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.Info
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic 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
- C07D513/02—Heterocyclic 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
- C07D513/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic 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
- A61K31/425—Thiazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic 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
- C07D307/18—Heterocyclic 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
- C07D307/20—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic 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
- C07D417/02—Heterocyclic 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
- C07D417/04—Heterocyclic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic 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
- C07D513/02—Heterocyclic 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
Landscapes
- 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.
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)
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)
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 |
-
2007
- 2007-10-06 BR BRPI0717741-0A2A patent/BRPI0717741A2/pt not_active Application Discontinuation
- 2007-10-16 KR KR1020097010038A patent/KR101486444B1/ko active IP Right Grant
- 2007-10-16 DK DK07873546.1T patent/DK2076132T3/da active
- 2007-10-16 PE PE2007001399A patent/PE20081105A1/es not_active Application Discontinuation
- 2007-10-16 AU AU2007353381A patent/AU2007353381B2/en not_active Ceased
- 2007-10-16 KR KR1020147026217A patent/KR101515077B1/ko active IP Right Grant
- 2007-10-16 ES ES07873546T patent/ES2390930T3/es active Active
- 2007-10-16 EA EA200970387A patent/EA017005B1/ru not_active IP Right Cessation
- 2007-10-16 NZ NZ576408A patent/NZ576408A/en not_active IP Right Cessation
- 2007-10-16 PL PL07873546T patent/PL2076132T3/pl unknown
- 2007-10-16 MY MYPI20091559 patent/MY150408A/en unknown
- 2007-10-16 US US11/873,202 patent/US7928085B2/en not_active Expired - Fee Related
- 2007-10-16 MX MX2009004028A patent/MX2009004028A/es active IP Right Grant
- 2007-10-16 PT PT07873546T patent/PT2076132E/pt unknown
- 2007-10-16 TW TW096138583A patent/TWI415854B/zh not_active IP Right Cessation
- 2007-10-16 JP JP2009533481A patent/JP5279715B2/ja not_active Expired - Fee Related
- 2007-10-16 EP EP07873546A patent/EP2076132B1/en not_active Not-in-force
- 2007-10-16 WO PCT/US2007/081526 patent/WO2008140549A1/en active Application Filing
- 2007-10-16 CA CA2666537A patent/CA2666537C/en not_active Expired - Fee Related
- 2007-10-16 CA CA2898225A patent/CA2898225A1/en not_active Abandoned
- 2007-10-17 AR ARP070104611A patent/AR063484A1/es unknown
- 2007-10-17 DO DO2007000131A patent/DOP2007000131A/es unknown
- 2007-10-17 UY UY30650A patent/UY30650A1/es not_active Application Discontinuation
-
2009
- 2009-04-16 IL IL198180A patent/IL198180A/en active IP Right Grant
- 2009-04-22 NO NO20091598A patent/NO20091598L/no not_active Application Discontinuation
-
2010
- 2010-01-05 HK HK10100028.4A patent/HK1132429A1/xx not_active IP Right Cessation
-
2011
- 2011-03-23 US US13/069,426 patent/US8193342B2/en active Active
-
2012
- 2012-09-28 CY CY20121100897T patent/CY1113368T1/el unknown
- 2012-11-19 IL IL223126A patent/IL223126A/en active IP Right Grant
-
2013
- 2013-05-21 JP JP2013107302A patent/JP5703334B2/ja not_active Expired - Fee Related
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MX2009004028A (es) | 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. | |
WO2006029081A3 (en) | Nucleoside-lipid conjugates, their method of preparation and uses thereof | |
EA201000552A1 (ru) | Производные пирроло[2,3-d]пиримидина в качестве ингибиторов протеинкиназы в | |
TN2009000215A1 (en) | Polymorphs of succinate salt of 2-[6-(3-amino-piperidin-1-yl)-3-methyl-2,4-dioxo-3,4-dihydro-2h-pyrimidin-1-ylmethy]-4-fluor-benzonitrile and methods of use therefor | |
EA201070929A1 (ru) | ФУРО- И ТИЕНО[3,2-c]ПИРИДИНЫ | |
BRPI0517426A (pt) | composto, processo para preparar o mesmo, composição farmacêutica, uso de um composto, e, métodos para produzir um efeito anti-proliferação celular, para produzir um efeito inibitório de cdk2, e para tratar uma doença em um animal de sangue quente | |
BRPI0513513A (pt) | composto ou um sal farmaceuticamente aceitável do mesmo, processo para preparar o mesmo, composição farmacêutica, uso de um composto ou um sal farmaceuticamente aceitável do mesmo, e, métodos para produzir um efeito inibitório de eg5 e um efeito anticáncer em um animal de sangue quente, e para tratar carcinomas em um animal de sangue quente | |
SG170828A1 (en) | Deazapurines useful as inhibitors of janus kinases | |
EA200701808A1 (ru) | Производные тетрагидроиндолона и тетрагидроиндазолона | |
WO2006066074A3 (en) | Lung-targeted drugs | |
TW200630366A (en) | Organic compounds | |
WO2006124413A3 (en) | Methods for treating drug resistant cancer | |
NO20055209L (no) | Peptabody for cancerbehandling | |
WO2007076087A3 (en) | 3-aryl-substituted quinazolones, and uses thereof | |
WO2010022201A3 (en) | Folinic acid derivatives for promoting bone growth | |
WO2010025135A3 (en) | Trimeprazine and ethopropazine derivatives for promoting bone growth | |
MX2007014297A (es) | Derivados de purina y su uso para el tratamiento de enfermedades autoinmunes. | |
WO2004060902A3 (en) | Novel nucleoside transport inhibitors | |
WO2007039919A8 (en) | Crystalline forms of anastrozole | |
EA201170702A1 (ru) | Способ получения производных дезоксирибофуранозы | |
EA200800575A1 (ru) | Производные 5-пиридинил-1-азабицикло [3.2.1] октана, их получение и их применение в терапии | |
WO2010011599A3 (en) | Pimethixene derivatives for promoting bone growth | |
WO2008087340A3 (fr) | UTILISATION D' OLIGO-β-(1,3)-GLUCANES MODIFIES POUR LE TRAITEMENT DE MALADIES DU SYSTEME IMMUNITAIRE, OLIGO-β-(1,3)-GLUCANE-(1,3)- MANNOSE, OLIGO-β-(1.3)-GLUCANE-(1,3)- MANNITOL ET LEURS DERIVES, LEURS PROCEDES DE PREPARATION ET MEDICAMENTS LES CONTENANT | |
ZA200903372B (en) | P-toluene sulfonic acid salt of 5-amino-3-(2'-O-acetyl-3'-deoxy-²-D-ribofuranosyl)-3H-thizaole [4, 5-D] pyrimidine-2-one and methods for preparation | |
WO2010019549A3 (en) | Indoprofen derivatives for promoting bone growth |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant or registration |