BG61511B1 - Ензимен метод за стереоселективно получаване на енантиомер на хетеробицикличен алкохол - Google Patents

Ензимен метод за стереоселективно получаване на енантиомер на хетеробицикличен алкохол Download PDF

Info

Publication number
BG61511B1
BG61511B1 BG98305A BG9830593A BG61511B1 BG 61511 B1 BG61511 B1 BG 61511B1 BG 98305 A BG98305 A BG 98305A BG 9830593 A BG9830593 A BG 9830593A BG 61511 B1 BG61511 B1 BG 61511B1
Authority
BG
Bulgaria
Prior art keywords
enantiomer
compound
general formula
alcohol
atom
Prior art date
Application number
BG98305A
Other languages
Bulgarian (bg)
English (en)
Other versions
BG98305A (bg
Inventor
Nicolaas Buizer
Chris Kruse
Der Laan Melle Van
Georges Langrand
Scharrenburg Gustaaf Van
Maria Snoek
Original Assignee
Duphar International Research B.V.
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 Duphar International Research B.V. filed Critical Duphar International Research B.V.
Publication of BG98305A publication Critical patent/BG98305A/bg
Publication of BG61511B1 publication Critical patent/BG61511B1/bg

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/281,4-Oxazines; Hydrogenated 1,4-oxazines
    • C07D265/341,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings
    • C07D265/361,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings condensed with one six-membered ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D319/00Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D319/101,4-Dioxanes; Hydrogenated 1,4-dioxanes
    • C07D319/141,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
    • C07D319/161,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D319/201,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring with substituents attached to the hetero ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D327/00Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
    • C07D327/02Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms one oxygen atom and one sulfur atom
    • C07D327/06Six-membered rings
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/02Oxygen as only ring hetero atoms
    • C12P17/06Oxygen as only ring hetero atoms containing a six-membered hetero ring, e.g. fluorescein
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/14Nitrogen or oxygen as hetero atom and at least one other diverse hetero ring atom in the same ring
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/003Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/004Processes 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
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/582Recycling of unreacted starting or intermediate materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
BG98305A 1992-12-21 1993-12-16 Ензимен метод за стереоселективно получаване на енантиомер на хетеробицикличен алкохол BG61511B1 (bg)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP92204043 1992-12-21

Publications (2)

Publication Number Publication Date
BG98305A BG98305A (bg) 1994-07-29
BG61511B1 true BG61511B1 (bg) 1997-10-31

Family

ID=8211159

Family Applications (1)

Application Number Title Priority Date Filing Date
BG98305A BG61511B1 (bg) 1992-12-21 1993-12-16 Ензимен метод за стереоселективно получаване на енантиомер на хетеробицикличен алкохол

Country Status (24)

