JPS5663977A - Secoprostaglandin i2 derivative and its preparation - Google Patents
Secoprostaglandin i2 derivative and its preparationInfo
- Publication number
- JPS5663977A JPS5663977A JP13938479A JP13938479A JPS5663977A JP S5663977 A JPS5663977 A JP S5663977A JP 13938479 A JP13938479 A JP 13938479A JP 13938479 A JP13938479 A JP 13938479A JP S5663977 A JPS5663977 A JP S5663977A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- secoprostaglandin
- derivative
- kinds
- compound
- 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)
- Furan Compounds (AREA)
Abstract
NEW MATERIAL:A secoprostaglandin I2 derivative of formula I (R is H, 1W6C alkyl, etc.; Z is H or protecting group).
EXAMPLE: dl-11,12-Seco-PG I2 methyl ester.
USE: Pharmaceuticals having possibilities to suppress lipid metabolism, inflammation, and some kinds of cancer when applied to cardiac vessel, kidney, digestive tracts, etc.
PROCESS: The compound of formula I is prepared by the dehydrohalogenation of a compound of formula II (X is Br or I) with a base (e.g. Na2CO3). The amount of the base is 1W100 times equivalent to the raw material. Two or more kinds of bases may be used at the same time. The reaction temperature is -20W+150°C, and the reaction completes usually within 10min.W100hr.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13938479A JPS5663977A (en) | 1979-10-30 | 1979-10-30 | Secoprostaglandin i2 derivative and its preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13938479A JPS5663977A (en) | 1979-10-30 | 1979-10-30 | Secoprostaglandin i2 derivative and its preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5663977A true JPS5663977A (en) | 1981-05-30 |
Family
ID=15244050
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13938479A Pending JPS5663977A (en) | 1979-10-30 | 1979-10-30 | Secoprostaglandin i2 derivative and its preparation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5663977A (en) |
-
1979
- 1979-10-30 JP JP13938479A patent/JPS5663977A/en active Pending
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