KR890017223A - 2-아릴프로피온산의 에난티오머를 수득하는 방법 - Google Patents
2-아릴프로피온산의 에난티오머를 수득하는 방법 Download PDFInfo
- Publication number
- KR890017223A KR890017223A KR1019890005931A KR890005931A KR890017223A KR 890017223 A KR890017223 A KR 890017223A KR 1019890005931 A KR1019890005931 A KR 1019890005931A KR 890005931 A KR890005931 A KR 890005931A KR 890017223 A KR890017223 A KR 890017223A
- Authority
- KR
- South Korea
- Prior art keywords
- arylpropionic acid
- ibuprofen
- salt
- enantiomer
- acid
- Prior art date
Links
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
- C07C61/08—Saturated compounds having a carboxyl group bound to a six-membered 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
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/88—Carbazoles; Hydrogenated carbazoles 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 ring system
-
- 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)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (8)
- 광학적 활성형태의 트레오 - 1 - P - 니트로페닐 - 2 - 아미노프로판 - 1.3 - 디올을 사용하여 2 - 아릴프로피온산의 라세미체를 디아스테레오머염으로 전환시키고, 이들염을 분리한후, 수득된 순수한 디아스테레오머를 에난티오머 형태의 2 - 아릴프로피온산 또는 그의 염의 유리산으로 전환시키는 것을 특징으로하는, 2 - 아릴프로피온산의 라세미 혼합물을 아민 - 에난티오머와 반응시켜 2 - 아릴프로피온산의 에난티오머를 수득하는 방법.
- 제 1 항에 있어서, 2 - 아릴프로피온산이 플루트비프로펜, 페노프로펜, 케토프로펜, 나프록센, 베녹사프로펜 및 이부프로펜으로부터 선택된 것임을 특징으로 하는 방법.
- 제 2 항에 있어서, 이부프로펜이 2 - 아릴프로피온산으로서 사용되는 것을 특징으로 하는 방법.
- 제 1 항 또는 제 2 항에 있어서, 결정화를 이용하여 디아스테레오머염을 절단하는 것을 특징으로 하는 방법.
- 전술한 항들중 어느 한 항에 있어서, 2 - 아릴프로피온산을 D(-) - 트레오 - 1 - P - 니트로페닐 - 1 - 아미노프로판 - 1, 3 - 디올과 반응시키는 것을 특징으로 하는 방법.
- 전술한 항들중 어느 한 항에 있어서, 광학적 대장체의 염을 침전시킨후 잔류 모액을 농축시키고, 임의로 분리된 대장체의 재결정화 모액을 가하여 수화알칼리와의 슬러리를 형성시킨후, 그로부터 아미노 알코올을 분리하는것을 특징으로 하는 방법.
- 전술한 항들중 어느 한 항에 있어서, 침전된 광학 대장체와 아미노 알코올의 염을 분리한 후 수득된 2 - 아릴프로피온산의 에난티오머 용액을 다시 라세미화시키고, 상기 용액을 공정에 재순환시키는 것을 특징으로 하는 방법.
- 전술한 항들중 어느 한 항에 있어서, 이부프로펜이 라세미 혼합물로서 사용되고, 그로부터 S(+) - 이부프로펜이 수득되는 것을 특징으로 하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3814887A DE3814887C1 (ko) | 1988-05-02 | 1988-05-02 | |
DEP3814887.0 | 1988-05-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR890017223A true KR890017223A (ko) | 1989-12-15 |
Family
ID=6353411
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019890005931A KR890017223A (ko) | 1988-05-02 | 1989-05-02 | 2-아릴프로피온산의 에난티오머를 수득하는 방법 |
Country Status (13)
Country | Link |
---|---|
US (1) | US4973745A (ko) |
EP (1) | EP0340663A3 (ko) |
JP (1) | JPH02138237A (ko) |
KR (1) | KR890017223A (ko) |
CN (1) | CN1037503A (ko) |
AU (1) | AU607856B2 (ko) |
DD (1) | DD283802A5 (ko) |
DE (1) | DE3814887C1 (ko) |
FI (1) | FI892007A (ko) |
HU (1) | HU204492B (ko) |
IL (1) | IL90090A0 (ko) |
NO (1) | NO171783C (ko) |
ZA (1) | ZA893107B (ko) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5191112A (en) * | 1989-10-17 | 1993-03-02 | Nissan Chemical Industries, Ltd. | Process for optical resolution of (±)-2-(3-benzoyl)-phenylpropionic acid |
WO1991006295A1 (en) * | 1989-11-06 | 1991-05-16 | Sepracor, Inc. | Analgesic composition containing optically pure s(+) flurbiprofen |
HU219242B (en) | 1991-05-13 | 2001-03-28 | Boots Co Plc | S(+)-ibuprofen sodium salt dihydrate, pharmaceutical composition comprising this compound and process for production of them |
US5756096A (en) * | 1991-07-25 | 1998-05-26 | Idec Pharmaceuticals Corporation | Recombinant antibodies for human therapy |
MX9204374A (es) * | 1991-07-25 | 1993-03-01 | Idec Pharma Corp | Anticuerpo recombinante y metodo para su produccion. |
US6136310A (en) * | 1991-07-25 | 2000-10-24 | Idec Pharmaceuticals Corporation | Recombinant anti-CD4 antibodies for human therapy |
DE4137773A1 (de) * | 1991-11-16 | 1993-05-19 | Degussa | Herstellung und verwendung von salzen der reinen enantiomere der (alpha)-liponsaeure |
US5235101A (en) * | 1992-01-24 | 1993-08-10 | Ethyl Corporation | Preparation by flotation of optically active aliphatic carboxylic acids |
US5235100A (en) * | 1992-01-24 | 1993-08-10 | Ethyl Corporation | Preparation of optically active aliphatic carboxylic acids |
US5220053A (en) * | 1992-01-24 | 1993-06-15 | Ethyl Corporation | Preparation of optically active aliphatic carboxylic acids |
US5235095A (en) * | 1992-01-24 | 1993-08-10 | Ethyl Corporation | Preparation of optically active aliphatic carboxylic acids |
US5331000A (en) * | 1992-03-09 | 1994-07-19 | Sepracor Inc. | Antipyretic and analgesic methods and compositions containing optically pure R(-) ketoprofen |
US5248813A (en) * | 1992-10-14 | 1993-09-28 | Ethyl Corporation | Enantiomeric resolution |
US5260482A (en) * | 1992-10-14 | 1993-11-09 | Ethyl Corporation | Enantiomeric resolution |
US5256816A (en) * | 1992-10-14 | 1993-10-26 | Ethyl Corporation | Enantiomeric resolution |
US5278337A (en) * | 1992-10-14 | 1994-01-11 | Ethyl Corporation | Enantiomeric resolution of aryl-substituted aliphatic carboxylic acids |
US5380867A (en) * | 1992-12-02 | 1995-01-10 | Hoechst Celanese Corporation | Selective precipitation of α-aryl carboxylic acid salts |
US5442117A (en) * | 1993-12-13 | 1995-08-15 | Albemarle Corporation | Enantiomeric resolution |
IT1271800B (it) * | 1994-12-27 | 1997-06-09 | Zambon Spa | Processo di preparazione degli enantiomeri dell'acido 2- (2-fluoro- 4-bifenil) propionico |
US6013808A (en) * | 1998-06-16 | 2000-01-11 | Pfizer Inc. | Method of purifying carbazole ester precursors of 6-chloro-α-methyl-carbazole-2-acetic acid |
ITMI981583A1 (it) * | 1998-07-10 | 2000-01-10 | Bracco Spa | Processo per la preparazione dell'acido 4 -carbossi-5,8,11-tris (carbossimetil)-1-fenil-2-oxa-5,8,11-triazatridecan-13-oico |
US6656730B1 (en) * | 1999-06-15 | 2003-12-02 | Isis Pharmaceuticals, Inc. | Oligonucleotides conjugated to protein-binding drugs |
HU230004B1 (en) | 2001-06-21 | 2015-04-28 | Sanofi Aventis | Resolution process for (r)-(-)-2-hydroxy-2-(2-chlorophenyl)-acetic acid |
TW200628439A (en) * | 2004-11-09 | 2006-08-16 | Novartis Ag | Organic compounds |
GB0811851D0 (en) * | 2008-06-30 | 2008-07-30 | Aesica Pharmaceuticals Ltd | Process |
CN108586413B (zh) * | 2018-06-11 | 2020-04-21 | 上海应用技术大学 | 一种光学纯(s)-6-甲氧基苯并二氢吡喃-3-羧酸的制备方法 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ZA70809B (en) * | 1969-03-24 | 1971-09-29 | Syntex Corp | Amine salts of 2-(6'-methoxy-2'-naphthyl)propionic acids and processes for the preparation thereof |
SU408943A1 (ru) * | 1971-02-25 | 1973-11-30 | Всесоюзный научно исследовательский институт целлюлозно бумажной промышленности | Способ получения l-винной кислоты |
DE2362687C3 (de) * | 1973-12-17 | 1982-01-14 | Degussa Ag, 6000 Frankfurt | Verfahren zur Gewinnung der optischen Isomeren des Penicillamins |
US4209638A (en) * | 1977-03-08 | 1980-06-24 | The Boots Company Limited | Preparation of therapeutic agents |
IT1194152B (it) * | 1983-03-07 | 1988-09-14 | Secifarma Spa | Procedimento di risoluzione enantiomerica di miscele di acidi d- e l-6-metossi-alfa-metil-2-naftalenacetici ed agenti di risoluzione per detto procedimento |
JPS61266579A (ja) * | 1985-05-22 | 1986-11-26 | Nippon Dakuro Shamrock:Kk | 金属表面処理法 |
-
1988
- 1988-05-02 DE DE3814887A patent/DE3814887C1/de not_active Expired
-
1989
- 1989-04-25 IL IL90090A patent/IL90090A0/xx unknown
- 1989-04-26 AU AU33339/89A patent/AU607856B2/en not_active Ceased
- 1989-04-26 ZA ZA893107A patent/ZA893107B/xx unknown
- 1989-04-27 FI FI892007A patent/FI892007A/fi not_active Application Discontinuation
- 1989-04-27 DD DD89328036A patent/DD283802A5/de not_active IP Right Cessation
- 1989-04-28 NO NO891793A patent/NO171783C/no unknown
- 1989-04-28 EP EP19890107758 patent/EP0340663A3/de not_active Withdrawn
- 1989-04-28 HU HU892042A patent/HU204492B/hu not_active IP Right Cessation
- 1989-05-01 US US07/345,716 patent/US4973745A/en not_active Expired - Fee Related
- 1989-05-01 JP JP1114025A patent/JPH02138237A/ja active Pending
- 1989-05-02 KR KR1019890005931A patent/KR890017223A/ko not_active Application Discontinuation
- 1989-05-02 CN CN89103035A patent/CN1037503A/zh active Pending
Also Published As
Publication number | Publication date |
---|---|
JPH02138237A (ja) | 1990-05-28 |
EP0340663A2 (de) | 1989-11-08 |
IL90090A0 (en) | 1989-12-15 |
AU607856B2 (en) | 1991-03-14 |
AU3333989A (en) | 1989-11-02 |
DE3814887C1 (ko) | 1989-09-21 |
US4973745A (en) | 1990-11-27 |
HU204492B (en) | 1992-01-28 |
EP0340663A3 (de) | 1991-07-03 |
CN1037503A (zh) | 1989-11-29 |
ZA893107B (en) | 1990-01-31 |
FI892007A (fi) | 1989-11-03 |
HUT50090A (en) | 1989-12-28 |
NO891793D0 (no) | 1989-04-28 |
DD283802A5 (de) | 1990-10-24 |
NO171783B (no) | 1993-01-25 |
NO171783C (no) | 1993-05-05 |
FI892007A0 (fi) | 1989-04-27 |
NO891793L (no) | 1989-11-03 |
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