NO127920B - - Google Patents
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- Publication number
- NO127920B NO127920B NO00773/72*[A NO77372A NO127920B NO 127920 B NO127920 B NO 127920B NO 77372 A NO77372 A NO 77372A NO 127920 B NO127920 B NO 127920B
- Authority
- NO
- Norway
- Prior art keywords
- dimethyl
- methoxy
- ergoline
- methyl
- pyrroyloxymethyl
- Prior art date
Links
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical group 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 239000003880 polar aprotic solvent Substances 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 150000003512 tertiary amines Chemical class 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 238000002844 melting Methods 0.000 description 21
- 230000008018 melting Effects 0.000 description 21
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 12
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 11
- 239000002904 solvent Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- UCTWMZQNUQWSLP-UHFFFAOYSA-N adrenaline Chemical compound CNCC(O)C1=CC=C(O)C(O)=C1 UCTWMZQNUQWSLP-UHFFFAOYSA-N 0.000 description 4
- -1 pyrrole radical Chemical group 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 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
- 239000002244 precipitate Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 230000002908 adrenolytic effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- YYROPELSRYBVMQ-UHFFFAOYSA-N p-toluenesulfonyl chloride Substances CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 2
- DOYOPBSXEIZLRE-UHFFFAOYSA-N pyrrole-3-carboxylic acid Chemical compound OC(=O)C=1C=CNC=1 DOYOPBSXEIZLRE-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- CTEWKXYQIKKNAH-HCGVIMEBSA-N (6ar,10ar)-9-methoxy-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline Chemical compound C1=CC([C@@H]2[C@H](NCC(C2)OC)C2)=C3C2=CNC3=C1 CTEWKXYQIKKNAH-HCGVIMEBSA-N 0.000 description 1
- HSKWOJUVXHOUQF-IKJNGHJTSA-N (6ar,10as)-10a-methoxy-4,7,9-trimethyl-6,6a,8,10-tetrahydroindolo[4,3-fg]quinoline-9-ol Chemical compound C1=CC([C@]2(OC)[C@H](N(C)CC(C)(O)C2)C2)=C3C2=CN(C)C3=C1 HSKWOJUVXHOUQF-IKJNGHJTSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- UUYNZCLYPLJBTG-UHFFFAOYSA-N 1,3,5-trimethylpyrrole-2-carboxylic acid Chemical compound CC=1C=C(C)N(C)C=1C(O)=O UUYNZCLYPLJBTG-UHFFFAOYSA-N 0.000 description 1
- KDYMOUGNHJDZKT-UHFFFAOYSA-N 1-butylpyrrole-2-carboxylic acid Chemical compound CCCCN1C=CC=C1C(O)=O KDYMOUGNHJDZKT-UHFFFAOYSA-N 0.000 description 1
- XCOJUFQICAEQEP-UHFFFAOYSA-N 1-ethylpyrrole-2-carboxylic acid Chemical compound CCN1C=CC=C1C(O)=O XCOJUFQICAEQEP-UHFFFAOYSA-N 0.000 description 1
- ILAOVOOZLVGAJF-UHFFFAOYSA-N 1-methylpyrrole-2-carboxylic acid Chemical compound CN1C=CC=C1C(O)=O ILAOVOOZLVGAJF-UHFFFAOYSA-N 0.000 description 1
- GMLCQPJLSFPJMX-UHFFFAOYSA-N 1-phenylpyrrole-2-carboxylic acid Chemical compound OC(=O)C1=CC=CN1C1=CC=CC=C1 GMLCQPJLSFPJMX-UHFFFAOYSA-N 0.000 description 1
- XBPJVSRTTKVMEN-UHFFFAOYSA-N 2,4-dimethyl-1h-pyrrole-3-carboxylic acid Chemical compound CC1=CNC(C)=C1C(O)=O XBPJVSRTTKVMEN-UHFFFAOYSA-N 0.000 description 1
- YBJBJOLFTYIFKP-UHFFFAOYSA-N 2-methyl-1h-pyrrole-3-carboxylic acid Chemical compound CC=1NC=CC=1C(O)=O YBJBJOLFTYIFKP-UHFFFAOYSA-N 0.000 description 1
- XFUFEHARKXXQGR-UHFFFAOYSA-N 3,4,5-tribromo-1-methylpyrrole-2-carboxylic acid Chemical compound CN1C(Br)=C(Br)C(Br)=C1C(O)=O XFUFEHARKXXQGR-UHFFFAOYSA-N 0.000 description 1
- LMXSZWFRGRIPQR-UHFFFAOYSA-N 3,4,5-trichloro-1h-pyrrole-2-carboxylic acid Chemical compound OC(=O)C=1NC(Cl)=C(Cl)C=1Cl LMXSZWFRGRIPQR-UHFFFAOYSA-N 0.000 description 1
- PENUMIKIRFKVKW-UHFFFAOYSA-N 3,4-dibromo-1-methylpyrrole-2-carboxylic acid Chemical compound CN1C=C(Br)C(Br)=C1C(O)=O PENUMIKIRFKVKW-UHFFFAOYSA-N 0.000 description 1
- PHQXHIWKCSGYDM-UHFFFAOYSA-N 3,4-dichloro-1h-pyrrole-2-carboxylic acid Chemical compound OC(=O)C=1NC=C(Cl)C=1Cl PHQXHIWKCSGYDM-UHFFFAOYSA-N 0.000 description 1
- XQGVQRPSTODODM-UHFFFAOYSA-N 3,5-dimethyl-1h-pyrrole-2-carboxylic acid Chemical compound CC1=CC(C)=C(C(O)=O)N1 XQGVQRPSTODODM-UHFFFAOYSA-N 0.000 description 1
- HAEVZKQRENIKEV-UHFFFAOYSA-N 4-bromo-3,5-dimethyl-1h-pyrrole-2-carboxylic acid Chemical compound CC=1NC(C(O)=O)=C(C)C=1Br HAEVZKQRENIKEV-UHFFFAOYSA-N 0.000 description 1
- DXKYHAPIBYYLJR-UHFFFAOYSA-N 4-ethoxycarbonyl-3,5-dimethyl-1h-pyrrole-2-carboxylic acid Chemical compound CCOC(=O)C1=C(C)NC(C(O)=O)=C1C DXKYHAPIBYYLJR-UHFFFAOYSA-N 0.000 description 1
- JMDVLCHZHALXPK-UHFFFAOYSA-N 4-methoxy-1h-pyrrole-2-carboxylic acid Chemical compound COC1=CNC(C(O)=O)=C1 JMDVLCHZHALXPK-UHFFFAOYSA-N 0.000 description 1
- QFLMHTCEGRXTNL-UHFFFAOYSA-N 4-methoxy-1h-pyrrole-3-carboxylic acid Chemical compound COC1=CNC=C1C(O)=O QFLMHTCEGRXTNL-UHFFFAOYSA-N 0.000 description 1
- PKYXJNNPHVMPDQ-UHFFFAOYSA-N 5-bromo-1-methylpyrrole-2-carboxylic acid Chemical compound CN1C(Br)=CC=C1C(O)=O PKYXJNNPHVMPDQ-UHFFFAOYSA-N 0.000 description 1
- SWLUNFAAJVHVFI-UHFFFAOYSA-N 5-chloro-1h-pyrrole-2-carboxylic acid Chemical compound OC(=O)C1=CC=C(Cl)N1 SWLUNFAAJVHVFI-UHFFFAOYSA-N 0.000 description 1
- VZZQCXPDRSMKPM-UHFFFAOYSA-N 5-ethoxycarbonyl-2,4-dimethyl-1h-pyrrole-3-carboxylic acid Chemical compound CCOC(=O)C=1NC(C)=C(C(O)=O)C=1C VZZQCXPDRSMKPM-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical class [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 241000700198 Cavia Species 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 208000001953 Hypotension Diseases 0.000 description 1
- 239000012359 Methanesulfonyl chloride Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 230000000794 anti-serotonin Effects 0.000 description 1
- 239000003420 antiserotonin agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- HESHRHUZIWVEAJ-JGRZULCMSA-N dihydroergotamine Chemical compound C([C@H]1C(=O)N2CCC[C@H]2[C@]2(O)O[C@@](C(N21)=O)(C)NC(=O)[C@H]1CN([C@H]2[C@@H](C3=CC=CC4=NC=C([C]34)C2)C1)C)C1=CC=CC=C1 HESHRHUZIWVEAJ-JGRZULCMSA-N 0.000 description 1
- 229960004704 dihydroergotamine Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 208000021822 hypotensive Diseases 0.000 description 1
- 230000001077 hypotensive effect Effects 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 230000001665 lethal effect Effects 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 150000003109 potassium Chemical class 0.000 description 1
- BBFCIBZLAVOLCF-UHFFFAOYSA-N pyridin-1-ium;bromide Chemical compound Br.C1=CC=NC=C1 BBFCIBZLAVOLCF-UHFFFAOYSA-N 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000000932 sedative agent Substances 0.000 description 1
- 230000001624 sedative effect Effects 0.000 description 1
- 210000001625 seminal vesicle Anatomy 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 230000003033 spasmogenic effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- 201000010653 vesiculitis Diseases 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D457/00—Heterocyclic compounds containing indolo [4, 3-f, g] quinoline ring systems, e.g. derivatives of ergoline, of the formula:, e.g. lysergic acid
- C07D457/02—Heterocyclic compounds containing indolo [4, 3-f, g] quinoline ring systems, e.g. derivatives of ergoline, of the formula:, e.g. lysergic acid with hydrocarbon or substituted hydrocarbon radicals, attached in position 8
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT2171371 | 1971-03-13 | ||
| IT3105971A IT1045256B (it) | 1971-11-13 | 1971-11-13 | Derivati del lumilisergolo |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO127920B true NO127920B (hu) | 1973-09-03 |
Family
ID=26327977
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO00773/72*[A NO127920B (hu) | 1971-03-13 | 1972-03-10 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US3966739A (hu) |
| JP (1) | JPS5133920B1 (hu) |
| AT (1) | AT322119B (hu) |
| AU (1) | AU461957B2 (hu) |
| BE (1) | BE780473A (hu) |
| CA (1) | CA967958A (hu) |
| CH (1) | CH567505A5 (hu) |
| DE (1) | DE2211397B2 (hu) |
| DK (1) | DK140479B (hu) |
| ES (1) | ES400683A1 (hu) |
| FR (1) | FR2130140B1 (hu) |
| GB (1) | GB1333024A (hu) |
| HU (1) | HU163400B (hu) |
| IE (1) | IE36207B1 (hu) |
| IL (1) | IL38936A (hu) |
| NL (1) | NL159384B (hu) |
| NO (1) | NO127920B (hu) |
| SE (1) | SE394281B (hu) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7400790A (hu) * | 1973-02-02 | 1974-08-06 | ||
| CH619709A5 (en) * | 1975-03-14 | 1980-10-15 | Siphar Sa | Process for the preparation of carbamates of 2-halogenoergolines and 2-halogenoergolenes |
| JPS5316315U (hu) * | 1976-07-22 | 1978-02-10 | ||
| YU40004B (en) * | 1977-07-21 | 1985-06-30 | Lek Tovarna Farmacevtskih | Praocess for preparing n-substituted esters of 9,10-dihydrlysergic acid |
| IT1094965B (it) * | 1978-04-05 | 1985-08-10 | Corvi Mora E | Procedimento di preparazione di derivati del lisergolo |
| JPS5823990U (ja) * | 1981-08-10 | 1983-02-15 | アイカ工業株式会社 | ドア用パネル板の構造 |
| EP2832233A1 (en) * | 2013-07-30 | 2015-02-04 | IMAX Discovery GmbH | 1H-pyrrole-2,4-dicarbonyl-derivatives and their use as flavoring agents |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3155667A (en) * | 1964-11-03 | Process for the preparation of | ||
