KR960703836A - D-키로-이노시톨 제조방법 - Google Patents
D-키로-이노시톨 제조방법Info
- Publication number
- KR960703836A KR960703836A KR1019960700719A KR19960700719A KR960703836A KR 960703836 A KR960703836 A KR 960703836A KR 1019960700719 A KR1019960700719 A KR 1019960700719A KR 19960700719 A KR19960700719 A KR 19960700719A KR 960703836 A KR960703836 A KR 960703836A
- Authority
- KR
- South Korea
- Prior art keywords
- inositol
- kasugamycin
- acidic
- exchange resin
- reaction solution
- Prior art date
Links
- 229960000367 inositol Drugs 0.000 title claims abstract 11
- 238000004519 manufacturing process Methods 0.000 title claims 2
- 230000002378 acidificating effect Effects 0.000 claims abstract 27
- 238000006243 chemical reaction Methods 0.000 claims abstract 21
- 239000000243 solution Substances 0.000 claims abstract 19
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 claims abstract 18
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 claims abstract 16
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims abstract 15
- 239000003456 ion exchange resin Substances 0.000 claims abstract 15
- 229920003303 ion-exchange polymer Polymers 0.000 claims abstract 15
- CDAISMWEOUEBRE-LKPKBOIGSA-N 1D-chiro-inositol Chemical compound O[C@H]1[C@@H](O)[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O CDAISMWEOUEBRE-LKPKBOIGSA-N 0.000 claims abstract 12
- 239000007864 aqueous solution Substances 0.000 claims abstract 9
- 239000011347 resin Substances 0.000 claims abstract 7
- 229920005989 resin Polymers 0.000 claims abstract 7
- 239000013078 crystal Substances 0.000 claims abstract 3
- 150000003839 salts Chemical class 0.000 claims abstract 3
- SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 claims abstract 2
- 238000006460 hydrolysis reaction Methods 0.000 claims abstract 2
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 claims abstract 2
- 238000000034 method Methods 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims 2
- 239000012141 concentrate Substances 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 239000002245 particle Substances 0.000 claims 2
- 239000012266 salt solution Substances 0.000 claims 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims 1
- 238000000151 deposition Methods 0.000 claims 1
- 230000007062 hydrolysis Effects 0.000 claims 1
- 239000012535 impurity Substances 0.000 claims 1
- 230000001376 precipitating effect Effects 0.000 claims 1
- 230000007935 neutral effect Effects 0.000 abstract 2
- 239000003929 acidic solution Substances 0.000 abstract 1
- 238000011084 recovery Methods 0.000 abstract 1
- 238000010586 diagram Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C35/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C35/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic
- C07C35/08—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic containing a six-membered rings
- C07C35/14—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic containing a six-membered rings with more than one hydroxy group bound to the ring
- C07C35/16—Inositols
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/09—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
- C07C29/10—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Saccharide Compounds (AREA)
Abstract
Description
Claims (4)
- 카수가마이신 또는 이의 염 수용액을 H+-형의 강산성 이온 교환 수지의 입자와 혼합하여, 이 혼합물을 상압 또는 가압하에서 가열하여 카수가마이신의 가수 분해를 행하고, 반응 종료후에, 생성된 D-키로-이노시톨을 함유하는 산성 반응 용액을 강산성 이온 교환 수지와 분리하여, D-키로-이노시톨을 함유하는 산성 반응 용액을 얻는 다음, 이 산성 반응 용액으로부터 D-키토-이노시톨을 회수함을 특징으로 하는 D-키로-이노시톨의 제조방법.
- 카수가마이신 또는 이의 염 수용액을 H+-형의 강산성 이온 교환 수지로 충전된 컬럼에 연속적으로 도입하고, 상압 또는 가압하에 상기 컬럼내의 카수가마이신 수용액과 수지를 가열하여 카수가마이신의 가수분해를 행하고, 이 수지 컬럼으로부터, 생성된 D-키로-이노시톨을 함유하는 산성 반응용액을 유출시키고, 상기 산성반응 용액으로부터 D-키로-이노시톨을 회수함을 특징으로 하는 D-키로-이노시톨의 제조방법.
- 다음 제1공정 내지 제4공정 : 제1공정 : 카수가마이신 또는 이의 염 수용액을 H+-형의 강산성 이온 교환 수지의 입자와 혼합하여, 이 혼합물을 상압 또는 가압하에 가열하여 카수가마이신의 가수분해를 행하고, 반응 종료후에 생성된 D-키로-이노시톨을 함유하는 산성 반응 용액을 강산성 이온 교환 수지와 분리시켜서, D-키로-이노시톨을 함유하는 산성반응 용액을 얻는 과정, 제2공정 : 제1공정에서 얻은 산성 반응 용액을, H+-형의 강산성 이온 교환 수지로 충전된 컬럼으로 통과시켜서 이에 미반응 카수가마이신이 잔유하면, 상기 반응 용액으로부터 미반응 카수가마이신을 제거하여 D-키로-이노시톨을 함유하는 산성 수용액을 얻는 공정, 제3공정 : 제2공정에서 얻은 산성 수용액을 OH-형의 강염기성 교환수지로 충전된 컬럼으로 통과시켜서, D-키로-이노시톨을 함유하는 중화된 용출액을 얻는 공정, 제4공정 : 제3공정에서 얻은 용출액을 농축하고, 이 농축액으로부터 고순도의 D-키로-이노시톨 결정을 석출시키는 공정을 연속적으로 행함을 특징으로 하는 D-키로-이노시톨의 제조방법.
- 다음 제1공정 내지 제4공정 : 제1공정 : 카수가마이신 또는 이의 염 수용액을 H+-형의 강산성 이온 교환 수지로 충전된 컬럼에 연속적으로 도입하고, 상압 또는 가압하에 컬럼내에 카수가마이신 수용액과 수지를 가열하여 카수가마이신의 가수분해를 행하고, 수지컬럼으로부터 생성된 D-키로-이노시톨을 함유하는 산성 반응 용액을 유출시켜서 D-키로-이노시톨을 함유하는 산성 반응 용액을 얻는 공정, 제2공정 : 제1공정에서 얻은 산성 반응 용액을 H+-형의 강산성 이온 교환 수지로 충전된 컬럼에 통과시켜서 상기 반응 용액에 함유되어 있는 염기성 불순물을 제거하고 경우에 따라서, 미반응 카수가마이신이 잔유해 있으면, 상기 반응용액으로부터 미반응 카수가마이신을 제거하여 D-키로-이노시톨을 함유하는 산성 수용액을 얻는 공정, 제3공정 : 제2공정에서 얻은 산성 수용액을 OH+-형의 강염기성 이온 교환수지로 충전된 컬럼에 통과시켜서 D-키로-이노시톨을 함유하는 중화된 용출액을 얻는 공정, 제4공정 : 제3공정에서 얻은 용출액을 농축하여 미 농축액에서 고순도의 D-키로-이노시톨 결정을 석출시키는 공정으로 행함을 특징으로 하는 D-키로-이노시톨의 제조방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP93-217926 | 1993-08-11 | ||
JP5217926A JP3053510B2 (ja) | 1993-08-11 | 1993-08-11 | D−キロ−イノシトールの製造法 |
JP05288827A JP3113770B2 (ja) | 1993-10-26 | 1993-10-26 | D−キロ−イノシトールの製造方法 |
JP93-288827 | 1993-10-26 | ||
JP94-152181 | 1994-07-04 | ||
JP06152181A JP3113776B2 (ja) | 1994-07-04 | 1994-07-04 | D−キロ−イノシトールの製造方法 |
PCT/JP1994/001304 WO1995004711A1 (fr) | 1993-08-11 | 1994-08-08 | Procede de production de d-chiro-inositol |
Publications (2)
Publication Number | Publication Date |
---|---|
KR960703836A true KR960703836A (ko) | 1996-08-31 |
KR100332144B1 KR100332144B1 (ko) | 2002-11-13 |
Family
ID=27320233
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019960700719A KR100332144B1 (ko) | 1993-08-11 | 1994-08-08 | D-키로-이노시톨제조방법 |
Country Status (11)
Country | Link |
---|---|
US (1) | US5714643A (ko) |
EP (1) | EP0712827B1 (ko) |
KR (1) | KR100332144B1 (ko) |
CN (1) | CN1072637C (ko) |
AT (1) | ATE176779T1 (ko) |
CA (1) | CA2168953A1 (ko) |
DE (1) | DE69416594T2 (ko) |
DK (1) | DK0712827T3 (ko) |
ES (1) | ES2130440T3 (ko) |
TW (1) | TW350837B (ko) |
WO (1) | WO1995004711A1 (ko) |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH10509148A (ja) * | 1994-11-10 | 1998-09-08 | アボツト・ラボラトリーズ | D−chiro−イノシトールの改良製造方法 |
US5932774A (en) * | 1995-11-06 | 1999-08-03 | Abbott Laboratories | Processes for the preparation of D-chiro-inositol |
JP2001215294A (ja) * | 1999-11-22 | 2001-08-10 | Japan Organo Co Ltd | 復水脱塩装置 |
US6342645B2 (en) * | 1999-12-30 | 2002-01-29 | Insmed Pharmaceuticals, Inc. | Methods for the production and isolation of D-chiro-inositol from kasugamycin and the use of D-chiro-inositol obtained therefrom |
US6660891B2 (en) * | 2000-05-15 | 2003-12-09 | Insmed Incorporated | Methods for the production of D-chiro-inositol and the use of D-chiro inositol obtained therefrom |
US6408277B1 (en) * | 2000-06-21 | 2002-06-18 | Banter Limited | System and method for automatic task prioritization |
US7521481B2 (en) | 2003-02-27 | 2009-04-21 | Mclaurin Joanne | Methods of preventing, treating and diagnosing disorders of protein aggregation |
WO2006053428A1 (en) * | 2004-11-17 | 2006-05-26 | Joanne Mclaurin | Compositions comprising scyllo-inositol derivatives and methods to treat disorders of protein aggregation |
WO2007119108A2 (en) * | 2005-10-13 | 2007-10-25 | Waratah Pharmaceuticals Inc. | Inositol derivatives and their uses in the treatment of diseases characterized by abnormal protein folding or aggregation or amyloid formation, deposition, accumulation or persistence |
US20070197452A1 (en) * | 2006-02-17 | 2007-08-23 | Mclaurin Joanne | Treatment of amyloid-related diseases |
EP1996175A4 (en) * | 2006-03-09 | 2009-06-10 | Waratah Pharmaceuticals Inc | CYCLOHEXAN POLYALKOHOL FORMULATION FOR THE TREATMENT OF PROTEIN AGGREGATION DISORDERS |
CA2652449A1 (en) * | 2006-05-19 | 2007-11-29 | Waratah Pharmaceuticals Inc. | Screening methods for amyloid beta modulators |
WO2008034244A1 (en) * | 2006-09-21 | 2008-03-27 | Waratah Pharmaceuticals Inc. | The combination of a cyclohexanehexol and a nsaid for the treatment of neurodegenerative diseases |
US20080103116A1 (en) * | 2006-11-01 | 2008-05-01 | Jennings-Spring Barbara L | Method of treatment and compositions of D-chiro inositol and phosphates thereof |
US20090214474A1 (en) * | 2006-11-01 | 2009-08-27 | Barbara Brooke Jennings | Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development |
US20110218176A1 (en) | 2006-11-01 | 2011-09-08 | Barbara Brooke Jennings-Spring | Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development |
US20100292157A1 (en) * | 2006-11-24 | 2010-11-18 | Antonio Cruz | Combination Treatments for Alzheimer's Disease and Similar Diseases |
CA2683548A1 (en) * | 2007-04-12 | 2008-10-23 | Joanne Mclaurin | Use of cyclohexanehexol derivatives for the treatment of polyglutamine diseases |
WO2008124931A1 (en) * | 2007-04-12 | 2008-10-23 | Joanne Mclaurin | Use of cyclohexanehexol derivatives in the treatment of amyotrophic lateral sclerosis |
EP2656839A1 (en) * | 2007-04-12 | 2013-10-30 | Waratah Pharmaceuticals, Inc. | Use of Cyclohexanehexol Derivatives in the Treatment of Ocular Diseases |