Country Link
US (1) US5914263A (fr)
EP (2) EP0939135A1 (fr)
JP (1) JPH06237790A (fr)
KR (1) KR940014808A (fr)
CN (1) CN1255496A (fr)
AT (1) ATE182367T1 (fr)
AU (1) AU674547B2 (fr)
BG (1) BG61511B1 (fr)
CA (1) CA2111607A1 (fr)
CZ (2) CZ286077B6 (fr)
DE (1) DE69325698T2 (fr)
DK (1) DK0605033T3 (fr)
ES (1) ES2134241T3 (fr)
FI (1) FI935676A (fr)
GR (1) GR3031446T3 (fr)
IL (1) IL108090A (fr)
NO (1) NO934652L (fr)
NZ (1) NZ250478A (fr)
PL (2) PL178517B1 (fr)
RO (1) RO112517B1 (fr)
RU (1) RU2124506C1 (fr)
SK (1) SK143793A3 (fr)
TW (1) TW381120B (fr)
ZA (1) ZA939435B (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2724184B1 (fr) * 1994-09-05 1997-01-03 Rhone Poulenc Chimie Procede de resolution d'un melange d'alcools stereoisomeres
AU701883B2 (en) * 1996-01-25 1999-02-11 Duphar International Research B.V. Process for the stereoselective preparation of a hetero-bicyclic alcohol enantiomer
DE19706337A1 (de) 1997-02-19 1998-08-20 Basf Ag Verfahren zur Herstellung von enantiomerenreinen Estern
JP5080716B2 (ja) * 2001-07-20 2012-11-21 サイコジェニックス・インコーポレーテッド 注意欠陥・多動性障害の治療
FR2853327B1 (fr) 2003-04-04 2012-07-27 Solvay Procede pour la fabrication de derives de beta-aminoacides enantiopurs et derives de beta-aminoacides enantiopurs
KR100527231B1 (ko) * 2003-06-03 2005-11-08 엔자이텍 주식회사 무수숙신산에 의한 광학활성 1,2-디올 유도체와 이의 에스테르 제조방법
JP5547865B2 (ja) 2003-10-29 2014-07-16 ワイス・エルエルシー アプリンドルおよびその誘導体を含む持続放出型医薬組成物
DE102004004719A1 (de) * 2004-01-29 2005-08-18 Basf Ag Verfahren zur Herstellung von enantiomerenreinen Aminoalkoholen
TW200811182A (en) * 2006-05-25 2008-03-01 Wyeth Corp Oxindoledioxans, synthesis thereof, and intermediates thereto
CZ2009687A3 (cs) * 2009-10-21 2010-12-15 Mikrobiologický ústav AV CR, v.v.i. Zpusob výroby opticky cistých stereomeru silybinu A a silybinu B
PL3080284T3 (pl) * 2013-12-11 2018-05-30 F.Hoffmann-La Roche Ag Sposób wytwarzania chiralnej 2-(4-aminofenylo)morfoliny

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3692775A (en) * 1969-03-17 1972-09-19 Allied Chem Racemization of d-or l-{60 -amino-caprolactam in the presence of metal ions
GB1389217A (en) * 1971-06-02 1975-04-03 Glaxo Lab Ltd Phenylglycine derivatives
FR2479825A1 (fr) * 1980-04-04 1981-10-09 Fabre Sa Pierre Benzodioxanne 1,4 methoxy-2 propanolamines, leur preparation et leur application en tant que medicaments
FR2523961B1 (fr) * 1982-03-23 1985-08-30 Centre Nat Rech Scient Procede de preparation d'un alpha-amino-acide libre l
US4659671A (en) * 1983-07-01 1987-04-21 Massachusetts Institute Of Technology Enzymatic separation of racemic mixtures of hydroxy compounds
AU577802B2 (en) * 1983-10-17 1988-10-06 Duphar International Research B.V. Blood-pressure lowering piperazine derivatives
DE3586794T2 (de) * 1984-12-21 1993-05-27 Duphar Int Res Arzneimittel mit psychotroper wirkung.
EP0185429A1 (fr) * 1984-12-21 1986-06-25 Duphar International Research B.V Pipérazines bicycliques
IT1201408B (it) * 1985-03-22 1989-02-02 Montedison Spa Processo per la preparazione biotecnologica di acidi alfa-arilalcanoici otticamente attivi
IE74200B1 (en) * 1987-09-11 1997-07-16 Duphar Int Res Anxiolytically active piperazine derivatives
NZ231631A (en) * 1988-12-08 1992-07-28 Duphar Int Res Heterocyclically-substituted piperazine and diazepine derivatives and anxiolytic compositions
US5166062A (en) * 1990-01-26 1992-11-24 University Of New Mexico Methods for separating diol and triol stereoisomers from a stereoisomer mixture

