ES2067148T3 - Procedimiento e intermedios para 2r-bencil-cromano-6-carbaldehido. - Google Patents

Procedimiento e intermedios para 2r-bencil-cromano-6-carbaldehido.

Info

Publication number
ES2067148T3
ES2067148T3 ES91301891T ES91301891T ES2067148T3 ES 2067148 T3 ES2067148 T3 ES 2067148T3 ES 91301891 T ES91301891 T ES 91301891T ES 91301891 T ES91301891 T ES 91301891T ES 2067148 T3 ES2067148 T3 ES 2067148T3
Authority
ES
Spain
Prior art keywords
bencil
chroman
carbaldehyde
intermediates
procedure
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
ES91301891T
Other languages
English (en)
Inventor
Frank John Urban
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.)
PFIZER
Pfizer Inc
Original Assignee
PFIZER
Pfizer Inc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=23973911&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ES2067148(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by PFIZER, Pfizer Inc filed Critical PFIZER
Application granted granted Critical
Publication of ES2067148T3 publication Critical patent/ES2067148T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • 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
    • C07D311/58Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • 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
    • C07D311/58Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • C07D311/66Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biotechnology (AREA)
  • Analytical Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Genetics & Genomics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Pyrane Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

LOS (C SUB 1 ATOS OPTICAMENTE ACTIVOS SE PREPARAN MEDIANTE HIDROLISIS PARCIAL DEL CORRESPONDIENTE ESTER RACEMICO USANDO UNA LIPASA MICROBIANA COMO CATALIZADOR. DICHO 2R TE MEDIANTE UN 2R ROMETILOSULFONILOXIMETILO)CROMAN E INTERMEDIARIOS DE 2R ILOCROMAN EN 2R RBALDEIDO, UN COMPUESTO DE RECONOCIDA UTILIDAD EN LA FABRICACION DE CIERTOS AGENTES HIPOGLICEMICOS.
ES91301891T 1990-03-21 1991-03-07 Procedimiento e intermedios para 2r-bencil-cromano-6-carbaldehido. Expired - Lifetime ES2067148T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/496,737 US5089637A (en) 1990-03-21 1990-03-21 Process and intermediates for 2r-benzyl-chroman-6-carbaldehyde

Publications (1)

Publication Number Publication Date
ES2067148T3 true ES2067148T3 (es) 1995-03-16

Family

ID=23973911

Family Applications (1)

Application Number Title Priority Date Filing Date
ES91301891T Expired - Lifetime ES2067148T3 (es) 1990-03-21 1991-03-07 Procedimiento e intermedios para 2r-bencil-cromano-6-carbaldehido.

Country Status (20)

Country Link
US (1) US5089637A (es)
EP (1) EP0448254B1 (es)
JP (1) JPH0764838B2 (es)
KR (1) KR940005601B1 (es)
AT (1) ATE117299T1 (es)
AU (1) AU620756B2 (es)
CA (1) CA2038610C (es)
DE (1) DE69106753T2 (es)
DK (1) DK0448254T3 (es)
ES (1) ES2067148T3 (es)
FI (1) FI97385C (es)
GR (1) GR3015390T3 (es)
HU (1) HUT61603A (es)
IE (1) IE64066B1 (es)
IL (1) IL97549A0 (es)
MY (1) MY106374A (es)
NO (1) NO179680C (es)
NZ (1) NZ237466A (es)
PT (1) PT97070B (es)
ZA (1) ZA912063B (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5658796A (en) * 1995-06-07 1997-08-19 Seprachem, Inc. Optical resolution of alkyl chroman-2-carboxylates
JP2002512807A (ja) * 1998-04-28 2002-05-08 ノボ ノルディスク アクティーゼルスカブ (−)−3.4−トランス−ジアリールクロマンを得るための酵素的分割
US6184005B1 (en) 1998-04-28 2001-02-06 Novo Nordisk A/S Enzymatic resolvation for obtaining a (−)-3,4-trans-diarylchroman
JPWO2003040382A1 (ja) * 2001-11-09 2005-03-03 株式会社カネカ 光学活性クロマン誘導体の製造法および中間体
EP1634958B1 (en) * 2003-06-04 2009-02-18 Mitsubishi Gas Chemical Company, Inc. Method for producing optically active chroman-carboxylate
WO2006116165A1 (en) * 2005-04-22 2006-11-02 Wyeth Chromane and chromene derivatives and uses thereof
KR100784850B1 (ko) * 2006-10-19 2007-12-14 충북대학교 산학협력단 크로만-2-카복실산 아릴아마이드 유도체, 그 제조방법 및이를 포함하는 NF-κB 저해제
IT1402974B1 (it) 2010-11-30 2013-09-27 Menarini Int Operations Lu Sa Processo per la preparazione del nebivololo.
FR2986804A1 (fr) * 2012-02-09 2013-08-16 Servier Lab Procede de synthese enzymatique de l'acide (7s) 3,4-dimethoxybicyclo[4.2.0]octa-1,3,5-triene 7-carboxylique ou de ses esters, et application a la synthese de l'ivabradine et de ses sels
EP2968814B1 (en) 2013-03-15 2017-09-27 Airway Control Technologies, LLC Medical breathing apparatus

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4654362A (en) * 1983-12-05 1987-03-31 Janssen Pharmaceutica, N.V. Derivatives of 2,2'-iminobisethanol
KR930005004B1 (ko) * 1985-04-15 1993-06-11 쟈안센 파아마슈우티카 엔. 부이. 치환된 n-[(4-피페리디닐)알킬]이환 축합 옥사졸아민 및 티아졸아민의 제조방법
HU210339B (en) * 1985-05-21 1995-03-28 Pfizer Process for preparing thiazolidinediones and their pharmaceutical compositions haring hypoglycemic effect
US5037747A (en) * 1988-01-26 1991-08-06 Hoffmann-La Roche Inc. Production of benzopyran-2-carboxylic acids and esters by enzymatic hydrolysis

Also Published As

Publication number Publication date
MY106374A (en) 1995-05-30
IE64066B1 (en) 1995-07-12
FI97385B (fi) 1996-08-30
CA2038610A1 (en) 1991-09-22
HUT61603A (en) 1993-01-28
NO179680B (no) 1996-08-19
ZA912063B (en) 1992-10-28
EP0448254A3 (en) 1991-12-18
PT97070B (pt) 2001-05-31
NO179680C (no) 1996-11-27
DK0448254T3 (da) 1995-03-20
EP0448254A2 (en) 1991-09-25
NZ237466A (en) 1992-04-28
JPH04234871A (ja) 1992-08-24
PT97070A (pt) 1991-10-31
AU7369691A (en) 1991-11-14
CA2038610C (en) 1999-03-09
HU910939D0 (en) 1991-10-28
EP0448254B1 (en) 1995-01-18
US5089637A (en) 1992-02-18
AU620756B2 (en) 1992-02-20
KR910016939A (ko) 1991-11-05
FI911356A0 (fi) 1991-03-20
DE69106753T2 (de) 1995-05-18
FI911356L (fi) 1991-09-22
IL97549A0 (en) 1992-06-21
NO911101D0 (no) 1991-03-19
JPH0764838B2 (ja) 1995-07-12
NO911101L (no) 1991-09-23
KR940005601B1 (ko) 1994-06-21
FI97385C (fi) 1996-12-10
IE910938A1 (en) 1991-09-25
DE69106753D1 (de) 1995-03-02
ATE117299T1 (de) 1995-02-15
GR3015390T3 (en) 1995-06-30

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