MXPA03007853A - Metodo para la sintesis de 2',3'-didesoxi-2',3'-dideshidronucleosidos. - Google Patents
Metodo para la sintesis de 2',3'-didesoxi-2',3'-dideshidronucleosidos.Info
- Publication number
- MXPA03007853A MXPA03007853A MXPA03007853A MXPA03007853A MXPA03007853A MX PA03007853 A MXPA03007853 A MX PA03007853A MX PA03007853 A MXPA03007853 A MX PA03007853A MX PA03007853 A MXPA03007853 A MX PA03007853A MX PA03007853 A MXPA03007853 A MX PA03007853A
- Authority
- MX
- Mexico
- Prior art keywords
- dideoxy
- halonucleoside
- haloacylation
- bgr
- didehydro
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 2
- 230000015572 biosynthetic process Effects 0.000 title 1
- 238000003786 synthesis reaction Methods 0.000 title 1
- 239000002777 nucleoside Substances 0.000 abstract 2
- 238000005864 bromoacetylation reaction Methods 0.000 abstract 1
- 239000005549 deoxyribonucleoside Substances 0.000 abstract 1
- 238000010511 deprotection reaction Methods 0.000 abstract 1
- 125000000524 functional group Chemical group 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000002243 precursor Substances 0.000 abstract 1
- 238000006894 reductive elimination reaction Methods 0.000 abstract 1
- 239000002342 ribonucleoside Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/067—Pyrimidine radicals with ribosyl as the saccharide radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
-
- 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
- A61P31/10—Antimycotics
-
- 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
- A61P31/18—Antivirals for RNA viruses for HIV
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Oncology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Virology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Saccharide Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
La presente invencion es una ruta de sintesis eficiente para 2',3'-didesoxi-2',3'- dideshidro-nucleosidos a partir de precursores disponibles con la opcion de introducir grupos funcionales segun se necesite, tales como los analogos 2',3'-didesoxi y 2'- o 3'- desoxirribonucleosido asi como los derivados adicionales obtenidos por manipulaciones subsiguientes de grupo funcional. En breve, la presente invencion describe un metodo para preparar '-D- y '-L-2',3'-didesoxi-2',3'-dideshideshidro-nucleosidos partiendo de los ribonucleosidos sustituidos apropiadamente en dos, opcionalmente en tres pasos: Paso (1) una halogenoacilacion, tal como halogenoacetilacion, y en particular, bromoacetilacion; Paso (2) una eliminacion reductiva; y opcionalmente, Paso (3) una desproteccion. La halogenoacilacion del paso (1) puede formar el 2'-acil-3'-halogenonucleosido, el 3'-acil-2'-halogenonucleosido, o una mezcla de los mismos.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US27243401P | 2001-03-01 | 2001-03-01 | |
| US27244101P | 2001-03-01 | 2001-03-01 | |
| PCT/US2002/006460 WO2002070533A2 (en) | 2001-03-01 | 2002-03-01 | Method for the synthesis of 2',3'-dideoxy-2',3'-didehydronucleosides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA03007853A true MXPA03007853A (es) | 2004-05-24 |
