SK140898A3 - Improved process for the production of enantiomerically-pure azetidine-2-carboxylic acid - Google Patents

Improved process for the production of enantiomerically-pure azetidine-2-carboxylic acid Download PDF

Info

Publication number
SK140898A3
SK140898A3 SK1408-98A SK140898A SK140898A3 SK 140898 A3 SK140898 A3 SK 140898A3 SK 140898 A SK140898 A SK 140898A SK 140898 A3 SK140898 A3 SK 140898A3
Authority
SK
Slovakia
Prior art keywords
azeoh
acid
aldehyde
range
tartrate
Prior art date
Application number
SK1408-98A
Other languages
English (en)
Slovak (sk)
Inventor
Philipp Barth
Armin Pfenninger
Original Assignee
Astra Ab
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 Astra Ab filed Critical Astra Ab
Publication of SK140898A3 publication Critical patent/SK140898A3/sk

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B57/00—Separation of optically-active compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
SK1408-98A 1996-04-26 1997-04-22 Improved process for the production of enantiomerically-pure azetidine-2-carboxylic acid SK140898A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE9601600A SE9601600D0 (sv) 1996-04-26 1996-04-26 Improved process
PCT/SE1997/000675 WO1997041084A1 (fr) 1996-04-26 1997-04-22 Procede ameliore permettant de produire de l'acide azetine-2-carboxylique ne contenant pas d'enantiomeres

Publications (1)

Publication Number Publication Date
SK140898A3 true SK140898A3 (en) 1999-05-07

Family

ID=20402360

Family Applications (1)

Application Number Title Priority Date Filing Date
SK1408-98A SK140898A3 (en) 1996-04-26 1997-04-22 Improved process for the production of enantiomerically-pure azetidine-2-carboxylic acid

Country Status (32)

Country Link
US (1) US6143903A (fr)
EP (1) EP0906255B1 (fr)
JP (2) JP2000509068A (fr)
KR (1) KR100447072B1 (fr)
CN (1) CN1071292C (fr)
AR (1) AR006639A1 (fr)
AT (1) ATE200889T1 (fr)
AU (1) AU713519B2 (fr)
BR (1) BR9708872A (fr)
CA (1) CA2253711C (fr)
CZ (1) CZ339998A3 (fr)
DE (1) DE69704708T2 (fr)
DK (1) DK0906255T3 (fr)
EE (1) EE9800365A (fr)
EG (1) EG20975A (fr)
ES (1) ES2158557T3 (fr)
GR (1) GR3036303T3 (fr)
HU (1) HUP9901665A3 (fr)
ID (1) ID16840A (fr)
IL (1) IL126717A (fr)
IN (1) IN186439B (fr)
IS (1) IS4860A (fr)
MY (1) MY132450A (fr)
NO (1) NO310404B1 (fr)
NZ (1) NZ332155A (fr)
PL (1) PL329685A1 (fr)
PT (1) PT906255E (fr)
SE (1) SE9601600D0 (fr)
SK (1) SK140898A3 (fr)
TR (1) TR199802146T2 (fr)
WO (1) WO1997041084A1 (fr)
ZA (1) ZA973156B (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1308519B1 (fr) * 1997-01-24 2006-04-19 Sumitomo Chemical Company, Limited Procédé pour améliorer de dérivés optiquement actives de l'acide azetidine-2-carboxylique
SE9802939D0 (sv) 1998-09-01 1998-09-01 Astra Ab New process
SE9901712D0 (sv) * 1999-05-11 1999-05-11 Astra Ab New process
WO2005103005A1 (fr) * 2004-04-26 2005-11-03 Astellas Pharma Inc. PROCÉDÉ SERVANT À PRODUIRE SÉLECTIVEMENT UN ISOMÈRE OPTIQUEMENT ACTIF DE LA β-PYRIDYLALANINE
EP2334620B1 (fr) * 2008-09-05 2018-09-05 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Procédé pour l'énantioséparation de systèmes chiraux avec préparation d'un composé à l'aide de deux étapes de cristallisation ultérieures
JP2013241339A (ja) * 2010-09-09 2013-12-05 Mitsubishi Gas Chemical Co Inc 光学活性アミノ酸の製造方法
JP2013241338A (ja) * 2010-09-09 2013-12-05 Mitsubishi Gas Chemical Co Inc 光学活性２−アミノ酪酸の製造方法
CN103204783B (zh) * 2013-04-18 2015-09-02 张家港市华昌药业有限公司 一种d-赖氨酸盐酸盐的制备方法
JPWO2016021711A1 (ja) * 2014-08-07 2017-06-01 株式会社エーピーアイ コーポレーション アミノ酸誘導体の製造方法

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE795874A (fr) * 1972-02-25 1973-08-23 Glaxo Lab Ltd Procede de preparation d'esters optiquement actifs d'alpha-amino-acides
JPS5139219B2 (fr) * 1972-06-08 1976-10-26
US4072698A (en) * 1976-12-02 1978-02-07 The Upjohn Company Resolution of aminonitriles
JPS56104866A (en) * 1980-01-24 1981-08-20 Mitsubishi Chem Ind Ltd Production of (2r,4r)-4-alkyl-2-piperidinecarboxylic acid or its l-tartarate salt
DE3303112A1 (de) * 1983-01-31 1984-08-09 Hoechst Ag, 6230 Frankfurt Verfahren zur racemattrennung optisch aktiver bicyclischer imino-(alpha)-carbonsaeuren
US4923983A (en) * 1989-07-31 1990-05-08 Eli Lilly And Company Method of resolving cis 3-amino-4-[2-(2-furyl)eth-1-yl]-1-methoxycarbonylmethyl-azetidin-2-one
EP0499376A1 (fr) * 1991-01-31 1992-08-19 Hoechst Celanese Corporation Transformation asymmétrique des amino acides chiraux et leurs sels induis par précipitation
GB9420246D0 (en) * 1994-10-07 1994-11-23 Chiroscience Ltd Asymmetric crystallisation
IN187238B (fr) * 1995-06-30 2002-03-09 Astra Ab
EP0827954B1 (fr) * 1996-09-06 2003-06-04 Sumitomo Chemical Company Limited Procédé de préparation d'acide azétidine-2-carboxylique optiquement actif

Also Published As

Publication number Publication date
MY132450A (en) 2007-10-31
DK0906255T3 (da) 2001-08-13
DE69704708T2 (de) 2001-12-06
ES2158557T3 (es) 2001-09-01
KR20000065019A (ko) 2000-11-06
KR100447072B1 (ko) 2004-10-14
CZ339998A3 (cs) 1999-03-17
HUP9901665A2 (hu) 1999-09-28
TR199802146T2 (xx) 1999-01-18
NO310404B1 (no) 2001-07-02
SE9601600D0 (sv) 1996-04-26
CA2253711C (fr) 2005-08-23
NO984681D0 (no) 1998-10-07
PT906255E (pt) 2001-10-30
NO984681L (no) 1998-10-07
AU2719497A (en) 1997-11-19
DE69704708D1 (de) 2001-06-07
IL126717A0 (en) 1999-08-17
US6143903A (en) 2000-11-07
BR9708872A (pt) 1999-08-03
WO1997041084A1 (fr) 1997-11-06
PL329685A1 (en) 1999-04-12
IN186439B (fr) 2001-09-01
GR3036303T3 (en) 2001-10-31
IL126717A (en) 2002-11-10
CA2253711A1 (fr) 1997-11-06
JP2009120611A (ja) 2009-06-04
JP2000509068A (ja) 2000-07-18
NZ332155A (en) 2000-07-28
EP0906255A1 (fr) 1999-04-07
EP0906255B1 (fr) 2001-05-02
ID16840A (id) 1997-11-13
AU713519B2 (en) 1999-12-02
HUP9901665A3 (en) 1999-11-29
CN1216972A (zh) 1999-05-19
CN1071292C (zh) 2001-09-19
EG20975A (en) 2000-08-30
ATE200889T1 (de) 2001-05-15
EE9800365A (et) 1999-04-15
IS4860A (is) 1998-10-06
AR006639A1 (es) 1999-09-08
ZA973156B (en) 1997-11-06

Similar Documents

Publication Publication Date Title
JP2009120611A (ja) エナンチオマーとして純粋なアゼチジン−２−カルボン酸の改良された製造方法
JP2008247922A (ja) エナンチオマーとして純粋なアゼチジン−２−カルボン酸の製造方法
HUE026124T2 (en) Procedure for producing ramipril
HU226475B1 (en) Process for producing (1r,4s)- and (1s,4r)-1-amino-4-hydroxymethyl-2-cyclopentene and the new intermediates
EP0623104B1 (fr) Resolution du profene
EP0173921B1 (fr) Procédé de racémisation d'un acide alpha-amino-carboxylique
IE920307A1 (en) Precipitation-induced asymmetric transformation of chiral¹alpha-amino acids and salts thereof
US6054594A (en) Process for the production of enantiomerically enriched N-acylazetidine-2-carboxylic acids
HU203716B (en) Process for producing optically active amino-acids
EP0174358A1 (fr) Nouveaux sels diastereomeres de phenylalanine et ses derives n-acyliques et procede de separation de phenylalanine optiquement actives et de ses derives n-acyliques
MXPA98008788A (en) Improved process for the production of azetidin-2- carboxylic acid enantiomerically p
JPH0623149B2 (ja) 高純度ｎ−アセチル−ｄｌ−アミノ酸の製造方法
EP1484315A1 (fr) Procede de production de beta-phenylalamine optiquement active
EP0432204A1 (fr) Derives et precurseurs de captopril et ses analogues
JPH0940621A (ja) 光学活性インダニルメチルアミン誘導体及びその製造法
MXPA97010269A (es) Proceso para la produccion de acido azetidin-2-carboxilico enantiomericamente puro
HU177583B (en) Process for resolving alkali salts and lactone of raceme cys-2-hydroxy-cyclopent-4-ene-1-yl-acetic acid with optically active alpha-phenyl-ethylamine