DK1756052T3 - Forbedret fremgangsmåde til at fremstille 3-hydroxy-4-hydroxymethyl-pyrrolidin-forbindelser - Google Patents

Forbedret fremgangsmåde til at fremstille 3-hydroxy-4-hydroxymethyl-pyrrolidin-forbindelser

Info

Publication number
DK1756052T3
DK1756052T3 DK05757531T DK05757531T DK1756052T3 DK 1756052 T3 DK1756052 T3 DK 1756052T3 DK 05757531 T DK05757531 T DK 05757531T DK 05757531 T DK05757531 T DK 05757531T DK 1756052 T3 DK1756052 T3 DK 1756052T3
Authority
DK
Denmark
Prior art keywords
hydroxy
preparing
hydroxymethyl
improved process
pyrrolidine compounds
Prior art date
Application number
DK05757531T
Other languages
English (en)
Inventor
Gary Brian Evans
Peter Charles Tyler
Dirk Henning Lenz
Jennifer Mary Mason
Keith Clinch
Original Assignee
Ind Res 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 Ind Res Ltd filed Critical Ind Res Ltd
Application granted granted Critical
Publication of DK1756052T3 publication Critical patent/DK1756052T3/da

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • 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
    • C07D207/04—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 no double bonds between ring members or between ring members and non-ring members
    • C07D207/10—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 no double bonds between ring members or between ring members and non-ring members 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
    • C07D207/12—Oxygen or sulfur atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
DK05757531T 2004-06-04 2005-06-03 Forbedret fremgangsmåde til at fremstille 3-hydroxy-4-hydroxymethyl-pyrrolidin-forbindelser DK1756052T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
NZ533360A NZ533360A (en) 2004-06-04 2004-06-04 Improved method for preparing 3-hydroxy-4-hydroxymethyl-pyrrolidine compounds
PCT/NZ2005/000114 WO2005118532A1 (en) 2004-06-04 2005-06-03 Improved method for preparing 3-hydroxy-4-hydroxymethyl-pyrrolidine compounds

Publications (1)

Publication Number Publication Date
DK1756052T3 true DK1756052T3 (da) 2009-03-09

Family

ID=35462865

Family Applications (1)

Application Number Title Priority Date Filing Date
DK05757531T DK1756052T3 (da) 2004-06-04 2005-06-03 Forbedret fremgangsmåde til at fremstille 3-hydroxy-4-hydroxymethyl-pyrrolidin-forbindelser

Country Status (20)

Country Link
US (1) US8183019B2 (da)
EP (1) EP1756052B1 (da)
JP (2) JP5219506B2 (da)
KR (1) KR101294732B1 (da)
CN (1) CN101018768B (da)
AT (1) ATE417036T1 (da)
AU (1) AU2005250308B2 (da)
CA (1) CA2568836C (da)
CY (1) CY1108866T1 (da)
DE (1) DE602005011609D1 (da)
DK (1) DK1756052T3 (da)
ES (1) ES2318504T3 (da)
HK (1) HK1106518A1 (da)
IL (1) IL179749A (da)
MX (1) MXPA06014139A (da)
NZ (1) NZ533360A (da)
PL (1) PL1756052T3 (da)
PT (1) PT1756052E (da)
SI (1) SI1756052T1 (da)
WO (1) WO2005118532A1 (da)