Family
ID=26955519
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA03007853A MXPA03007853A (es) | 2001-03-01 | 2002-03-01 | Metodo para la sintesis de 2',3'-didesoxi-2',3'-dideshidronucleosidos. |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US6927291B2 (es) |
| EP (1) | EP1363927A2 (es) |
| JP (1) | JP2004527504A (es) |
| KR (1) | KR20030092006A (es) |
| CN (1) | CN1505635A (es) |
| AU (1) | AU2002255654B2 (es) |
| BR (1) | BR0207746A (es) |
| CA (1) | CA2439836A1 (es) |
| IL (1) | IL157478A0 (es) |
| MX (1) | MXPA03007853A (es) |
| NZ (1) | NZ540956A (es) |
| RU (1) | RU2003129164A (es) |
| WO (1) | WO2002070533A2 (es) |
Families Citing this family (72)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001079246A2 (en) | 2000-04-13 | 2001-10-25 | Pharmasset, Ltd. | 3'-or 2'-hydroxymethyl substituted nucleoside derivatives for treatment of hepatitis virus infections |
| MY164523A (en) | 2000-05-23 | 2017-12-29 | Univ Degli Studi Cagliari | Methods and compositions for treating hepatitis c virus |
| IL153020A0 (en) | 2000-05-26 | 2003-06-24 | Idenix Cayman Ltd | Methods and compositions for treating flaviviruses and pestiviruses |
| NZ537662A (en) | 2002-06-28 | 2007-10-26 | Idenix Cayman Ltd | 2'-C-methyl-3'-O-L-valine ester ribofuranosyl cytidine for treatment of flaviviridae infections |
| US7608600B2 (en) | 2002-06-28 | 2009-10-27 | Idenix Pharmaceuticals, Inc. | Modified 2′ and 3′-nucleoside prodrugs for treating Flaviviridae infections |
| BR0312278A (pt) | 2002-06-28 | 2007-06-19 | Idenix Cayman Ltd | éster 2'-c-metil-3'-o-l-valina de ribofuranosil citidina para tratamento de infecções por flaviviridae |
| SG174624A1 (en) | 2002-08-01 | 2011-10-28 | Pharmasset Inc | Compounds with the bicyclo[4.2.1]nonane system for the treatment of flaviviridae infections |
| BR0316363A (pt) | 2002-11-15 | 2005-10-04 | Idenix Cayman Ltd | Nucleosìdeos 2'-ramificado e mutação de flaviviridae |
| EP2319853B1 (en) | 2002-12-12 | 2014-03-12 | IDENIX Pharmaceuticals, Inc. | Process for the production of 2'-branched nucleosides |
| PL3521297T3 (pl) | 2003-05-30 | 2022-04-04 | Gilead Pharmasset Llc | Zmodyfikowane fluorowane analogi nukleozydów |
| CA2634749C (en) | 2005-12-23 | 2014-08-19 | Idenix Pharmaceuticals, Inc. | Process for preparing a synthetic intermediate for preparation of branched nucleosides |
| MX2008009022A (es) * | 2006-01-13 | 2008-09-24 | Wyeth Corp | 1h-indoles sustituidos por sulfonilo como ligandos para los receptores 5-hidroxitriptamina. |
| US7951789B2 (en) | 2006-12-28 | 2011-05-31 | Idenix Pharmaceuticals, Inc. | Compounds and pharmaceutical compositions for the treatment of viral infections |
| ATE525068T1 (de) | 2007-02-28 | 2011-10-15 | Conatus Pharmaceuticals Inc | Verfahren zur behandlung von chronischer viraler hepatitis c mithilfe von ro 113-0830 |
| WO2008106167A1 (en) * | 2007-02-28 | 2008-09-04 | Conatus Pharmaceuticals, Inc. | Combination therapy comprising matrix metalloproteinase inhibitors and caspase inhibitors for the treatment of liver diseases |
| WO2009020480A2 (en) * | 2007-04-26 | 2009-02-12 | The Scripps Research Institute | Genomic mutation inhibitors that inhibit y family dna polymerases |
| AU2009277172B2 (en) * | 2008-07-02 | 2014-05-29 | Idenix Pharmaceuticals, Inc. | Compounds and pharmaceutical compositions for the treatment of viral infections |
| JP5690286B2 (ja) | 2009-03-04 | 2015-03-25 | イデニク プハルマセウティカルス,インコーポレイテッド | ホスホチオフェン及びホスホチアゾールhcvポリメラーゼ阻害剤 |
| CA2769652A1 (en) | 2009-08-05 | 2011-02-10 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors useful against viral infections, particularly hcv |
| US20110117055A1 (en) | 2009-11-19 | 2011-05-19 | Macdonald James E | Methods of Treating Hepatitis C Virus with Oxoacetamide Compounds |
| KR20120118008A (ko) | 2009-12-18 | 2012-10-25 | 아이데닉스 파마슈티칼스, 인코포레이티드 | 5,5-융합 아릴렌 또는 헤테로아릴렌 간염 c 바이러스 억제제 |
| CA2795054A1 (en) | 2010-04-01 | 2011-10-06 | Idenix Pharmaceuticals, Inc. | Compounds and pharmaceutical compositions for the treatment of viral infections |
| WO2012080050A1 (en) | 2010-12-14 | 2012-06-21 | F. Hoffmann-La Roche Ag | Solid forms of a phenoxybenzenesulfonyl compound |
| WO2012109398A1 (en) | 2011-02-10 | 2012-08-16 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors, pharmaceutical compositions thereof, and their use for treating hcv infections |
| US20120252721A1 (en) | 2011-03-31 | 2012-10-04 | Idenix Pharmaceuticals, Inc. | Methods for treating drug-resistant hepatitis c virus infection with a 5,5-fused arylene or heteroarylene hepatitis c virus inhibitor |
| EP2691409B1 (en) | 2011-03-31 | 2018-02-21 | Idenix Pharmaceuticals LLC. | Compounds and pharmaceutical compositions for the treatment of viral infections |
| FR2978441A1 (fr) * | 2011-07-25 | 2013-02-01 | Diverchim | Nouveaux analogues de ceramides, leurs procedes de preparation et leurs applications dans les compositions pharmaceutiques et cosmetiques |
| WO2013039855A1 (en) | 2011-09-12 | 2013-03-21 | Idenix Pharmaceuticals, Inc. | Compounds and pharmaceutical compositions for the treatment of viral infections |
| US9403863B2 (en) | 2011-09-12 | 2016-08-02 | Idenix Pharmaceuticals Llc | Substituted carbonyloxymethylphosphoramidate compounds and pharmaceutical compositions for the treatment of viral infections |
| WO2013056046A1 (en) | 2011-10-14 | 2013-04-18 | Idenix Pharmaceuticals, Inc. | Substituted 3',5'-cyclic phosphates of purine nucleotide compounds and pharmaceutical compositions for the treatment of viral infections |
| ES3018133T3 (en) | 2011-11-30 | 2025-05-14 | Univ Emory | Jak inhibitors for use in the prevention or treatment of a viral disease caused by a coronaviridae |
| WO2013133927A1 (en) | 2012-02-13 | 2013-09-12 | Idenix Pharmaceuticals, Inc. | Pharmaceutical compositions of 2'-c-methyl-guanosine, 5'-[2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)thio]ethyl n-(phenylmethyl)phosphoramidate] |
| EP2852604B1 (en) | 2012-05-22 | 2017-04-12 | Idenix Pharmaceuticals LLC | 3',5'-cyclic phosphoramidate prodrugs for hcv infection |
| EP2852605B1 (en) | 2012-05-22 | 2018-01-31 | Idenix Pharmaceuticals LLC | 3',5'-cyclic phosphate prodrugs for hcv infection |
| EP2852603B1 (en) | 2012-05-22 | 2021-05-12 | Idenix Pharmaceuticals LLC | D-amino acid compounds for liver disease |
| SG11201407336PA (en) | 2012-05-25 | 2015-03-30 | Janssen Sciences Ireland Uc | Uracyl spirooxetane nucleosides |
| EP2900682A1 (en) | 2012-09-27 | 2015-08-05 | IDENIX Pharmaceuticals, Inc. | Esters and malonates of sate prodrugs |
| AU2013329521B2 (en) | 2012-10-08 | 2018-04-19 | Centre National De La Recherche Scientifique | 2'-chloro nucleoside analogs for HCV infection |
| US20140112886A1 (en) | 2012-10-19 | 2014-04-24 | Idenix Pharmaceuticals, Inc. | Dinucleotide compounds for hcv infection |
| US10723754B2 (en) | 2012-10-22 | 2020-07-28 | Idenix Pharmaceuticals Llc | 2′,4′-bridged nucleosides for HCV infection |
| WO2014078427A1 (en) | 2012-11-14 | 2014-05-22 | Idenix Pharmaceuticals, Inc. | D-alanine ester of rp-nucleoside analog |
| WO2014078436A1 (en) | 2012-11-14 | 2014-05-22 | Idenix Pharmaceuticals, Inc. | D-alanine ester of sp-nucleoside analog |
| US9211300B2 (en) | 2012-12-19 | 2015-12-15 | Idenix Pharmaceuticals Llc | 4′-fluoro nucleosides for the treatment of HCV |
| CN103936637B (zh) * | 2013-01-18 | 2016-04-06 | 北京大学 | E-3,4-二羟苯乙烯基亚砜类化合物的制备方法及其作为神经保护药物的应用 |
| US9309275B2 (en) | 2013-03-04 | 2016-04-12 | Idenix Pharmaceuticals Llc | 3′-deoxy nucleosides for the treatment of HCV |
| WO2014137930A1 (en) | 2013-03-04 | 2014-09-12 | Idenix Pharmaceuticals, Inc. | Thiophosphate nucleosides for the treatment of hcv |
| US20140271547A1 (en) | 2013-03-13 | 2014-09-18 | Idenix Pharmaceuticals, Inc. | Amino acid phosphoramidate pronucleotides of 2'-cyano, azido and amino nucleosides for the treatment of hcv |
| US9187515B2 (en) | 2013-04-01 | 2015-11-17 | Idenix Pharmaceuticals Llc | 2′,4′-fluoro nucleosides for the treatment of HCV |
| EP3004130B1 (en) | 2013-06-05 | 2019-08-07 | Idenix Pharmaceuticals LLC. | 1',4'-thio nucleosides for the treatment of hcv |
| WO2015017713A1 (en) | 2013-08-01 | 2015-02-05 | Idenix Pharmaceuticals, Inc. | D-amino acid phosphoramidate pronucleotides of halogeno pyrimidine compounds for liver disease |
| LT3041854T (lt) | 2013-08-08 | 2020-03-25 | The Scripps Research Institute | Nukleorūgščių specifinės vietos žymėjimo fermentais in vitro būdas, įvedant nenatūralius nukleotidus |
| WO2015042375A1 (en) | 2013-09-20 | 2015-03-26 | Idenix Pharmaceuticals, Inc. | Hepatitis c virus inhibitors |
| WO2015061683A1 (en) | 2013-10-25 | 2015-04-30 | Idenix Pharmaceuticals, Inc. | D-amino acid phosphoramidate and d-alanine thiophosphoramidate pronucleotides of nucleoside compounds useful for the treatment of hcv |
| EP3063165A1 (en) | 2013-11-01 | 2016-09-07 | Idenix Pharmaceuticals LLC | D-alanine phosphoramidate pronucleotides of 2'-methyl 2'-fluoro guanosine nucleoside compounds for the treatment of hcv |
| EP3074399A1 (en) | 2013-11-27 | 2016-10-05 | Idenix Pharmaceuticals LLC | 2'-dichloro and 2'-fluoro-2'-chloro nucleoside analogues for hcv infection |
| US10683321B2 (en) | 2013-12-18 | 2020-06-16 | Idenix Pharmaceuticals Llc | 4′-or nucleosides for the treatment of HCV |
