MX2009004028A - Sal acido p-toluensulfonico de 5-amino-3-(2'-o-acetil-3'-desoxi-be ta-d-ribofuranosil)-3h-tiazolo[4,5-d]pirimidin-2-ona y metodos de preparacion. - Google Patents

Sal acido p-toluensulfonico de 5-amino-3-(2'-o-acetil-3'-desoxi-be ta-d-ribofuranosil)-3h-tiazolo[4,5-d]pirimidin-2-ona y metodos de preparacion.

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Publication number
MX2009004028A
MX2009004028A MX2009004028A MX2009004028A MX2009004028A MX 2009004028 A MX2009004028 A MX 2009004028A MX 2009004028 A MX2009004028 A MX 2009004028A MX 2009004028 A MX2009004028 A MX 2009004028A MX 2009004028 A MX2009004028 A MX 2009004028A
Authority
MX
Mexico
Prior art keywords
ribofuranosyl
deoxy
acetyl
amino
sulfonic acid
Prior art date
Application number
MX2009004028A
Other languages
English (en)
Inventor
Fritz Blatter
Gregory J Haley
Erik J Rueden
David Kucera
Tingmin Wag
Martin Viertelhaus
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 MX2009004028A publication Critical patent/MX2009004028A/es

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    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/20Antivirals for DNA viruses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D307/18Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings 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
    • C07D307/20Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04Ortho-condensed systems
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Virology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Molecular Biology (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

La presente invención se refiere a la sal ácido p-toluensulfónico de 5-amino-3-(2´-O-acetil-3´-desoxi-ß-D-ribo-furanosil)-3H-tiazolo [4,5-d]pirimidin-2-ona y a su uso en el tratamiento de condiciones tales como infecciones virales, tumores y cáncer. Se describe también un método para preparar la sal ácido p-toluensulfónico de 5-amino-3-(2´-O-acetil-3´-desoxi-ß-D-ribofura nosil)-3H-tiazolo[4,5-d]pirimidin-2-ona y métodos para producir compuestos de furanosa que son intermediarios útiles en la preparación de compuestos farmacéuticos tales como sal ácido p-toluensulfónico de 5-amino-3-(2´-O-acetil-3´-desoxi-ß-D-ribofura nosil)-3H-tiazolo[4,5-d]pirimidin-2-ona y similares.
MX2009004028A 2006-10-17 2007-10-16 Sal acido p-toluensulfonico de 5-amino-3-(2'-o-acetil-3'-desoxi-be ta-d-ribofuranosil)-3h-tiazolo[4,5-d]pirimidin-2-ona y metodos de preparacion. MX2009004028A (es)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US85200206P 2006-10-17 2006-10-17
US89940507P 2007-02-05 2007-02-05
US95359707P 2007-08-02 2007-08-02
PCT/US2007/081526 WO2008140549A1 (en) 2006-10-17 2007-10-16 P-TOLUENE SULFONIC ACID SALT OF 5-AMINO-3-(2'-O-ACETYL-3'-DEOXY-β-D-RIBOFURANOSYL)-3H-THIAZOLE [4, 5-D] PYRIMIDINE-2-ONE AND METHODS FOR PREPARATION

Publications (1)

Publication Number Publication Date
MX2009004028A true MX2009004028A (es) 2009-05-11

Family

ID=39472747

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2009004028A MX2009004028A (es) 2006-10-17 2007-10-16 Sal acido p-toluensulfonico de 5-amino-3-(2'-o-acetil-3'-desoxi-be ta-d-ribofuranosil)-3h-tiazolo[4,5-d]pirimidin-2-ona y metodos de preparacion.

Country Status (25)

Country Link
US (2) US7928085B2 (es)
EP (1) EP2076132B1 (es)
JP (2) JP5279715B2 (es)
KR (2) KR101486444B1 (es)
AR (1) AR063484A1 (es)
AU (1) AU2007353381B2 (es)
BR (1) BRPI0717741A2 (es)
CA (2) CA2666537C (es)
CY (1) CY1113368T1 (es)
DK (1) DK2076132T3 (es)
DO (1) DOP2007000131A (es)
EA (1) EA017005B1 (es)
ES (1) ES2390930T3 (es)
HK (1) HK1132429A1 (es)
IL (2) IL198180A (es)
MX (1) MX2009004028A (es)
MY (1) MY150408A (es)
NO (1) NO20091598L (es)
NZ (1) NZ576408A (es)
PE (1) PE20081105A1 (es)
PL (1) PL2076132T3 (es)
PT (1) PT2076132E (es)
TW (1) TWI415854B (es)
UY (1) UY30650A1 (es)
WO (1) WO2008140549A1 (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101461604B1 (ko) 2006-06-22 2014-11-18 애나디스 파마슈티칼스, 인코포레이티드 5-아미노-3-(3''-데옥시-β-D-리보퓨라노실)-티아졸로[4,5-d]파이리미딘-2,7-다이온의 프로드럭
US20110166092A1 (en) * 2007-08-20 2011-07-07 Anadys Pharmaceuticals, Inc. Dosing methods for treating disease
UA124184C2 (uk) 2014-12-08 2021-08-04 Ф. Хоффманн-Ля Рош Аг 3-ЗАМІЩЕНІ 5-АМІНО-6H-ТІАЗОЛО[4,5-d]ПІРИМІДИН-2,7-ДІОНОВІ СПОЛУКИ ДЛЯ ЛІКУВАННЯ І ПРОФІЛАКТИКИ ВІРУСНИХ ІНФЕКЦІЙ
US9676793B2 (en) 2014-12-23 2017-06-13 Hoffmann-Laroche Inc. Co-crystals of 5-amino-2-oxothiazolo[4,5-d]pyrimidin-3(2H)-yl-5-hydroxymethyl tetrahydrofuran-3-yl acetate and methods for preparing and using the same
EP3845227A1 (en) 2015-03-16 2021-07-07 F. Hoffmann-La Roche AG Combined treatment with a tlr7 agonist and an hbv capsid assembly inhibitor
CN107743491B (zh) 2015-05-08 2020-08-21 豪夫迈·罗氏有限公司 用于治疗和预防病毒感染的新的氧硫杂环戊烷甲酸及其衍生物
EP3294746B1 (en) 2015-05-12 2021-10-06 F. Hoffmann-La Roche AG Substituted aminothiazolopyrimidinedione derivatives for the treatment and prophylaxis of virus infection
JP6839104B2 (ja) 2015-06-30 2021-03-03 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft ウイルス感染の治療及び予防のための新規な置換アミノチアゾロピリミジンジオン
EP3568400A1 (en) * 2017-01-06 2019-11-20 H. Hoffnabb-La Roche Ag PROCESS FOR THE PREPARATION OF 3-SUBSTITUTED 5-AMINO-6H-THIAZOLO[4,5-d]PYRIMIDINE-2-7-DIONE COMPOUNDS
CN110007010A (zh) * 2018-01-05 2019-07-12 大鹏药品工业株式会社 源自曲氟尿苷的类似物质的检测方法

