BRPI0413498A - método para produzir um éster de ácido carboxìlico substituìdo por hidróxi, ciano vicinal a partir de um éster de ácido carboxìlico substituìdo por hidróxi, halo vicinal, e, composição - Google Patents
método para produzir um éster de ácido carboxìlico substituìdo por hidróxi, ciano vicinal a partir de um éster de ácido carboxìlico substituìdo por hidróxi, halo vicinal, e, composiçãoInfo
- Publication number
- BRPI0413498A BRPI0413498A BRPI0413498-2A BRPI0413498A BRPI0413498A BR PI0413498 A BRPI0413498 A BR PI0413498A BR PI0413498 A BRPI0413498 A BR PI0413498A BR PI0413498 A BRPI0413498 A BR PI0413498A
- Authority
- BR
- Brazil
- Prior art keywords
- vicinal
- carboxylic acid
- acid ester
- halo
- hydroxy substituted
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 125000003262 carboxylic acid ester group Chemical class [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 title 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 title 2
- 125000001475 halogen functional group Chemical group 0.000 title 1
- 150000001733 carboxylic acid esters Chemical class 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 3
- -1 4-substituted-3-hydroxybutyric acid Chemical class 0.000 abstract 1
- 229930194542 Keto Natural products 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 108010013164 halohydrin dehalogenase Proteins 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical class [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000000468 ketone group Chemical group 0.000 abstract 1
Classifications
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- 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
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- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/002—Nitriles (-CN)
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- 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
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
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- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/02—Amides, e.g. chloramphenicol or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes
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- 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/62—Carboxylic acid esters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
"MéTODO PARA PRODUZIR UM éSTER DE áCIDO CARBOXìLICO SUBSTITUìDO POR HIDRóXI, CIANO VICINAL A PARTIR DE UM éSTER DE áCIDO CARBOXìLICO SUBSTITUìDO POR HIDRóXI, HALO VICINAL, E, COMPOSIçãO". A presente invenção proporciona métodos e composição para a preparação de derivados de ácido 4-substituído-3-hidróxi-butírico por meio de conversão de derivados de ácido 4-halo-3-hidróxi-butírico catalisada por haloidrina-desalogenase. A presente invenção proporciona adicionalmente métodos e composições para a preparação de derivados de ácido 4-halo-3-hidróxi-butírico por meio de conversão de derivados de ácido 4-halo-3-cetohidróxi-butírico catalisada por ceto-redutase. A presente invenção também proporciona métodos e composições para a preparação de ésteres de ácido carboxílico substituído por hidróxi, ciano vicinal.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/639,159 US7125693B2 (en) | 2002-08-09 | 2003-08-11 | Enzymatic processes for the production of 4-substituted 3-hydroxybutyric acid derivatives |
| PCT/US2004/004819 WO2005018579A2 (en) | 2003-08-11 | 2004-02-18 | Enzymatic processes for the production of 4-substituted 3-hydroxybutyric acid derivatives and vicinal cyano, hydroxy substituted carboxylic acid esters |
| US10/782,258 US7132267B2 (en) | 2002-08-09 | 2004-02-18 | Enzymatic processes for the production of 4-substituted 3-hydroxybutyric acid derivatives and vicinal cyano, hydroxy substituted carboxylic acid esters |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0413498A true BRPI0413498A (pt) | 2006-10-17 |
Family
ID=34221830
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0413498-2A BRPI0413498A (pt) | 2003-08-11 | 2004-02-18 | método para produzir um éster de ácido carboxìlico substituìdo por hidróxi, ciano vicinal a partir de um éster de ácido carboxìlico substituìdo por hidróxi, halo vicinal, e, composição |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US7132267B2 (pt) |
| EP (1) | EP1660669A4 (pt) |
| JP (1) | JP2007502111A (pt) |
| KR (1) | KR20060071397A (pt) |
| AU (1) | AU2004266100A1 (pt) |
| BR (1) | BRPI0413498A (pt) |
| CA (1) | CA2535353A1 (pt) |
| MX (1) | MXPA06001718A (pt) |
| NO (1) | NO20060544L (pt) |
| WO (1) | WO2005018579A2 (pt) |
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| JP4012299B2 (ja) | 1998-02-25 | 2007-11-21 | ダイセル化学工業株式会社 | ハロゲン置換を含む光学活性アルコールの製造方法 |
| CA2329893A1 (en) * | 1998-04-30 | 1999-11-11 | Kaneka Corporation | Process for producing 6-cyanomethyl-1,3-dioxane-4-acetic acid derivatives |
| CA2305564C (en) * | 1998-08-05 | 2008-06-17 | Kaneka Corporation | Process for the preparation of optically active 2-[6-(hydroxymethyl)-1,3-dioxan-4-yl]acetic acid derivatives |
| JP2000236883A (ja) * | 1998-12-21 | 2000-09-05 | Daicel Chem Ind Ltd | 新規なカルボニル還元酵素、該酵素の製造方法、該酵素をコードするdnaおよびこれを利用したアルコールの製造方法 |
| JP2003504070A (ja) * | 1999-07-09 | 2003-02-04 | フォルシュングスツェントルム ユーリッヒ ゲゼルシャフト ミット ベシュレンクテル ハフツング | ケトカルボン酸及びそのエステルの還元のための方法 |
| AU1551701A (en) * | 1999-12-03 | 2001-06-12 | Kaneka Corporation | Novel carbonyl reductase, gene thereof and method of using the same |
| EP1158054A1 (en) | 2000-05-25 | 2001-11-28 | Rijksuniversiteit te Groningen | Enzymatic conversion of epoxides |
| EP1201647B1 (en) * | 2000-10-31 | 2004-09-22 | Sumitomo Chemical Company, Limited | Process for producing 4-cyano-4oxobutanoate and 4-cyano-3-hydroxybutanoate |
| IL159368A0 (en) | 2001-07-02 | 2004-06-01 | Kaneka Corp | Method of modifying enzyme and oxidoreductase variant |
| CA2493941A1 (en) | 2002-08-09 | 2004-02-19 | Codexis, Inc. | Enzymatic processes for the production of 4-substituted 3-hydroxybutyric acid derivatives |
| EP1654354A1 (en) | 2003-08-11 | 2006-05-10 | Codexis, Inc. | Improved ketoreductase polypeptides and related polynucleotides |
| EP1654356A1 (en) * | 2003-08-11 | 2006-05-10 | Codexis, Inc. | Improved halohydrin dehalogenases and related polynucleotides |
| EP1660669A4 (en) | 2003-08-11 | 2008-10-01 | Codexis Inc | ENZYMATIC PROCEDURES FOR THE PREPARATION OF 4-SUBSTITUTED 3-HYDROXYBUTYLIC ACID DERIVATIVES AND OF VICINAL CYANO, HYDROXY-SUBSTITUTED CARBOXYLIC ACID ESTERS |
| US7541171B2 (en) * | 2003-08-11 | 2009-06-02 | Codexis, Inc. | Halohydrin dehalogenases and related polynucleotides |
| JP2007502114A (ja) | 2003-08-11 | 2007-02-08 | コデクシス, インコーポレイテッド | 改良されたグルコースデヒドロゲナーゼポリペプチドおよび関連ポリヌクレオチド |
| US7588928B2 (en) * | 2003-08-11 | 2009-09-15 | Codexis, Inc. | Halohydrin dehalogenases and related polynucleotides |
-
2004
- 2004-02-18 EP EP04712399A patent/EP1660669A4/en not_active Withdrawn
- 2004-02-18 AU AU2004266100A patent/AU2004266100A1/en not_active Abandoned
- 2004-02-18 JP JP2006523171A patent/JP2007502111A/ja not_active Withdrawn
- 2004-02-18 CA CA002535353A patent/CA2535353A1/en not_active Abandoned
- 2004-02-18 WO PCT/US2004/004819 patent/WO2005018579A2/en not_active Ceased
- 2004-02-18 US US10/782,258 patent/US7132267B2/en not_active Expired - Lifetime
- 2004-02-18 BR BRPI0413498-2A patent/BRPI0413498A/pt not_active IP Right Cessation
- 2004-02-18 MX MXPA06001718A patent/MXPA06001718A/es not_active Application Discontinuation
- 2004-02-18 KR KR1020067002920A patent/KR20060071397A/ko not_active Ceased
-
2006
- 2006-02-02 NO NO20060544A patent/NO20060544L/no not_active Application Discontinuation
- 2006-08-10 US US11/502,745 patent/US7807423B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| NO20060544L (no) | 2006-03-13 |
| US7807423B2 (en) | 2010-10-05 |
| AU2004266100A1 (en) | 2005-03-03 |
| WO2005018579A3 (en) | 2005-04-14 |
| US20040214297A1 (en) | 2004-10-28 |
| EP1660669A4 (en) | 2008-10-01 |
| US7132267B2 (en) | 2006-11-07 |
| US20070161094A1 (en) | 2007-07-12 |
| CA2535353A1 (en) | 2005-03-03 |
| KR20060071397A (ko) | 2006-06-26 |
| WO2005018579A2 (en) | 2005-03-03 |
| MXPA06001718A (es) | 2006-05-19 |
| EP1660669A2 (en) | 2006-05-31 |
| JP2007502111A (ja) | 2007-02-08 |
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