JPS57106662A - Preparation of erythro 2-(4-benzylpiperidino)-1-(4- hydroxyphenyl)propanol - Google Patents
Preparation of erythro 2-(4-benzylpiperidino)-1-(4- hydroxyphenyl)propanolInfo
- Publication number
- JPS57106662A JPS57106662A JP55182094A JP18209480A JPS57106662A JP S57106662 A JPS57106662 A JP S57106662A JP 55182094 A JP55182094 A JP 55182094A JP 18209480 A JP18209480 A JP 18209480A JP S57106662 A JPS57106662 A JP S57106662A
- Authority
- JP
- Japan
- Prior art keywords
- diborane
- hydroxyl group
- erythro
- hydroxyphenyl
- propanol
- 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
- Hydrogenated Pyridines (AREA)
Abstract
PURPOSE: To obtain the titled compound useful as an improver for cerabral blood stream, etc. streoselectively easely and in high yield, by reducing a piperidinoalkanone having a phenolic hydroxyl group containing no protecting group with diborane directly.
CONSTITUTION: Piperidinoalkanone shown by the formulaIis reduced with diborane, to give erythro 2-(4-piperidino)-1-(hydroxyphenyl) propanol shown by the formula II. Since the compound shown by the formulaIis reduced diborane while the phenolic hydroxyl group is not being protected, the process to remove the hydroxyl group is omitted. An erythro form is obtained in high selectivity. Diborane is usually produced by reacting a solution of diboranetetrahydrofuran on the market or sodium boron hydride or lithium boron hydride with Lewis acid. and used.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55182094A JPS57106662A (en) | 1980-12-24 | 1980-12-24 | Preparation of erythro 2-(4-benzylpiperidino)-1-(4- hydroxyphenyl)propanol |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55182094A JPS57106662A (en) | 1980-12-24 | 1980-12-24 | Preparation of erythro 2-(4-benzylpiperidino)-1-(4- hydroxyphenyl)propanol |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57106662A true JPS57106662A (en) | 1982-07-02 |
JPS6366313B2 JPS6366313B2 (en) | 1988-12-20 |
Family
ID=16112240
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP55182094A Granted JPS57106662A (en) | 1980-12-24 | 1980-12-24 | Preparation of erythro 2-(4-benzylpiperidino)-1-(4- hydroxyphenyl)propanol |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57106662A (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5528903A (en) * | 1978-08-18 | 1980-02-29 | Grelan Pharmaceut Co Ltd | Preparation of piperidinoalkanol |
-
1980
- 1980-12-24 JP JP55182094A patent/JPS57106662A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5528903A (en) * | 1978-08-18 | 1980-02-29 | Grelan Pharmaceut Co Ltd | Preparation of piperidinoalkanol |
Also Published As
Publication number | Publication date |
---|---|
JPS6366313B2 (en) | 1988-12-20 |
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