NO133137B - - Google Patents
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- Publication number
- NO133137B NO133137B NO2954/71A NO295471A NO133137B NO 133137 B NO133137 B NO 133137B NO 2954/71 A NO2954/71 A NO 2954/71A NO 295471 A NO295471 A NO 295471A NO 133137 B NO133137 B NO 133137B
- Authority
- NO
- Norway
- Prior art keywords
- acid
- dioxocyclohexanecarboxylic
- isothiocyanate
- dione
- alkoxy
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 10
- HJSLFCCWAKVHIW-UHFFFAOYSA-N cyclohexane-1,3-dione Chemical compound O=C1CCCC(=O)C1 HJSLFCCWAKVHIW-UHFFFAOYSA-N 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- QKFJKGMPGYROCL-UHFFFAOYSA-N phenyl isothiocyanate Chemical class S=C=NC1=CC=CC=C1 QKFJKGMPGYROCL-UHFFFAOYSA-N 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- 239000005864 Sulphur Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000012948 isocyanate Substances 0.000 claims description 4
- 150000002513 isocyanates Chemical class 0.000 claims description 4
- 150000002540 isothiocyanates Chemical class 0.000 claims description 4
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical class O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- 229940117953 phenylisothiocyanate Drugs 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- LDUQUHXCYGDUFJ-UHFFFAOYSA-N 2,6-dioxocyclohexane-1-carboxylic acid Chemical compound OC(=O)C1C(=O)CCCC1=O LDUQUHXCYGDUFJ-UHFFFAOYSA-N 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
- 239000013543 active substance Substances 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 241001465754 Metazoa Species 0.000 description 4
- 229960000583 acetic acid Drugs 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000012362 glacial acetic acid Substances 0.000 description 4
- 241000283690 Bos taurus Species 0.000 description 3
- 241001494479 Pecora Species 0.000 description 3
- -1 nitro, methyl Chemical group 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- GRQAXLYUJPTODT-UHFFFAOYSA-N 2,6-dioxo-n-phenylcyclohexane-1-carbothioamide Chemical compound O=C1CCCC(=O)C1C(=S)NC1=CC=CC=C1 GRQAXLYUJPTODT-UHFFFAOYSA-N 0.000 description 2
- SOPQSPVALWUPDD-UHFFFAOYSA-N 2,6-dioxocyclohexane-1-carbothioic S-acid Chemical compound O=C1C(C(CCC1)=O)C(O)=S SOPQSPVALWUPDD-UHFFFAOYSA-N 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 2
- 206010017533 Fungal infection Diseases 0.000 description 2
- 241000545744 Hirudinea Species 0.000 description 2
- 208000031888 Mycoses Diseases 0.000 description 2
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 230000000843 anti-fungal effect Effects 0.000 description 2
- 244000052616 bacterial pathogen Species 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 244000309464 bull Species 0.000 description 2
- 230000000973 chemotherapeutic effect Effects 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000000338 in vitro Methods 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 210000004185 liver Anatomy 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- XINQFOMFQFGGCQ-UHFFFAOYSA-L (2-dodecoxy-2-oxoethyl)-[6-[(2-dodecoxy-2-oxoethyl)-dimethylazaniumyl]hexyl]-dimethylazanium;dichloride Chemical compound [Cl-].[Cl-].CCCCCCCCCCCCOC(=O)C[N+](C)(C)CCCCCC[N+](C)(C)CC(=O)OCCCCCCCCCCCC XINQFOMFQFGGCQ-UHFFFAOYSA-L 0.000 description 1
- DRBGWCMNNQMIAL-UHFFFAOYSA-N (4-chlorophenyl)carbamoyl acetate Chemical compound C(C)(=O)OC(NC1=CC=C(C=C1)Cl)=O DRBGWCMNNQMIAL-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- ADAKRBAJFHTIEW-UHFFFAOYSA-N 1-chloro-4-isocyanatobenzene Chemical compound ClC1=CC=C(N=C=O)C=C1 ADAKRBAJFHTIEW-UHFFFAOYSA-N 0.000 description 1
