ES2111124T3 - Procedimiento para separar enantiomeros de ester benzoilico de 1,2-isopropilidenglicerol. - Google Patents
Procedimiento para separar enantiomeros de ester benzoilico de 1,2-isopropilidenglicerol.Info
- Publication number
- ES2111124T3 ES2111124T3 ES93200395T ES93200395T ES2111124T3 ES 2111124 T3 ES2111124 T3 ES 2111124T3 ES 93200395 T ES93200395 T ES 93200395T ES 93200395 T ES93200395 T ES 93200395T ES 2111124 T3 ES2111124 T3 ES 2111124T3
- Authority
- ES
- Spain
- Prior art keywords
- ester
- benzoilic
- isopropylidenglycerol
- procedure
- separating enantiomers
- 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.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title abstract 3
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical compound C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 title 1
- 150000002148 esters Chemical class 0.000 title 1
- PHIQHXFUZVPYII-ZCFIWIBFSA-N (R)-carnitine Chemical compound C[N+](C)(C)C[C@H](O)CC([O-])=O PHIQHXFUZVPYII-ZCFIWIBFSA-N 0.000 abstract 1
- 229940035676 analgesics Drugs 0.000 abstract 1
- 239000000730 antalgic agent Substances 0.000 abstract 1
- 239000003443 antiviral agent Substances 0.000 abstract 1
- 239000002876 beta blocker Substances 0.000 abstract 1
- 229940097320 beta blocking agent Drugs 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000002425 crystallisation Methods 0.000 abstract 1
- 230000008025 crystallization Effects 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000007071 enzymatic hydrolysis Effects 0.000 abstract 1
- 238000006047 enzymatic hydrolysis reaction Methods 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 239000013067 intermediate product Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/02—Oxygen as only ring hetero atoms
- C12P17/04—Oxygen as only ring hetero atoms containing a five-membered hetero ring, e.g. griseofulvin, vitamin C
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
- C12N11/02—Enzymes or microbial cells immobilised on or in an organic carrier
- C12N11/04—Enzymes or microbial cells immobilised on or in an organic carrier entrapped within the carrier, e.g. gel or hollow fibres
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
- C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
- C12P41/004—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of alcohol- or thiol groups in the enantiomers or the inverse reaction
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Genetics & Genomics (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- General Health & Medical Sciences (AREA)
- Biotechnology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Biomedical Technology (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
SE DESCRIBE UN PROCESO PARA SEPARAR LOS ISOMEROS OPTICOS DEL 1,2-ISOPROPILIDENOGLICEROL, DE LA FORMULA I, EL PROCESO COMPRENDE LA HIDROLISIS ENZIMATICA PARCIAL Y ESTEROSELECTIVA DE UN ESTER DE BENZOIL DE 1,2-ISOPROPILIDENOGLICEROL (II) CATALIZADA POR UNA LIPASA LIBRE O INMOVILIZADA, LA HIDROLISIS SE CONDUCE EN LA PRESENCIA DE UN COSOLVENTE Y ES SEGUIDA POR UNA CRISTALIZACION QUE HACE POSIBLE QUE SE OBTENGAN CRITALES DE (II) EN FORMA DE RACIMO Y LICOR MADRE QUE CONTENGA (II) EN FORMA DE ENANTIOMERO PURO. EL COMPUESTO (I) ES AMPLIAMENTE USADO DE FORMA INDUSTRIAL COMO PRODUCTO INTERMEDIO EN LA SINTESIS DE DROGAS QUIRALES TALES COMO LA R-(-)-CARNITINA, (S)-BLOQUEADORES BETA, AGENTES ANTIVIRALES (S), DROGAS ANALGESICAS, ETC.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ITMI920331A IT1254463B (it) | 1992-02-17 | 1992-02-17 | Processo per la preparazione di (r) e (s)-1,2-isopropilidenglicerolo |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2111124T3 true ES2111124T3 (es) | 1998-03-01 |
Family
ID=11361994
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES93200395T Expired - Lifetime ES2111124T3 (es) | 1992-02-17 | 1993-02-12 | Procedimiento para separar enantiomeros de ester benzoilico de 1,2-isopropilidenglicerol. |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5332674A (es) |
| EP (1) | EP0556909B1 (es) |
| JP (1) | JP3195108B2 (es) |
| AT (1) | ATE161290T1 (es) |
| CA (1) | CA2089626C (es) |
| DE (1) | DE69315720T2 (es) |
| DK (1) | DK0556909T3 (es) |
| ES (1) | ES2111124T3 (es) |
| IT (1) | IT1254463B (es) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6300176B1 (en) * | 1994-07-22 | 2001-10-09 | Semiconductor Energy Laboratory Co., Ltd. | Laser processing method |
| ITMI20022273A1 (it) * | 2002-10-25 | 2004-04-26 | Prime Europ Therapeuticals | Sintesi enzimatica di (s)-1, 2-0-1, 2-0-isopropilidenglicerolo. |
| DE10336270B3 (de) * | 2003-08-07 | 2005-04-14 | Consortium für elektrochemische Industrie GmbH | Verfahren zur enantioselektiven Herstellung von sekundären Alkoholen durch lipasenkatalysierte Solvolyse der korrespondierenden Acetessigester |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4957868A (en) * | 1984-12-24 | 1990-09-18 | Chiyoda Chemical Engineering & Constructions Co., Ltd. | Cylindrical hollow carriers for microorganisms made of nonwoven fabric |
| IL82416A0 (en) * | 1986-05-08 | 1987-11-30 | Gist Brocades Nv | Process for the preparation of r-2,2-r1,r2-1,3-dioxolane-4-methanol |
| EP0401704B1 (en) * | 1989-06-03 | 1995-02-15 | Mitsubishi Rayon Co., Ltd | Process for the preparation of organic esters |
-
1992
- 1992-02-17 IT ITMI920331A patent/IT1254463B/it active
-
1993
- 1993-02-12 ES ES93200395T patent/ES2111124T3/es not_active Expired - Lifetime
- 1993-02-12 EP EP93200395A patent/EP0556909B1/en not_active Expired - Lifetime
- 1993-02-12 DK DK93200395T patent/DK0556909T3/da active
- 1993-02-12 DE DE69315720T patent/DE69315720T2/de not_active Expired - Fee Related
- 1993-02-12 US US08/016,882 patent/US5332674A/en not_active Expired - Fee Related
- 1993-02-12 AT AT93200395T patent/ATE161290T1/de not_active IP Right Cessation
- 1993-02-16 CA CA002089626A patent/CA2089626C/en not_active Expired - Fee Related
- 1993-02-17 JP JP05141193A patent/JP3195108B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| ITMI920331A1 (it) | 1993-08-17 |
| EP0556909B1 (en) | 1997-12-17 |
| US5332674A (en) | 1994-07-26 |
| JPH067195A (ja) | 1994-01-18 |
| JP3195108B2 (ja) | 2001-08-06 |
| CA2089626A1 (en) | 1993-08-18 |
| DE69315720T2 (de) | 1998-07-23 |
| CA2089626C (en) | 2001-01-16 |
| ITMI920331A0 (it) | 1992-02-17 |
| ATE161290T1 (de) | 1998-01-15 |
| IT1254463B (it) | 1995-09-25 |
| DK0556909T3 (da) | 1998-08-24 |
| DE69315720D1 (de) | 1998-01-29 |
| EP0556909A1 (en) | 1993-08-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
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