JPS572282A - Synthesis of fortimicins - Google Patents
Synthesis of fortimicinsInfo
- Publication number
- JPS572282A JPS572282A JP7516180A JP7516180A JPS572282A JP S572282 A JPS572282 A JP S572282A JP 7516180 A JP7516180 A JP 7516180A JP 7516180 A JP7516180 A JP 7516180A JP S572282 A JPS572282 A JP S572282A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- derivative
- fortamine
- purpurosamine
- 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.)
- Granted
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: The condensation reaction between a purpurosamine saccharide and a fortamine derivative is conducted in the presence of catalyst in a dry atmosphere, then the protecting groups are removed to produce a fortimicin used as an aminoglycoside antibiotic or its synthetic intermediate.
CONSTITUTION: After condensation reaction between a compound of formula I (R1, R2 are H, methyl; R, R6 are protecting group; X is halogen) and another compound of formula II (R3, R4 are H, protected amino group; R5 is H, protected hydroxyl) in the presence of a catalyst under anhydrous conditions, the protecting groups are removed to give a compound of formula III (R3', R4' are H, NH2; R5' is H, hydroxyl). Fortimicin B or sporaricin B are obtained from the compound of formula IV (R is 2,4-dinitrophenyl) and another compound of formula V or 2-deoxy-1-epi- fortamine and sannamycin B is synthesized from a 6-N-methyl-purpurosamine C derivative and a 2-deoxyfortamine B derivative.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55075161A JPS6019918B2 (en) | 1980-06-04 | 1980-06-04 | Synthesis method of fortemisins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55075161A JPS6019918B2 (en) | 1980-06-04 | 1980-06-04 | Synthesis method of fortemisins |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS572282A true JPS572282A (en) | 1982-01-07 |
JPS6019918B2 JPS6019918B2 (en) | 1985-05-18 |
Family
ID=13568195
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP55075161A Expired JPS6019918B2 (en) | 1980-06-04 | 1980-06-04 | Synthesis method of fortemisins |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6019918B2 (en) |
-
1980
- 1980-06-04 JP JP55075161A patent/JPS6019918B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS6019918B2 (en) | 1985-05-18 |
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