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AR058210A1 - Procedimiento para preparar 5-amino-3h-tiazolo[4,5-d]pirimidin-2-ona, un intermediario util para la preparacion de ciertos nucleosidos de tiazolo[4,5-d]pirimidina que actuan como inmunomoduladores. - Google Patents

Procedimiento para preparar 5-amino-3h-tiazolo[4,5-d]pirimidin-2-ona, un intermediario util para la preparacion de ciertos nucleosidos de tiazolo[4,5-d]pirimidina que actuan como inmunomoduladores.

Info

Publication number
AR058210A1
AR058210A1 ARP060105089A ARP060105089A AR058210A1 AR 058210 A1 AR058210 A1 AR 058210A1 AR P060105089 A ARP060105089 A AR P060105089A AR P060105089 A ARP060105089 A AR P060105089A AR 058210 A1 AR058210 A1 AR 058210A1
Authority
AR
Argentina
Prior art keywords
amino
formula
thiazolo
pyrimidin
tiazolo
Prior art date
Application number
ARP060105089A
Other languages
English (en)
Inventor
T Wang
J S Ng
S E Webber
Original Assignee
Anadys 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 Anadys Pharmaceuticals Inc filed Critical Anadys Pharmaceuticals Inc
Publication of AR058210A1 publication Critical patent/AR058210A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Reivindicacion 1: Un procedimiento para la preparacion de 5-amino-3H-tiazolo[4,5-d]pirimidin-2-ona que posee la formula (1) caracterizado porque comprende: (i) halogenacion de una 2,4-diaminopirimidina de formula (2) para formar un 2,4-diamino-5- halo-pirimidina de formula (3) en donde X representa halo seleccionado de F, Cl, Br e I; (ii) ciclocondensacion de 2,4-diamino-5-halo-pirimidina para formar 5-amino-3H-tiazolo[4,5-d]pirimidin-2-tiona de formula (4); y (iii) oxidar la 5-amino-3H- tiazolo[4,5-d]pirimidin-2-tiona para formar 5-amino-3H-tiazolo[4,5-d]pirimidin-2-ona. Reivindicacion 12: Un procedimiento para la ciclocondensacion de 2,4-diamino-5-halo-pirimidina de formula (3) caracterizado porque X es halo seleccionado de F, Cl, Br, e I; para formar 5-amino-3H-tiazolo[4,5-d]pirimidin-2-tiona de formula (4) en donde la ciclocondensacion es realizada en presencia de un compuesto xantogenato que tiene la formula (5) en donde M es un cation de metal y R1es un grupo alquilo; y en donde la reaccion comprende calentar la solucion e los reactivos anteriores en presencia de un solvente inerte. Reivindicacion 17: Un procedimiento para oxidar 5-amino-3H-tiazolo[4,5-d]pirimidin-2-tiona de formula (4) para formar 5-amino-3- tiazolo[4,5-d]pirimidin-2-ona de formula (1) en donde el procedimiento comprende: hacer reaccionar 5-amino-3H-tiazolo[4,5-d]pirimidin-2-tiona con un agente oxidante bajo condiciones básicas y una hidrolisis ácida subsiguiente.
ARP060105089A 2005-11-21 2006-11-21 Procedimiento para preparar 5-amino-3h-tiazolo[4,5-d]pirimidin-2-ona, un intermediario util para la preparacion de ciertos nucleosidos de tiazolo[4,5-d]pirimidina que actuan como inmunomoduladores. AR058210A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US73805505P 2005-11-21 2005-11-21

Publications (1)

Publication Number Publication Date
AR058210A1 true AR058210A1 (es) 2008-01-23

Family

ID=37908057

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP060105089A AR058210A1 (es) 2005-11-21 2006-11-21 Procedimiento para preparar 5-amino-3h-tiazolo[4,5-d]pirimidin-2-ona, un intermediario util para la preparacion de ciertos nucleosidos de tiazolo[4,5-d]pirimidina que actuan como inmunomoduladores.

Country Status (18)

