DE69937374D1 - Verfahren zur Herstellung von 3,5-dihydroxy substituierten Estern als Zwischenprodukte zur Herstellung optisch aktiver 2-(6-(Hydroxymethyl)-1,3-dioxan-4-yl)-essigsäure-Derivate - Google Patents

Verfahren zur Herstellung von 3,5-dihydroxy substituierten Estern als Zwischenprodukte zur Herstellung optisch aktiver 2-(6-(Hydroxymethyl)-1,3-dioxan-4-yl)-essigsäure-Derivate

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Publication number
DE69937374D1
DE69937374D1 DE69937374T DE69937374T DE69937374D1 DE 69937374 D1 DE69937374 D1 DE 69937374D1 DE 69937374 T DE69937374 T DE 69937374T DE 69937374 T DE69937374 T DE 69937374T DE 69937374 D1 DE69937374 D1 DE 69937374D1
Authority
DE
Germany
Prior art keywords
preparation
dioxan
hydroxymethyl
optically active
acetic acid
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
Application number
DE69937374T
Other languages
English (en)
Other versions
DE69937374T2 (de
Inventor
Noriyuki Kizaki
Yukio Yamada
Yoshihiko Yasohara
Akira Nishiyama
Makoto Miyazaki
Masaru Mitsuda
Takeshi Kondo
Noboru Ueyama
Kenji Inoue
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kaneka Corp
Original Assignee
Kaneka Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kaneka Corp filed Critical Kaneka Corp
Application granted granted Critical
Publication of DE69937374D1 publication Critical patent/DE69937374D1/de
Publication of DE69937374T2 publication Critical patent/DE69937374T2/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
    • C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00—Preparation of carboxylic acid nitriles
    • C07C253/30—Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • 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
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Zoology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
DE69937374T 1998-08-05 1999-08-05 Verfahren zur Herstellung von 3,5-dihydroxy substituierten Estern als Zwischenprodukte zur Herstellung optisch aktiver 2-(6-(Hydroxymethyl)-1,3-dioxan-4-yl)-essigsäure-Derivate Expired - Lifetime DE69937374T2 (de)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP22149598 1998-08-05
JP22149598 1998-08-05
JP15803399 1999-06-04
JP15803399 1999-06-04

Publications (2)

Publication Number Publication Date
DE69937374D1 true DE69937374D1 (de) 2007-11-29
DE69937374T2 DE69937374T2 (de) 2008-07-24

Family

ID=26485288

Family Applications (3)

Application Number Title Priority Date Filing Date
DE69937374T Expired - Lifetime DE69937374T2 (de) 1998-08-05 1999-08-05 Verfahren zur Herstellung von 3,5-dihydroxy substituierten Estern als Zwischenprodukte zur Herstellung optisch aktiver 2-(6-(Hydroxymethyl)-1,3-dioxan-4-yl)-essigsäure-Derivate
DE69942897T Expired - Lifetime DE69942897D1 (de) 1998-08-05 1999-08-05 Verfahren zur Herstellung optisch aktiver 2-Ä6-(Hydroxymethyl)-1,3-Dioxan-4-ylÜ-Essigsäure-Derivate
DE69917204T Expired - Lifetime DE69917204T2 (de) 1998-08-05 1999-08-05 Verfahren zur herstellung optisch aktiver 2-(6-(hydroxymethyl)-1,3-dioxan-4-yl) -essigsäure-derivate

Family Applications After (2)

Application Number Title Priority Date Filing Date
DE69942897T Expired - Lifetime DE69942897D1 (de) 1998-08-05 1999-08-05 Verfahren zur Herstellung optisch aktiver 2-Ä6-(Hydroxymethyl)-1,3-Dioxan-4-ylÜ-Essigsäure-Derivate
DE69917204T Expired - Lifetime DE69917204T2 (de) 1998-08-05 1999-08-05 Verfahren zur herstellung optisch aktiver 2-(6-(hydroxymethyl)-1,3-dioxan-4-yl) -essigsäure-derivate

Country Status (14)

