Preparation method of 3-piperidine-2-yl-azetidine-3-ol derivative
The invention discloses a preparation method of a 3-piperidine-2-yl-azetidine-3-ol derivative, which comprises the following steps: adopting a compound disclosed in the invention as a starting material, sequentially carrying out a three-membered ring forming reaction, a protecting group adding react...
Gespeichert in:
Hauptverfasser: | , , , , |
---|---|
Format: | Patent |
Sprache: | chi ; eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The invention discloses a preparation method of a 3-piperidine-2-yl-azetidine-3-ol derivative, which comprises the following steps: adopting a compound disclosed in the invention as a starting material, sequentially carrying out a three-membered ring forming reaction, a protecting group adding reaction, a ring opening reaction, a substitution reaction, an addition reaction and a cyclization reaction to obtain the 3-piperidine-2-yl-azetidine-3-ol derivative. The preparation method of the 3-piperidine-2-yl-azetidine-3-ol derivative has the advantages of simple operation, mild reaction conditions, high yield, few impurities and the like, is easy to amplify, and is suitable for industrial production.
本发明公开了一种3-哌啶-2-基-氮杂环丁烷-3-醇衍生物的制备方法,包括以下步骤:以为起始原料,依次进行成三元环反应、上保护基反应、开环反应、取代反应、加成反应和环化反应,即可得到3-哌啶-2-基-氮杂环丁烷-3-醇衍生物。本发明的3-哌啶-2-基-氮杂环丁烷-3-醇衍生物制备方法具有操作简单、反应条件温和、收率高、杂质少等优点,易放大,适于工业化生产。 |
---|