JPS5838244A - 核置換シンナモイルアントラニル酸塩およびその製造方法 - Google Patents
核置換シンナモイルアントラニル酸塩およびその製造方法Info
- Publication number
- JPS5838244A JPS5838244A JP56137344A JP13734481A JPS5838244A JP S5838244 A JPS5838244 A JP S5838244A JP 56137344 A JP56137344 A JP 56137344A JP 13734481 A JP13734481 A JP 13734481A JP S5838244 A JPS5838244 A JP S5838244A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- general formula
- nuclear
- represented
- compound represented
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- JUUPYFMXANQBND-UHFFFAOYSA-N 3-phenylprop-2-enoyl 2-aminobenzoate Chemical class NC1=CC=CC=C1C(=O)OC(=O)C=CC1=CC=CC=C1 JUUPYFMXANQBND-UHFFFAOYSA-N 0.000 title claims description 11
- 238000002360 preparation method Methods 0.000 title abstract description 3
- 238000004519 manufacturing process Methods 0.000 claims abstract description 33
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 29
- 239000003960 organic solvent Substances 0.000 claims abstract description 10
- -1 cyclic amine Chemical class 0.000 claims abstract description 8
- 150000003934 aromatic aldehydes Chemical class 0.000 claims abstract description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
- 239000002253 acid Substances 0.000 claims abstract description 3
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 21
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 230000018044 dehydration Effects 0.000 claims description 2
- 238000006297 dehydration reaction Methods 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 5
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 38
- 238000006243 chemical reaction Methods 0.000 abstract description 23
- 239000013078 crystal Substances 0.000 abstract description 13
- 238000000034 method Methods 0.000 abstract description 9
- 239000000203 mixture Substances 0.000 abstract description 8
- NIVAFQOSMWPNDU-UHFFFAOYSA-N 2-[3-(3,4-dimethoxyphenyl)prop-2-enoylamino]benzoate;piperidin-1-ium Chemical compound C1CC[NH2+]CC1.C1=C(OC)C(OC)=CC=C1C=CC(=O)NC1=CC=CC=C1C([O-])=O NIVAFQOSMWPNDU-UHFFFAOYSA-N 0.000 abstract description 3
- 230000003266 anti-allergic effect Effects 0.000 abstract description 3
- ZAYGCNHJXNYVAJ-UHFFFAOYSA-N 2-(2-anilino-2-oxoethyl)-2-hydroxypropanedioic acid Chemical compound OC(=O)C(O)(C(O)=O)CC(=O)NC1=CC=CC=C1 ZAYGCNHJXNYVAJ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 1
- 239000000047 product Substances 0.000 description 11
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 10
- 238000002844 melting Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 238000000862 absorption spectrum Methods 0.000 description 8
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 8
- LZEMYXZYMHWMMN-UHFFFAOYSA-N 2-(phenylcarbamoyl)propanedioic acid Chemical compound OC(=O)C(C(O)=O)C(=O)NC1=CC=CC=C1 LZEMYXZYMHWMMN-UHFFFAOYSA-N 0.000 description 7
- 238000000921 elemental analysis Methods 0.000 description 7
- 238000001914 filtration Methods 0.000 description 7
- NQRYJNQNLNOLGT-UHFFFAOYSA-O Piperidinium(1+) Chemical compound C1CC[NH2+]CC1 NQRYJNQNLNOLGT-UHFFFAOYSA-O 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 238000010992 reflux Methods 0.000 description 5
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