Country Link
US (1) US7781581B2 (es)
EP (1) EP1973920B1 (es)
JP (1) JP5117391B2 (es)
KR (1) KR20080090400A (es)
CN (1) CN101365705A (es)
AR (1) AR058210A1 (es)
AT (1) ATE474842T1 (es)
AU (1) AU2006318260B2 (es)
BR (1) BRPI0618789A2 (es)
CA (1) CA2630463C (es)
DE (1) DE602006015700D1 (es)
EA (1) EA200801404A1 (es)
ES (1) ES2345904T3 (es)
IL (1) IL191568A0 (es)
NO (1) NO20082365L (es)
SG (1) SG152296A1 (es)
TW (1) TWI383987B (es)
WO (1) WO2007062355A2 (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7709448B2 (en) 2006-06-22 2010-05-04 Anadys Pharmaceuticals, Inc. Prodrugs of 5-amino-3-(3′-deoxy-β-D-ribofuranosyl)-thiazolo[4,5-d]pyrimidin-2,7-dione
WO2012102366A1 (ja) * 2011-01-28 2012-08-02 日本たばこ産業株式会社 新規ピペラジン化合物の製造方法
CN103012284A (zh) * 2012-12-26 2013-04-03 无锡捷化医药科技有限公司 一种2-氨基-5-溴嘧啶类化合物的制备方法
US9441008B2 (en) 2014-12-08 2016-09-13 Hoffmann-La Roche Inc. 3-substituted 5-amino-6H-thiazolo[4,5-D]pyrimidine-2,7-dione compounds for the treatment and prophylaxis of virus infection
CN110139868B (zh) 2017-01-06 2021-07-09 豪夫迈·罗氏有限公司 制备3-取代的5-氨基-6H-噻唑并[4,5-d]嘧啶-2,7-二酮化合物的方法
CN111635368B (zh) * 2020-06-12 2021-06-29 东莞市东阳光仿制药研发有限公司 一种胺化合物的制备方法

Family Cites Families (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4643992A (en) 1982-11-09 1987-02-17 Scripps Clinic And Research Foundation Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives
US4539205A (en) 1982-11-09 1985-09-03 Scripps Clinic And Research Foundation Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives
US5166141A (en) 1983-11-01 1992-11-24 Scripps Clinic And Research Foundation Immunostimulating 7-deaza-7-oxa- and 7-deaza-7-oxo-analogs of 8-substituted-guanine-9-(1'-beta-D-aldoglycosidyl) derivatives and methods of treating test animals
US4746651A (en) 1983-11-01 1988-05-24 Scripps Clinic And Research Foundation Antimicrobial chemotherapeutic potentiation using substituted nucleoside derivatives
US5011828A (en) 1985-11-15 1991-04-30 Michael Goodman Immunostimulating guanine derivatives, compositions and methods
GB8712745D0 (en) 1987-05-30 1987-07-01 Wellcome Found Antiviral compounds
US5041426A (en) 1987-12-21 1991-08-20 Brigham Young University Immune system enhancing 3-β-d-ribofuranosylthiazolo[4,5-d]pyridimine nucleosides and nucleotides
US4880784A (en) 1987-12-21 1989-11-14 Brigham Young University Antiviral methods utilizing ribofuranosylthiazolo[4,5-d]pyrimdine derivatives
US5041542A (en) 1988-06-03 1991-08-20 Nucleic Acid Research Institute Substituted pyrimido[5,4-d]pyrimidine nucleosides
GB9015914D0 (en) 1990-07-19 1990-09-05 Wellcome Found Heterocyclic compounds
US5248672A (en) 1990-11-01 1993-09-28 The Regents Of The University Of Michigan Polysubstituted benzimidazole nucleosides as antiviral agents
GB9105899D0 (en) 1991-03-20 1991-05-08 Wellcome Found Therapeutic nucleosides
AU5165793A (en) 1992-10-01 1994-04-26 Mcneilab, Inc. Derivatives of 7,8-disubstituted guanosines
GB9301000D0 (en) 1993-01-20 1993-03-10 Glaxo Group Ltd Chemical compounds
US5395937A (en) 1993-01-29 1995-03-07 Minnesota Mining And Manufacturing Company Process for preparing quinoline amines
US5446045A (en) 1993-12-20 1995-08-29 Revankar; Ganapathi R. Antiviral guanine analogs
US5994321A (en) 1993-12-20 1999-11-30 Aronex Pharmaceuticals, Inc. Antiviral guanine analogs
US5496816A (en) 1994-03-14 1996-03-05 Merck & Co., Inc. Carbapenem antibacterial compounds, compositions containing such compounds and methods of treatment
EP0882727B9 (en) 1996-07-03 2005-06-15 Sumitomo Pharmaceuticals Company, Limited Novel purine derivatives
US6509320B1 (en) 1996-10-16 2003-01-21 Icn Pharmaceuticals, Inc. Purine L-nucleosides, analogs and uses thereof
HUP0001186A3 (en) 1996-10-16 2002-04-29 Icn Pharmaceuticals Inc Costa Purine l-nucleosides,analogs and pharmaceutical compositions thereof
NZ335124A (en) 1996-10-25 2001-02-23 Minnesota Mining & Mfg Immune response modifier compounds for treatment of TH2 mediated and related diseases
US6329381B1 (en) 1997-11-28 2001-12-11 Sumitomo Pharmaceuticals Company, Limited Heterocyclic compounds
TW572758B (en) 1997-12-22 2004-01-21 Sumitomo Pharma Type 2 helper T cell-selective immune response inhibitors comprising purine derivatives
JP2002510695A (ja) * 1998-04-03 2002-04-09 デュポン ファーマシューティカルズ カンパニー 副腎皮質刺激ホルモン放出因子(CRF)拮抗剤としてのチアゾロ[4,5−d]ピリミジンおよびピリジン
US6444652B1 (en) 1998-08-10 2002-09-03 Novirio Pharmaceuticals Limited β-L-2'-deoxy-nucleosides for the treatment of hepatitis B
US6667312B2 (en) 2000-12-08 2003-12-23 3M Innovative Properties Company Thioether substituted imidazoquinolines
US6664260B2 (en) 2000-12-08 2003-12-16 3M Innovative Properties Company Heterocyclic ether substituted imidazoquinolines
US6664264B2 (en) 2000-12-08 2003-12-16 3M Innovative Properties Company Thioether substituted imidazoquinolines
US6545016B1 (en) 2000-12-08 2003-04-08 3M Innovative Properties Company Amide substituted imidazopyridines
US6545017B1 (en) 2000-12-08 2003-04-08 3M Innovative Properties Company Urea substituted imidazopyridines
US20020086871A1 (en) 2000-12-29 2002-07-04 O'neill Brian Thomas Pharmaceutical composition for the treatment of CNS and other disorders
ATE404561T1 (de) 2001-04-17 2008-08-15 Dainippon Sumitomo Pharma Co Neue adeninderivate
YU45204A (sh) 2001-11-27 2006-08-17 Anadys Pharmaceuticals Inc. 3-BETA-D-RIBOFURANOZILTIAZOLO/4,5-d/ PIRIMIDINSKI NUKLEOZIDII NJIHOVA UPOTREBA
US7321033B2 (en) * 2001-11-27 2008-01-22 Anadys Pharmaceuticals, Inc. 3-B-D-ribofuranosylthiazolo [4,5-d] pyrimidine nucleosides and uses thereof
BR0309581A (pt) 2002-05-06 2005-03-29 Genelabs Tech Inc Derivados de nucleosìdeo para tratamento de infecção por vìrus de hepatite c
PA8577501A1 (es) * 2002-07-25 2004-02-07 Warner Lambert Co Inhibidores de quinasas
WO2005016235A2 (en) 2003-04-14 2005-02-24 The Regents Of The University Of California Combined use of impdh inhibitors with toll-like receptor agonists
AU2004247559B2 (en) * 2003-06-12 2009-08-27 Astellas Pharma Inc. Benzamide derivative or salt thereof
WO2005025583A2 (en) 2003-09-05 2005-03-24 Anadys Pharmaceuticals, Inc. Tlr7 ligands for the treatment of hepatitis c
AU2005221140A1 (en) * 2004-03-08 2005-09-22 Amgen Inc. Therapeutic modulation of PPAR (gamma) activity
JP2008516978A (ja) 2004-10-15 2008-05-22 バイエル・フアーマシユーチカルズ・コーポレーシヨン 肥満症の処置のためのビフェニル−4−イル−カルボニルアミノ酸誘導体の製造および使用
PL1824482T3 (pl) * 2004-12-17 2014-07-31 Anadys Pharmaceuticals Inc 3,5-Dipodstawione oraz 3,5,7-tripodstawione związki 3H-oksazolo- oraz 3H-tiazolo[4,5-d]pirymidyn-2-onowe i ich proleki
JP2008540549A (ja) 2005-05-09 2008-11-20 ハイドラ バイオサイエンシズ インコーポレイテッド Trpv3機能調節用化合物
US7709448B2 (en) 2006-06-22 2010-05-04 Anadys Pharmaceuticals, Inc. Prodrugs of 5-amino-3-(3′-deoxy-β-D-ribofuranosyl)-thiazolo[4,5-d]pyrimidin-2,7-dione
JP5225991B2 (ja) 2006-07-18 2013-07-03 アナディス ファーマシューティカルズ インク チアゾロ[4,5−d]ピリミジンのカーボネート及びカルバメートプロドラッグ

Also Published As

Publication number Publication date
DE602006015700D1 (de) 2010-09-02
CA2630463A1 (en) 2007-05-31
KR20080090400A (ko) 2008-10-08
BRPI0618789A2 (pt) 2016-08-30
JP5117391B2 (ja) 2013-01-16
WO2007062355A2 (en) 2007-05-31
ATE474842T1 (de) 2010-08-15
NO20082365L (no) 2008-08-18
EP1973920B1 (en) 2010-07-21
US7781581B2 (en) 2010-08-24
EP1973920A2 (en) 2008-10-01
SG152296A1 (en) 2009-05-29
CN101365705A (zh) 2009-02-11
CA2630463C (en) 2015-01-06
JP2009516709A (ja) 2009-04-23
EA200801404A1 (ru) 2008-10-30
WO2007062355A3 (en) 2007-07-26
TWI383987B (zh) 2013-02-01
AU2006318260B2 (en) 2012-05-17
AU2006318260A1 (en) 2007-05-31
TW200736265A (en) 2007-10-01
ES2345904T3 (es) 2010-10-05
US20070117979A1 (en) 2007-05-24
IL191568A0 (en) 2008-12-29

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