AR247891A1 - Procedimiento para preparar nuevos derivados de 2'-halometilidencitidina y uridina - Google Patents
Procedimiento para preparar nuevos derivados de 2'-halometilidencitidina y uridinaInfo
- Publication number
- AR247891A1 AR247891A1 AR89315416A AR31541689A AR247891A1 AR 247891 A1 AR247891 A1 AR 247891A1 AR 89315416 A AR89315416 A AR 89315416A AR 31541689 A AR31541689 A AR 31541689A AR 247891 A1 AR247891 A1 AR 247891A1
- Authority
- AR
- Argentina
- Prior art keywords
- formula
- uridine
- halogen
- halomethylidene
- ethenylidene
- 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
- 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
-
- 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
- A61P35/00—Antineoplastic agents
-
- 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)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
FABRICACION DE COMPUESTOS DE 2'-HALOMETILIDENCITIDINA O URIDINA DE FORMULA I EN LA QUE X1 Y X2 SON H O HALOGENO, SIENDO UNA DE ELLAS HALOGENO Y B TIENE FORMULA II DONDE Y5 ES AMINO O ALCOXILO O SALES FARMACEUTICAMENTE ACEPTABLES DE LOS MISMOS, QUE COMPRENDE LAS ETAPAS DE: A) HACER REACCIONAR UN DERIVADO DE 3, 5-0-TETRAISOPROPILIDENSILOXANO-1, 3-DIIL-2-CETONUCLEOSIDO DE FORMULA III CON UNAMETILIDENFOSFOROILIDA DE FORMULA IV EN LA QUE XHAL ES HALOGENO, XO ES XHAL O AR-SO2-, DONDE AR ES FENILO; LP ES FENIL-P(O)<, PARA OBTENER 3, 5-0-TETRAISOPROPILSILOXAN- 1, 3-DIIL-HALOMETILIDEN-NUCLEOSIDOS DE FORMULA V; B) HACERLOS REACCIONAR CON F- O ACIDOS PARA SEPARAR EL GRUPO BLOQUEANTE TETRAISOPROPILDISILOXANO PARA FORMAR LOS NUCLEOSIDOS DE FORMULA VI; C) SEPARAR EL GRUPO AR-SO2- POR AMALGAMA DE MERCURIO, AMALGAMA DE SODIO/MERCURIO O HIDRURO DE TRIBUTILESTANO/AZO-BISISOBUTILNITRILO, PARA DAR NUCLEOSIDOS DONDE XO ES H; Y D) CONVERTIR EL GRUPO ALCOXI DONDE Y5 ES AMINO O HO (CETO), HACIENDO REACCI ONAR LOS COMPUESTOS OBTENIDOS CON AMONIACO O UNA BASE.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27147988A | 1988-11-15 | 1988-11-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR247891A1 true AR247891A1 (es) | 1995-04-28 |
Family
ID=23035764
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AR89315416A AR247891A1 (es) | 1988-11-15 | 1989-11-10 | Procedimiento para preparar nuevos derivados de 2'-halometilidencitidina y uridina |
Country Status (19)
Country | Link |
---|---|
EP (1) | EP0372268B1 (es) |
JP (1) | JP2802947B2 (es) |
KR (1) | KR0144865B1 (es) |
CN (1) | CN1022248C (es) |
AR (1) | AR247891A1 (es) |
AT (1) | ATE105297T1 (es) |
AU (1) | AU621160B2 (es) |
CA (1) | CA2002648C (es) |
DE (1) | DE68915128T2 (es) |
DK (1) | DK171844B1 (es) |
ES (1) | ES2056180T3 (es) |
FI (1) | FI92588C (es) |
HU (3) | HU205134B (es) |
IE (1) | IE63563B1 (es) |
IL (1) | IL92293A (es) |
NO (1) | NO172240C (es) |
NZ (1) | NZ231365A (es) |
PT (1) | PT92309B (es) |
ZA (1) | ZA898567B (es) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6458772B1 (en) | 1909-10-07 | 2002-10-01 | Medivir Ab | Prodrugs |
KR910008800B1 (ko) * | 1987-03-19 | 1991-10-21 | 야마사 쇼오유 가부시끼가이샤 | 2'-알킬리덴 피리미딘 누클레오시드 유도체, 그 제조법, 및 그 용도 |
NZ234534A (en) * | 1989-07-17 | 1994-12-22 | Univ Birmingham | Pyrimidine 4'-thionucleoside derivatives and their preparation; intermediates therefor |
US5521163A (en) * | 1990-07-13 | 1996-05-28 | University Of Birmingham | Antiviral pyrimidine nucleosides and methods for using same |
FR2668153B1 (fr) * | 1990-10-22 | 1995-03-31 | Pasteur Merieux Serums Vacc | Nouveaux composes ribonucleosides, leur procede de preparation et les medicaments les contenant. |
WO1993022327A1 (en) * | 1992-04-23 | 1993-11-11 | Yoshitomi Pharmaceutical Industries, Ltd. | 2'-methylidenenucleoside compound and pharmaceutical use thereof |
US5589587A (en) * | 1992-05-12 | 1996-12-31 | Merrell Pharmaceuticals Inc. | Process for the preparation of ribonucleotide reductase inhibitors |
EP0640092B1 (en) * | 1992-05-12 | 1996-12-11 | Merrell Pharmaceuticals Inc. | A process for the preparation of ribonucleotide reductase inhibitors |
AU678789B2 (en) * | 1992-12-03 | 1997-06-12 | Merrell Dow Pharmaceuticals Inc. | Compositions containing acyclovir-like compounds and 2'-vinyl substituted nucleoside analogs for the treatment of viral infections |
CN1043231C (zh) * | 1994-01-07 | 1999-05-05 | 默里尔药物公司 | (E)-α-去氧-α-(氟亚甲基)胞苷的一水合物 |
US5627053A (en) * | 1994-03-29 | 1997-05-06 | Ribozyme Pharmaceuticals, Inc. | 2'deoxy-2'-alkylnucleotide containing nucleic acid |
AU2768295A (en) * | 1994-07-11 | 1996-02-09 | Hoechst Marion Roussel, Inc. | Method of treating a neoplastic disease state by conjunctive therapy with 2'-fluoromethylidene derivatives and radiation or chemotherapy |
EP0770621A4 (en) * | 1994-07-12 | 1998-01-28 | Yamasa Corp | 2'-DESOXY-2 '- (METHYLIDENE SUBSTITUTED OR NON-SUBSTITUTED) -4'-THIONUCLEOSIDE |
WO2003026675A1 (en) * | 2001-09-28 | 2003-04-03 | Idenix (Cayman) Limited | Methods and compositions for treating flaviviruses and pestiviruses using 4'-modified nucleoside |
BR0307712A (pt) * | 2002-02-14 | 2005-05-24 | Pharmasset Ltd | Composto, composição e uso dos mesmos no tratamento de infecções por flaviviridae e proliferação celular anormal |
KR20040036417A (ko) * | 2002-10-25 | 2004-04-30 | 정낙신 | 항암 활성을 갖는 티오뉴클레오시드 유도체 및 이를함유하는 약학적 조성물 |
CN100389119C (zh) * | 2004-10-27 | 2008-05-21 | 北京东华康明生物科技有限公司 | (反式)-2-脱氧-2-(氟亚甲基)-4-r酰胞苷化合物及其制备方法 |
GEP20166496B (en) | 2011-12-22 | 2016-06-27 | Alios Biopharma Inc | Substituted nucleosides, nucleotides and analogs thereof |
US9441007B2 (en) | 2012-03-21 | 2016-09-13 | Alios Biopharma, Inc. | Substituted nucleosides, nucleotides and analogs thereof |
USRE48171E1 (en) | 2012-03-21 | 2020-08-25 | Janssen Biopharma, Inc. | Substituted nucleosides, nucleotides and analogs thereof |
MX2015006248A (es) * | 2012-11-19 | 2015-08-14 | Merck Sharp & Dohme | Derivados de nucleosido 2'-alquinilo sustituido para el tratamiento de enfermedades virales. |
WO2018092107A1 (en) * | 2016-11-21 | 2018-05-24 | Munisekhar Medasani | Novel anti-viral and anti-cancer molecule |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR910008800B1 (ko) * | 1987-03-19 | 1991-10-21 | 야마사 쇼오유 가부시끼가이샤 | 2'-알킬리덴 피리미딘 누클레오시드 유도체, 그 제조법, 및 그 용도 |
-
1989
- 1989-11-09 CA CA002002648A patent/CA2002648C/en not_active Expired - Lifetime
- 1989-11-09 ZA ZA898567A patent/ZA898567B/xx unknown
- 1989-11-10 AR AR89315416A patent/AR247891A1/es active
- 1989-11-10 AU AU44611/89A patent/AU621160B2/en not_active Ceased
- 1989-11-13 IL IL9229389A patent/IL92293A/en not_active IP Right Cessation
- 1989-11-13 NZ NZ231365A patent/NZ231365A/en unknown
- 1989-11-14 PT PT92309A patent/PT92309B/pt not_active IP Right Cessation
- 1989-11-14 DK DK570089A patent/DK171844B1/da not_active IP Right Cessation
- 1989-11-14 NO NO894539A patent/NO172240C/no not_active IP Right Cessation
- 1989-11-14 IE IE365189A patent/IE63563B1/en not_active IP Right Cessation
- 1989-11-14 FI FI895417A patent/FI92588C/fi not_active IP Right Cessation
- 1989-11-14 KR KR1019890016636A patent/KR0144865B1/ko not_active IP Right Cessation
- 1989-11-14 HU HU895900A patent/HU205134B/hu not_active IP Right Cessation
- 1989-11-15 JP JP1297225A patent/JP2802947B2/ja not_active Expired - Fee Related
- 1989-11-15 EP EP89121139A patent/EP0372268B1/en not_active Expired - Lifetime
- 1989-11-15 ES ES89121139T patent/ES2056180T3/es not_active Expired - Lifetime
- 1989-11-15 DE DE68915128T patent/DE68915128T2/de not_active Expired - Fee Related
- 1989-11-15 CN CN89108557A patent/CN1022248C/zh not_active Expired - Fee Related
- 1989-11-15 AT AT8989121139T patent/ATE105297T1/de not_active IP Right Cessation
-
1994
- 1994-11-14 HU HU94P/P00045P patent/HU210343A9/hu unknown
- 1994-11-14 HU HU94P/P00045P patent/HU00045A9/hu unknown
Also Published As
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