| US3228943A (en) * | 1962-06-11 | 1966-01-11 | Lumilysergol derivatives | |
| GB1053507A (hu) * | 1964-04-14 | |||
| US3418360A (en) * | 1964-12-14 | 1968-12-24 | Gulf Research Development Co | Esterification in the presence of alkanoic acid amides |
| FR1439953A (fr) * | 1965-01-28 | 1966-05-27 | Sandoz Sa | Nouveaux dérivés de l'ergolène et leur préparation |
| US3341575A (en) * | 1965-03-19 | 1967-09-12 | Union Oil Co | Preparation of esters from alkyl chlorides and carboxylic acid salts in the presenceof amide solvent and a soluble iodide compound |
| US3461156A (en) * | 1965-09-24 | 1969-08-12 | Union Oil Co | Process of preparating esters |
| US3551571A (en) * | 1967-05-19 | 1970-12-29 | Endo Lab | Methods for reducing pain,reducing fever and alleviating inflammatory syndromes with heteroaromatic pyrrol-3-yl ketones |
| DE1936410A1 (de) * | 1969-07-17 | 1971-02-11 | Hoechst Ag | O-Acyl-lysergole und Verfahren zu ihrer Herstellung |
-
1972
- 1972-03-03 NL NL7202845.A patent/NL159384B/xx not_active IP Right Cessation
- 1972-03-07 US US05/232,605 patent/US3966739A/en not_active Expired - Lifetime
- 1972-03-08 IL IL38936A patent/IL38936A/xx unknown
- 1972-03-08 IE IE293/72A patent/IE36207B1/xx unknown
- 1972-03-08 CA CA136,871A patent/CA967958A/en not_active Expired
- 1972-03-08 GB GB1069872A patent/GB1333024A/en not_active Expired
- 1972-03-09 FR FR7208204A patent/FR2130140B1/fr not_active Expired
- 1972-03-09 DE DE2211397A patent/DE2211397B2/de active Granted
- 1972-03-10 SE SE7203051A patent/SE394281B/xx unknown
- 1972-03-10 AU AU39871/72A patent/AU461957B2/en not_active Expired
- 1972-03-10 BE BE780473A patent/BE780473A/xx not_active IP Right Cessation
- 1972-03-10 AT AT202072A patent/AT322119B/de not_active IP Right Cessation
- 1972-03-10 CH CH358172A patent/CH567505A5/xx not_active IP Right Cessation
- 1972-03-10 DK DK111172AA patent/DK140479B/da unknown
- 1972-03-10 NO NO00773/72*[A patent/NO127920B/no unknown
- 1972-03-11 JP JP47024431A patent/JPS5133920B1/ja active Pending
- 1972-03-11 HU HUFA905A patent/HU163400B/hu unknown
- 1972-03-11 ES ES400683A patent/ES400683A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DK140479C (hu) | 1980-03-17 |
| NL7202845A (hu) | 1972-09-15 |
| AU461957B2 (en) | 1975-06-12 |
| IE36207L (en) | 1972-09-13 |
| GB1333024A (en) | 1973-10-10 |
| DE2211397C3 (hu) | 1978-11-09 |
| AT322119B (de) | 1975-05-12 |
| SE394281B (sv) | 1977-06-20 |
| DK140479B (da) | 1979-09-10 |
| JPS5133920B1 (hu) | 1976-09-22 |
| US3966739A (en) | 1976-06-29 |
| FR2130140B1 (hu) | 1975-08-01 |
| HU163400B (hu) | 1973-08-28 |
| DE2211397A1 (de) | 1972-09-21 |
| NL159384B (nl) | 1979-02-15 |
| IL38936A (en) | 1975-04-25 |
| BE780473A (fr) | 1972-09-11 |
| FR2130140A1 (hu) | 1972-11-03 |
| IL38936A0 (en) | 1972-05-30 |
| ES400683A1 (es) | 1975-07-16 |
| CH567505A5 (hu) | 1975-10-15 |
| IE36207B1 (en) | 1976-09-15 |
| CA967958A (en) | 1975-05-20 |
| AU3987172A (en) | 1973-09-13 |
| DE2211397B2 (de) | 1978-03-16 |
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