KR860004003A - 알파-나프틸-프로피온산 라세미혼합물의 새로운 광학적 분할방법 - Google Patents
알파-나프틸-프로피온산 라세미혼합물의 새로운 광학적 분할방법 Download PDFInfo
- Publication number
- KR860004003A KR860004003A KR1019850008756A KR850008756A KR860004003A KR 860004003 A KR860004003 A KR 860004003A KR 1019850008756 A KR1019850008756 A KR 1019850008756A KR 850008756 A KR850008756 A KR 850008756A KR 860004003 A KR860004003 A KR 860004003A
- Authority
- KR
- South Korea
- Prior art keywords
- carbon atoms
- naphthyl
- methoxy
- hydroxy
- scheme
- 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.)
- Ceased
Links
- 238000000034 method Methods 0.000 title claims 9
- 239000000203 mixture Substances 0.000 title claims 7
- 230000003287 optical effect Effects 0.000 title claims 3
- 230000011218 segmentation Effects 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 14
- -1 benzoyloxy, substituted benzoyloxy, sulfonyloxy, benzenesulfonyloxy, 4-methyl-benzenesulfonyloxy, 2-imidazolyl-carbonyl Chemical group 0.000 claims 9
- 150000001408 amides Chemical class 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 6
- 229910052736 halogen Inorganic materials 0.000 claims 6
- 239000002904 solvent Substances 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 4
- 239000003513 alkali Substances 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- 239000000463 material Substances 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- UVPBNWOIJKXKEA-UHFFFAOYSA-N 2-(5-bromo-6-methoxynaphthalen-2-yl)propanamide Chemical compound C1=C(C(C)C(N)=O)C=CC2=C(Br)C(OC)=CC=C21 UVPBNWOIJKXKEA-UHFFFAOYSA-N 0.000 claims 2
- VKCNNDPZFOVURD-UHFFFAOYSA-N 2-naphthalen-1-ylpropanoic acid Chemical compound C1=CC=C2C(C(C(O)=O)C)=CC=CC2=C1 VKCNNDPZFOVURD-UHFFFAOYSA-N 0.000 claims 2
- 150000004703 alkoxides Chemical class 0.000 claims 2
- 150000001414 amino alcohols Chemical class 0.000 claims 2
- 239000007864 aqueous solution Substances 0.000 claims 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 2
- 238000009835 boiling Methods 0.000 claims 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Substances OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 125000004464 hydroxyphenyl group Chemical group 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 239000003960 organic solvent Substances 0.000 claims 2
- 235000019260 propionic acid Nutrition 0.000 claims 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims 2
- 239000011541 reaction mixture Substances 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- ZCSPYHPIRDRSPR-UHFFFAOYSA-N 2-(6-methoxynaphthalen-2-yl)propanamide Chemical compound C1=C(C(C)C(N)=O)C=CC2=CC(OC)=CC=C21 ZCSPYHPIRDRSPR-UHFFFAOYSA-N 0.000 claims 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical group [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- BUDQDWGNQVEFAC-UHFFFAOYSA-N Dihydropyran Chemical compound C1COC=CC1 BUDQDWGNQVEFAC-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 238000005903 acid hydrolysis reaction Methods 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 239000002585 base Substances 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 238000003776 cleavage reaction Methods 0.000 claims 1
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 238000001914 filtration Methods 0.000 claims 1
- 150000008282 halocarbons Chemical class 0.000 claims 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims 1
- 150000004678 hydrides Chemical class 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 125000001041 indolyl group Chemical group 0.000 claims 1
- 150000007522 mineralic acids Chemical class 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 1
- 230000000737 periodic effect Effects 0.000 claims 1