Also Published As

Publication number Publication date
GR3031446T3 (en) 2000-01-31
ZA939435B (en) 1994-08-09
SK143793A3 (en) 1994-09-07
RU2124506C1 (ru) 1999-01-10
CZ278493A3 (en) 1994-07-13
PL178517B1 (pl) 2000-05-31
NO934652D0 (no) 1993-12-16
TW381120B (en) 2000-02-01
EP0605033B1 (fr) 1999-07-21
AU674547B2 (en) 1997-01-02
AU5250293A (en) 1994-06-30
ES2134241T3 (es) 1999-10-01
PL177831B1 (pl) 2000-01-31
IL108090A (en) 1998-10-30
BG98305A (bg) 1994-07-29
CA2111607A1 (fr) 1994-06-22
IL108090A0 (en) 1994-04-12
CN1255496A (zh) 2000-06-07
JPH06237790A (ja) 1994-08-30
ATE182367T1 (de) 1999-08-15
EP0605033A1 (fr) 1994-07-06
US5914263A (en) 1999-06-22
KR940014808A (ko) 1994-07-19
FI935676A0 (fi) 1993-12-16
PL301539A1 (en) 1994-06-27
RO112517B1 (ro) 1997-10-30
CZ286162B6 (cs) 2000-01-12
DE69325698T2 (de) 2000-01-27
NZ250478A (en) 1995-03-28
DE69325698D1 (de) 1999-08-26
DK0605033T3 (da) 2000-02-07
CZ286077B6 (cs) 2000-01-12
EP0939135A1 (fr) 1999-09-01
NO934652L (no) 1994-06-22
FI935676A (fi) 1994-06-22

Similar Documents

Publication Publication Date Title
BG61511B1 (bg) Ензимен метод за стереоселективно получаване на енантиомер на хетеробицикличен алкохол
RU2241040C2 (ru) Способ ферментативного разделения энантиомеров 3 (s)-гидрокси-1-метил-4-(2,4,6-триметоксифенил) - 1,2,3,6 -тетрагидропиридина, а также r-сложных эфиров карбоновой кислоты
EP1211254A1 (fr) Procede de preparation de derives de benzoxazine et de leurs intermediaires
AU2001230192B2 (en) Method for the enzymatic resolution of the racemates of aminomethyl-aryl-cyclohexanol derivatives
EP0328125A2 (fr) Procédé de séparation enzymatique d'isomères optiques d'alcools primaires racémiques alpha-alcoyle-substitués
EP2218788B1 (fr) Procédé de préparation de cyclopenténones optiquement actifs
EP1283200A2 (fr) Présurseurs de la paroxétine optiquement purs
KR101399551B1 (ko) 광학적으로 활성인 사이클로펜텐온의 제조방법 및 그로부터제조된 사이클로펜텐온
US5731464A (en) Process for preparation of indenol
EP0763023A1 (fr) Composes chiraux et leur resolution
HU213569B (en) Enzymatic process for the stereoselective preparation of a heterobicyclic alcohol enantiomer
EP0579370B1 (fr) 2,4-0-Isopropylidène-2,4-dihydroxypentane 1,5-disubstitué optiquement actif et procédé pour sa préparation
US5661014A (en) Chiral compounds and their resolution synthesis using enantioselective esterases
JP3814766B2 (ja) 光学活性な2−ハロ−1−(置換フェニル)エタノールの製造法
IE903437A1 (en) Enantioselective enzymatic synthesis of s(-)- and¹r(+)-esters of 4-hydroxy-2-cyclopenten-1-one and its ketal¹formed with 2,2-dimethyl- propane-1,3-diol
JPH08113550A (ja) 光学活性3−ヒドロキシヘキサン酸類の製造方法
Wei et al. Chemoenzymatic synthesis of Ro 25-8210 and Ro 25-6630
JPWO2011061934A1 (ja) 酵素を用いた光学活性ビシクロ[3.1.0]ヘキサン誘導体の製造方法
EP1601778A1 (fr) Procede chimioenzymatique stereoselectif pour la preparation de phenylglycidates optiquement enrichis
EP0490407A2 (fr) Procédé de séparation enzymatique d'isomères optiques de tosyloxyalcanols
MXPA00007811A (en) Method for enzymatic enantiomer-separation of 3(r)- and 3(s)-hydroxy-1- methyl-4-(2,4, 6-trimethoxyphenyl)-1, 2,3,6- tetrahydro-pyridine or its carboxylic acid esters
JPH07322889A (ja) 光学活性な2,5−ピロリジンジオン誘導体の製造法