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US5985848A (en) 1997-10-14 1999-11-16 Albert Einstein College Of Medicine Of Yeshiva University Inhibitors of nucleoside metabolism
ATE425165T1 (de) 1999-04-08 2009-03-15 Ind Res Ltd Verfahren zur zubereitung von inhibitoren des nukleosid-metabolismus
SI1539783T1 (sl) 2002-08-21 2011-08-31 Einstein Coll Med Inhibitorji nukleozidnih fosforilaz in nukleozidaz
NZ523970A (en) * 2003-02-04 2005-02-25 Ind Res Ltd Process for preparing inhibitors of nucleoside phoshorylases and nucleosidases
CN1329374C (zh) * 2004-06-09 2007-08-01 上海靶点药物有限公司 作为ccr5拮抗剂的化合物
US8541567B2 (en) * 2005-07-27 2013-09-24 Albert Einstein College Of Medicine Of Yeshiva University Transition state structure of 5′-methylthioadenosine/s-adenosylhomocysteine nucleosidases
NZ544187A (en) * 2005-12-15 2008-07-31 Ind Res Ltd Deazapurine analogs of 1'-aza-l-nucleosides
WO2007097643A1 (en) * 2006-02-22 2007-08-30 Industrial Research Limited Analogues of coformycin and their use for treating protozoan parasite infections
WO2007097648A1 (en) * 2006-02-24 2007-08-30 Industrial Research Limited Methods of treating diseases using inhibitors of nucleoside phosphorylases and nucleosidases
US8916571B2 (en) 2006-02-24 2014-12-23 Albert Einstein College Of Medicine Of Yeshiva University Methods of treating cancer using inhibitors of 5′-methylthioadenosine phosphorylase
CN101094080B (zh) * 2006-06-22 2012-06-20 华为技术有限公司 一种即按即通系统中的计费方法
AU2007293774C1 (en) 2006-09-07 2014-12-18 Albert Einstein College Of Medicine, Inc. Acyclic amine inhibitors of nucleoside phosphorylases and hydrolases
CA2662626C (en) 2006-09-07 2016-07-26 Industrial Research Limited Acyclic amine inhibitors of 5'-methylthioadenosine phosphorylase and nucleosidase
KR20090101278A (ko) * 2006-12-22 2009-09-24 인더스트리얼 리서치 리미티드 누클레오시다제 및 포스포릴라제 억제제의 아제티딘 유사체
CA2706575C (en) * 2008-01-25 2015-07-14 Xenoport, Inc. Enantiomerically resolving acyloxyalkyl thiocarbonates used in synthesizing acyloxyalkyl carbamate prodrugs
WO2010033236A2 (en) * 2008-09-22 2010-03-25 Albert Einstein College Of Medicine Of Yeshiva University Methods and compositions for treating bacterial infections by inhibiting quorum sensing
US9493465B2 (en) 2009-07-17 2016-11-15 Victoria Link Limited 3-hydroxypyrrolidine inhibitors of 5′-methylthioadenosine phosphorylase and nucleosidase
WO2012074912A1 (en) 2010-11-29 2012-06-07 Albert Einstein College Of Medicine Of Yeshiva University Methods, assays and compounds for treating bacterial infections by inhibiting methylthioinosine phosphorylase
JP6063571B2 (ja) 2012-08-07 2017-01-18 アルバート アインシュタイン カレッジ オブ メディシン，インコーポレイティド ヘリコバクター・ピロリ感染の治療
US9994574B2 (en) 2012-11-12 2018-06-12 Victoria Link Limited Salt and polymorphic forms of (3R,4S)-L-((4-amino-5H-pyrrolo[3,2,-d]pyrimidin-7-yl)methyl)-4(methylthiomethyl)pyrodin-3-ol(MTDIA)
SG11201606595RA (en) 2014-02-12 2016-09-29 Einstein Coll Med Treatment of h. pylori infections using mtan inhibitors
CN104529814A (zh) * 2014-12-15 2015-04-22 上海同昌生物医药科技有限公司 一种合成n-苄基羟胺盐酸盐的方法
CN111793017B (zh) * 2019-04-04 2024-01-16 广东东阳光药业股份有限公司 一种内酰胺化合物的制备方法

