IL235978B - Oligonucleotide synthesis method utilizing liquid support in high dispersive phase - Google Patents

Oligonucleotide synthesis method utilizing liquid support in high dispersive phase

Info

Publication number
IL235978B
IL235978B IL235978A IL23597814A IL235978B IL 235978 B IL235978 B IL 235978B IL 235978 A IL235978 A IL 235978A IL 23597814 A IL23597814 A IL 23597814A IL 235978 B IL235978 B IL 235978B
Authority
IL
Israel
Prior art keywords
synthesis method
oligonucleotide synthesis
phase support
highly dispersible
dispersible liquid
Prior art date
Application number
IL235978A
Other languages
English (en)
Hebrew (he)
Other versions
IL235978A0 (en
Original Assignee
Hokkaido System Science Co Ltd
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 Hokkaido System Science Co Ltd filed Critical Hokkaido System Science Co Ltd
Publication of IL235978A0 publication Critical patent/IL235978A0/en
Publication of IL235978B publication Critical patent/IL235978B/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • C07H21/04—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H1/00—Processes for the preparation of sugar derivatives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H1/00—Processes for the preparation of sugar derivatives
    • C07H1/02—Phosphorylation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H1/00—Processes for the preparation of sugar derivatives
    • C07H1/02—Phosphorylation
    • C07H1/04—Introducing polyphosphoric acid radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/06—Pyrimidine radicals
    • C07H19/073—Pyrimidine radicals with 2-deoxyribosyl as the saccharide radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • C07H21/02—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with ribosyl as saccharide radical
    • Y—GENERAL 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
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Saccharide Compounds (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
IL235978A 2012-05-30 2014-11-27 Oligonucleotide synthesis method utilizing liquid support in high dispersive phase IL235978B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2012/063921 WO2013179412A1 (ja) 2012-05-30 2012-05-30 高分散性液相支持体を用いたオリゴヌクレオチド合成法

Publications (2)

Publication Number Publication Date
IL235978A0 IL235978A0 (en) 2015-02-01
IL235978B true IL235978B (en) 2018-02-28

Family

ID=49672666

Family Applications (1)

Application Number Title Priority Date Filing Date
IL235978A IL235978B (en) 2012-05-30 2014-11-27 Oligonucleotide synthesis method utilizing liquid support in high dispersive phase

Country Status (7)

Country Link
US (1) US9284344B2 (enExample)
EP (1) EP2857412B1 (enExample)
DK (1) DK2857412T3 (enExample)
IL (1) IL235978B (enExample)
IN (1) IN2014DN10144A (enExample)
SG (1) SG11201407967TA (enExample)
WO (1) WO2013179412A1 (enExample)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0923225A2 (pt) 2008-12-02 2016-10-04 Chiralgen Ltd metodo para sintese de acidos nucleicos modificados no atomo de fosforo
EP2451461A4 (en) 2009-07-06 2013-05-29 Ontorii Inc NOVEL NUCLEIC ACID PRODRUGS AND METHOD OF USE THEREOF
DK2620428T3 (da) 2010-09-24 2019-07-01 Wave Life Sciences Ltd Asymmetrisk hjælpegruppe
CN107365339A (zh) 2011-07-19 2017-11-21 波涛生命科学有限公司 合成官能化核酸的方法
US8846885B2 (en) 2012-02-17 2014-09-30 Ajinomoto Co., Inc. Oligonucleotide with protected base
IN2014DN06768A (enExample) * 2012-02-17 2015-05-22 Ajinomoto Kk
DK2872147T3 (da) 2012-07-13 2023-02-20 Wave Life Sciences Ltd Fremgangsmåde til fremstilling af kirale oligonukleotider
SG11201500243WA (en) 2012-07-13 2015-04-29 Shin Nippon Biomedical Lab Ltd Chiral nucleic acid adjuvant
WO2014010250A1 (en) 2012-07-13 2014-01-16 Chiralgen, Ltd. Asymmetric auxiliary group
EP3095461A4 (en) 2014-01-15 2017-08-23 Shin Nippon Biomedical Laboratories, Ltd. Chiral nucleic acid adjuvant having immunity induction activity, and immunity induction activator
WO2015108046A1 (ja) 2014-01-15 2015-07-23 株式会社新日本科学 抗アレルギー作用を有するキラル核酸アジュバンド及び抗アレルギー剤
EP3095459A4 (en) 2014-01-15 2017-08-23 Shin Nippon Biomedical Laboratories, Ltd. Chiral nucleic acid adjuvant having antitumor effect and antitumor agent
EP3094728B1 (en) 2014-01-16 2022-03-09 Wave Life Sciences Ltd. Chiral design
CN108350018A (zh) 2015-11-17 2018-07-31 日产化学工业株式会社 寡核苷酸的制造方法
EP3398955B1 (en) * 2015-12-16 2026-06-03 Ajinomoto Co., Inc. Oligonucleotide production method, and nucleoside, nucleotide, or oligonucleotide
JPWO2017111137A1 (ja) 2015-12-22 2018-10-18 味の素株式会社 オリゴヌクレオチドの製造方法
CN113423715A (zh) 2019-02-15 2021-09-21 味之素株式会社 寡核苷酸的制造方法
CN113490679A (zh) 2019-02-28 2021-10-08 富士胶片株式会社 肽化合物的制造方法、保护基形成用试药及芳香族杂环化合物
KR102668387B1 (ko) 2019-02-28 2024-05-22 후지필름 가부시키가이샤 펩타이드 화합물의 제조 방법, 보호기 형성용 시약, 및 축합 다환 방향족 탄화 수소 화합물
EP3950698A4 (en) 2019-03-28 2023-01-25 Ajinomoto Co., Inc. METHOD OF PREPARING AN OLIGONUCLEOTIDE WITH PHOSPHOROTHIOATE SITE
CN114206897B (zh) * 2019-05-08 2024-09-20 比奥根Ma公司 寡核苷酸的汇聚液相合成
WO2021039935A1 (ja) * 2019-08-29 2021-03-04 富士フイルム株式会社 核酸化合物の製造方法、及び、核酸化合物
US12649761B2 (en) 2020-03-31 2026-06-09 Janssen Biopharma, Inc. Synthesis of oligonucleotides and related compounds
FR3111896A1 (fr) 2020-06-24 2021-12-31 Strainchem Procédés de synthèses en solution de macromolécules à partir d’unités de dérivés de glucides
CN113583069B (zh) * 2021-09-09 2023-06-06 北京大学 核苷磷脂类化合物及其化学合成方法和在核酸递送中的应用
WO2024083746A1 (en) 2022-10-17 2024-04-25 Bachem Holding Ag Method and composition for oligonucleotide synthesis
WO2024137756A1 (en) * 2022-12-23 2024-06-27 Hongene Biotech Corporation Compounds and methods for liquid phase oligonucleotide synthesis
EP4678626A1 (en) 2023-03-06 2026-01-14 Spera Pharma, Inc. Long-chain alkenyloxy-substituted benzoyl derivative and oligonucleotide synthesis method using same
EP4695265A1 (en) 2023-10-16 2026-02-18 Bachem Holding AG Method and composition for oligonucleotide synthesis

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7094943B2 (en) 1998-04-27 2006-08-22 Hubert Köster Solution phase biopolymer synthesis
JP2003002895A (ja) 2001-05-30 2003-01-08 Tokyo Inst Of Technol 核酸の合成法
JP4963665B2 (ja) 2007-11-27 2012-06-27 株式会社ミツバ 扁平型コミュテータ及びその製造方法
JP5548852B2 (ja) * 2009-05-29 2014-07-16 国立大学法人東京農工大学 疎水性基結合ヌクレオシド、疎水性基結合ヌクレオシド溶液、及び疎水性基結合オリゴヌクレオチド合成方法
US9029528B2 (en) 2011-05-17 2015-05-12 Ajinomoto Co., Inc. Solution-based method of making oligonucleotides via phosphoramidite coupling
IN2014DN06768A (enExample) 2012-02-17 2015-05-22 Ajinomoto Kk

Also Published As

Publication number Publication date
US20150112053A1 (en) 2015-04-23
SG11201407967TA (en) 2015-01-29
DK2857412T3 (en) 2017-04-03
EP2857412A1 (en) 2015-04-08
EP2857412B1 (en) 2017-01-11
WO2013179412A1 (ja) 2013-12-05
IL235978A0 (en) 2015-02-01
EP2857412A4 (en) 2015-10-21
IN2014DN10144A (enExample) 2015-08-21
US9284344B2 (en) 2016-03-15

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