US20100331267A1 (en) * | 2007-04-12 | 2010-12-30 | Mclaurin Joanne | Use of cyclohexanehexol derivatives in the treatment of alpha-synucleinopathies |
WO2010040232A1 (en) * | 2008-10-09 | 2010-04-15 | Waratah Pharmaceuticals Inc. | Use of scyllo-inositols for the treatment of macular degeneration-related disorders |
KR101447579B1 (ko) | 2012-09-26 | 2014-10-15 | 주식회사 디와이내츄럴 | 미생물을 이용한 d-카이로 이노시톨의 생산 방법 |
CN104961628A (zh) * | 2015-06-30 | 2015-10-07 | 天津科技大学 | 一种由d-松醇转化为d-手性肌醇的方法 |
CN105669376B (zh) * | 2016-02-27 | 2019-03-12 | 诸城市浩天药业有限公司 | 制备高结晶度、粒径大的肌醇的结晶工艺及应用 |
JP6934069B2 (ja) * | 2017-12-21 | 2021-09-08 | オルガノ株式会社 | 非水液状物質の精製方法及びイオン交換樹脂充填カートリッジの作製方法 |
JP7530388B2 (ja) * | 2019-05-03 | 2024-08-07 | ボノ アンド ディッタ エスピーエイ | キャロブエキスからピニトールを分離するためのプロセス |
DE102022004733A1 (de) | 2022-12-15 | 2024-06-20 | Forschungszentrum Jülich GmbH | Genetisch modifizierter Mikroorganismus und dessen Verwendung zur Herstellung von D-Chiro-Inositol |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS572381B2 (ko) * | 1974-11-18 | 1982-01-16 | ||
US5091596A (en) * | 1990-12-20 | 1992-02-25 | Univ. Of Va. Alumni Patents Foundation | Method for producing chiro-inositol |
-
1994
- 1994-08-08 CN CN94193030A patent/CN1072637C/zh not_active Expired - Fee Related
- 1994-08-08 CA CA002168953A patent/CA2168953A1/en not_active Abandoned
- 1994-08-08 WO PCT/JP1994/001304 patent/WO1995004711A1/ja active IP Right Grant
- 1994-08-08 US US08/596,131 patent/US5714643A/en not_active Expired - Fee Related
- 1994-08-08 KR KR1019960700719A patent/KR100332144B1/ko not_active IP Right Cessation
- 1994-08-08 DK DK94923085T patent/DK0712827T3/da active
- 1994-08-08 DE DE69416594T patent/DE69416594T2/de not_active Expired - Fee Related
- 1994-08-08 AT AT94923085T patent/ATE176779T1/de not_active IP Right Cessation
- 1994-08-08 EP EP94923085A patent/EP0712827B1/en not_active Expired - Lifetime
- 1994-08-08 ES ES94923085T patent/ES2130440T3/es not_active Expired - Lifetime
- 1994-09-02 TW TW083108097A patent/TW350837B/zh active
Also Published As
Publication number | Publication date |
---|---|
EP0712827A4 (en) | 1996-11-06 |
EP0712827B1 (en) | 1999-02-17 |
US5714643A (en) | 1998-02-03 |
CN1128986A (zh) | 1996-08-14 |
CN1072637C (zh) | 2001-10-10 |
DE69416594T2 (de) | 1999-09-23 |
KR100332144B1 (ko) | 2002-11-13 |
EP0712827A1 (en) | 1996-05-22 |
ES2130440T3 (es) | 1999-07-01 |
WO1995004711A1 (fr) | 1995-02-16 |
TW350837B (en) | 1999-01-21 |
ATE176779T1 (de) | 1999-03-15 |
CA2168953A1 (en) | 1995-02-16 |
DK0712827T3 (da) | 1999-09-20 |
DE69416594D1 (de) | 1999-03-25 |
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