ES2320364T3 - Procedimiento de preparacion de beta-lactamas protegidas por n-carbamato opticamente activo por resolucion optica por medio de una lipasa de candida antarctica. - Google Patents

Procedimiento de preparacion de beta-lactamas protegidas por n-carbamato opticamente activo por resolucion optica por medio de una lipasa de candida antarctica. Download PDF

Info

Publication number
ES2320364T3
ES2320364T3 ES05826088T ES05826088T ES2320364T3 ES 2320364 T3 ES2320364 T3 ES 2320364T3 ES 05826088 T ES05826088 T ES 05826088T ES 05826088 T ES05826088 T ES 05826088T ES 2320364 T3 ES2320364 T3 ES 2320364T3
Authority
ES
Spain
Prior art keywords
lipase
protected
lactam
diyl
carbamate
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
ES05826088T
Other languages
English (en)
Spanish (es)
Inventor
Ankush Argade
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.)
Rigel Pharmaceuticals Inc
Original Assignee
Rigel Pharmaceuticals 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
Application filed by Rigel Pharmaceuticals Inc filed Critical Rigel Pharmaceuticals Inc
Application granted granted Critical
Publication of ES2320364T3 publication Critical patent/ES2320364T3/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
    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/10Nitrogen as only ring hetero atom
    • 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
    • C12P13/04Alpha- or beta- amino acids
    • 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
    • C12P41/006Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures
    • 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

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)
  • Genetics & Genomics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
ES05826088T 2004-11-15 2005-11-15 Procedimiento de preparacion de beta-lactamas protegidas por n-carbamato opticamente activo por resolucion optica por medio de una lipasa de candida antarctica. Expired - Lifetime ES2320364T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US62840104P 2004-11-15 2004-11-15
US628401P 2004-11-15

Publications (1)

Publication Number Publication Date
ES2320364T3 true ES2320364T3 (es) 2009-05-21

Family

ID=36190809

Family Applications (1)

Application Number Title Priority Date Filing Date
ES05826088T Expired - Lifetime ES2320364T3 (es) 2004-11-15 2005-11-15 Procedimiento de preparacion de beta-lactamas protegidas por n-carbamato opticamente activo por resolucion optica por medio de una lipasa de candida antarctica.

Country Status (10)

Country Link
US (1) US7459301B2 (enExample)
EP (1) EP1812581B1 (enExample)
JP (1) JP4738416B2 (enExample)
AT (1) ATE421996T1 (enExample)
CA (1) CA2580151C (enExample)
DE (1) DE602005012597D1 (enExample)
DK (1) DK1812581T3 (enExample)
ES (1) ES2320364T3 (enExample)
PT (1) PT1812581E (enExample)
WO (1) WO2006055528A2 (enExample)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1763514A2 (en) 2004-05-18 2007-03-21 Rigel Pharmaceuticals, Inc. Cycloalkyl substituted pyrimidinediamine compounds and their uses
GB2420559B (en) * 2004-11-15 2008-08-06 Rigel Pharmaceuticals Inc Stereoisomerically enriched 3-aminocarbonyl bicycloheptene pyrimidinediamine compounds and their uses
EP1960372B1 (en) 2005-12-15 2015-12-09 Rigel Pharmaceuticals, Inc. Kinase inhibitors and their uses
HU227663B1 (en) * 2007-07-09 2011-10-28 Univ Szegedi Resolution process
CN102264368B (zh) 2008-12-22 2014-09-10 米伦纽姆医药公司 极光激酶抑制剂与抗cd20抗体的组合
EP2489663A1 (en) 2011-02-16 2012-08-22 Almirall, S.A. Compounds as syk kinase inhibitors
US10335494B2 (en) 2013-12-06 2019-07-02 Millennium Pharmaceuticals, Inc. Combination of aurora kinase inhibitors and anti-CD30 antibodies
JP2018524292A (ja) 2015-07-21 2018-08-30 ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. オーロラキナーゼインヒビターと化学療法剤の投与
WO2019195658A1 (en) 2018-04-05 2019-10-10 Dana-Farber Cancer Institute, Inc. Sting levels as a biomarker for cancer immunotherapy
WO2019201279A1 (zh) * 2018-04-18 2019-10-24 广东东阳光药业有限公司 一种桥环化合物的制备方法
WO2021041532A1 (en) 2019-08-26 2021-03-04 Dana-Farber Cancer Institute, Inc. Use of heparin to promote type 1 interferon signaling