- NZHGWWWHIYHZNX-UHFFFAOYSA-N 2-((3-(3,4-dimethoxyphenyl)-1-oxo-2-propenyl)amino)benzoic acid Chemical compound C1=C(OC)C(OC)=CC=C1C=CC(=O)NC1=CC=CC=C1C(O)=O NZHGWWWHIYHZNX-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- OAVFKCUALRMNQB-UHFFFAOYSA-N 2-[3-(3,4-dimethoxyphenyl)prop-2-enoylamino]benzoate;morpholin-4-ium Chemical compound C1COCC[NH2+]1.C1=C(OC)C(OC)=CC=C1C=CC(=O)NC1=CC=CC=C1C([O-])=O OAVFKCUALRMNQB-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- JVTZFYYHCGSXJV-UHFFFAOYSA-N isovanillin Chemical compound COC1=CC=C(C=O)C=C1O JVTZFYYHCGSXJV-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- RKGQUTNLMXNUME-UHFFFAOYSA-N methanetricarboxylic acid Chemical compound OC(=O)C(C(O)=O)C(O)=O RKGQUTNLMXNUME-UHFFFAOYSA-N 0.000 description 2
- JJVNINGBHGBWJH-UHFFFAOYSA-N ortho-vanillin Chemical compound COC1=CC=CC(C=O)=C1O JJVNINGBHGBWJH-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- PKZJLOCLABXVMC-UHFFFAOYSA-N 2-Methoxybenzaldehyde Chemical compound COC1=CC=CC=C1C=O PKZJLOCLABXVMC-UHFFFAOYSA-N 0.000 description 1
- DMPUNCUVRGJYGL-UHFFFAOYSA-N 2-ethoxy-3-methoxybenzaldehyde Chemical compound CCOC1=C(OC)C=CC=C1C=O DMPUNCUVRGJYGL-UHFFFAOYSA-N 0.000 description 1
- HAQLHRYUDBKTJG-UHFFFAOYSA-N 3,5-dihydroxybenzaldehyde Chemical compound OC1=CC(O)=CC(C=O)=C1 HAQLHRYUDBKTJG-UHFFFAOYSA-N 0.000 description 1
- NOJXRHBIVBIMQY-UHFFFAOYSA-N 3-anilino-3-oxopropanoic acid Chemical compound OC(=O)CC(=O)NC1=CC=CC=C1 NOJXRHBIVBIMQY-UHFFFAOYSA-N 0.000 description 1
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 1
- 239000005746 Carboxin Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-O Pyrrolidinium ion Chemical compound C1CC[NH2+]C1 RWRDLPDLKQPQOW-UHFFFAOYSA-O 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 238000006114 decarboxylation reaction Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- BTXNYTINYBABQR-UHFFFAOYSA-N hypericin Chemical compound C12=C(O)C=C(O)C(C(C=3C(O)=CC(C)=C4C=33)=O)=C2C3=C2C3=C4C(C)=CC(O)=C3C(=O)C3=C(O)C=C(O)C1=C32 BTXNYTINYBABQR-UHFFFAOYSA-N 0.000 description 1
- 229940005608 hypericin Drugs 0.000 description 1
- PHOKTTKFQUYZPI-UHFFFAOYSA-N hypericin Natural products Cc1cc(O)c2c3C(=O)C(=Cc4c(O)c5c(O)cc(O)c6c7C(=O)C(=Cc8c(C)c1c2c(c78)c(c34)c56)O)O PHOKTTKFQUYZPI-UHFFFAOYSA-N 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-O morpholinium Chemical compound [H+].C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-O 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- SSKVDVBQSWQEGJ-UHFFFAOYSA-N pseudohypericin Natural products C12=C(O)C=C(O)C(C(C=3C(O)=CC(O)=C4C=33)=O)=C2C3=C2C3=C4C(C)=CC(O)=C3C(=O)C3=C(O)C=C(O)C1=C32 SSKVDVBQSWQEGJ-UHFFFAOYSA-N 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
- C07D295/027—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Dental Preparations (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Hydrogenated Pyridines (AREA)
Priority Applications (15)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56137344A JPS5838244A (ja) | 1981-09-01 | 1981-09-01 | 核置換シンナモイルアントラニル酸塩およびその製造方法 |
| AU87148/82A AU562861B2 (en) | 1981-09-01 | 1982-08-13 | Cinnamoylanthranilic acid compounds |
| DE8282304389T DE3268129D1 (en) | 1981-09-01 | 1982-08-19 | A method for the production of nuclear substituted cinnamoylanthranilic acid derivatives and intermediates thereof |
| AT82304389T ATE17115T1 (de) | 1981-09-01 | 1982-08-19 | Verfahren zur herstellung von kernsubstituierten derivaten der cinnamoylanthranilsaeure und deren zwischenprodukte. |
| EP82304389A EP0074725B1 (en) | 1981-09-01 | 1982-08-19 | A method for the production of nuclear substituted cinnamoylanthranilic acid derivatives and intermediates thereof |
| PT75452A PT75452B (en) | 1981-09-01 | 1982-08-23 | A method for the preparation of nuclear substituted cinnamoylathranilic acid derivatives |
| FI822953A FI75148C (fi) | 1981-09-01 | 1982-08-25 | Foerfarande foer framstaellning av ringsubstituerade cinnamoylantranilsyraderivat. |
| CA000410210A CA1189090A (en) | 1981-09-01 | 1982-08-26 | Method for the production of nuclear substituted cinnamoylanthranilic acid derivatives |
| NO822943A NO159849C (no) | 1981-09-01 | 1982-08-31 | Fremgangsmaate ved fremstilling av kjernesubstituerte kanelantranilsyrederivater. |
| HU822794A HU186968B (en) | 1981-09-01 | 1982-08-31 | Process for preparing cinnamoly-anthranilic acid derivatives substituted in the nucleus |
| ES515401A ES8307208A1 (es) | 1981-09-01 | 1982-08-31 | Un procedimiento para la produccion de un derivado de acido cinamoilantralinico sustituido en el nucleo. |
| DK389582A DK158467C (da) | 1981-09-01 | 1982-08-31 | Fremgangsmaade til fremstilling af cinnamoylanthranilsyrederivater |
| US06/577,758 US4486597A (en) | 1981-09-01 | 1984-02-07 | Method for the production of nuclear substituted cinnamoylanthranilic acid derivatives |
| US06/640,588 US4623724A (en) | 1981-09-01 | 1984-08-14 | Method for the production of nuclear substituted cinnamoylanthranilic acid salts |
| US06/654,231 US4587356A (en) | 1981-09-01 | 1984-09-25 | Process for the production of nuclear substituted cinnamoylanthranilic acid derivatives |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56137344A JPS5838244A (ja) | 1981-09-01 | 1981-09-01 | 核置換シンナモイルアントラニル酸塩およびその製造方法 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63220233A Division JPH01246249A (ja) | 1988-09-02 | 1988-09-02 | 核置換シンナモイルアントラニル酸塩およびその製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5838244A true JPS5838244A (ja) | 1983-03-05 |
| JPH0136462B2 JPH0136462B2 (en, 2012) | 1989-07-31 |
Family
ID=15196441
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56137344A Granted JPS5838244A (ja) | 1981-09-01 | 1981-09-01 | 核置換シンナモイルアントラニル酸塩およびその製造方法 |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US4486597A (en, 2012) |
| EP (1) | EP0074725B1 (en, 2012) |
| JP (1) | JPS5838244A (en, 2012) |
| AT (1) | ATE17115T1 (en, 2012) |
| AU (1) | AU562861B2 (en, 2012) |
| CA (1) | CA1189090A (en, 2012) |
| DE (1) | DE3268129D1 (en, 2012) |
| DK (1) | DK158467C (en, 2012) |
| ES (1) | ES8307208A1 (en, 2012) |
| FI (1) | FI75148C (en, 2012) |
| HU (1) | HU186968B (en, 2012) |
| NO (1) | NO159849C (en, 2012) |
| PT (1) | PT75452B (en, 2012) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60214766A (ja) * | 1984-04-04 | 1985-10-28 | Terumo Corp | アミド誘導体およびこれを有効成分として含有する５−リポキシゲナ−ゼ作用阻害剤 |
| JP2006514931A (ja) * | 2002-11-25 | 2006-05-18 | ジムリス ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディットゲゼルシャフト | 化粧用及び医薬用活性化合物としてのアントラニル酸アミド類及びそれらの誘導体 |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4536346A (en) * | 1983-05-06 | 1985-08-20 | American Cyanamid Company | Aralkanamidophenyl compounds |
| JPH0784424B2 (ja) * | 1987-04-15 | 1995-09-13 | 味の素株式会社 | チロシン誘導体及びその用途 |
| KR970006473B1 (ko) * | 1987-06-08 | 1997-04-28 | 오노 화아마슈티칼 캄파니 리미팃드 | 신나모일아미드 유도체, 그들의 제조방법, 그들을 함유하는 제약학적 조성물 및 그들의 사용 |
| WO2002055454A2 (en) * | 2001-01-10 | 2002-07-18 | Smithkline Beecham Corporation | Process and product |
| DE10208778B4 (de) * | 2002-02-28 | 2004-08-12 | Thyssenkrupp Stahl Ag | Aus Stahl-Hohlprofilen gebildete Tragstruktur für Fahrzeuge |
| NZ584613A (en) * | 2007-12-21 | 2011-07-29 | Fibrotech Therapeutics Pty Ltd | Halogenated cinnamoylbenzamide derivatives for anti-fibrotic drugs |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS50140413A (en, 2012) * | 1974-04-18 | 1975-11-11 | ||
| JPS568858A (en) * | 1980-06-23 | 1981-01-29 | Hitachi Ltd | Resin sealing type semiconductor device |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3755603A (en) * | 1970-07-01 | 1973-08-28 | Syntex Corp | Biphenylyloxyacetic acids in pharmaceutical compositions |
| JPS5640710B2 (en, 2012) * | 1973-01-18 | 1981-09-22 | ||
| JPS511440A (ja) * | 1974-04-18 | 1976-01-08 | Kissei Pharmaceutical | Shinkihokozokukarubonsanjudotai no seizohoho |
| US4337270A (en) * | 1980-05-21 | 1982-06-29 | Hisamitsu Pharmaceutical Co., Inc. | Novel anthranilic acid derivatives |
-
1981
- 1981-09-01 JP JP56137344A patent/JPS5838244A/ja active Granted
-
1982
- 1982-08-13 AU AU87148/82A patent/AU562861B2/en not_active Expired
- 1982-08-19 EP EP82304389A patent/EP0074725B1/en not_active Expired
- 1982-08-19 DE DE8282304389T patent/DE3268129D1/de not_active Expired
- 1982-08-19 AT AT82304389T patent/ATE17115T1/de not_active IP Right Cessation
- 1982-08-23 PT PT75452A patent/PT75452B/pt not_active IP Right Cessation
- 1982-08-25 FI FI822953A patent/FI75148C/fi not_active IP Right Cessation
- 1982-08-26 CA CA000410210A patent/CA1189090A/en not_active Expired
- 1982-08-31 DK DK389582A patent/DK158467C/da not_active IP Right Cessation
- 1982-08-31 HU HU822794A patent/HU186968B/hu unknown
- 1982-08-31 ES ES515401A patent/ES8307208A1/es not_active Expired
- 1982-08-31 NO NO822943A patent/NO159849C/no not_active IP Right Cessation
-
1984
- 1984-02-07 US US06/577,758 patent/US4486597A/en not_active Expired - Lifetime
- 1984-08-14 US US06/640,588 patent/US4623724A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS50140413A (en, 2012) * | 1974-04-18 | 1975-11-11 | ||
| JPS568858A (en) * | 1980-06-23 | 1981-01-29 | Hitachi Ltd | Resin sealing type semiconductor device |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60214766A (ja) * | 1984-04-04 | 1985-10-28 | Terumo Corp | アミド誘導体およびこれを有効成分として含有する５−リポキシゲナ−ゼ作用阻害剤 |
| JP2006514931A (ja) * | 2002-11-25 | 2006-05-18 | ジムリス ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディットゲゼルシャフト | 化粧用及び医薬用活性化合物としてのアントラニル酸アミド類及びそれらの誘導体 |
Also Published As
| Publication number | Publication date |
|---|---|
| NO822943L (no) | 1983-03-02 |
| NO159849B (no) | 1988-11-07 |
| PT75452B (en) | 1984-11-19 |
| DK158467B (da) | 1990-05-21 |
| HU186968B (en) | 1985-10-28 |
| EP0074725B1 (en) | 1985-12-27 |
| EP0074725A1 (en) | 1983-03-23 |
| ES515401A0 (es) | 1983-07-01 |
| US4486597A (en) | 1984-12-04 |
| FI822953A0 (fi) | 1982-08-25 |
| ES8307208A1 (es) | 1983-07-01 |
| FI75148C (fi) | 1988-05-09 |
| DK158467C (da) | 1990-10-22 |
| FI822953L (fi) | 1983-03-02 |
| ATE17115T1 (de) | 1986-01-15 |
| NO159849C (no) | 1989-02-15 |
| US4623724A (en) | 1986-11-18 |
| AU562861B2 (en) | 1987-06-18 |
| AU8714882A (en) | 1983-03-10 |
| PT75452A (en) | 1982-09-01 |
| FI75148B (fi) | 1988-01-29 |
| JPH0136462B2 (en, 2012) | 1989-07-31 |
| CA1189090A (en) | 1985-06-18 |
| DE3268129D1 (en) | 1986-02-06 |
| DK389582A (da) | 1983-03-02 |
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