Country Link
US (2) US6472544B1 (de)
EP (3) EP1024139B1 (de)
JP (1) JP3803551B2 (de)
KR (1) KR100654115B1 (de)
CN (2) CN1162422C (de)
AT (3) ATE375989T1 (de)
CA (1) CA2305564C (de)
DE (3) DE69937374T2 (de)
DK (1) DK1619191T3 (de)
ES (2) ES2294236T3 (de)
HU (1) HUP0101122A3 (de)
NO (1) NO325591B1 (de)
PT (1) PT1619191E (de)
WO (1) WO2000008011A1 (de)

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CZ20012792A3 (cs) 1999-12-03 2002-03-13 Kaneka Corporation Polypeptid, polynukleotid kódující polypeptid, expresní vektor, transformant a způsob přípravy
GB0011120D0 (en) * 2000-05-09 2000-06-28 Avecia Ltd Process
KR20020068496A (ko) * 2000-06-05 2002-08-27 카네카 코포레이션 광학 활성 2-[6-(히드록시메틸)-1,3-디옥산-4-일]아세트산유도체의 제조 방법
AU2006203127B2 (en) * 2000-07-19 2008-06-19 Astrazeneca Uk Limited Process for the preparation of 2-(6-substituted-1,3-dioxane-4-yl) acetic acid derivatives
NL1015744C2 (nl) 2000-07-19 2002-01-22 Dsm Nv Werkwijze voor de bereiding van 2-(6-gesubstitueerde-1,3-dioxan-4-yl) azijnzuurderivaten.
EP1406860A1 (de) * 2001-07-06 2004-04-14 Teva Pharmaceutical Industries Limited Produkte natürlichen ursprungs mit organisch gebundenem iod
DE60218678T2 (de) 2001-07-12 2008-02-14 Dsm Ip Assets B.V. Verfahren zur herstellung von 2,4-didesoxyhexosen und 2,4,6-tridesoxyhexosen
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EP1375493A1 (de) 2002-06-17 2004-01-02 Dsm N.V. Verfahren zur Herstellung von Dioxanessigsäureester
EP1537222B1 (de) * 2002-08-09 2011-03-09 Codexis, Inc. Enzymatische verfahren zur herstellung 4-substituierter 3-hydroxybuttersäure-derivate
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MXPA06001719A (es) * 2003-08-11 2006-05-19 Codexis Inc Polipeptidos de glucosa deshidrogenasa mejorados, y polinucleotidos relacionados.
JP2007502111A (ja) * 2003-08-11 2007-02-08 コデクシス， インコーポレイテッド ４−置換３−ヒドロキシ酪酸誘導体およびビシナルなシアノ，ヒドロキシ置換カルボン酸エステルの生成のための酵素的プロセス
US7588928B2 (en) * 2003-08-11 2009-09-15 Codexis, Inc. Halohydrin dehalogenases and related polynucleotides
BRPI0413501A (pt) 2003-08-11 2006-10-10 Codexis Inc polipetìdeo, polinucleotìdeo isolado ou recombinante, vetor de expressão, célula hospedeira, e, método de preparar um polipetìdeo de hhdh
EP1654354A1 (de) * 2003-08-11 2006-05-10 Codexis, Inc. Verbesserte ketoreduktase polypeptide und entsprechende polynukleotide
US7541171B2 (en) * 2003-08-11 2009-06-02 Codexis, Inc. Halohydrin dehalogenases and related polynucleotides
CN101528917B (zh) * 2006-10-02 2015-07-29 科德克希思公司 用于制备立体异构纯的他汀类及其合成中间体的组合物和方法
KR101130717B1 (ko) * 2008-05-14 2012-03-28 웰이앤씨 주식회사 ＨＭＧ-ＣｏＡ 환원 저해제의 제조를 위한 키랄 중간체의제조방법
SG172231A1 (en) 2008-12-18 2011-07-28 Codexis Inc Recombinant halohydrin dehalogenase polypeptides
CN101624390B (zh) * 2009-03-09 2014-06-11 鲁南制药集团股份有限公司 一种瑞舒伐他汀钙侧链关键中间体的制备方法
KR101157314B1 (ko) * 2009-06-05 2012-06-15 주식회사종근당 로수바스타틴의 신규한 제조방법, 이 제조에 유용한 중간체 화합물 및 그의 제조방법
GB2474687A (en) * 2009-10-23 2011-04-27 Phoenix Chemicals Ltd A continuous process for the production of (R)-6-cyano-5-hydroxy-3-oxo-hexanoic acid tert-butyl ester (and derivatives)
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PL2665722T3 (pl) 2011-01-18 2017-03-31 Dsm Sinochem Pharmaceuticals Netherlands B.V. Sposób otrzymywania diolosulfonów
MX357470B (es) 2011-01-18 2018-07-11 Dsm Sinochem Pharm Nl Bv Procedimiento para la preparación de estatinas en presencia de base.
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CN102180862B (zh) * 2011-03-24 2013-08-28 烟台万润精细化工股份有限公司 一种(4R-cis)-6-取代-2,2-二甲基-1,3-二氧六环-4-乙酸叔丁酯的制备方法
TWI551592B (zh) 2011-04-01 2016-10-01 隆沙有限公司 以兩步驟來製備３，５－二側氧己酸酯
EP2734513A4 (de) 2011-07-19 2014-11-26 Sunshine Lake Pharma Co Ltd Zwischenprodukt von statin-arzneimitteln und ihre herstellung
WO2013083719A1 (en) 2011-12-09 2013-06-13 Dsm Sinochem Pharmaceuticals Netherlands B.V. Process for the preparation of a thioprecursor for statins
CN102643757B (zh) * 2011-12-29 2013-09-11 浙江工业大学 生物催化制备6-氰基-(3r,5r)-二羟基己酸叔丁酯及菌株
GB201212777D0 (en) * 2012-07-18 2012-08-29 Bakhu Pharma Ltd Process for crossed claisen condensation reactions promoted by lithium amide in liquid ammonia
CN103435592B (zh) * 2013-08-12 2015-02-04 南京欧信医药技术有限公司 2-((4r,6s)-6-甲醛基-2,2-二甲基-1,3二氧六环-4-基)-乙酸甲酯的制备方法
CN105622566B (zh) * 2014-11-19 2018-07-27 上海弈柯莱生物医药科技有限公司 一种3,5-二取代羟基-6-取代己酸酯衍生物的制备方法
CN105669637A (zh) * 2014-11-21 2016-06-15 南京博优康远生物医药科技有限公司 一种3,5,6-取代己酸酯衍生物的制备方法
CN104789505B (zh) * 2015-04-23 2018-03-06 苏州东和盛昌生物科技有限公司 还原制备顺式3,5‑二羟基己酸酯化合物的方法及菌种
CN106011094B (zh) * 2016-07-27 2020-11-03 苏州汉酶生物技术有限公司 工程化酮还原酶多肽及其用于制备(3r,5s)-6-氯-3,5-二羟基己酸叔丁酯的方法