- 150000003138 primary alcohols Chemical class 0.000 claims 1
- 238000011084 recovery Methods 0.000 claims 1
- 230000007017 scission Effects 0.000 claims 1
- 150000003333 secondary alcohols Chemical class 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 125000001412 tetrahydropyranyl group Chemical class 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C61/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C61/12—Saturated polycyclic compounds
- C07C61/125—Saturated polycyclic compounds having a carboxyl group bound to a condensed ring system
- C07C61/13—Saturated polycyclic compounds having a carboxyl group bound to a condensed ring system having two rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/487—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to chemical modification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Fertilizers (AREA)
- Treatment Of Sludge (AREA)
- Treating Waste Gases (AREA)
- Cephalosporin Compounds (AREA)
- Detergent Compositions (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT23689/84A IT1196334B (it) | 1984-11-22 | 1984-11-22 | Processo per la risoluzione ottica di miscugli racemi di acidi alfanaftil-propionici |
| IT84-23689A | 1984-11-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR860004003A true KR860004003A (ko) | 1986-06-16 |
Family
ID=11209167
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019850008756A Ceased KR860004003A (ko) | 1984-11-22 | 1985-11-22 | 알파-나프틸-프로피온산 라세미혼합물의 새로운 광학적 분할방법 |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4622419A (cg-RX-API-DMAC7.html) |
| EP (1) | EP0182279B1 (cg-RX-API-DMAC7.html) |
| JP (2) | JPS61129148A (cg-RX-API-DMAC7.html) |
| KR (1) | KR860004003A (cg-RX-API-DMAC7.html) |
| AT (1) | ATE50558T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU591880B2 (cg-RX-API-DMAC7.html) |
| CA (2) | CA1264765A (cg-RX-API-DMAC7.html) |
| DE (2) | DE3576152D1 (cg-RX-API-DMAC7.html) |
| DK (1) | DK537485A (cg-RX-API-DMAC7.html) |
| ES (1) | ES8609194A1 (cg-RX-API-DMAC7.html) |
| FI (1) | FI83074C (cg-RX-API-DMAC7.html) |
| GR (1) | GR852798B (cg-RX-API-DMAC7.html) |
| HU (2) | HU910941D0 (cg-RX-API-DMAC7.html) |
| IL (1) | IL76952A (cg-RX-API-DMAC7.html) |
| IT (1) | IT1196334B (cg-RX-API-DMAC7.html) |
| NO (1) | NO162815C (cg-RX-API-DMAC7.html) |
| NZ (1) | NZ214137A (cg-RX-API-DMAC7.html) |
| PT (1) | PT81530B (cg-RX-API-DMAC7.html) |
| YU (1) | YU45288B (cg-RX-API-DMAC7.html) |
| ZA (1) | ZA858383B (cg-RX-API-DMAC7.html) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU611699B2 (en) * | 1987-07-31 | 1991-06-20 | American Home Products Corporation | Naphthalene propionic acid derivatives |
| US4937373A (en) * | 1988-12-08 | 1990-06-26 | Hoffmann-La Roche Inc. | Substituted naphthalene carboxylic acids |
| US5196575A (en) * | 1992-02-19 | 1993-03-23 | Hoechst Celanese Corp. | Supercritical separation of isomers of functional organic compounds at moderate conditions |
| IT1271800B (it) * | 1994-12-27 | 1997-06-09 | Zambon Spa | Processo di preparazione degli enantiomeri dell'acido 2- (2-fluoro- 4-bifenil) propionico |
| DE19624604A1 (de) * | 1996-06-20 | 1998-01-02 | Hoechst Ag | Verfahren zur Herstellung chiraler, nicht racemischer (4-Aryl-2,5-dioxoimidazolidin-1-yl)essigsäuren |
| US5936118A (en) * | 1997-04-04 | 1999-08-10 | Albemarle Corporation | Process for chiral enrichment of optically active carboxylic acids or salts or esters thereof |
| CA2542969A1 (en) * | 2003-10-27 | 2005-06-06 | Holzindustrie Leitinger Gesellschaft M.B.H. | Method for quality assurance of long timber |
