EE03044B1 - Nukleosiidide diastereoselektiivse sünteesi protsess - Google Patents
Nukleosiidide diastereoselektiivse sünteesi protsessInfo
- Publication number
- EE03044B1 EE03044B1 EE9400283A EE9400283A EE03044B1 EE 03044 B1 EE03044 B1 EE 03044B1 EE 9400283 A EE9400283 A EE 9400283A EE 9400283 A EE9400283 A EE 9400283A EE 03044 B1 EE03044 B1 EE 03044B1
- Authority
- EE
- Estonia
- Prior art keywords
- nucleosides
- diastereoselective synthesis
- diastereoselective
- processes
- synthesis
- Prior art date
Links
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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
-
- 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
- C07D307/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/32—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/32—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings 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
- C07D317/34—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
- C07D327/02—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms one oxygen atom and one sulfur atom
- C07D327/04—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D339/00—Heterocyclic compounds containing rings having two sulfur atoms as the only ring hetero atoms
- C07D339/02—Five-membered rings
- C07D339/06—Five-membered rings having the hetero atoms in positions 1 and 3, e.g. cyclic dithiocarbonates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D411/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D411/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D411/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
-
- 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
-
- 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)
- Organic Chemistry (AREA)
- Health & Medical Sciences (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)
- Public Health (AREA)
- Communicable Diseases (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Saccharide Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Catalysts (AREA)
- Furan Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US70337991A | 1991-05-21 | 1991-05-21 | |
| PCT/CA1992/000211 WO1992020669A1 (en) | 1991-05-21 | 1992-05-20 | Processes for the diastereoselective synthesis of nucleosides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EE03044B1 true EE03044B1 (et) | 1997-10-15 |
Family
ID=24825144
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EE9400283A EE03044B1 (et) | 1991-05-21 | 1994-10-20 | Nukleosiidide diastereoselektiivse sünteesi protsess |
Country Status (34)
| Country | Link |
|---|---|
| US (5) | US5756706A (xx) |
| EP (2) | EP0515156B1 (xx) |
| JP (3) | JP3330972B2 (xx) |
| KR (3) | KR0160144B1 (xx) |
| CN (6) | CN1035555C (xx) |
| AT (2) | ATE157662T1 (xx) |
| AU (4) | AU1691392A (xx) |
| BG (2) | BG61695B1 (xx) |
| CA (2) | CA2069063C (xx) |
| CZ (3) | CZ280857B6 (xx) |
| DE (2) | DE69208144T2 (xx) |
| DK (2) | DK0515156T3 (xx) |
| EE (1) | EE03044B1 (xx) |
| ES (2) | ES2084937T3 (xx) |
| FI (3) | FI109025B (xx) |
| GR (2) | GR3018941T3 (xx) |
| GT (1) | GT199800047A (xx) |
| HK (1) | HK132196A (xx) |
| HU (2) | HU221850B1 (xx) |
| IE (2) | IE76741B1 (xx) |
| IL (6) | IL101931A (xx) |
| MD (1) | MD1155C2 (xx) |
| MX (2) | MX9202395A (xx) |
| NO (2) | NO301010B1 (xx) |
| NZ (2) | NZ242818A (xx) |
| OA (1) | OA10212A (xx) |
| PL (3) | PL176026B1 (xx) |
| RO (1) | RO116812B1 (xx) |
| RU (4) | RU2105009C1 (xx) |
| SG (1) | SG43863A1 (xx) |
| SK (2) | SK279438B6 (xx) |
| TW (4) | TW366349B (xx) |
| WO (2) | WO1992020696A1 (xx) |
| ZA (2) | ZA923640B (xx) |
Families Citing this family (111)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6903224B2 (en) | 1988-04-11 | 2005-06-07 | Biochem Pharma Inc. | Substituted 1,3-oxathiolanes |
| US6350753B1 (en) | 1988-04-11 | 2002-02-26 | Biochem Pharma Inc. | 2-Substituted-4-substituted-1,3-dioxolanes and use thereof |
| US5684164A (en) * | 1988-04-11 | 1997-11-04 | Biochem Pharma Inc. | Processes for preparing substituted 1,3-oxathiolanes with antiviral properties |
| US5466806A (en) * | 1989-02-08 | 1995-11-14 | Biochem Pharma Inc. | Processes for preparing substituted 1,3-oxathiolanes with antiviral properties |
| EP0674634B1 (en) * | 1989-02-08 | 2003-04-16 | Biochem Pharma Inc | Process for preparing substituted 1,3-oxathiolanes with antiviral properties |
| US5827727A (en) | 1990-02-01 | 1998-10-27 | Emory University | Method of resolution of 1,3-oxathiolane nucleoside enantiomers |
| US5276151A (en) * | 1990-02-01 | 1994-01-04 | Emory University | Method of synthesis of 1,3-dioxolane nucleosides |
| US5204466A (en) * | 1990-02-01 | 1993-04-20 | Emory University | Method and compositions for the synthesis of bch-189 and related compounds |
| US6703396B1 (en) | 1990-02-01 | 2004-03-09 | Emory University | Method of resolution and antiviral activity of 1,3-oxathiolane nuclesoside enantiomers |
| US5914331A (en) * | 1990-02-01 | 1999-06-22 | Emory University | Antiviral activity and resolution of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane |
| US5587480A (en) * | 1990-11-13 | 1996-12-24 | Biochem Pharma, Inc. | Substituted 1,3-oxathiolanes and substituted 1,3-dithiolanes with antiviral properties |
| US5444063A (en) * | 1990-12-05 | 1995-08-22 | Emory University | Enantiomerically pure β-D-dioxolane nucleosides with selective anti-Hepatitis B virus activity |
| US5925643A (en) * | 1990-12-05 | 1999-07-20 | Emory University | Enantiomerically pure β-D-dioxolane-nucleosides |
| US6812233B1 (en) | 1991-03-06 | 2004-11-02 | Emory University | Therapeutic nucleosides |
| US5817667A (en) * | 1991-04-17 | 1998-10-06 | University Of Georgia Research Foudation | Compounds and methods for the treatment of cancer |
| ZA923640B (en) * | 1991-05-21 | 1993-02-24 | Iaf Biochem Int | Processes for the diastereoselective synthesis of nucleosides |
| US6005107A (en) * | 1992-12-23 | 1999-12-21 | Biochem Pharma, Inc. | Antiviral compounds |
| US6444656B1 (en) | 1992-12-23 | 2002-09-03 | Biochem Pharma, Inc. | Antiviral phosphonate nucleotides |
| GB9226879D0 (en) * | 1992-12-23 | 1993-02-17 | Iaf Biochem Int | Anti-viral compounds |
| GB9226927D0 (en) * | 1992-12-24 | 1993-02-17 | Iaf Biochem Int | Dideoxy nucleoside analogues |
| US5627160A (en) * | 1993-05-25 | 1997-05-06 | Yale University | L-2',3'-dideoxy nucleoside analogs as anti-hepatitis B (HBV) and anti-HIV agents |
| 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 |
| GB9311709D0 (en) * | 1993-06-07 | 1993-07-21 | Iaf Biochem Int | Stereoselective synthesis of nucleoside analogues using bicycle intermediate |
| US20020120130A1 (en) | 1993-09-10 | 2002-08-29 | Gilles Gosselin | 2' or 3' -deoxy and 2', 3' -dideoxy-beta-L-pentofuranonucleo-side compounds, method of preparation and application in therapy, especially as anti- viral agents |
| CA2171550C (en) | 1993-09-10 | 2008-08-26 | Raymond F. Schinazi | Nucleosides with anti-hepatitis b virus activity |
| US5587362A (en) * | 1994-01-28 | 1996-12-24 | Univ. Of Ga Research Foundation | L-nucleosides |
| IL113432A (en) * | 1994-04-23 | 2000-11-21 | Glaxo Group Ltd | Process for the diastereoselective synthesis of nucleoside analogues |
| GB9413724D0 (en) * | 1994-07-07 | 1994-08-24 | Wellcome Found | Therapeutic nucleosides |
| US6448235B1 (en) | 1994-07-11 | 2002-09-10 | University Of Virginia Patent Foundation | Method for treating restenosis with A2A adenosine receptor agonists |
| US6514949B1 (en) | 1994-07-11 | 2003-02-04 | University Of Virginia Patent Foundation | Method compositions for treating the inflammatory response |
| IL115156A (en) | 1994-09-06 | 2000-07-16 | Univ Georgia | Pharmaceutical compositions for the treatment of cancer comprising 1-(2-hydroxymethyl-1,3-dioxolan-4-yl) cytosines |
| US6391859B1 (en) | 1995-01-27 | 2002-05-21 | Emory University | [5-Carboxamido or 5-fluoro]-[2′,3′-unsaturated or 3′-modified]-pyrimidine nucleosides |
| 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 |
| US5808040A (en) * | 1995-01-30 | 1998-09-15 | Yale University | L-nucleosides incorporated into polymeric structure for stabilization of oligonucleotides |
| US5869461A (en) * | 1995-03-16 | 1999-02-09 | Yale University | Reducing toxicity of L-nucleosides with D-nucleosides |
| GB9506644D0 (en) * | 1995-03-31 | 1995-05-24 | Wellcome Found | Preparation of nucleoside analogues |
| ATE346651T1 (de) | 1995-06-07 | 2006-12-15 | Univ Emory | Nucleoside mit anti-hepatitis b virus wirksamkeit |
| KR100213932B1 (ko) * | 1995-11-02 | 1999-08-02 | 김충환 | 새로운 뉴클레오시드 유도체 및 그 제조방법 |
| GB9600143D0 (en) | 1996-01-05 | 1996-03-06 | Wellcome Found | Therapeutic compounds |
| EP0799834A1 (en) * | 1996-04-04 | 1997-10-08 | Novartis AG | Modified nucleotides |
| US6005097A (en) * | 1996-06-14 | 1999-12-21 | Vion Pharmaceuticals, Inc. | Processes for high-yield diastereoselective synthesis of dideoxynucleosides |
| US5753789A (en) * | 1996-07-26 | 1998-05-19 | Yale University | Oligonucleotides containing L-nucleosides |
| US6022876A (en) | 1996-11-15 | 2000-02-08 | Yale University | L-β-dioxolane uridine analogs and methods for treating and preventing Epstein-Barr virus infections |
| CA2280761A1 (en) | 1997-02-13 | 1998-08-20 | Stanley Dawes Chamberlain | Benzimidazole derivatives |
| JP2001518899A (ja) | 1997-04-07 | 2001-10-16 | トライアングル ファーマシューティカルズ,インコーポレイティド | 他の抗ウイルス剤との組合せにおけるmkc−442の使用 |
| DK0994890T3 (da) | 1997-06-10 | 2003-12-01 | Univ Michigan | Benzimidazolderivater |
| PL338454A1 (en) | 1997-07-30 | 2000-11-06 | Univ Michigan | Lixofuranosilbenzimidazoles as antiviral agents |
| US20030220234A1 (en) * | 1998-11-02 | 2003-11-27 | Selvaraj Naicker | Deuterated cyclosporine analogs and their use as immunodulating agents |
| YU44900A (sh) | 1998-01-31 | 2003-01-31 | Glaxo Group Limited | Derivati 2-(purin-9-il)tetrahidrofuran-3,4-diola |
| CN1141305C (zh) | 1998-08-12 | 2004-03-10 | 三角药物公司 | 生产1,3-氧硫戊环核苷的方法 |
| US6979561B1 (en) | 1998-10-09 | 2005-12-27 | Gilead Sciences, Inc. | Non-homogeneous systems for the resolution of enantiomeric mixtures |
| OA11741A (en) | 1998-12-23 | 2005-05-13 | Iaf Biochem Int | Antiviral nucleoside analogues. |
| US7635690B2 (en) | 1999-01-22 | 2009-12-22 | Emory University | HIV-1 mutations selected for by β-2′,3′-didehydro-2′,3′-dideoxy-5-fluorocytidine |
| US7115584B2 (en) | 1999-01-22 | 2006-10-03 | Emory University | HIV-1 mutations selected for by β-2′,3′-didehydro-2′,3′-dideoxy-5-fluorocytidine |
| US7427606B2 (en) * | 1999-02-01 | 2008-09-23 | University Of Virginia Patent Foundation | Method to reduce inflammatory response in transplanted tissue |
| US7378400B2 (en) * | 1999-02-01 | 2008-05-27 | University Of Virginia Patent Foundation | Method to reduce an inflammatory response from arthritis |
| US6232297B1 (en) | 1999-02-01 | 2001-05-15 | University Of Virginia Patent Foundation | Methods and compositions for treating inflammatory response |
| YU25500A (sh) | 1999-05-11 | 2003-08-29 | Pfizer Products Inc. | Postupak za sintezu analoga nukleozida |
| US6322771B1 (en) | 1999-06-18 | 2001-11-27 | University Of Virginia Patent Foundation | Induction of pharmacological stress with adenosine receptor agonists |
| DE60011637T2 (de) * | 1999-09-24 | 2004-11-11 | Shire Biochem Inc., Laval | Dioxolan nukleosidanalogen zur behandlung und vorbeugung von viralen infektionen |
| AU1262001A (en) | 1999-11-04 | 2001-05-14 | Biochem Pharma Inc. | Method for the treatment or prevention of flaviviridae viral infection using nucleoside analogues |
| US6436948B1 (en) | 2000-03-03 | 2002-08-20 | University Of Georgia Research Foundation Inc. | Method for the treatment of psoriasis and genital warts |
| CA2308559C (en) * | 2000-05-16 | 2005-07-26 | Brantford Chemicals Inc. | 1,3-oxathiolan-5-ones useful in the production of antiviral nucleoside analogues |
| JP5105689B2 (ja) | 2001-03-01 | 2012-12-26 | ギリード・サイエンシズ・インコーポレーテッド | 多形型および他の結晶型のシス−ftc |
| CA2351049C (en) | 2001-06-18 | 2007-03-13 | Brantford Chemicals Inc. | Process for recovery of the desired cis-1,3-oxathiolane nucleosides from their undesired trans-isomers |
| JP4514452B2 (ja) * | 2001-10-01 | 2010-07-28 | ユニバーシティ オブ バージニア パテント ファウンデーション | A2aアゴニスト活性を有する2−プロピルアデノシン・アナログおよびその組成物 |
| CN100334106C (zh) * | 2001-10-19 | 2007-08-29 | 伊索泰克尼卡股份有限公司 | 环孢菌素类似物的合成 |
| ITMI20012317A1 (it) * | 2001-11-06 | 2003-05-06 | Recordati Ind Chimica E Farma | Processo diastereoselettivo per la preparazione del'agente antivirale4-amino-1-(2r-idrossimetil-/1,3/ossatiolan-5s-i1)-1h-pirimidin-2-one |
| CN1620295A (zh) * | 2001-12-14 | 2005-05-25 | 法玛塞特有限公司 | 制备用于合成抗病毒核苷的中间体 |
| JP4441265B2 (ja) | 2002-01-25 | 2010-03-31 | シャー バイオケム インコーポレイティッド | ジオキソランヌクレオシド類似体の製造方法 |
| US7365173B2 (en) * | 2002-02-04 | 2008-04-29 | American National Red Cross | Method for the production of pure virally inactivated butyrylcholinesterase |
| US6855821B2 (en) | 2002-08-06 | 2005-02-15 | Pharmasset, Ltd. | Processes for preparing 1,3-dioxolane nucleosides |
| US20040224917A1 (en) | 2003-01-14 | 2004-11-11 | Gilead Sciences, Inc. | Compositions and methods for combination antiviral therapy |
| ITMI20030578A1 (it) * | 2003-03-24 | 2004-09-25 | Clariant Lsm Italia Spa | Processo ed intermedi per la preparazione di emtricitabina |
| EP1720840B1 (en) | 2004-02-03 | 2016-02-03 | Emory University | Methods to manufacture 1,3-dioxolane nucleosides |
| CA2576826C (en) * | 2004-08-02 | 2014-09-30 | University Of Virginia Patent Foundation | 2-propynyl adenosine analogs with modified 5'-ribose groups having a2a agonist activity |
| US7442687B2 (en) * | 2004-08-02 | 2008-10-28 | The University Of Virginia Patent Foundation | 2-polycyclic propynyl adenosine analogs having A2A agonist activity |
| US7576069B2 (en) * | 2004-08-02 | 2009-08-18 | University Of Virginia Patent Foundation | 2-polycyclic propynyl adenosine analogs having A2A agonist activity |
| US7970631B2 (en) * | 2004-08-31 | 2011-06-28 | Ethicon Endo-Surgery, Inc. | Medical effector system |
| US7250416B2 (en) | 2005-03-11 | 2007-07-31 | Supergen, Inc. | Azacytosine analogs and derivatives |
| RU2430919C2 (ru) * | 2005-03-14 | 2011-10-10 | Шайр Канада Инк. | Способы получения оптически активного цис-2-гидроксиметил-4-(цитозин-1'-ил)-1,3-оксатиолана или его фармацевтически приемлемых солей |
| TWI471145B (zh) | 2005-06-13 | 2015-02-01 | Bristol Myers Squibb & Gilead Sciences Llc | 單一式藥學劑量型 |
| TWI375560B (en) | 2005-06-13 | 2012-11-01 | Gilead Sciences Inc | Composition comprising dry granulated emtricitabine and tenofovir df and method for making the same |
| US7700567B2 (en) | 2005-09-29 | 2010-04-20 | Supergen, Inc. | Oligonucleotide analogues incorporating 5-aza-cytosine therein |
| WO2007077505A2 (en) * | 2005-12-30 | 2007-07-12 | Ranbaxy Laboratories Limited | Crystalline l-menthyl (2r, 5s)-5-(4-amino-5-fluoro-2-oxo-2h-pyrimidin-1-yl)[1, 3]oxathiolan-2-carboxylate and process for preparation thereof |
| WO2007120972A2 (en) * | 2006-02-10 | 2007-10-25 | University Of Virginia Patent Foundation | Method to treat sickle cell disease |
| US8188063B2 (en) * | 2006-06-19 | 2012-05-29 | University Of Virginia Patent Foundation | Use of adenosine A2A modulators to treat spinal cord injury |
| CA2667891A1 (en) * | 2006-10-30 | 2008-05-08 | Lupin Limited | An improved process for the manufacture of lamivudine |
| JP2010540556A (ja) | 2007-09-26 | 2010-12-24 | マウント サイナイ スクール オブ メディシン | アザシチジン類似体およびその使用 |
| CN101918416A (zh) * | 2007-11-29 | 2010-12-15 | 兰贝克赛实验室有限公司 | 制备取代的1,3-氧硫杂环戊烷,尤其是拉米夫定的方法和中间体 |
| AU2008331166B2 (en) * | 2007-11-29 | 2013-10-10 | Ranbaxy Laboratories Limited | Process for the preparation of substituted 1,3-oxathiolanes |
| US8350030B2 (en) | 2007-12-07 | 2013-01-08 | Matrix Laboratories Limited | Process for producing 5-fluoro-1-(2R, 5S)-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]cytosine |
| US8058259B2 (en) * | 2007-12-20 | 2011-11-15 | University Of Virginia Patent Foundation | Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9H-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as A2AR agonists |
| HRP20151357T1 (hr) | 2008-05-02 | 2016-01-29 | Gilead Sciences, Inc. | Upotreba äśestica äśvrstog nosaäśa kako bi se poboljšala procesabilnost farmaceutskog agensa |
| WO2010082128A1 (en) | 2009-01-19 | 2010-07-22 | Aurobindo Pharma Limited | Process for the preparation of cis-nucleoside derivative |
| EA021313B1 (ru) | 2009-02-06 | 2015-05-29 | Джилид Сайэнс, Инк. | Таблетки для комбинированной терапии |
| CA2786227A1 (en) * | 2010-01-08 | 2011-07-14 | Hetero Research Foundation | Improved process for nucleosides |
| NZ627827A (en) | 2010-01-27 | 2016-02-26 | Viiv Healthcare Co | Antiviral combinations involving (3s, 11ar)-n-[(2,4-difluorophenyl)methyl]-2,3,5,7,11,11a-hexahydro-6-hydroxy-3-methyl-5,7-dioxo-oxazolo[3,2-a]pyrido[1,2-d]pyrazine-8-carboxamide |
| WO2011095987A1 (en) * | 2010-02-03 | 2011-08-11 | Matrix Laboratories Ltd. | Novel process for the preparation of cis-nucleoside derivative |
| PL2542551T3 (pl) | 2010-03-04 | 2015-01-30 | Ranbaxy Laboratories Ltd | Sposób stereoselektywnego otrzymywania 5-fluoro-1-(2R,SS)-[2-(hydroksymetylo)-1,3-oksatiolan--5-ylo]cytozyny |
| EP2377862A1 (en) | 2010-03-29 | 2011-10-19 | Esteve Química, S.A. | Process for obtaining emtricitabine |
| WO2011141805A2 (en) | 2010-05-14 | 2011-11-17 | Lupin Limited | An improved process for the manufacture of lamivudine |
| WO2012062835A1 (en) | 2010-11-12 | 2012-05-18 | Glaxo Wellcome Manufacturing Pte Ltd | Novel pharmaceutical compositions |
| EP2739620A1 (en) | 2011-08-05 | 2014-06-11 | Lupin Limited | A stereoselective process for preparation of 1,3-oxathiolane nucleosides |
| BR112014004779B1 (pt) | 2011-08-30 | 2022-01-18 | Astex Pharmaceuticals, Inc | Formulações de derivados de decitabina, kit e processos relacionados |
| CN103242243B (zh) * | 2013-01-08 | 2015-08-19 | 北京大学 | 一种碱基乙酸甘油醚酯分子,其化学合成方法及其在基因治疗领域的应用 |
| CN103288806A (zh) * | 2013-07-02 | 2013-09-11 | 山东大学 | 一种曲沙他滨的合成方法 |
| MX2018000016A (es) | 2015-07-02 | 2019-01-31 | Otsuka Pharma Co Ltd | Composiciones farmaceuticas liofilizadas. |
| CN105037340B (zh) * | 2015-07-14 | 2018-08-10 | 福建广生堂药业股份有限公司 | 一种拉米夫定关键中间体手性异构体杂质的制备方法 |
| MX2020001233A (es) | 2017-08-03 | 2020-07-20 | Otsuka Pharma Co Ltd | Compuesto farmaceutico y metodos de purificacion del mismo. |
| CN120665607A (zh) * | 2023-04-21 | 2025-09-19 | 中南大学 | 一种用于对映选择性反胶团萃取的手性表面活性剂 |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2895965A (en) | 1959-07-21 | Process for the production of | ||
| FR1445013A (fr) * | 1964-07-09 | 1966-07-08 | Thomae Gmbh Dr K | Procédé pour fabriquer des nouveaux acides dioxolano-2-carboxyliques |
| DE2508312A1 (de) * | 1975-02-24 | 1976-09-02 | Schering Ag | Neues verfahren zur herstellung von nucleosiden |
| US4383114A (en) * | 1977-02-09 | 1983-05-10 | Regents Of The University Of Minnesota | Adenosine deaminase resistant antiviral purine arabinonucleosides |
| US4182718A (en) | 1977-10-25 | 1980-01-08 | Monsanto Company | 1,3-Dioxolane and 1,3-dioxane polycarboxylates, and precursors thereof |
| US4212860A (en) | 1978-11-08 | 1980-07-15 | Schering Corporation | 4-O-(2,3,5-Trideoxy-5-amino-α-D-pentofuranosyl)-6-O-aminoglycosyl-1,3-diaminocyclitois, methods for their preparation, pharmaceutical formulations thereof and their use as antibacterial agents |
| US4231945A (en) * | 1978-11-08 | 1980-11-04 | Schering Corporation | S-5-(Azidomethyl or aminomethyl)-2-lower-alkoxytetrahydrofurans |
| US4479942A (en) * | 1981-08-10 | 1984-10-30 | Fujisawa Pharmaceutical Co., Ltd. | Tetrahydrofurnancarboxylic acid derivatives, processes for preparation thereof and pharmaceutical compositions thereof |
| US4855304A (en) * | 1985-01-10 | 1989-08-08 | Repligen Corporation | Dinucleoside pyrophosphates and pyrophosphate homologs as plant antivirals |
| DK363987A (da) * | 1986-08-08 | 1988-02-09 | Hoffmann La Roche | Pyrimidinderivater |
| GB8621268D0 (en) * | 1986-09-03 | 1986-10-08 | Univ Strathclyde | Separation of substances |
| US4997818A (en) * | 1987-09-21 | 1991-03-05 | The University Hospital | Therapeutic method for selectively treating terminal deoxynucleotidyl transferase-positive neoplastic leukemias and lymphomas |
| SE8704298D0 (sv) * | 1987-11-03 | 1987-11-03 | Astra Ab | Compounds for use in therapy |
| US4908440A (en) * | 1987-11-12 | 1990-03-13 | Bristol Myers Company | 2',3'-dideoxy-2'-fluoroarabinopyrimidine nucleosides |
| US4997926A (en) * | 1987-11-18 | 1991-03-05 | Scripps Clinic And Research Foundation | Deaminase-stable anti-retroviral 2-halo-2',3'-dideoxy |
| JPH022349A (ja) * | 1988-02-17 | 1990-01-08 | Takeda Chem Ind Ltd | ピリミジンアナログ耐性化遺伝子dnaおよびその用途 |
| US4904770A (en) * | 1988-03-24 | 1990-02-27 | Bristol-Myers Company | Production of 2',3'-dideoxy-2',3'-didehydronucleosides |
| NZ228645A (en) * | 1988-04-11 | 1991-09-25 | Iaf Biochem Int | 1,3-dioxolane derivatives substituted in the 5th position by a purine or pyrimidine radical; treatment of viral infections |
| US5047407A (en) * | 1989-02-08 | 1991-09-10 | Iaf Biochem International, Inc. | 2-substituted-5-substituted-1,3-oxathiolanes with antiviral properties |
| GB8815265D0 (en) * | 1988-06-27 | 1988-08-03 | Wellcome Found | Therapeutic nucleosides |
| DE3823127A1 (de) * | 1988-07-08 | 1990-01-11 | Rheinische Braunkohlenw Ag | Vorrichtung und verfahren zur reinigung von abwasser |
| US4987224A (en) * | 1988-08-02 | 1991-01-22 | University Of Georgia Research Foundation, Inc. | Method of preparation of 2',3'-dideoxynucleosides |
| DE3827134A1 (de) * | 1988-08-10 | 1990-03-15 | Bayer Ag | Substituierte triazolyl- bzw. imidazolyl-hydroxyalkyldioxolane, verfahren zu ihrer herstellung und ihre verwendung als mikrobizide, oxiranyldioxolane, dioxolanylketone, oxiranylketone und (alpha)-halogenketone als zwischenprodukte und verfahren zu deren herstellung |
| US5075225A (en) * | 1989-04-06 | 1991-12-24 | The Texas A&M University System | Process for the enzymatic synthesis of nucleosides |
| NZ233197A (en) * | 1989-04-13 | 1991-11-26 | Richard Thomas Walker | Aromatically substituted nucleotide derivatives, intermediates therefor and pharmaceutical compositions |
| NZ234534A (en) * | 1989-07-17 | 1994-12-22 | Univ Birmingham | Pyrimidine 4'-thionucleoside derivatives and their preparation; intermediates therefor |
| IE904378A1 (en) * | 1989-12-20 | 1991-07-03 | Abbott Lab | Analogs of oxetanyl purines and pyrimidines |
| US5204466A (en) * | 1990-02-01 | 1993-04-20 | Emory University | Method and compositions for the synthesis of bch-189 and related compounds |
| GB9009861D0 (en) * | 1990-05-02 | 1990-06-27 | Glaxo Group Ltd | Chemical compounds |
| GB9014090D0 (en) * | 1990-06-25 | 1990-08-15 | Zaadunie Bv | Improvements in or relating to organic compounds |
| WO1992010496A1 (en) * | 1990-12-05 | 1992-06-25 | University Of Georgia Research Foundation, Inc. | ENANTIOMERICALLY PURE β-L-(-)-1,3-OXATHIOLANE NUCLEOSIDES |
| NZ250842A (en) * | 1991-02-22 | 1996-03-26 | Univ Emory | Resolution of a racemic mixture of nucleoside enantiomers such as 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane (ftc) |
| WO1992018517A1 (en) * | 1991-04-17 | 1992-10-29 | Yale University | Method of treating or preventing hepatitis b virus |
| GB9109506D0 (en) * | 1991-05-02 | 1991-06-26 | Wellcome Found | Therapeutic nucleosides |
| ZA923640B (en) * | 1991-05-21 | 1993-02-24 | Iaf Biochem Int | Processes for the diastereoselective synthesis of nucleosides |
-
1992
- 1992-05-19 ZA ZA923640A patent/ZA923640B/xx unknown
- 1992-05-19 ZA ZA923641A patent/ZA923641B/xx unknown
- 1992-05-20 IL IL10193192A patent/IL101931A/en not_active IP Right Cessation
- 1992-05-20 CZ CZ932493A patent/CZ280857B6/cs not_active IP Right Cessation
- 1992-05-20 PL PL92309052A patent/PL176026B1/pl unknown
- 1992-05-20 CZ CZ962224A patent/CZ284975B6/cs not_active IP Right Cessation
- 1992-05-20 RU RU93058554A patent/RU2105009C1/ru not_active IP Right Cessation
- 1992-05-20 NO NO921988A patent/NO301010B1/no not_active IP Right Cessation
- 1992-05-20 NO NO921989A patent/NO300593B1/no unknown
- 1992-05-20 ES ES92304551T patent/ES2084937T3/es not_active Expired - Lifetime
- 1992-05-20 SG SG1996003228A patent/SG43863A1/en unknown
- 1992-05-20 WO PCT/CA1992/000209 patent/WO1992020696A1/en not_active Ceased
- 1992-05-20 AU AU16913/92A patent/AU1691392A/en not_active Abandoned
- 1992-05-20 PL PL92301339A patent/PL168910B1/pl not_active IP Right Cessation
- 1992-05-20 SK SK1293-93A patent/SK279438B6/sk not_active IP Right Cessation
- 1992-05-20 ES ES92304552T patent/ES2104832T3/es not_active Expired - Lifetime
- 1992-05-20 CA CA002069063A patent/CA2069063C/en not_active Expired - Lifetime
- 1992-05-20 KR KR1019920008507A patent/KR0160144B1/ko not_active Expired - Fee Related
- 1992-05-20 MD MD95-0172A patent/MD1155C2/ro unknown
- 1992-05-20 AU AU16394/92A patent/AU655973B2/en not_active Expired
- 1992-05-20 US US08/142,389 patent/US5756706A/en not_active Expired - Fee Related
- 1992-05-20 RU RU93058362A patent/RU2140925C1/ru active
- 1992-05-20 KR KR1019920008694A patent/KR100232012B1/ko not_active Expired - Lifetime
- 1992-05-20 IL IL11610992A patent/IL116109A/en not_active IP Right Cessation
- 1992-05-20 EP EP92304551A patent/EP0515156B1/en not_active Expired - Lifetime
- 1992-05-20 IL IL101932A patent/IL101932A/xx not_active IP Right Cessation
- 1992-05-20 AU AU16908/92A patent/AU1690892A/en not_active Abandoned
- 1992-05-20 IL IL116176A patent/IL116176A/en not_active IP Right Cessation
- 1992-05-20 RO RO93-01554A patent/RO116812B1/ro unknown
- 1992-05-20 CZ CZ932492A patent/CZ285220B6/cs not_active IP Right Cessation
- 1992-05-20 PL PL92301340A patent/PL170869B1/pl unknown
- 1992-05-20 SK SK1294-93A patent/SK281954B6/sk not_active IP Right Cessation
- 1992-05-20 AT AT92304552T patent/ATE157662T1/de active
- 1992-05-20 NZ NZ242818A patent/NZ242818A/en not_active IP Right Cessation
- 1992-05-20 NZ NZ242817A patent/NZ242817A/en not_active IP Right Cessation
- 1992-05-20 DE DE69208144T patent/DE69208144T2/de not_active Expired - Fee Related
- 1992-05-20 RU RU96119766/04A patent/RU2163909C2/ru not_active IP Right Cessation
- 1992-05-20 EP EP92304552A patent/EP0515157B1/en not_active Expired - Lifetime
- 1992-05-20 DK DK92304551.2T patent/DK0515156T3/da active
- 1992-05-20 DE DE69221936T patent/DE69221936T2/de not_active Expired - Lifetime
- 1992-05-20 WO PCT/CA1992/000211 patent/WO1992020669A1/en not_active Ceased
- 1992-05-20 AT AT92304551T patent/ATE133958T1/de not_active IP Right Cessation
- 1992-05-20 AU AU16395/92A patent/AU668086B2/en not_active Ceased
- 1992-05-20 HU HU9303297A patent/HU221850B1/hu active IP Right Grant
- 1992-05-20 CA CA002069024A patent/CA2069024C/en not_active Expired - Fee Related
- 1992-05-20 HU HU9303296A patent/HU223838B1/hu not_active IP Right Cessation
- 1992-05-20 DK DK92304552.0T patent/DK0515157T3/da active
- 1992-05-20 RU RU99115480/04A patent/RU2223960C2/ru active
- 1992-05-21 CN CN92103924A patent/CN1035555C/zh not_active Expired - Fee Related
- 1992-05-21 MX MX9202395A patent/MX9202395A/es unknown
- 1992-05-21 JP JP12916392A patent/JP3330972B2/ja not_active Expired - Fee Related
- 1992-05-21 CN CN92103921A patent/CN1038591C/zh not_active Expired - Lifetime
- 1992-05-21 US US08/142,387 patent/US5696254A/en not_active Expired - Lifetime
- 1992-05-21 MX MX9202404A patent/MX9202404A/es unknown
- 1992-05-21 JP JP12915592A patent/JP3229013B2/ja not_active Expired - Lifetime
- 1992-06-02 TW TW081104321A patent/TW366349B/zh not_active IP Right Cessation
- 1992-06-02 TW TW088109433A patent/TWI245046B/zh not_active IP Right Cessation
- 1992-06-02 TW TW081104323A patent/TW366350B/zh not_active IP Right Cessation
- 1992-06-02 TW TW088109374A patent/TW467907B/zh not_active IP Right Cessation
- 1992-07-01 IE IE921619A patent/IE76741B1/en not_active IP Right Cessation
- 1992-07-01 IE IE161892A patent/IE921618A1/en not_active IP Right Cessation
-
1993
- 1993-11-19 FI FI935150A patent/FI109025B/fi active
- 1993-11-19 FI FI935151A patent/FI106377B/fi not_active IP Right Cessation
- 1993-11-19 OA OA60440A patent/OA10212A/en unknown
- 1993-12-20 BG BG98310A patent/BG61695B1/bg unknown
- 1993-12-20 BG BG98311A patent/BG61696B1/bg unknown
-
1994
- 1994-10-20 EE EE9400283A patent/EE03044B1/xx unknown
-
1995
- 1995-03-10 CN CN95102412A patent/CN1050603C/zh not_active Expired - Lifetime
- 1995-06-05 US US08/464,960 patent/US5744596A/en not_active Expired - Fee Related
- 1995-06-05 US US08/460,856 patent/US5663320A/en not_active Expired - Lifetime
- 1995-06-05 US US08/464,317 patent/US5693787A/en not_active Expired - Lifetime
- 1995-11-23 IL IL11610995A patent/IL116109A0/xx unknown
- 1995-11-28 IL IL11617695A patent/IL116176A0/xx unknown
-
1996
- 1996-02-08 GR GR960400299T patent/GR3018941T3/el unknown
- 1996-07-18 HK HK132196A patent/HK132196A/en not_active IP Right Cessation
-
1997
- 1997-09-04 GR GR970400204T patent/GR3024617T3/el unknown
-
1998
- 1998-03-04 GT GT199800047A patent/GT199800047A/es unknown
- 1998-12-03 CN CN98122385A patent/CN1083450C/zh not_active Expired - Lifetime
- 1998-12-03 CN CN98122383A patent/CN1109030C/zh not_active Expired - Lifetime
- 1998-12-03 CN CN98122384A patent/CN1097049C/zh not_active Expired - Lifetime
-
1999
- 1999-07-12 KR KR1019990027976A patent/KR100242921B1/ko not_active Expired - Lifetime
-
2000
- 2000-08-29 FI FI20001900A patent/FI20001900L/fi unknown
-
2001
- 2001-05-07 JP JP2001136217A patent/JP3704055B2/ja not_active Expired - Lifetime
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EE03044B1 (et) | Nukleosiidide diastereoselektiivse sünteesi protsess | |
| RU93058554A (ru) | Способы диастереоселективного синтеза нуклеозидов | |
| RU93058362A (ru) | Способы диастереоселективного синтеза нуклеозидов, промежуточные соединения, способы получения промежуточных соединений | |
| FI101793B1 (fi) | Menetelmä uusien, terapeuttisesti käyttökelpoisten 9-purinyylifosfonihappojohdannaisten valmistamiseksi | |
| PT97478A (pt) | Processo de producao de derivados n-(3-fluoro-2-fosfonilmetoxipropilo) de bases puricas e pirimidicas heterociclicas e de composicoes farmaceuticas que os contem | |
| DK1091001T3 (da) | Fremgangsmåde til rensning af S-adenosyl-L-methionin og til fremstilling af farmaceutiske acceptable salte deraf | |
| NO974512L (no) | Fremgangsmåte for syntese av nukleosid-analoger | |
| FI960286L (fi) | Välituotteita nukleosidien diastereoselektiivisiin synteesimenetelmiin | |
| IT8721511A0 (it) | Processo per la produzione di atenololo elevata purezza |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| KB4A | Valid patent at the end of a year |
Effective date: 20021231 |
|
| KB4A | Valid patent at the end of a year |
Effective date: 20031231 |
|
| KB4A | Valid patent at the end of a year |
Effective date: 20041231 |
|
| KB4A | Valid patent at the end of a year |
Effective date: 20051231 |
|
| HC1A | Change of owner name | ||
| KB4A | Valid patent at the end of a year |
Effective date: 20061231 |
|
| KB4A | Valid patent at the end of a year |
Effective date: 20071231 |
|
| HC1A | Change of owner name | ||
| KB4A | Valid patent at the end of a year |
Effective date: 20081231 |
|
| KB4A | Valid patent at the end of a year |
Effective date: 20091231 |
|
| KB4A | Valid patent at the end of a year |
Effective date: 20101231 |