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002520027A (ja) * 1998-07-09 2002-07-09 ロンザ ア−ゲ− (1r,4s)−2−アザビシクロ[2.2.1]ヘプタ−5−エン−3−オン誘導体の製造方法

Also Published As

Publication number Publication date
WO2006055528A3 (en) 2006-08-31
EP1812581A2 (en) 2007-08-01
CA2580151A1 (en) 2006-05-26
WO2006055528A2 (en) 2006-05-26
US7459301B2 (en) 2008-12-02
ATE421996T1 (de) 2009-02-15
DE602005012597D1 (de) 2009-03-19
JP4738416B2 (ja) 2011-08-03
US20060166308A1 (en) 2006-07-27
PT1812581E (pt) 2009-04-22
CA2580151C (en) 2014-02-04
JP2008520206A (ja) 2008-06-19
DK1812581T3 (da) 2009-05-11
EP1812581B1 (en) 2009-01-28

Similar Documents

Publication Publication Date Title
ES2320364T3 (es) Procedimiento de preparacion de beta-lactamas protegidas por n-carbamato opticamente activo por resolucion optica por medio de una lipasa de candida antarctica.
ES2331140T3 (es) Metodo para la preparacion enzimatica de acido (s)-3-ciano-5-metilhexanoico.
Csomós et al. Biocatalysis for the preparation of optically active β-lactam precursors of amino acids
Kirihara et al. Efficient synthesis of (R)-and (S)-1-amino-2, 2-difluorocyclopropanecarboxylic acid via lipase-catalyzed desymmetrization of prochiral precursors
Sanfilippo et al. Resolution of racemic amines via lipase-catalyzed benzoylation: Chemoenzymatic synthesis of the pharmacologically active isomers of labetalol
Kámán et al. Enzymatic resolution of alicyclic β-lactams
Szymanski et al. Studies on the application of the Passerini reaction and enzymatic procedures to the synthesis of tripeptide mimetics
Li et al. Burkholderia cepacia lipase and activated β-lactams in β-dipeptide and β-amino amide synthesis
CN109790121B (zh) 用于制备btk抑制剂的方法和中间体
Banfi et al. Synthesis of asymmetrized 2-benzyl-1, 3-diaminopropane by a chemoenzymatic route: a tool for combinatorially developing peptidomimetics
Szymanski et al. Toward stereocontrolled, chemoenzymatic synthesis of unnatural peptides
Lundell et al. Enantiomers of adrenaline-type amino alcohols by Burkholderia cepacia lipase-catalyzed asymmetric acylation
ES2258394B1 (es) Procedimiento enzimatico para la preparacion de un compuesto intermedio y su uso en la sintesis de tamsulosina clorhidrato.
Kamal et al. Lipase-catalyzed resolution of 1-chloro-3-[(4-morpholin-4-yl-1, 2, 5-thiadiazole-3-yl) oxy] propan-2-ol: Synthesis of (R)-and (S)-timolol
JP4242647B2 (ja) アミンおよびヒドロキシドの酵素脱保護
Matsuo et al. A practical synthesis of enantiopure N-carbobenzyloxy-N′-phthaloyl-cis-1, 2-cyclohexanediamine by asymmetric reductive amination and the Curtius rearrangement
D’Antona et al. A novel chemo-multienzymatic synthesis of bioactive cyclophellitol and epi-cyclophellitol in both enantiopure forms
Panunzio et al. Enantioselective synthesis of protected d-serine from tetrahydrooxazin-4-one via a hetero Diels–Alder reaction
EP1536017B1 (en) Process for producing optically active octahydro-1H-indole-2-carboxylic acid
JP2612671B2 (ja) 光学活性なプロピオン酸エステルの製造法
JP3192791B2 (ja) 光学活性なD−N−ピペロニル−2−アミノ−(ベンゾ[b]チオフェン−3−イル)−プロピオニルアミドの製造法
JPS63502960A (ja) ラセミ体の分割方法
JP2003002872A (ja) リジン誘導体の製造方法
HU227663B1 (en) Resolution process
Klempier et al. Nitrilase‐and Nitrile Hydratase‐Catalyzed Enantioselective Preparation of Non‐Proteinogenic Amino Acids