JPS5564576A - Preparation of musimol derivative - Google Patents
Preparation of musimol derivativeInfo
- Publication number
- JPS5564576A JPS5564576A JP13694678A JP13694678A JPS5564576A JP S5564576 A JPS5564576 A JP S5564576A JP 13694678 A JP13694678 A JP 13694678A JP 13694678 A JP13694678 A JP 13694678A JP S5564576 A JPS5564576 A JP S5564576A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- formula
- musimol
- derivative
- halogen
- 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
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
PURPOSE: To obtain the title compound useful as a medicine having a psychotropic action in short steps, starting from a readily available 3-hydroxy-5-methylisoxazole.
CONSTITUTION: A compound of formula I: (R is H, aryl, or halogen) is reacted with a compound of the formula R'-X (R' is acyl or benzenesulfonyl group; X is halogen) to give a compound of formula II, Which is brominated with N-bromo- succinimide, etc., to form a compound of formula III. The resulting compound is aminated with conc. aqueous anmonia, and the protecting group R' is eliminated to give a musimol of formula IV and its derivative, which is an antiepileptic or cerebral physiological study reagent. The method requires a readily available raw material, produced in large amounts as a pesticide, short steps, and the amination step at normal temperature and pressure. The intermediate is not necessarily purified.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13694678A JPS5564576A (en) | 1978-11-07 | 1978-11-07 | Preparation of musimol derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13694678A JPS5564576A (en) | 1978-11-07 | 1978-11-07 | Preparation of musimol derivative |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5564576A true JPS5564576A (en) | 1980-05-15 |
JPS6159307B2 JPS6159307B2 (en) | 1986-12-16 |
Family
ID=15187210
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13694678A Granted JPS5564576A (en) | 1978-11-07 | 1978-11-07 | Preparation of musimol derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5564576A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58194867A (en) * | 1982-05-10 | 1983-11-12 | Sankyo Co Ltd | Preparation of isoxazole derivative |
-
1978
- 1978-11-07 JP JP13694678A patent/JPS5564576A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58194867A (en) * | 1982-05-10 | 1983-11-12 | Sankyo Co Ltd | Preparation of isoxazole derivative |
JPH0411543B2 (en) * | 1982-05-10 | 1992-02-28 |
Also Published As
Publication number | Publication date |
---|---|
JPS6159307B2 (en) | 1986-12-16 |
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