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07224081A (ja) * 1994-02-10 1995-08-22 Kobayashi Koryo Kk デオキシリボフラノシルハライド誘導体の製造方法
US5532374A (en) * 1995-06-06 1996-07-02 Hitachi Chemical Company, Ltd. Method of preparation of bis-quinolines
JP4067226B2 (ja) * 1999-04-01 2008-03-26 三井化学株式会社 1―ハロゲノ−2−デオキシリボフラノース誘導体の製造方法
JP2000327693A (ja) * 1999-05-21 2000-11-28 Mitsui Chemicals Inc 2’−デオキシ−β−シチジン誘導体の製造方法
US6649761B2 (en) 2001-05-30 2003-11-18 Merck & Co., Inc. Process for preparing piperazinepentaneamide HIV protease inhibitors
KR100718371B1 (ko) * 2001-11-27 2007-05-14 애나디스 파마슈티칼스, 인코포레이티드 3-β-D-리보푸라노실티아졸로[4,5-d]피리디민누클레오시드 및 이의 용도
WO2004052892A1 (en) 2002-12-09 2004-06-24 Texcontor Etablissement Anhydrous crystalline form of valacyclovir hydrochloride
ES2342069T4 (es) * 2003-09-05 2011-01-26 Anadys Pharmaceuticals, Inc. Ligandos de tlr7 para el tratamiento de la hepatitis c.
US20080070852A1 (en) * 2004-06-07 2008-03-20 Averett Devron R 3-Beta-D-Ribofuranosylthiazolo[ 4,5-D] Pyridimine Nucleosides and Uses Thereof
AR052995A1 (es) * 2004-12-17 2007-04-18 Anadys Pharmaceuticals Inc Compuestos de 3h-oxazolo y 3h-tiazolo[4, 5 - d]pirimidin-2-ona3, 5-disustituidos y 3, 5, 7-trisustituidos con actividad inmunomoduladora, sus profarmacos, composiciones farmaceuticas que los contienen y su empleo en el tratamiento de enfermedades de origen viral
US7501526B2 (en) * 2005-01-20 2009-03-10 Taigen Biotechnology Synthesis of polyamine compounds
KR101461604B1 (ko) 2006-06-22 2014-11-18 애나디스 파마슈티칼스, 인코포레이티드 5-아미노-3-(3''-데옥시-β-D-리보퓨라노실)-티아졸로[4,5-d]파이리미딘-2,7-다이온의 프로드럭
JP5550234B2 (ja) * 2006-12-08 2014-07-16 株式会社エーピーアイ コーポレーション フラノース誘導体の製造方法

Also Published As

Publication number Publication date
KR20090074237A (ko) 2009-07-06
CA2666537A1 (en) 2008-11-20
EP2076132A1 (en) 2009-07-08
JP5703334B2 (ja) 2015-04-15
KR101515077B1 (ko) 2015-04-24
IL223126A (en) 2016-08-31
KR20140119203A (ko) 2014-10-08
CY1113368T1 (el) 2016-06-22
PT2076132E (pt) 2012-10-03
UY30650A1 (es) 2008-05-31
WO2008140549A1 (en) 2008-11-20
EP2076132A4 (en) 2011-05-04
US7928085B2 (en) 2011-04-19
AR063484A1 (es) 2009-01-28
EA017005B1 (ru) 2012-09-28
MY150408A (en) 2014-01-15
JP2010506947A (ja) 2010-03-04
US20110172447A1 (en) 2011-07-14
AU2007353381A1 (en) 2008-11-20
PL2076132T3 (pl) 2013-01-31
IL198180A0 (en) 2009-12-24
PE20081105A1 (es) 2008-08-15
JP2013166782A (ja) 2013-08-29
BRPI0717741A2 (pt) 2014-04-08
DK2076132T3 (da) 2012-09-10
JP5279715B2 (ja) 2013-09-04
DOP2007000131A (es) 2008-09-15
AU2007353381B2 (en) 2013-07-04
NO20091598L (no) 2009-07-10
IL223126A0 (en) 2012-12-31
CA2666537C (en) 2015-12-08
KR101486444B1 (ko) 2015-01-26
EA200970387A1 (ru) 2009-10-30
IL198180A (en) 2015-06-30
EP2076132B1 (en) 2012-07-11
CA2898225A1 (en) 2008-11-20
ES2390930T3 (es) 2012-11-19
TWI415854B (zh) 2013-11-21
US8193342B2 (en) 2012-06-05
US20090197826A1 (en) 2009-08-06
HK1132429A1 (es) 2010-02-26
NZ576408A (en) 2012-04-27
TW200833699A (en) 2008-08-16

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