| WO2015134561A1 (en) | 2014-03-05 | 2015-09-11 | Idenix Pharmaceuticals, Inc. | Pharmaceutical compositions comprising a 5,5-fused heteroarylene flaviviridae inhibitor and their use for treating or preventing flaviviridae infection |
| EP3114122A1 (en) | 2014-03-05 | 2017-01-11 | Idenix Pharmaceuticals LLC | Solid forms of a flaviviridae virus inhibitor compound and salts thereof |
| TWI638047B (zh) | 2014-04-09 | 2018-10-11 | 史基普研究協會 | 藉由核酸三磷酸酯轉運子將非天然或經修飾的核苷三磷酸酯輸入至細胞中 |
| WO2015161137A1 (en) | 2014-04-16 | 2015-10-22 | Idenix Pharmaceuticals, Inc. | 3'-substituted methyl or alkynyl nucleosides for the treatment of hcv |
| WO2017106767A1 (en) | 2015-12-18 | 2017-06-22 | The Scripps Research Institute | Production of unnatural nucleotides using a crispr/cas9 system |
| HUE060123T2 (hu) | 2016-06-24 | 2023-01-28 | Scripps Research Inst | Új nukleozid-trifoszfát-transzporter és alkalmazásai |
| EP3651774A4 (en) | 2017-07-11 | 2021-07-07 | The Scripps Research Institute | INTEGRATION OF INNATURAL NUCLEOTIDES AND APPLICATION METHODS IN VIVO |
| KR20250171416A (ko) | 2017-07-11 | 2025-12-08 | 신톡스, 인크. | 비천연 뉴클레오티드의 도입 및 그의 방법 |
| BR112020002272A2 (pt) | 2017-08-03 | 2020-07-28 | Synthorx, Inc. | conjugados de citocina para o tratamento de doenças autoimunes |
| CN112105627B (zh) | 2017-12-29 | 2024-07-02 | 斯克利普斯研究所 | 非天然碱基对组合物及使用方法 |
| TWI834636B (zh) | 2018-02-26 | 2024-03-11 | 美商欣爍克斯公司 | Il-15結合物及其用途 |
| TW202031284A (zh) | 2018-11-08 | 2020-09-01 | 美商新索思股份有限公司 | 介白素10結合物及其用途 |
| US20200246467A1 (en) | 2019-02-06 | 2020-08-06 | Synthorx, Inc. | Il-2 conjugates and methods of use thereof |
| JP7728181B2 (ja) | 2019-06-14 | 2025-08-22 | ザ スクリプス リサーチ インスティテュート | 半合成生物における複製、転写および翻訳のための試薬ならびに方法 |
| BR112022003046A8 (pt) | 2019-08-23 | 2024-02-06 | Synthorx Inc | Conjugado de il-15, seu método de preparo e seus usos, bem como composição farmacêutica e método in vitro de expansão de uma ou mais das populações de células t |
| EP4028060A1 (en) | 2019-09-10 | 2022-07-20 | Synthorx, Inc. | Il-2 conjugates and methods of use to treat autoimmune diseases |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3817982A (en) | 1971-12-29 | 1974-06-18 | Syntex Inc | 2{40 ,3{40 -unsaturated nucleosides and method of making |
| US4594339A (en) | 1982-04-06 | 1986-06-10 | Sloan-Kettering Institute For Cancer Research | Anti-herpes virus compositions containing 5-substituted 1-2'(deoxy-2-'-substituted-β-d-arabinofuranosyl)pyrimedene nucleosides |
| US5455339A (en) | 1986-05-01 | 1995-10-03 | University Of Georgia Research Foundation, Inc. | Method for the preparation of 2',3'-dideoxy and 2',3'-dideoxydide-hydro nucleosides |
| JPS6339893A (ja) | 1986-08-05 | 1988-02-20 | Daikin Ind Ltd | 5−フルオロウリジン類およびその製法 |
| US5384396A (en) | 1988-02-23 | 1995-01-24 | The University Of Georgia Research Foundation, Inc. | Process for the deoxygenation of nucleosides |
| US4904770A (en) | 1988-03-24 | 1990-02-27 | Bristol-Myers Company | Production of 2',3'-dideoxy-2',3'-didehydronucleosides |
| US5130421A (en) | 1988-03-24 | 1992-07-14 | Bristol-Myers Company | Production of 2',3'-dideoxy-2',3'-didehydronucleosides |
| US4900828A (en) | 1988-05-12 | 1990-02-13 | Hoffmann-Laroche Inc. | Intermediate compounds and an improved procedure for the synthesis of 2',3'-dideoxycytidine |
| US4987224A (en) | 1988-08-02 | 1991-01-22 | University Of Georgia Research Foundation, Inc. | Method of preparation of 2',3'-dideoxynucleosides |
| NL8901258A (nl) | 1989-05-19 | 1990-12-17 | Stichting Rega V Z W | 5-halogeno-2',3'-dideoxycytidinederivaten in geneesmiddelen voor het behandelen van retrovirus-infecties. |
| DD293498A5 (de) | 1989-07-20 | 1991-09-05 | Zi Fuer Molekularbiologie Der Adw,De | Verfahren zur herstellung eines mittels fuer die behandlung oder prophylaxe von hepatits-infektionen bei mensch und tier |
| US5212298A (en) | 1989-08-16 | 1993-05-18 | Monsanto Company | Method for producing synthetic N-linked glycoconjugates |
| US5200514A (en) | 1990-01-19 | 1993-04-06 | University Of Georgia Research Foundation, Inc. | Synthesis of 2'-deoxypyrimidine nucleosides |
| US5175267A (en) | 1990-03-02 | 1992-12-29 | University Of Georgia Research Foundation, Inc. | Stereoselective glycosylation of hetercyclic bases |
| FR2674064B1 (fr) * | 1991-03-13 | 1993-06-04 | Alsthom Gec | Dispositif de varistance et de resistance pour la chambre de coupure d'un disjoncteur. |
| JPH04295475A (ja) * | 1991-03-22 | 1992-10-20 | Japan Tobacco Inc | 2’,3’−ジデオキシ−2’,3’− ジデヒドロヌクレオシド類の製法 |
| JP3042073B2 (ja) | 1991-06-19 | 2000-05-15 | 味の素株式会社 | ヌクレオシド誘導体とその製造方法 |
| TW374087B (en) | 1993-05-25 | 1999-11-11 | Univ Yale | L-2',3'-dideoxy nucleotide analogs as anti-hepatitis B(HBV) and anti-HIV agents |
| US5539099A (en) | 1993-11-15 | 1996-07-23 | Bristol-Myers Squibb Company | Process for large-scale preparation of 2',3'-didehydro-2',3'-dideoxynucleosides |
| US5703058A (en) | 1995-01-27 | 1997-12-30 | Emory University | Compositions containing 5-fluoro-2',3'-didehydro-2',3'-dideoxycytidine or a mono-, di-, or triphosphate thereof and a second antiviral agent |
| MXPA00008348A (es) | 1998-02-25 | 2005-07-15 | Univ Emory | 2-fluronucleosidos. |
-
2002
- 2002-03-01 CN CNA028089146A patent/CN1505635A/zh active Pending
- 2002-03-01 BR BR0207746-9A patent/BR0207746A/pt not_active IP Right Cessation
- 2002-03-01 RU RU2003129164/04A patent/RU2003129164A/ru not_active Application Discontinuation
- 2002-03-01 AU AU2002255654A patent/AU2002255654B2/en not_active Ceased
- 2002-03-01 NZ NZ540956A patent/NZ540956A/en unknown
- 2002-03-01 US US10/087,112 patent/US6927291B2/en not_active Expired - Lifetime
- 2002-03-01 IL IL15747802A patent/IL157478A0/xx unknown
- 2002-03-01 KR KR10-2003-7011287A patent/KR20030092006A/ko not_active Ceased
- 2002-03-01 MX MXPA03007853A patent/MXPA03007853A/es not_active Application Discontinuation
- 2002-03-01 EP EP02725067A patent/EP1363927A2/en not_active Withdrawn
- 2002-03-01 JP JP2002569852A patent/JP2004527504A/ja active Pending
- 2002-03-01 WO PCT/US2002/006460 patent/WO2002070533A2/en not_active Ceased
- 2002-03-01 CA CA002439836A patent/CA2439836A1/en not_active Abandoned