- NRSSOFNMWSJECS-UHFFFAOYSA-N 1-isocyanato-3,5-bis(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC(N=C=O)=CC(C(F)(F)F)=C1 NRSSOFNMWSJECS-UHFFFAOYSA-N 0.000 description 1
- BDPQUWSFKCFOST-UHFFFAOYSA-N 1-isothiocyanato-3-methylbenzene Chemical compound CC1=CC=CC(N=C=S)=C1 BDPQUWSFKCFOST-UHFFFAOYSA-N 0.000 description 1
- UDJIPUWKNJRKBB-UHFFFAOYSA-N 2,6-dioxo-N-phenylcyclohexane-1-carboxamide Chemical class O=C(Nc1ccccc1)C1C(=O)CCCC1=O UDJIPUWKNJRKBB-UHFFFAOYSA-N 0.000 description 1
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 241000242711 Fasciola hepatica Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 241000283903 Ovis aries Species 0.000 description 1
- ZLMJMSJWJFRBEC-LZFNBGRKSA-N Potassium-45 Chemical compound [45K] ZLMJMSJWJFRBEC-LZFNBGRKSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 241000242541 Trematoda Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000007059 acute toxicity Effects 0.000 description 1
- 231100000403 acute toxicity Toxicity 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 229940051881 anilide analgesics and antipyretics Drugs 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- OILAIQUEIWYQPH-UHFFFAOYSA-N cyclohexane-1,2-dione Chemical class O=C1CCCCC1=O OILAIQUEIWYQPH-UHFFFAOYSA-N 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 244000053095 fungal pathogen Species 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- KBMXZBWIWSRALH-UHFFFAOYSA-N n-(4-chlorophenyl)-2,6-dioxocyclohexane-1-carbothioamide Chemical compound C1=CC(Cl)=CC=C1NC(=S)C1C(=O)CCCC1=O KBMXZBWIWSRALH-UHFFFAOYSA-N 0.000 description 1
- ZOCYRJKGMXEYTN-UHFFFAOYSA-N n-(4-chlorophenyl)carbamoyl chloride Chemical compound ClC(=O)NC1=CC=C(Cl)C=C1 ZOCYRJKGMXEYTN-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- FNKMDTZNLLZDLZ-UHFFFAOYSA-N o-(phenylcarbamothioyl) n-phenylcarbamothioate Chemical class C=1C=CC=CC=1NC(=S)OC(=S)NC1=CC=CC=C1 FNKMDTZNLLZDLZ-UHFFFAOYSA-N 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- OPVOKTZBUWENMY-UHFFFAOYSA-N phenylcarbamoyl n-phenylcarbamate Chemical class C=1C=CC=CC=1NC(=O)OC(=O)NC1=CC=CC=C1 OPVOKTZBUWENMY-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C265/00—Derivatives of isocyanic acid
- C07C265/12—Derivatives of isocyanic acid having isocyanate groups bound to carbon atoms of six-membered aromatic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/70—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/82—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton with the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids
- C07C327/38—Amides of thiocarboxylic acids
- C07C327/46—Amides of thiocarboxylic acids having carbon atoms of thiocarboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19702039466 DE2039466C3 (de) | 1970-08-08 | Dioxocyclohexancaibonsäureanilide und -thioanilide und Verfahren zu ihrer Herstellung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO133137B true NO133137B (fi) | 1975-12-08 |
| NO133137C NO133137C (fi) | 1976-03-17 |
Family
ID=5779205
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO2954/71A NO133137C (fi) | 1970-08-08 | 1971-08-06 |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US3746765A (fi) |
| AT (1) | AT316504B (fi) |
| BE (1) | BE771060A (fi) |
| BG (1) | BG20345A3 (fi) |
| BR (1) | BR7105080D0 (fi) |
| CA (1) | CA980795A (fi) |
| CH (1) | CH560183A5 (fi) |
| CS (1) | CS162759B2 (fi) |
| DD (1) | DD95367A5 (fi) |
| DK (1) | DK137269C (fi) |
| EG (1) | EG11967A (fi) |
| ES (1) | ES393859A1 (fi) |
