JPS6429393A - Nucleoside analog - Google Patents
Nucleoside analogInfo
- Publication number
- JPS6429393A JPS6429393A JP62183659A JP18365987A JPS6429393A JP S6429393 A JPS6429393 A JP S6429393A JP 62183659 A JP62183659 A JP 62183659A JP 18365987 A JP18365987 A JP 18365987A JP S6429393 A JPS6429393 A JP S6429393A
- Authority
- JP
- Japan
- Prior art keywords
- derivative
- reacted
- acetylamine
- deoxy
- alkoxycarbonyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Abstract
NEW MATERIAL:A compound expressed by the formula (B is -CH= or -N=; X and Y are cyano, amino, alkoxycarbonyl, etc.; Z is H or alkoxycarbonyl; R<1> and R<2> are H or protecting groups of hydroxyl groups). EXAMPLE:4, 5-Diethoxycarbonyl-3-(3-deoxy-3-fluoro-2, 5-O-dibenzoyl-beta-D-ribofura nosyl)-1H-pyrazole. USE:An antitumor and antiviral agents. PREPARATION:For example, methyl 2,5-di-O-benzoyl-3-deoxy-3-fluoro-beta-D- ribofuranoside is dissolved in acetic acid and acetic anhydride, treated with hydrogen bromide and brominated. Mercuric cyanide is then added to provide a cyano derivative, which is subsequently reduced and reacted with acetic anhy dride to afford an acetylamine derivative. The resultant acetylamine derivative is then reacted with benzyl bromide to provide a dibenzyl derivative, which is subsequently treated with nitrogen dioxide in the presence of acetic acid, diazotized and reacted with diethyl acetylenedicarboxylate to afford the aimed compound expressed by the formula.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62183659A JPS6429393A (en) | 1987-07-24 | 1987-07-24 | Nucleoside analog |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62183659A JPS6429393A (en) | 1987-07-24 | 1987-07-24 | Nucleoside analog |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6429393A true JPS6429393A (en) | 1989-01-31 |
Family
ID=16139681
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62183659A Pending JPS6429393A (en) | 1987-07-24 | 1987-07-24 | Nucleoside analog |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6429393A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5157114A (en) * | 1988-08-19 | 1992-10-20 | Burroughs Wellcome Co. | 2',3'-dideoxy-3'-fluoro-5-ethyngluridine |
US5438131A (en) * | 1992-09-16 | 1995-08-01 | Bergstrom; Donald E. | 3-nitropyrrole nucleoside |
-
1987
- 1987-07-24 JP JP62183659A patent/JPS6429393A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5157114A (en) * | 1988-08-19 | 1992-10-20 | Burroughs Wellcome Co. | 2',3'-dideoxy-3'-fluoro-5-ethyngluridine |
US5438131A (en) * | 1992-09-16 | 1995-08-01 | Bergstrom; Donald E. | 3-nitropyrrole nucleoside |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU8551091A (en) | Process for the production of carboxylic acid anhydrides | |
JPS5227721A (en) | Process for preparation of substituted phosphonic acid derivatives | |
JPS6429393A (en) | Nucleoside analog | |
JPS57179147A (en) | Amidine derivative | |
AU1505892A (en) | Process for preparing hindered amine light stabilizers | |
GR3006438T3 (en) | ||
JPS57108072A (en) | Preparation of n-acylcarnosine | |
JPS55139336A (en) | Preparation of polycarboxylic acid and its ester | |
DK0493064T3 (en) | Deacetylcolchicine derivatives | |
JPS57192340A (en) | Isoprenylamine derivative | |
JPS55149299A (en) | N6-substituted cordicepin derivative and its preparation | |
JPS6483089A (en) | Production of vinylsilanes | |
JPS6419087A (en) | Production of 1,3,4-tri-o-acyl-2-deoxy-beta-d-erythro-pentapyranose | |
JPS5643287A (en) | Preparation of cephamycin derivative | |
JPS5256193A (en) | Process for copolyesterpolyol | |
JPS5714598A (en) | 5-substituted-1-beta-d-arabinofuranosyluracil derivative and its preparation | |
JPS5210207A (en) | Process for preparation of high purity pulenol | |
JPS55102548A (en) | Nitrosamine derivative | |
JPS5247893A (en) | Process for preparing hydroscopic polyamides | |
JPS6445392A (en) | Production of estradiol derivative | |
JPS51133296A (en) | Processes for preparing 7-acylamino- 3-hydroxymethyl-2-cephem-4-carbox ylic acid derivatives | |
JPS55115899A (en) | 3,18-o-cyclotylosin derivative | |
AU680325B2 (en) | Process for the carbonylation of an acetylenically unsaturated compound | |
JPS6431762A (en) | Dihalogenoindole derivative | |
JPS55102559A (en) | Production of 2-methoxy-5-sulfamoylbenzoic acid amide |