Method for synthesizing dimethyl cysteamine hydrochloride
The invention relates to a method for synthesizing dimethyl cysteamine hydrochloride. The method comprises the following steps: carrying out ring opening and ring closing reaction on 5, 5-dimethyl-2-isopropyl thiazolidine under the action of hydrochloric acid, a solvent, phenylhydrazine and aldehyde...
Gespeichert in:
1. Verfasser: | |
---|---|
Format: | Patent |
Sprache: | chi ; eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The invention relates to a method for synthesizing dimethyl cysteamine hydrochloride. The method comprises the following steps: carrying out ring opening and ring closing reaction on 5, 5-dimethyl-2-isopropyl thiazolidine under the action of hydrochloric acid, a solvent, phenylhydrazine and aldehyde to obtain 5, 5-dimethyl-2-substituted thiazolidine mother liquor; directly adding hydrochloric acidinto 5, 5-dimethyl-2-substituted thiazolidine mother liquor and carrying out ring opening reaction to obtain the dimethyl cysteamine hydrochloride. The invention discloses a one-pot preparation process, reaction steps are reduced and the purity is not reduced by controlling the material ratio and charging operation details.
本发明涉及一种合成二甲基半胱胺盐酸盐的方法,包括5,5-二甲基-2-异丙基噻唑烷在盐酸、溶剂、苯肼以及醛的作用下,经开环再关环反应得到5,5-二甲基-2-取代噻唑烷母液;直接向5,5-二甲基-2-取代噻唑烷母液中加入盐酸,经开环反应得到二甲基半胱胺盐酸盐。本发明公开了一锅法的制备工艺,减少了反应步骤,通过控制物料配比及加料操作细节,纯度并未降低。 |
---|