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JP3504026B2 (ja) 1995-06-16 2004-03-08 株式会社トクヤマ ピロリジン誘導体の製造方法
AU1739097A (en) * 1996-02-23 1997-09-10 Albert Einstein College Of Medicine Of Yeshiva University Enzyme detection/assay method and substrates
US5985848A (en) * 1997-10-14 1999-11-16 Albert Einstein College Of Medicine Of Yeshiva University Inhibitors of nucleoside metabolism
JP2002539195A (ja) 1999-03-15 2002-11-19 ノボ ノルディスク アクティーゼルスカブ （２ｒ，３ｒ，４ｒ）−３，４−ジヒドロキシ−２−ヒドロキシメチルピロリジンの新規塩
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ATE425165T1 (de) * 1999-04-08 2009-03-15 Ind Res Ltd Verfahren zur zubereitung von inhibitoren des nukleosid-metabolismus
US6448799B1 (en) * 1999-09-30 2002-09-10 Hitachi Electronics Engineering Co., Ltd. Timing adjustment method and apparatus for semiconductor IC tester
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MXPA04009026A (es) * 2002-03-18 2005-01-25 Kyorin Seiyaku Kk Derivados de acido 10- (3- ciclopropilaminometil -1-pirrolidinil) piridobenzoxazin- carboxilico efectivos contra bacterias resistentes a farmacos.
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SI1539783T1 (sl) * 2002-08-21 2011-08-31 Einstein Coll Med Inhibitorji nukleozidnih fosforilaz in nukleozidaz
NZ523970A (en) * 2003-02-04 2005-02-25 Ind Res Ltd Process for preparing inhibitors of nucleoside phoshorylases and nucleosidases
US20060216775A1 (en) 2003-06-17 2006-09-28 The Regents Of The University Of Califoenia Compositions and methods for analysis and manipulation of enzymes in biosynthetic proteomes
JP2007525480A (ja) * 2003-09-09 2007-09-06 イェシバ・ユニバーシティ リシンａ鎖の遷移状態類似体阻害剤
CN1329374C (zh) * 2004-06-09 2007-08-01 上海靶点药物有限公司 作为ccr5拮抗剂的化合物
JP2008508287A (ja) 2004-07-27 2008-03-21 バイオクリスト・フアーマシユーテイカルズ・インコーポレイテツド ５’−メチルチオアデノシンホスホリラーゼ及び５’メチルチオアデノシン／ｓ−アデノシルホモシステインヌクレオシダーゼの阻害剤
NZ540160A (en) 2005-05-20 2008-03-28 Einstein Coll Med Inhibitors of nucleoside phosphorylases
US8541567B2 (en) 2005-07-27 2013-09-24 Albert Einstein College Of Medicine Of Yeshiva University Transition state structure of 5′-methylthioadenosine/s-adenosylhomocysteine nucleosidases
NZ544187A (en) * 2005-12-15 2008-07-31 Ind Res Ltd Deazapurine analogs of 1'-aza-l-nucleosides
WO2007097648A1 (en) 2006-02-24 2007-08-30 Industrial Research Limited Methods of treating diseases using inhibitors of nucleoside phosphorylases and nucleosidases
US8916571B2 (en) * 2006-02-24 2014-12-23 Albert Einstein College Of Medicine Of Yeshiva University Methods of treating cancer using inhibitors of 5′-methylthioadenosine phosphorylase
EP2007718A2 (en) * 2006-03-29 2008-12-31 Medichem, S.A. Processes for preparing ezetimibe and intermediate compounds useful for the preparation thereof
CA2662626C (en) * 2006-09-07 2016-07-26 Industrial Research Limited Acyclic amine inhibitors of 5'-methylthioadenosine phosphorylase and nucleosidase
AU2007293774C1 (en) 2006-09-07 2014-12-18 Albert Einstein College Of Medicine, Inc. Acyclic amine inhibitors of nucleoside phosphorylases and hydrolases
CA2663562A1 (en) * 2006-09-26 2008-04-03 Vern L. Schramm Transition state structure of human 5'-methylthioadenosine phosphorylase
KR20090101278A (ko) 2006-12-22 2009-09-24 인더스트리얼 리서치 리미티드 누클레오시다제 및 포스포릴라제 억제제의 아제티딘 유사체
WO2009082247A1 (en) 2007-12-21 2009-07-02 Industrial Research Limited Process for preparing immucillins having a methylene link
WO2010033236A2 (en) 2008-09-22 2010-03-25 Albert Einstein College Of Medicine Of Yeshiva University Methods and compositions for treating bacterial infections by inhibiting quorum sensing
US9493465B2 (en) 2009-07-17 2016-11-15 Victoria Link Limited 3-hydroxypyrrolidine inhibitors of 5′-methylthioadenosine phosphorylase and nucleosidase

Also Published As

Publication number Publication date
CA2568836A1 (en) 2005-12-15
CN101018768A (zh) 2007-08-15
KR20070050037A (ko) 2007-05-14
MXPA06014139A (es) 2007-05-09
US8183019B2 (en) 2012-05-22
US20080280334A1 (en) 2008-11-13
NZ533360A (en) 2007-02-23
WO2005118532A1 (en) 2005-12-15
AU2005250308A1 (en) 2005-12-15
ATE417036T1 (de) 2008-12-15
CA2568836C (en) 2013-04-16
EP1756052A4 (en) 2007-08-22
CY1108866T1 (el) 2014-07-02
JP5219506B2 (ja) 2013-06-26
KR101294732B1 (ko) 2013-08-12
JP2008501682A (ja) 2008-01-24
PL1756052T3 (pl) 2009-05-29
HK1106518A1 (en) 2008-03-14
EP1756052B1 (en) 2008-12-10
DE602005011609D1 (de) 2009-01-22
PT1756052E (pt) 2009-02-11
SI1756052T1 (sl) 2009-04-30
IL179749A0 (en) 2007-05-15
IL179749A (en) 2011-07-31
EP1756052A1 (en) 2007-02-28
JP2012211136A (ja) 2012-11-01
CN101018768B (zh) 2012-11-21
ES2318504T3 (es) 2009-05-01
AU2005250308B2 (en) 2012-04-26

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