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Also Published As

Publication number Publication date
KR20010030819A (ko) 2001-04-16
DK1619191T3 (da) 2011-01-31
US6903225B2 (en) 2005-06-07
ATE486068T1 (de) 2010-11-15
CN100376682C (zh) 2008-03-26
WO2000008011A1 (en) 2000-02-17
HUP0101122A2 (hu) 2001-08-28
CN1274356A (zh) 2000-11-22
EP1619191B1 (de) 2010-10-27
ES2294236T3 (es) 2008-04-01
JP3803551B2 (ja) 2006-08-02
DE69937374T2 (de) 2008-07-24
ATE266656T1 (de) 2004-05-15
ES2221406T3 (es) 2004-12-16
EP1394157A2 (de) 2004-03-03
DE69942897D1 (de) 2010-12-09
CN1162422C (zh) 2004-08-18
US6472544B1 (en) 2002-10-29
EP1024139A1 (de) 2000-08-02
EP1024139A4 (de) 2002-04-17
EP1619191A3 (de) 2006-08-23
US20030040634A1 (en) 2003-02-27
NO20001703D0 (no) 2000-04-03
EP1394157B1 (de) 2007-10-17
CN1566351A (zh) 2005-01-19
EP1024139B1 (de) 2004-05-12
CA2305564C (en) 2008-06-17
HUP0101122A3 (en) 2006-02-28
EP1619191A2 (de) 2006-01-25
NO325591B1 (no) 2008-06-23
EP1394157A3 (de) 2004-03-17
PT1619191E (pt) 2010-12-21
ATE375989T1 (de) 2007-11-15
DE69917204D1 (de) 2004-06-17
NO20001703L (no) 2000-04-03
CA2305564A1 (en) 2000-02-17
KR100654115B1 (ko) 2006-12-05
DE69917204T2 (de) 2005-06-23

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