-
2005
- 2005-07-18 US US11/182,862 patent/US20050250946A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| NZ540956A (en) | 2007-01-26 |
| WO2002070533A3 (en) | 2002-12-19 |
| CA2439836A1 (en) | 2002-09-12 |
| WO2002070533A2 (en) | 2002-09-12 |
| RU2003129164A (ru) | 2005-03-20 |
| BR0207746A (pt) | 2004-06-29 |
| CN1505635A (zh) | 2004-06-16 |
| JP2004527504A (ja) | 2004-09-09 |
| IL157478A0 (en) | 2004-03-28 |
| EP1363927A2 (en) | 2003-11-26 |
| US20020198224A1 (en) | 2002-12-26 |
| AU2002255654B2 (en) | 2008-05-15 |
| US20050250946A1 (en) | 2005-11-10 |
| US6927291B2 (en) | 2005-08-09 |
| KR20030092006A (ko) | 2003-12-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MXPA03007853A (es) | Metodo para la sintesis de 2',3'-didesoxi-2',3'-dideshidronucleosidos. | |
| WO2002071827A3 (en) | Retinoid x receptor modulators | |
| MXPA02011370A (es) | Iminoazinas substituidas. | |
| MXPA02012033A (es) | Derivados de 2-aminocarbonil-9h-purina. | |
| UA66750C2 (en) | Substituted 1-phenylpirazole 3-carboxamides, a method for the preparation thereof and intermediary compounds, pharmaceutical composition having affinity to neurotensin receptors | |
| PL358887A1 (en) | Process for the preparation of substituted octanoyl amides | |
| BR0113286A (pt) | Pirazóis substituìdos | |
| ZA200202568B (en) | Process for the synthesis of silicoaluminophosphate molecular sieves. | |
| TR200102338T2 (tr) | Siklik ikame edilmiş bağlı pirolokarbazoller ve izoindolonlar. | |
| IL160045A0 (en) | Oxopyrrolidine compounds, preparation of said compounds and their use in the manufacturing of levetiracetam and analogues | |
| DK1301526T3 (da) | Fremgangsmåde til oxidation til fremstilling af mellemproduktet 6.alpha.,9alpha.-difluor-11.beta.,17.alpha.-dihydroxy-16.alpha.-methyl-androst-1,4-dien-3-on 17.beta-carboxylsyre | |
| PL371127A1 (en) | 6-aminomorphinane derivatives, method for the production and use thereof | |
| DK1255747T3 (da) | Syntese af 3,6-dialkyl-5,6-dihydro-4-hydroxy-pyran-2-on | |
| NO20024321L (no) | Fremgangsmate for fremstilling av krystallinsk form I av kabergolin | |
| EA200300579A1 (ru) | Соединение лактама | |
| TR200503401T1 (tr) | Kuetiapin (Quetiapine) Fumarat'ın yeni polimorfları | |
| UA66866C2 (uk) | Синтез морфолінових похідних | |
| IS2486B (is) | Aralkýl-tetrahýdró-pýridín, framleiðsla þeirra oglyfjasamsetningar sem innihalda þau | |
| WO2003035651A3 (fr) | Derives de l'artemisinine, et leurs utilisations dans le traitement du paludisme | |
| WO2004069774A3 (en) | Synthesis of 13c-labelled estrogen analogues | |
| EP1529783A3 (de) | Derivative von 9,10-Dihydro-9-oxa-10-phosphaphenanthren-10-oxid | |
| CA2258539A1 (en) | Ring-fused dihydropyranes, process for the preparation and use thereof | |
| BR0206502A (pt) | Antagonistas do receptor de histamina | |
| AU6726998A (en) | Method for producing 5-aminomethyl-2-chloropyridines | |
| ID27440A (id) | Proses untuk menyiapkan penengah-penengah |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HC | Change of company name or juridical status | ||
| FA | Abandonment or withdrawal |