JPS5452059A - Synthesis of tobramycin - Google Patents
Synthesis of tobramycinInfo
- Publication number
- JPS5452059A JPS5452059A JP11515277A JP11515277A JPS5452059A JP S5452059 A JPS5452059 A JP S5452059A JP 11515277 A JP11515277 A JP 11515277A JP 11515277 A JP11515277 A JP 11515277A JP S5452059 A JPS5452059 A JP S5452059A
- Authority
- JP
- Japan
- Prior art keywords
- group
- ring
- derivative
- amino group
- amino
- 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
- Saccharide Compounds (AREA)
Abstract
PURPOSE: To prepare the title compound by condensing a lividamine derivative with a hexopyranose derivative, converting the sulfonyloxy group to amino group, opening the ring to a dialdehyde, closing the ring with nitromethane to obtain a diol, and reducing the nitro group to the amino group.
CONSTITUTION: Tobramycin VI is prepared by (1) condensing a lividamine derivative I [R1 is -OSO2R2 (R2 is alkyl, aralkyl, aryl); Y' is an OH-protecting group; Z is an amino-protecting grup]with hexopyranose or pentofuranose derivative II (Y is an OH-protecting group; X is halonen, A is III or IV) to obtain the compound V, (2) converting the 6'-position to amino group through azide group, (3) opening the ring by treating with periodic acid (aslt) to obtain a dialdehyde compound, (4) closing the ring by reacting nitromethane to obtain a diol-containing ring, and finally (5) reducing the nitro group to amino group
COPYRIGHT: (C)1979,JPO&Japio
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11515277A JPS5452059A (en) | 1977-09-27 | 1977-09-27 | Synthesis of tobramycin |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11515277A JPS5452059A (en) | 1977-09-27 | 1977-09-27 | Synthesis of tobramycin |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5452059A true JPS5452059A (en) | 1979-04-24 |
Family
ID=14655597
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11515277A Pending JPS5452059A (en) | 1977-09-27 | 1977-09-27 | Synthesis of tobramycin |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5452059A (en) |
-
1977
- 1977-09-27 JP JP11515277A patent/JPS5452059A/en active Pending
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