PL4036244T3 - Enzymatyczny sposób wytwarzania kwasu (2s)-2-[(4r)-2-oxo-4-propylo-pirolidyn-1-ylo]masłowego i jego przemiana w briwaracetam - Google Patents

Enzymatyczny sposób wytwarzania kwasu (2s)-2-[(4r)-2-oxo-4-propylo-pirolidyn-1-ylo]masłowego i jego przemiana w briwaracetam

Info

Publication number
PL4036244T3
PL4036244T3 PL21159958.4T PL21159958T PL4036244T3 PL 4036244 T3 PL4036244 T3 PL 4036244T3 PL 21159958 T PL21159958 T PL 21159958T PL 4036244 T3 PL4036244 T3 PL 4036244T3
Authority
PL
Poland
Prior art keywords
brivaracetam
pyrrolidin
oxo
propyl
conversion
Prior art date
Application number
PL21159958.4T
Other languages
English (en)
Inventor
Satchandra Kiran Divi
Mysore Aswatha Narayana Rao
Shaik Nowshuddin
Original Assignee
Divi's Laboratories Limited
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 Divi's Laboratories Limited filed Critical Divi's Laboratories Limited
Publication of PL4036244T3 publication Critical patent/PL4036244T3/pl

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4015—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil having oxo groups directly attached to the heterocyclic ring, e.g. piracetam, ethosuximide
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/10—Nitrogen as only ring hetero atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or 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 to ring carbon atoms
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
    • C07D207/27—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
    • C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
    • C12N9/64—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue
    • C12N9/6421—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
    • C12N9/6424—Serine endopeptidases (3.4.21)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/005—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of carboxylic acid groups in the enantiomers or the inverse reaction
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y304/00—Hydrolases acting on peptide bonds, i.e. peptidases (3.4)
    • C12Y304/21—Serine endopeptidases (3.4.21)
    • C12Y304/21062—Subtilisin (3.4.21.62)
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D11/00—Solvent extraction
    • B01D11/04—Solvent extraction of solutions which are liquid
    • B01D11/0492—Applications, solvents used

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Molecular Biology (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrrole Compounds (AREA)
PL21159958.4T 2021-02-01 2021-03-01 Enzymatyczny sposób wytwarzania kwasu (2s)-2-[(4r)-2-oxo-4-propylo-pirolidyn-1-ylo]masłowego i jego przemiana w briwaracetam PL4036244T3 (pl)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IN202141004400 2021-02-01

Publications (1)

Publication Number Publication Date
PL4036244T3 true PL4036244T3 (pl) 2024-03-11

Family

ID=74844839

Family Applications (1)

Application Number Title Priority Date Filing Date
PL21159958.4T PL4036244T3 (pl) 2021-02-01 2021-03-01 Enzymatyczny sposób wytwarzania kwasu (2s)-2-[(4r)-2-oxo-4-propylo-pirolidyn-1-ylo]masłowego i jego przemiana w briwaracetam

Country Status (8)

Country Link
US (1) US11400074B1 (pl)
EP (1) EP4036244B1 (pl)
JP (1) JP7280984B2 (pl)
KR (1) KR102791352B1 (pl)
ES (1) ES2969331T3 (pl)
FI (1) FI4036244T3 (pl)
PL (1) PL4036244T3 (pl)
SI (1) SI4036244T1 (pl)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115851866A (zh) * 2022-12-22 2023-03-28 浙江普洛家园药业有限公司 一种布瓦西坦及其中间体的制备方法
WO2026040943A1 (zh) * 2024-08-19 2026-02-26 浙江华海药业股份有限公司 一种酶催化制备α-手性羧酸或α-手性酯的方法

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060252134A1 (en) 1999-10-29 2006-11-09 Novus International, Inc. Enantioselective oligomerization of alpha-hydroxy carboxylic acids and alpha-amino acids
GB0004297D0 (en) 2000-02-23 2000-04-12 Ucb Sa 2-oxo-1 pyrrolidine derivatives process for preparing them and their uses
AU2003247201A1 (en) 2003-07-25 2005-02-14 Posco Method of preparation of optically active alcohols
CN101263113B (zh) 2005-09-15 2012-06-13 Ucb医药有限公司 4-取代的-吡咯烷-2-酮及其用途
US8338621B2 (en) 2005-12-21 2012-12-25 Ucb S.A. Process for the preparation of 2-oxo-1-pyrrolidine derivatives
WO2009009117A2 (en) * 2007-07-11 2009-01-15 Bioverdant, Inc. Chemoenzymatic processes for preparation of levetiracetam
CN101284811B (zh) 2008-06-11 2010-06-16 常州恩滋生物科技有限公司 阿巴卡韦的手性碳环中间体的合成方法
WO2016075082A1 (en) * 2014-11-10 2016-05-19 Sandoz Ag Stereoselective reductive amination of alpha-chiral aldehydes using omega-transaminases for the synthesis of precursors of pregabalin and brivaracetam
JP6872500B2 (ja) 2015-05-25 2021-05-19 エステベ・キミカ・ソシエダッド・アノニマEsteve Quimica, S.A. ブリバラセタムを製造する方法
WO2018042393A1 (en) 2016-09-05 2018-03-08 Micro Labs Limited Novel process for the preparation of brivaracetam
WO2019087172A1 (en) * 2017-12-19 2019-05-09 Glenmark Pharmaceuticals Limited Process for preparation of brivaracetam
CN108101824B (zh) 2018-02-13 2020-04-03 扬州奥锐特药业有限公司 一种高手性纯度内酰胺中间体及布瓦西坦的制备方法

Also Published As

Publication number Publication date
US11400074B1 (en) 2022-08-02
JP7280984B2 (ja) 2023-05-24
KR20220111209A (ko) 2022-08-09
SI4036244T1 (sl) 2024-03-29
US20220241242A1 (en) 2022-08-04
EP4036244A1 (en) 2022-08-03
ES2969331T3 (es) 2024-05-17
KR102791352B1 (ko) 2025-04-03
EP4036244B1 (en) 2023-10-11
JP2022117945A (ja) 2022-08-12
FI4036244T3 (fi) 2023-12-18

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