| FI (1) | FI53306C (fi) |
| FR (1) | FR2102140B1 (fi) |
| GB (1) | GB1350816A (fi) |
| IE (1) | IE35497B1 (fi) |
| IL (1) | IL37464A (fi) |
| IT (1) | IT1043844B (fi) |
| NL (1) | NL147934B (fi) |
| NO (1) | NO133137C (fi) |
| PH (1) | PH9208A (fi) |
| PL (1) | PL83204B1 (fi) |
| RO (1) | RO63938A (fi) |
| SE (1) | SE386666B (fi) |
| SU (1) | SU415867A3 (fi) |
| YU (1) | YU204771A (fi) |
| ZA (1) | ZA715239B (fi) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3814505A1 (de) * | 1988-04-29 | 1989-11-09 | Bayer Ag | Substituierte cycloalkyl- bzw. heterocyclyl-carbonsaeureanilide |
| US7179943B2 (en) * | 2004-06-14 | 2007-02-20 | Wyeth | Bicyclic derivatives that modulate voltage-gated potassium channels and methods of use thereof |
-
1971
- 1971-07-31 EG EG336/71A patent/EG11967A/xx active
- 1971-08-03 ES ES393859A patent/ES393859A1/es not_active Expired
- 1971-08-03 NL NL717110697A patent/NL147934B/xx unknown
- 1971-08-04 CH CH1148071A patent/CH560183A5/xx not_active IP Right Cessation
- 1971-08-04 BG BG18241A patent/BG20345A3/xx unknown
- 1971-08-05 YU YU02047/71A patent/YU204771A/xx unknown
- 1971-08-05 FI FI2199/71A patent/FI53306C/fi active
- 1971-08-05 CS CS5705A patent/CS162759B2/cs unknown
- 1971-08-05 US US00169530A patent/US3746765A/en not_active Expired - Lifetime
- 1971-08-06 IT IT27270/71A patent/IT1043844B/it active
- 1971-08-06 DK DK386471A patent/DK137269C/da active
- 1971-08-06 BE BE771060A patent/BE771060A/xx unknown
- 1971-08-06 DD DD156990A patent/DD95367A5/xx unknown
- 1971-08-06 BR BR5080/71A patent/BR7105080D0/pt unknown
- 1971-08-06 SU SU1691587A patent/SU415867A3/ru active
- 1971-08-06 CA CA119,961A patent/CA980795A/en not_active Expired
- 1971-08-06 NO NO2954/71A patent/NO133137C/no unknown
- 1971-08-06 AT AT691671A patent/AT316504B/de not_active IP Right Cessation
- 1971-08-06 ZA ZA715239*7A patent/ZA715239B/xx unknown
- 1971-08-06 IE IE998/71A patent/IE35497B1/xx unknown
- 1971-08-06 SE SE7110084A patent/SE386666B/xx unknown
- 1971-08-06 IL IL37464A patent/IL37464A/xx unknown
- 1971-08-07 RO RO7100067931A patent/RO63938A/ro unknown
- 1971-08-07 PL PL1971149893A patent/PL83204B1/pl unknown
- 1971-08-09 FR FR7129063A patent/FR2102140B1/fr not_active Expired
- 1971-08-09 GB GB3739871A patent/GB1350816A/en not_active Expired
- 1971-08-16 PH PH12750*UA patent/PH9208A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL7110697A (fi) | 1972-02-10 |
| DK137269B (da) | 1978-02-13 |
| FI53306B (fi) | 1977-12-30 |
| IL37464A0 (en) | 1971-11-29 |
| BG20345A3 (fi) | 1975-11-05 |
| IT1043844B (it) | 1980-02-29 |
| BR7105080D0 (pt) | 1973-05-10 |
| DD95367A5 (fi) | 1973-02-05 |
| GB1350816A (en) | 1974-04-24 |
| ES393859A1 (es) | 1974-07-16 |
| AT316504B (de) | 1974-07-10 |
| IE35497L (en) | 1972-02-08 |
| SE386666B (sv) | 1976-08-16 |
| SU415867A3 (fi) | 1974-02-15 |
| CH560183A5 (fi) | 1975-03-27 |
| RO63938A (fr) | 1978-10-15 |
| IE35497B1 (en) | 1976-03-03 |
| DK137269C (da) | 1978-08-07 |
| EG11967A (en) | 1978-09-30 |
| NO133137C (fi) | 1976-03-17 |
| US3746765A (en) | 1973-07-17 |
| FR2102140B1 (fi) | 1974-09-06 |
| IL37464A (en) | 1974-06-30 |
| CS162759B2 (fi) | 1975-07-15 |
| NL147934B (nl) | 1975-12-15 |
| FI53306C (fi) | 1978-04-10 |
| FR2102140A1 (fi) | 1972-04-07 |
| PL83204B1 (fi) | 1975-12-31 |
| ZA715239B (en) | 1972-05-31 |
| CA980795A (en) | 1975-12-30 |
| DE2039466B2 (de) | 1976-05-26 |
| DE2039466A1 (de) | 1972-02-17 |
| PH9208A (en) | 1975-07-03 |
| YU204771A (en) | 1979-12-31 |
| BE771060A (fr) | 1971-12-16 |
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