Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Novel preparation method of 1-(2-hydroxyethyl)piperazine hydrochloride

A technology of hydroxyethyl and hydrochloride, applied in the field of preparing pharmaceutical intermediate 1-piperazine hydrochloride, can solve the problems of low total yield, difficult to use, time-consuming and the like

Inactive Publication Date: 2019-03-01
WUXI QIANHAO BIOPHARMA
View PDF0 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

These traditional process routes are long, time-consuming, and the total yield is low. They have great defects in industrial production and are difficult to adopt.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Novel preparation method of 1-(2-hydroxyethyl)piperazine hydrochloride

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0012] Heat 100 grams (1.2mol) of anhydrous piperazine and 240 grams (1.5mol) of piperazine dihydrochloride to 120 degrees Celsius, add dropwise 110 grams (1.2mol) of 2-chloroethanol, continue heating and stirring after adding, and heat up To 136-140 degrees Celsius, keep 1 hour, stop heating after TLC shows that the reaction is complete. When the temperature drops to 80 degrees Celsius, add 500 milliliters of 95% ethanol, cool overnight in the refrigerator, filter and recover piperazine dihydrochloride the next day, wash the filter cake fully with a small amount of ethanol, combine the filtrates, and add 30% sodium hydroxide solution 200 grams of alkalization, filtered out insoluble inorganic salts; concentrated to remove the solvent, extracted the residue with ethyl acetate, passed through dry hydrogen chloride gas, filtered and dried to obtain white solid 1-(2-hydroxyethyl)piperazine Hydrochloride; the solid content is already above 98%. After one recrystallization with 90...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a practical synthesis method for preparing an important medicine raw material 1-(2-hydroxyethyl)piperazine hydrochloride. In the presence of a proper solvent or in the absenceof a solvent, piperazine hydrochloride and 2-chloroethanol are stirred to react at 100-150 DEG C; 1-(2-hydroxyethyl)piperazine hydrochloride is directly obtained with high yield without protection ofone amino of piperazine.

Description

technical field [0001] The invention provides an economical and practical new method for preparing pharmaceutical intermediate 1-(2-hydroxyethyl)piperazine hydrochloride. Background technique [0002] Piperazine is an important component of many drugs. It is a six-membered heterocyclic ring containing two nitrogen atoms in the molecule. It is an ideal structural unit of nitrogen-rich heterocyclic compounds. It has the characteristics of high formation enthalpy and good thermal stability. In recent years, the application of piperazine compounds in organic synthesis and medicine has attracted widespread attention in the field of organic chemistry and pharmacy. Compared with traditional organic drugs, the piperazine ring has a symmetrical structure with better nitrogen balance. The introduction of piperazine rings in drug synthesis can be used as drug synergistic groups to improve the pharmacokinetic properties of drugs and increase the biological activity of drugs; compounds c...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C07D295/088
CPCC07D295/088
Inventor 彭海燕
Owner WUXI QIANHAO BIOPHARMA
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products