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

Preparation method of esomeprazole and magnesium salt thereof

A technology of esomeprazole and magnesium salt, which is applied in the field of pharmaceutical chemical synthesis, can solve the problems of less application and instability, and achieve the effects of improving the reaction system, being easy to realize, and improving oxidation efficiency

Active Publication Date: 2014-04-09
KAIFENG MINGREN PHARMA
View PDF5 Cites 11 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Generally, esomeprazole magnesium refers to esomeprazole magnesium (trihydrate), in addition to esomeprazole magnesium (dihydrate), but due to its instability, it is less used in daily production

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
  • Preparation method of esomeprazole and magnesium salt thereof
  • Preparation method of esomeprazole and magnesium salt thereof
  • Preparation method of esomeprazole and magnesium salt thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0042] b. Add methanol to the obtained compound II, the amount of methanol added is 3 times the mass of compound II, add methanol and stir and mix evenly to obtain compound II methanol solution;

[0043] Add methanol and sodium hydroxide solution to 5-methoxy-2-mercaptobenzimidazole, compound III, stir and mix evenly to obtain a compound III solution; the amount of methanol added is 3 times the mass of compound III, and the hydroxide The amount of sodium added is twice the molar number of compound III; the sodium hydroxide is formulated into a solution with a concentration of 50% by mass;

[0044] c. At 25°C, add the compound II methanol solution obtained in step b to the compound III solution dropwise. The volume ratio between the compound III solution and the compound II methanol solution is 1.5:1. Finally, the reaction was carried out at 25°C for 1.5 hours. After the reaction, crystallization, filtration, water washing and drying were carried out in sequence. After drying, ...

Embodiment 2

[0055] In step b: the amount of methanol added is twice the mass of compound II;

[0056] The amount of methanol added is twice the mass of compound III, and the amount of sodium hydroxide added is 1.5 times the molar number of compound III;

[0057] In step c: at 10°C, the compound II methanol solution obtained in step b is added dropwise to the compound III solution, the volume ratio between the compound III solution and the compound II methanol solution is 1.8:1, dropwise After completion, the reaction was carried out at 10°C, and the reaction time was 2 hours;

[0058] In step d: Stir evenly, raise the temperature to 50°C, keep warm at this temperature for 3h, then cool to room temperature, then add 1,3-propylenediamine, lower the temperature to -5~0°C, then slowly add peroxide After the tert-amyl benzoate and tert-amyl peroxybenzoate are added dropwise, the temperature is raised to 5-10°C for reaction, and the reaction lasts for 1.5 hours. After the reaction, the obtaine...

Embodiment 3

[0063] In step b: the amount of methanol added is 4 times the mass of compound II;

[0064] Add methanol and potassium hydroxide solution to 5-methoxy-2-mercaptobenzimidazole, i.e. compound III, the amount of methanol added is 4 times the mass of compound III, and the amount of potassium hydroxide added is the number of moles of compound III 3 times;

[0065] In step c: at 30°C, add the compound II methanol solution obtained in step b to the compound III solution dropwise, the volume ratio between the compound III solution and the compound II methanol solution is 1.2:1, drop After the addition, the reaction was carried out at 30°C, and the reaction time was 0.5h;

[0066] In step d: Stir evenly, raise the temperature to 70°C, keep warm at this temperature for 1.5h, then cool to room temperature, then add methylamine, lower the temperature to -15~-10°C, then slowly add disuccinic acid peroxide dropwise , After adding disuccinic acid peroxide dropwise, the temperature was rais...

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 preparation method of esomeprazole and a magnesium salt thereof. The preparation method comprises the steps: with 4-methoxy-2-hydroxymethyl-3,5-dimethyl pyridine as raw material, carrying out a reaction with hydrobromic acid to obtain 4-methoxy-2-bromomethyl-3,5-dimethyl pyridine, namely a compound II; dripping a methanol solution of the compound II into a methanol solution of a compound III, and carrying out a reaction to obtain 5-methoxy-2-(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl thio-1H-benzimidazole, namely a compound IV; dissolving the compound IV in dichloromethane, adding D-diethyl tartrate, tetrabutyl titanate and water for reaction, and thus obtaining esomeprazole; and carrying out a reaction of esomeprazole with magnesium methoxide to obtain magnesium esomeprazole. The method is utilized to prepare esomeprazole and the magnesium salt thereof, and can effectively reduce the production cost.

Description

technical field [0001] The invention relates to the technical field of pharmaceutical chemical synthesis, in particular to a preparation method of esomeprazole and its magnesium salt. Background technique [0002] Esomeprazole is a proton pump inhibitor that reduces gastric acid secretion and prevents the formation of gastric acid by inhibiting the H+ / K+-ATPase of gastric parietal cells. The chemical name of esomeprazole is 5-methoxy-2-((S)-((4-methoxy-3,5-dimethyl-2-pyridyl)methyl)sulfinyl) -1H-benzimidazole. [0003] The chemical name of esomeprazole magnesium is 5-methoxy-2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfinyl]benzimidazole-1 - Base Magnesium. Esomeprazole magnesium is suitable for the treatment of gastroesophageal reflux disease, erosive reflux esophagitis, long-term maintenance treatment of cured esophagitis patients to prevent recurrence and other diseases. Generally, esomeprazole magnesium refers to esomeprazole magnesium (trihydrate), in addition t...

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
IPC IPC(8): C07D401/12
CPCC07D401/12
Inventor 王艳侨翟腾李沁沁王国强杨晓霞张亚慧
Owner KAIFENG MINGREN PHARMA
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