KR910007949A - 아스코르브산의 2-인산 에스테르의 제조방법 - Google Patents
아스코르브산의 2-인산 에스테르의 제조방법 Download PDFInfo
- Publication number
- KR910007949A KR910007949A KR1019900017618A KR900017618A KR910007949A KR 910007949 A KR910007949 A KR 910007949A KR 1019900017618 A KR1019900017618 A KR 1019900017618A KR 900017618 A KR900017618 A KR 900017618A KR 910007949 A KR910007949 A KR 910007949A
- Authority
- KR
- South Korea
- Prior art keywords
- ascorbic acid
- optionally protected
- carried out
- reaction
- phosphorylation
- Prior art date
Links
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 title claims 28
- 229960005070 ascorbic acid Drugs 0.000 title claims 17
- 235000010323 ascorbic acid Nutrition 0.000 title claims 17
- 239000011668 ascorbic acid Substances 0.000 title claims 17
- 238000000034 method Methods 0.000 title claims 12
- 229910019142 PO4 Inorganic materials 0.000 title claims 2
- 239000010452 phosphate Substances 0.000 title claims 2
- 238000006366 phosphorylation reaction Methods 0.000 claims 5
- 239000011541 reaction mixture Substances 0.000 claims 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 239000011261 inert gas Substances 0.000 claims 2
- 150000007530 organic bases Chemical class 0.000 claims 2
- 229910052786 argon Inorganic materials 0.000 claims 1
- 238000010511 deprotection reaction Methods 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 230000026731 phosphorylation Effects 0.000 claims 1
- 230000000865 phosphorylative effect Effects 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/65515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a five-membered ring
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (12)
- 5- 및 6- 위치에서 임의로 보호된 아스코르브산을 반응 혼합물 중의 임의로 보호된 아스코르브산의 농도를 0.3M 미만으로 유지시키면서 인산화시키고 필요에 따라 보호기를 제거함을 특징으로 하는 아스코르브산의 2-인산 에스테르의 제조방법.
- 제1항에 있어서, 5- 및 6- 위치에서 임의로 보호된 아스코르브산 및 인산화제의 혼합물을 반응 혼합물에 간헐적으로 또는 연속적으로 적가하여 인산화 반응을 수행하는 방법.
- 제1항에 있어서, 인산화 반응을 유기 염기 존재하에 수행하는 방법.
- 제3항에 있어서, 유기 염기가 피리딘인 방법.
- 제1항에 있어서, 인산화 반응을 비활성 기체 대기 중에서 수행하는 방법.
- 제5항에 있어서, 비활성 기체가 질소 또는 아르곤인 방법.
- 제1항에 있어서, 임의로 보호된 아스코르부산이 아스코르브산, 5,6-0-이소프로필리덴 아스코르브산, 5,6-O-2차-부티리덴 아스코르브산, 5,6-O-1-에틸부티리덴 아스코르브산, 5,6-O-시클로펜틸리덴 아스코르브산 및 5,6-O-시클로헥실리덴 아스코르브산으로 구성된 군에서 선택된 화합물인 방법.
- 제1항에 있어서, 임의로 보호된 아스코르브산이 아스코르브산 또는 5,6-0-이소프로필리덴 아스코르브산인 방법.
- 제1항에 있어서, 반응 혼합물 중의 임의로 보호된 아스코르브산의 농도가 0.25M 이하인 방법.
- 제1항에 있어서, 임의로 보호된 아스코르브산의 사용량에 대해 약 1.5~약2.5배 당량의 인산화제를 사용하여 인산화반응을 수행하는 방법.
- 제1항에 있어서, 인산화 반응을 pH 12.5~13.5에서 수행하는 방법.
- 제1항에 있어서, 반응 혼합물의 pH를 1이하로 조정하여 탈보호 반응을 수행하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28580089 | 1989-10-31 | ||
JP1-285800 | 1989-10-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR910007949A true KR910007949A (ko) | 1991-05-30 |
Family
ID=17696243
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900017618A KR910007949A (ko) | 1989-10-31 | 1990-10-31 | 아스코르브산의 2-인산 에스테르의 제조방법 |
Country Status (7)
Country | Link |
---|---|
US (1) | US5118817A (ko) |
EP (1) | EP0426020A3 (ko) |
JP (1) | JP2935736B2 (ko) |
KR (1) | KR910007949A (ko) |
CN (1) | CN1025858C (ko) |
CA (1) | CA2028911A1 (ko) |
HU (1) | HU207091B (ko) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE125814T1 (de) * | 1990-03-07 | 1995-08-15 | Hoffmann La Roche | Verfahren zur herstellung von derivaten der ascorbinsäure. |
DE4232997A1 (de) * | 1992-10-01 | 1994-04-07 | Basf Ag | Verfahren zur Reduzierung des Phosphatgehaltes im Abwasser bei der Herstellung von Metallsalzen des Ascorbinsäure-2-monophosphats |
US5516919A (en) * | 1994-04-28 | 1996-05-14 | Wako Pure Chemical Industries, Ltd. | Process for producing ascorbic acid derivative |
DE19831056A1 (de) * | 1998-07-13 | 2000-01-20 | Basf Ag | Verfahren zur Herstellung von Salzen von Ascorbyl-2-phosphorsäureestern |
US20030162760A1 (en) * | 1999-01-26 | 2003-08-28 | Eiko Masatsuji | Dermal agent |
WO2003084345A1 (en) * | 2002-04-02 | 2003-10-16 | Ganado Research, L.L.C. | Composition and method to improve quality and yield of meat products |
US20060009698A1 (en) * | 2004-04-07 | 2006-01-12 | Triage Wireless, Inc. | Hand-held monitor for measuring vital signs |
US20050261598A1 (en) * | 2004-04-07 | 2005-11-24 | Triage Wireless, Inc. | Patch sensor system for measuring vital signs |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3671549A (en) * | 1970-03-05 | 1972-06-20 | Merck & Co Inc | Process for preparing ascorbyl-3-phosphate and salts thereof |
US3749680A (en) * | 1971-01-08 | 1973-07-31 | Merck & Co Inc | Novel derivatives of isoascorbic acid and methods of producing and using same |
US3718482A (en) * | 1971-05-06 | 1973-02-27 | Merck & Co Inc | A food composition with isoascorbic acid-phosphate as an antioxidant |
US4179445A (en) * | 1976-05-06 | 1979-12-18 | Kansas State University Research Foundation | Method of preparation of 2-phosphate esters of ascorbic acid |
JPS594438B2 (ja) * | 1976-05-06 | 1984-01-30 | カンサス・ステ−ト・ユニバ−シテイ・リサ−チ・フアンデ−シヨン | アスコルビン酸の燐酸エステルの製法 |
US4647672A (en) * | 1985-06-25 | 1987-03-03 | Kansas State University Research Foundation | Ascorbate 2-polyphosphate esters and method of making same |
US4939128A (en) * | 1988-04-25 | 1990-07-03 | Takeda Chemical Industries, Ltd. | Ester of ascorbic acid 2-phosphate and pharmaceutical use |
-
1990
- 1990-10-17 US US07/599,079 patent/US5118817A/en not_active Expired - Fee Related
- 1990-10-26 EP EP19900120540 patent/EP0426020A3/en not_active Withdrawn
- 1990-10-30 CA CA002028911A patent/CA2028911A1/en not_active Abandoned
- 1990-10-30 JP JP2294601A patent/JP2935736B2/ja not_active Expired - Lifetime
- 1990-10-31 KR KR1019900017618A patent/KR910007949A/ko not_active Application Discontinuation
- 1990-10-31 CN CN90108889A patent/CN1025858C/zh not_active Expired - Fee Related
- 1990-10-31 HU HU906965A patent/HU207091B/hu not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EP0426020A2 (en) | 1991-05-08 |
CA2028911A1 (en) | 1991-05-01 |
CN1051361A (zh) | 1991-05-15 |
JP2935736B2 (ja) | 1999-08-16 |
CN1025858C (zh) | 1994-09-07 |
HU207091B (en) | 1993-03-01 |
US5118817A (en) | 1992-06-02 |
JPH03204891A (ja) | 1991-09-06 |
EP0426020A3 (en) | 1991-07-03 |
HUT55400A (en) | 1991-05-28 |
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A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
E601 | Decision to refuse application |