| EP1589019B1 (de) * | 2004-04-20 | 2008-08-13 | Ratiopharm GmbH | Stereoselektives Verfahren zur Herstellung von Clopidogrel |
| USD815946S1 (en) | 2016-04-25 | 2018-04-24 | Piramal Glass-Usa, Inc. | Bottle |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3683015A (en) * | 1970-11-04 | 1972-08-08 | Norman H Dyson | Resolution of 2-(6-methoxy-2-naphthyl)propionic |
| CH641432A5 (de) * | 1978-07-19 | 1984-02-29 | Syntex Pharma Int | Verfahren zur aufspaltung von racemischer 6-methoxy-alpha-methyl-2-naphthalinessigsaeure in die optischen antipoden. |
| JPS569514A (en) * | 1979-07-02 | 1981-01-31 | Hiroomi Makita | Method of and apparatus for filling back soil and compaction by soil improving machine |
| JPS5822139B2 (ja) * | 1979-12-28 | 1983-05-06 | 日清製粉株式会社 | ｄｌ−２−（６−メトキシ−２−ナフチル）−プロピオン酸の光学分割法 |
| IT1154663B (it) * | 1980-07-30 | 1987-01-21 | Alfa Chimica Italiana Spa | Procedimento per la risoluzione in antipodi ottici di miscele di acidi d- e l-2-(6-metossi-2-naftil)-propionico |
| FI831820L (fi) * | 1982-05-27 | 1983-11-28 | Syntex Pharma Int | Foerfarande foer framstaellning av d-2-(6-metoxi-2-naftyl)-propionsyra och dess farmaceutiskt godtagbara salter samt av nya mellanprodukter anvaenda vid deras framstaellning |
| IT1208109B (it) * | 1983-11-23 | 1989-06-06 | Alfa Chem Ital | Procedimento per la risoluzione ottica di acidi arilpropionici |
-
1984
- 1984-11-22 IT IT23689/84A patent/IT1196334B/it active
-
1985
- 1985-10-31 ZA ZA858383A patent/ZA858383B/xx unknown
- 1985-11-05 IL IL76952A patent/IL76952A/xx unknown
- 1985-11-06 US US06/795,516 patent/US4622419A/en not_active Expired - Fee Related
- 1985-11-11 NZ NZ214137A patent/NZ214137A/xx unknown
- 1985-11-13 EP EP85114450A patent/EP0182279B1/en not_active Expired - Lifetime
- 1985-11-13 DE DE8585114450T patent/DE3576152D1/de not_active Expired - Fee Related
- 1985-11-13 DE DE198585114450T patent/DE182279T1/de active Pending
- 1985-11-13 AT AT85114450T patent/ATE50558T1/de not_active IP Right Cessation
- 1985-11-18 YU YU1795/85A patent/YU45288B/xx unknown
- 1985-11-20 GR GR852798A patent/GR852798B/el unknown
- 1985-11-21 NO NO854659A patent/NO162815C/no unknown
- 1985-11-21 DK DK537485A patent/DK537485A/da not_active Application Discontinuation
- 1985-11-21 HU HU91941A patent/HU910941D0/hu unknown
- 1985-11-21 JP JP60262359A patent/JPS61129148A/ja active Pending
- 1985-11-21 HU HU854447A patent/HU204247B/hu unknown
- 1985-11-21 PT PT81530A patent/PT81530B/pt not_active IP Right Cessation
- 1985-11-21 AU AU50256/85A patent/AU591880B2/en not_active Ceased
- 1985-11-21 CA CA000495846A patent/CA1264765A/en not_active Expired - Fee Related
- 1985-11-21 FI FI854596A patent/FI83074C/fi not_active IP Right Cessation
- 1985-11-21 ES ES549118A patent/ES8609194A1/es not_active Expired
- 1985-11-22 KR KR1019850008756A patent/KR860004003A/ko not_active Ceased
-
1989
- 1989-04-26 CA CA000597921A patent/CA1276177C/en not_active Expired - Fee Related
-
1991
- 1991-02-01 JP JP3012280A patent/JPH05246967A/ja active Pending
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19851122 |
|
| PG1501 | Laying open of application | ||
| A201 | Request for examination | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 19900324 Comment text: Request for Examination of Application Patent event code: PA02011R01I Patent event date: 19851122 Comment text: Patent Application |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 19920402 Patent event code: PE09021S01D |
|
| E601 | Decision to refuse application | ||
| PE0601 | Decision on rejection of patent |
Patent event date: 19920612 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 19920402 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |