JP4757632B2 - 2’−デオキシグアノシンから2−クロロ−2’−デオキシアデノシンを調製する方法 - Google Patents

2’−デオキシグアノシンから2−クロロ−2’−デオキシアデノシンを調製する方法 Download PDF

Info

Publication number
JP4757632B2
JP4757632B2 JP2005501990A JP2005501990A JP4757632B2 JP 4757632 B2 JP4757632 B2 JP 4757632B2 JP 2005501990 A JP2005501990 A JP 2005501990A JP 2005501990 A JP2005501990 A JP 2005501990A JP 4757632 B2 JP4757632 B2 JP 4757632B2
Authority
JP
Japan
Prior art keywords
group
chloro
aryl
alkyl
sulfonyl
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 - Fee Related
Application number
JP2005501990A
Other languages
English (en)
Japanese (ja)
Other versions
JP2006508183A (ja
Inventor
ジェイ. ロビンス、モリス
ジャネバ、ズラトコ
フランカム、ポーラ
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.)
Brigham Young University
Original Assignee
Brigham Young University
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 Brigham Young University filed Critical Brigham Young University
Publication of JP2006508183A publication Critical patent/JP2006508183A/ja
Application granted granted Critical
Publication of JP4757632B2 publication Critical patent/JP4757632B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/16Purine radicals
    • C07H19/167Purine radicals with ribosyl as the saccharide radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/16Purine radicals
    • C07H19/173Purine radicals with 2-deoxyribosyl as the saccharide radical
    • 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)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Saccharide Compounds (AREA)
JP2005501990A 2002-09-25 2003-09-25 2’−デオキシグアノシンから2−クロロ−2’−デオキシアデノシンを調製する方法 Expired - Fee Related JP4757632B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US41391502P 2002-09-25 2002-09-25
US60/413,915 2002-09-25
US41632902P 2002-10-04 2002-10-04
US60/416,329 2002-10-04
PCT/US2003/030386 WO2004028462A2 (en) 2002-09-25 2003-09-25 Method for the preparation of 2-halo-2'-deoxyadenosine compounds from 2'-deoxyguanosine

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2011051093A Division JP2011116782A (ja) 2002-09-25 2011-03-09 2’−デオキシグアノシンから2−クロロ−2’−デオキシアデノシンを調製する方法

Publications (2)

Publication Number Publication Date
JP2006508183A JP2006508183A (ja) 2006-03-09
JP4757632B2 true JP4757632B2 (ja) 2011-08-24

Family

ID=32045263

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2005501990A Expired - Fee Related JP4757632B2 (ja) 2002-09-25 2003-09-25 2’−デオキシグアノシンから2−クロロ−2’−デオキシアデノシンを調製する方法
JP2011051093A Pending JP2011116782A (ja) 2002-09-25 2011-03-09 2’−デオキシグアノシンから2−クロロ−2’−デオキシアデノシンを調製する方法

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2011051093A Pending JP2011116782A (ja) 2002-09-25 2011-03-09 2’−デオキシグアノシンから2−クロロ−2’−デオキシアデノシンを調製する方法

Country Status (7)

Country Link
US (2) US7572909B2 (enExample)
EP (1) EP1556400B1 (enExample)
JP (2) JP4757632B2 (enExample)
AU (1) AU2003275267A1 (enExample)
CA (1) CA2540158C (enExample)
ES (1) ES2405825T3 (enExample)
WO (1) WO2004028462A2 (enExample)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4757632B2 (ja) 2002-09-25 2011-08-24 ブリガム ヤング ユニバーシティー 2’−デオキシグアノシンから2−クロロ−2’−デオキシアデノシンを調製する方法
DK2805723T3 (da) 2004-12-22 2018-01-29 Merck Serono Sa Cladribin-regime til behandling af multipel sclerose
CA2649810A1 (en) 2006-05-24 2007-11-29 Laboratoires Serono S.A. Cladribine regimen for treating multiple sclerosis
SI1932918T1 (sl) 2006-12-15 2010-02-26 Explora Lab Sa Postopek izdelave kladribina
RU2324699C1 (ru) * 2007-02-05 2008-05-20 Институт биоорганической химии им. академиков М.М. Шемякина и Ю.А. Овчинникова Россиийской Академии Наук СПОСОБ ПОЛУЧЕНИЯ 2,6-ДИХЛОР-9-(2,3,5-ТРИ-O-АЦЕТИЛ-β-D-РИБОФУРАНОЗИЛ)ПУРИНА
EP2343074A1 (en) 2009-12-23 2011-07-13 Merck Serono S.A. Use of purine analogues for treating airway diseases
RU2649828C1 (ru) * 2017-06-07 2018-04-04 Государственное бюджетное учреждение здравоохранения города Москвы Московский клинический научно-практический центр им. А.С. Логинова Департамента здравоохранения города Москвы Способ лечения волосатоклеточного лейкоза
KR20250005506A (ko) 2017-11-24 2025-01-09 메르크 파텐트 게엠베하 진행 형태의 다발성 경화증의 치료에서 사용을 위한 클라드리빈 용법
IL301246A (en) 2020-09-10 2023-05-01 Merck Patent Gmbh Cladribine treatment regimen
EP4302091A1 (en) 2021-03-03 2024-01-10 Ares Trading S.A. Improved treatment methods using dmds for the treatment of autoimmune diseases, and biomarker for predicting and/or optimising said treatment methods
WO2025125527A1 (en) 2023-12-14 2025-06-19 Ares Trading S.A. Cladribine regimen for treating myasthenia gravis

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61106594A (ja) * 1984-08-06 1986-05-24 ブリガム ヤング ユニヴア−シテイ プリン誘導体およびその製造法
JPH05255378A (ja) * 1991-12-18 1993-10-05 Ortho Pharmaceut Corp 2−クロル−2′−デオキシアデノシンの製造法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4760137A (en) 1984-08-06 1988-07-26 Brigham Young University Method for the production of 2'-deoxyadenosine compounds
DE3924424A1 (de) * 1989-07-24 1991-01-31 Boehringer Mannheim Gmbh Nucleosid-derivate, verfahren zu deren herstellung, deren verwendung als arzneimittel sowie deren verwendung bei der nucleinsaeure-sequenzierung
US5602246A (en) * 1992-11-25 1997-02-11 Schering Aktiengesellschaft Process for the preparation of fludarabine or fludarabine phosphate from guanosine
US6252061B1 (en) * 1998-03-23 2001-06-26 Reliable Biopharmaceutical, Inc. Process for the production of 2-halo-6-aminopurine derivatives
US6541626B2 (en) * 2001-04-17 2003-04-01 Isis Pharmaceuticals, Inc. Process for selective N-acylation of purine nucleosides
JP4757632B2 (ja) * 2002-09-25 2011-08-24 ブリガム ヤング ユニバーシティー 2’−デオキシグアノシンから2−クロロ−2’−デオキシアデノシンを調製する方法

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61106594A (ja) * 1984-08-06 1986-05-24 ブリガム ヤング ユニヴア−シテイ プリン誘導体およびその製造法
JPH05255378A (ja) * 1991-12-18 1993-10-05 Ortho Pharmaceut Corp 2−クロル−2′−デオキシアデノシンの製造法

Also Published As

Publication number Publication date
EP1556400A4 (en) 2009-11-18
US8466275B2 (en) 2013-06-18
US20090270604A1 (en) 2009-10-29
US7572909B2 (en) 2009-08-11
US20070032645A1 (en) 2007-02-08
JP2011116782A (ja) 2011-06-16
AU2003275267A1 (en) 2004-04-19
WO2004028462A3 (en) 2004-06-10
CA2540158C (en) 2011-07-05
CA2540158A1 (en) 2004-04-08
EP1556400A2 (en) 2005-07-27
WO2004028462A2 (en) 2004-04-08
ES2405825T3 (es) 2013-06-03
EP1556400B1 (en) 2013-05-01
AU2003275267A8 (en) 2004-04-19
JP2006508183A (ja) 2006-03-09
WO2004028462A9 (en) 2010-08-26

Similar Documents

Publication Publication Date Title
JP2011116782A (ja) 2’−デオキシグアノシンから2−クロロ−2’−デオキシアデノシンを調製する方法
US6927291B2 (en) Method for the synthesis of 2′,3′-dideoxy-2′,3′-didehydronucleosides
AU710074B2 (en) Novel method of preparation of known and novel 2'-modified nucleosides by intramolecular nucleophilic displacement
JP5878758B2 (ja) Rna及びその誘導体合成のための新規保護基
AU2002255654A1 (en) Method for the synthesis of 2',3'-dideoxy -2',3'-didehydronucleosides
EP1645561A1 (en) Method of synthesizing cyclic bisdinucleoside
HU208149B (en) Process for producing deoxyfluoronucleoside derivatives
KR20170129228A (ko) 유기인-뉴클레오사이드의 탈아미노화
US20210332070A1 (en) Compositions and Methods for Synthesis of Phosphorylated Molecules
JP2011512390A (ja) 可溶性担体上での合成によりヌクレオチドおよびアナログを調製する方法、ならびにこうして調製された生物学的ツール
EP1620451A2 (en) Industrially scalable nucleoside synthesis
JPWO2004018494A1 (ja) 4’−チオヌクレオチド
US20150376219A1 (en) Selective Preparations of Purine Nucleosides and Nucleotides: Reagents and Methods
WO2006138396A2 (en) Methods for selective n-9 glycosylation of purines
JP2008195648A (ja) 4’−セレノヌクレオシド及び4’−セレノヌクレオチド
Maruyama et al. Synthesis and biological activity of fluorinated nucleosides
Xiao et al. A Convenient Route to Symmetric Phosphate, Phosphorothioate, and Phosphoroselenoate

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20060922

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20100209

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20100507

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20100514

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20100609

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20101109

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20110309

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20110310

A911 Transfer to examiner for re-examination before appeal (zenchi)

Free format text: JAPANESE INTERMEDIATE CODE: A911

Effective date: 20110405

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20110517

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20110601

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20140610

Year of fee payment: 3

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees