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)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (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 |
EP0310673B1 (en) * | 1987-03-19 | 1995-07-05 | Yamasa Shoyu Kabushiki Kaisha | 2'-alkylidenepyrimidine nucleoside derivatives, process for their preparation, and their use |
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 |
ATE146183T1 (de) * | 1992-05-12 | 1996-12-15 | Merrell Pharma Inc | Verfahren zur herstellung von ribonukleotid- reduktasehemmern |
US5589587A (en) * | 1992-05-12 | 1996-12-31 | Merrell Pharmaceuticals Inc. | Process for the preparation of ribonucleotide reductase inhibitors |
HUT72604A (en) * | 1992-12-03 | 1996-05-28 | Merrell Dow Pharma | Compositions containing acyclovir-like compounds and 2`-vinyl substituted nucleoside analogs for the treatment of viral infections |
WO1995018815A1 (en) * | 1994-01-07 | 1995-07-13 | Merrell Pharmaceuticals Inc. | Monohydrate of (e)-2'-deoxy-2'-(fluoromethylene)cytidine |
US5627053A (en) * | 1994-03-29 | 1997-05-06 | Ribozyme Pharmaceuticals, Inc. | 2'deoxy-2'-alkylnucleotide containing nucleic acid |
WO1996001638A1 (en) * | 1994-07-11 | 1996-01-25 | Hoechst Marion Roussel, Inc. | Method of treating a neoplastic disease state by conjunctive therapy with 2'-fluoromethylidene derivatives and radiation or chemotherapy |
US5811408A (en) * | 1994-07-12 | 1998-09-22 | Yamasa Corporation | 2'-deoxy-2'-(substituted or unsubstituted)methylidene-4'-thionucleosides |
JP2005536440A (ja) * | 2001-09-28 | 2005-12-02 | イデニクス(ケイマン)リミテツド | 4’位が修飾されたヌクレオシドを使用するフラビウイルスおよびペスチウイルスの治療のための方法および組成物 |
WO2003068162A2 (en) * | 2002-02-14 | 2003-08-21 | Pharmasset Ltd. | Modified fluorinated nucleoside analogues |
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 |
LT2794627T (lt) | 2011-12-22 | 2019-01-10 | Alios Biopharma, Inc. | Pakeistieji nukleozidai, nukleotidai ir jų analogai |
USRE48171E1 (en) | 2012-03-21 | 2020-08-25 | Janssen 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 |
WO2014078463A1 (en) * | 2012-11-19 | 2014-05-22 | Merck Sharp & Dohme Corp. | 2 -alkynyl substituted nucleoside derivatives for treating viral diseases |
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 |
---|---|---|---|---|
EP0310673B1 (en) * | 1987-03-19 | 1995-07-05 | Yamasa Shoyu Kabushiki Kaisha | 2'-alkylidenepyrimidine nucleoside derivatives, process for their preparation, and their use |
-
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 FI FI895417A patent/FI92588C/fi not_active IP Right Cessation
- 1989-11-14 IE IE365189A patent/IE63563B1/en not_active IP Right Cessation
- 1989-11-14 HU HU895900A patent/HU205134B/hu 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 KR KR1019890016636A patent/KR0144865B1/ko not_active IP Right Cessation
- 1989-11-15 AT AT8989121139T patent/ATE105297T1/de not_active IP Right Cessation
- 1989-11-15 DE DE68915128T patent/DE68915128T2/de not_active Expired - Fee Related
- 1989-11-15 ES ES89121139T patent/ES2056180T3/es not_active Expired - Lifetime
- 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 CN CN89108557A patent/CN1022248C/zh not_active Expired - Fee Related
-
1994
- 1994-11-14 HU HU94P/P00045P patent/HU00045A9/hu unknown
- 1994-11-14 HU HU94P/P00045P patent/HU210343A9/hu unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR247891A1 (es) | Procedimiento para preparar nuevos derivados de 2'-halometilidencitidina y uridina | |
FI104176B1 (fi) | Menetelmä nukleosidien uusien antiviraalisten forfolipidijohdannaisten valmistamiseksi | |
ES2133769T3 (es) | Procedimiento para la sintesis diastereoselectiva de analogos de nucleosidos. | |
GT199900043A (es) | Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxìlico. | |
DE69007337D1 (de) | Gaserzeugende Zusammensetzungen, die Salze der 5-Nitro-Barbitursäure oder Salze der Nitro-Orotsäure oder 5-Nitro-Uracil enthalten. | |
DE68902916D1 (de) | Herstellung von quecksilberfreiem synthesegas, reduktionsgas oder brenngas. | |
DK276789A (da) | Ethylenaminderivater | |
ATE53588T1 (de) | Herstellung von cytosin-nukleosiden. | |
IT1249732B (it) | Oligonucleotidi antisenso. | |
ES2056153T3 (es) | Expectorante que comprende un derivado hidroxialquilcisteina. | |
DK629889A (da) | Aminosyrederivater, deres fremstilling og anvendelse som laegemidler | |
ES2029879T3 (es) | Procedimiento para producir derivados de aminas sustituidas. | |
ES2012736A6 (es) | Procedimiento para la preparacion de derivados triciclicos de 3-oxopropanonitrilo. | |
ES8606321A1 (es) | Un procedimiento para preparar un derivado de 2-hidroxi-3- (4-fenilpiperazimil)propoxi-benzofurano | |
ES2128554T3 (es) | Nuevos derivados del acido glutamico, procedimiento para su preparacion y su utilizacion como medicamentos para el aumento de la memoria y aprendizaje. | |
DE69111607D1 (de) | Reine kristalline form von rifapentin. | |
EP0598910A4 (en) | METHOD FOR PRODUCING NUCLEOSIDE DERIVATIVES. | |
AR002003A1 (es) | Oligorribonucleotidos de sentido inverso con estructuras unidas por grupos amida, compuestos intermediarios, composicion farmaceutica que los contiene,un proceso para la elaboracion de dicha composicion farmaceutica y el grupo de dichos compuestos como medicamentos. | |
IT8422635A0 (it) | Scambiatore di calore per raffreddare gas caldi, provenienti specialmente dalla sintesi dell'ammoniaca. | |
ES474759A1 (es) | Procedimiento de produccion de 3',4'-didesoxikanamicina b. | |
ES2038323T3 (es) | Metodo para producir cristales simples de sulfuro sodico anhidro. | |
ES8607304A1 (es) | Un procedimiento para la preparacion de derivados de espiro-hidantoina | |
ATE41769T1 (de) | Immunwirksame verbindungen. | |
DE3672253D1 (de) | Hexensaeuren. | |
DK0971907T3 (da) | Fremgangsmåde til fremstilling af 1,3-disubstituerede 2-nitroguanidiner |