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

Reference compounds for flupirtine maleate analysis

A technology of flupirtine maleate and its compound, which is applied in the application field of flupirtine maleate drug analysis, can solve the problems affecting the accuracy of samples, flupirtine maleate instability, easy discoloration, etc., to achieve High accuracy, improved purity and content, and good reproducibility

Active Publication Date: 2014-07-09
TIANJIN CHASE SUN PHARM CO LTD
View PDF4 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0015] During the experiment, we found that flupirtine maleate is extremely unstable, and the sample is very easy to change color during the placement process, which will affect the accuracy of the sample measurement. Therefore, it needs to be operated under specific conditions, such as: avoiding light, mixing samples Store in a dark place at a lower temperature

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
  • Reference compounds for flupirtine maleate analysis
  • Reference compounds for flupirtine maleate analysis
  • Reference compounds for flupirtine maleate analysis

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0080] Weigh 20.0 g of flupirtine maleate, add 200 mL of anhydrous methanol, heat to 80°C, stir to dissolve, and keep the temperature for 48 hours. Filtration, column chromatography, eluting with dichloromethane:methanol 100:1 respectively, to obtain impurity A and impurity B.

Embodiment 2

[0082] Dissolve 20g ANFP (2-amino-3-nitro-6-p-fluorobenzylaminopyridine) in anhydrous methanol, add 5% palladium carbon, complete the reaction under 20 kg pressure, spin dry, dissolve in dichloromethane 13 mL of triethylamine was added, methyl chloroformate was added at 0-25°C, and compound C was obtained by spin-drying.

Embodiment 3

[0084] Weigh 20.0 g of compound C, add 200 mL of dimethylformamide: water (20:1), heat to 110°C, stir to dissolve, and keep the temperature for 48 hours. Filtration, column chromatography, eluting with dichloromethane:methanol 100:1 respectively, to obtain impurity D and impurity E.

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 belongs to the technical field of medicine and relates to impurity compounds A, B, C, D and E for flupirtine maleate analysis and a use of the impurity compounds in flupirtine maleate drug analysis.

Description

technical field [0001] The invention belongs to the technical field of medicine, and in particular relates to impurity compounds A, B, C, D and E used in the analysis of flupirtine maleate and their application in the analysis of flupirtine maleate. Background technique [0002] Flupirtine maleate, chemical name 2-amino-3-acetylamino-6-(p-fluorophenylamino)-pyridine, ethyl-2-amino-6-[(p-fluorophenyl)amino]- 3-Pyridine-carbamate maleate: [0003] [0004] Molecular formula: C 15 h 17 FN 4 o 2 ·C 4 h 4 o 4 , molecular weight: 420.41 [0005] Flupirtine maleate is a selective neuronal potassium channel opener and a non-opioid analgesic that acts on the central nervous system without producing dependence and tolerance. Flupirtine maleate activates G protein-coupled K on nerve cell membrane + Channel.K + Efflux stabilizes the resting membrane potential. Cell membrane activity is reduced, thereby indirectly inhibiting the activation of NMDA receptors. Therapeutic 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): C07D213/75G01N30/02
CPCC07D213/75G01N30/02G01N2030/027
Inventor 张存彦韩冬董凯孙长海姚小青
Owner TIANJIN CHASE SUN PHARM CO LTD
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com