piperalines - with analgesic antipyretic antiinflammatory and hypotensive activity |
| BE792182A (fr) * | 1971-12-03 | 1973-06-01 | Hoffmann La Roche | 5-nitro-imidazoles |
| US3927000A (en) | 1972-08-21 | 1975-12-16 | Sterling Drug Inc | 1(OR 3) Perfluoroalkyl-3,4-dihydro-2(1H)-isoquinolinecarbonitriles and intermediates |
| IL44350A0 (en) * | 1973-04-05 | 1974-06-30 | Sparamedica Ag | New imidazole derivatives,their manufacture and pharmaceutical compositions containing them |
| US3984470A (en) | 1974-01-15 | 1976-10-05 | Labaz | Amidoxime derivatives and process for preparing the same |
| FR2257273B1 (es) | 1974-01-15 | 1978-01-13 | Labaz | |
| GB1477607A (en) | 1975-03-13 | 1977-06-22 | Roche Products Ltd | 2-amidino-4-hydroxy-1,2,3,4-tetrahydroisoquinoline and salts thereof |
| CH623971B5 (de) * | 1976-06-04 | 1982-01-15 | Hoechst Ag | Verfahren zur herstellung neuer benzofuranderivate und deren verwendung als optische aufheller. |
| US4048176A (en) * | 1976-07-23 | 1977-09-13 | Morton-Norwich Products, Inc. | 2-(3-Methyl-4-phenyl-1,2,3,4-tetrahydro-2-isoquinolyl)-acetamidoxime dihydrochloride |
| GB1602110A (en) * | 1977-04-21 | 1981-11-04 | Lafon Labor | Acetamidoxime derivatives |
| US4265911A (en) | 1979-10-09 | 1981-05-05 | Synthelabo | Propionamidoxime derivatives |
| FR2506767A1 (fr) * | 1981-05-26 | 1982-12-03 | Synthelabo | Derives heterocycliques d'amidoximes, leur preparation et leur application en therapeutique |
-
1981
- 1981-05-26 FR FR8110428A patent/FR2506767A1/fr active Granted
-
1982
- 1982-05-18 AT AT82400920T patent/ATE15894T1/de active
- 1982-05-18 EP EP82400920A patent/EP0067094B1/fr not_active Expired
- 1982-05-18 DE DE8282400920T patent/DE3266640D1/de not_active Expired
- 1982-05-24 AR AR289500A patent/AR230047A1/es active
- 1982-05-25 DK DK234182A patent/DK234182A/da not_active Application Discontinuation
- 1982-05-25 US US06/381,749 patent/US4438121A/en not_active Expired - Fee Related
- 1982-05-25 JP JP57089610A patent/JPS57206663A/ja active Granted
- 1982-05-25 CA CA000403620A patent/CA1185603A/en not_active Expired
- 1982-05-25 ES ES512520A patent/ES8304086A1/es not_active Expired
- 1982-05-25 AU AU84157/82A patent/AU550769B2/en not_active Ceased
- 1982-05-25 IL IL65876A patent/IL65876A/xx unknown
- 1982-05-25 NO NO821725A patent/NO821725L/no unknown
- 1982-05-25 ZA ZA823628A patent/ZA823628B/xx unknown
- 1982-05-25 GR GR68258A patent/GR76445B/el unknown
- 1982-05-25 PT PT74952A patent/PT74952B/pt unknown
- 1982-05-25 NZ NZ200729A patent/NZ200729A/en unknown
- 1982-05-25 FI FI821857A patent/FI821857A0/fi not_active Application Discontinuation
- 1982-05-25 HU HU821693A patent/HU186515B/hu unknown
-
1983
- 1983-10-25 US US06/545,159 patent/US4530843A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| ES512520A0 (es) | 1983-02-16 |
| DK234182A (da) | 1982-11-27 |
| GR76445B (es) | 1984-08-10 |
| JPS57206663A (en) | 1982-12-18 |
| FR2506767B1 (es) | 1984-02-10 |
| EP0067094A1 (fr) | 1982-12-15 |
| HU186515B (en) | 1985-08-28 |
| IL65876A0 (en) | 1982-08-31 |
| NZ200729A (en) | 1984-07-31 |
| ATE15894T1 (de) | 1985-10-15 |
| AR230047A1 (es) | 1984-02-29 |
| JPS625423B2 (es) | 1987-02-04 |
| FR2506767A1 (fr) | 1982-12-03 |
| DE3266640D1 (en) | 1985-11-07 |
| ES8304086A1 (es) | 1983-02-16 |
| US4438121A (en) | 1984-03-20 |
| PT74952B (fr) | 1985-05-16 |
| AU8415782A (en) | 1982-12-02 |
| IL65876A (en) | 1985-09-29 |
| CA1185603A (en) | 1985-04-16 |
| US4530843A (en) | 1985-07-23 |
| ZA823628B (en) | 1983-03-30 |
| PT74952A (fr) | 1982-06-01 |
| EP0067094B1 (fr) | 1985-10-02 |
| AU550769B2 (en) | 1986-04-10 |
| FI821857A0 (fi) | 1982-05-25 |
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