IL143229A0 - Method for producing optically active 1-amino-4-(hydroxymethyl)-cyclopent-2-ene derivatives - Google Patents

Method for producing optically active 1-amino-4-(hydroxymethyl)-cyclopent-2-ene derivatives

Info

Publication number
IL143229A0
IL143229A0 IL14322999A IL14322999A IL143229A0 IL 143229 A0 IL143229 A0 IL 143229A0 IL 14322999 A IL14322999 A IL 14322999A IL 14322999 A IL14322999 A IL 14322999A IL 143229 A0 IL143229 A0 IL 143229A0
Authority
IL
Israel
Prior art keywords
cyclopent
hydroxymethyl
amino
optically active
ene derivatives
Prior art date
Application number
IL14322999A
Original Assignee
Lonza Ag
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 Lonza Ag filed Critical Lonza Ag
Publication of IL143229A0 publication Critical patent/IL143229A0/en

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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
    • 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
    • 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
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/02Amides, e.g. chloramphenicol or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes

Abstract

The invention discloses a new method for producing enantiomer-enriched 1-amino-4-(hydroxymethyl)-cyclopent-2-ene derivatives of the general formulae (I) and (II) in which R1 is hydrogen or a possibly substituted C1-8 alkyl radical, aryl radical or cycloalkyl radical and R2 is acyl. According to said method a racemic 1-amino-4-(hydroxymethyl)-cyclopent-2-ene derivative of general formula (III), in which R1 has the meaning given above, is converted using a hydrolase and in the presence of an acylation agent
IL14322999A 1998-12-23 1999-12-23 Method for producing optically active 1-amino-4-(hydroxymethyl)-cyclopent-2-ene derivatives IL143229A0 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP98124570 1998-12-23
US14599999P 1999-07-29 1999-07-29
PCT/EP1999/010382 WO2000039324A2 (en) 1998-12-23 1999-12-23 Method for producing optically active 1-amino-4-(hydroxymethyl)-cyclopent-2-ene derivatives

Publications (1)

Publication Number Publication Date
IL143229A0 true IL143229A0 (en) 2002-04-21

Family

ID=26149931

Family Applications (1)

Application Number Title Priority Date Filing Date
IL14322999A IL143229A0 (en) 1998-12-23 1999-12-23 Method for producing optically active 1-amino-4-(hydroxymethyl)-cyclopent-2-ene derivatives

Country Status (20)

Country Link
US (1) US6524844B2 (en)
EP (1) EP1141374B1 (en)
JP (1) JP4633934B2 (en)
KR (1) KR100685195B1 (en)
CN (1) CN1189569C (en)
AT (1) ATE253125T1 (en)
AU (1) AU2102600A (en)
CA (1) CA2354382C (en)
CZ (1) CZ301107B6 (en)
DE (1) DE59907569D1 (en)
DK (1) DK1141374T3 (en)
ES (1) ES2211216T3 (en)
HU (1) HUP0104547A3 (en)
IL (1) IL143229A0 (en)
MX (1) MXPA01006428A (en)
NO (1) NO326058B1 (en)
PL (1) PL196857B1 (en)
PT (1) PT1141374E (en)
SK (1) SK285795B6 (en)
WO (1) WO2000039324A2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2354382C (en) * 1998-12-23 2010-09-07 Lonza Ag Process for preparing optically active 1-amino-4-(hydroxymethyl) cyclopent-2-ene derivatives
GB0306267D0 (en) 2003-03-19 2003-04-23 Ineos Fluor Ltd Process
WO2006117057A1 (en) * 2005-05-02 2006-11-09 Dsm Fine Chemicals Austria Nfg Gmbh & Co Kg Process for preparing enantiomerically enriched e-(2s)- and (2r)-alkyl-5-halopent-4-enecarboxylic acids or their esters

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2756790B2 (en) * 1988-07-18 1998-05-25 富士薬品工業株式会社 Method for producing optically active cyclopentenol derivative
GB9108376D0 (en) * 1991-04-19 1991-06-05 Enzymatix Ltd Cyclopentenes
WO1997045529A1 (en) * 1996-05-30 1997-12-04 Lonza Ag Process for the preparation of amino alcohols and derivatives thereof
SK285229B6 (en) * 1997-05-13 2006-09-07 Lonza Ag Process for the preparation of a (1R, 4S)- or (1S, 4R)-1-amino-4- (hydroxymethyl)-2-cyclopentene derivative and an enantiomer of a (1R,4S)-N-butyryl-1-amino-4-(hydroxymethyl)-2-cyclopenten
SK284594B6 (en) * 1997-11-27 2005-07-01 Lonza Ag Process for the preparation of aminoalcohol derivatives and their salts
CA2354382C (en) * 1998-12-23 2010-09-07 Lonza Ag Process for preparing optically active 1-amino-4-(hydroxymethyl) cyclopent-2-ene derivatives

Also Published As

Publication number Publication date
DE59907569D1 (en) 2003-12-04
US6524844B2 (en) 2003-02-25
PL196857B1 (en) 2008-02-29
WO2000039324A3 (en) 2000-09-21
EP1141374B1 (en) 2003-10-29
MXPA01006428A (en) 2002-06-21
HUP0104547A2 (en) 2002-03-28
PT1141374E (en) 2004-03-31
PL349388A1 (en) 2002-07-15
CZ20012168A3 (en) 2001-11-14
NO20013037L (en) 2001-06-19
WO2000039324A2 (en) 2000-07-06
AU2102600A (en) 2000-07-31
ATE253125T1 (en) 2003-11-15
CA2354382A1 (en) 2000-07-06
CZ301107B6 (en) 2009-11-11
DK1141374T3 (en) 2004-02-16
SK8812001A3 (en) 2002-01-07
CA2354382C (en) 2010-09-07
US20020042108A1 (en) 2002-04-11
ES2211216T3 (en) 2004-07-01
CN1352695A (en) 2002-06-05
KR20010099861A (en) 2001-11-09
EP1141374A2 (en) 2001-10-10
NO20013037D0 (en) 2001-06-19
NO326058B1 (en) 2008-09-08
KR100685195B1 (en) 2007-02-22
JP2003520018A (en) 2003-07-02
HUP0104547A3 (en) 2003-12-29
CN1189569C (en) 2005-02-16
JP4633934B2 (en) 2011-02-16
SK285795B6 (en) 2007-08-02

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