Esomeprazole sodium polymorph, preparation method and application thereof

A technology of esomeprazole sodium and polymorphs, applied in the field of medicinal chemistry, can solve the problems that impurities are difficult to reach 0.1%, solvents are difficult to meet the pharmacopoeia standards, and are not suitable for industrial production. The purity is good and the product purity is easy. Controlled, quality reproducible results

Active Publication Date: 2012-10-24
JIANGSU AOSAIKANG PHARMA CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0012] (1) It is difficult for a single impurity to reach less than 0.1%;
[0013] (2) Solvent residues are difficult to meet the pharmacopoeia standards;
[0014] (3) The solubility is not ideal;
[0015] (4) The operation is cumbersome and not suitable for industrial production;

Method used

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  • Esomeprazole sodium polymorph, preparation method and application thereof
  • Esomeprazole sodium polymorph, preparation method and application thereof
  • Esomeprazole sodium polymorph, preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0087] Embodiment 1: the preparation of esomeprazole sodium polymorph

[0088] Take 20g of esomeprazole and place it in a reaction flask, add 100mL of 2-butanone, stir until completely dissolved, filter, transfer the filtrate to the reaction flask, add 30% sodium hydroxide aqueous solution dropwise at an internal temperature of 20-25°C 8.1mL, after the dropwise addition, continue to stir the reaction at the same temperature for 5h, you can see that the color of the reaction becomes lighter. The reaction solution was concentrated under reduced pressure at 40°C, and the organic solvent was removed by concentration to obtain 40 g of a yellow oil. Slowly add 80g of diethyl ether to the yellow oil, crystallize at room temperature (21°C) for 3h, a large amount of white solid precipitates, then cool to 0°C for 1h to complete the crystallization. Suction filtration, the filter cake was washed with ether and dried. The solid was dried at 40°C under reduced pressure (-0.09MPa) to ob...

Embodiment 2

[0089] Embodiment 2: the preparation of esomeprazole sodium polymorph

[0090] Take 50g of esomeprazole and place it in a reaction flask, add 500mL of 2-butanone, stir well until it is completely dissolved, filter, transfer the filtrate to the reaction flask, and add 30% sodium hydroxide aqueous solution dropwise at an internal temperature of 10-15°C 20.3mL, after the dropwise addition, continue to stir and react at the same temperature for 10h. The reaction solution was concentrated under reduced pressure at 40°C, and the organic solvent was removed by concentration to obtain 52.6 g of a yellow oil. Slowly add 105.2 g of 2-butanone to the yellow oil, crystallize at room temperature (23°C) for 4 hours, and a large amount of white solid precipitates, then cool to 5°C and crystallize for 2 hours to complete the crystallization. Suction filtration, the filter cake was washed with 2-butanone and sucked dry. The solid was dried at 40°C under reduced pressure (-0.09MPa) to obtai...

Embodiment 3

[0091] Embodiment 3: the preparation of esomeprazole sodium polymorph

[0092] Take 5g of esomeprazole and place it in a reaction flask, add 40mL of 2-butanone, stir well until it is completely dissolved, filter, transfer the filtrate to the reaction flask, and add 30% sodium hydroxide aqueous solution dropwise at an internal temperature of 25-30°C 2.0mL, after the dropwise addition, continue to stir and react at the same temperature for 8h. The reaction solution was concentrated under reduced pressure at 40°C, and the organic solvent was removed by concentration to obtain 4.9 g of a yellow oil. Add 10 g of isopropyl ether to the yellow oil, cool to room temperature (20°C) and crystallize for 3 hours, a large amount of white solid precipitates, then cool to 10°C and crystallize for 2 hours to complete the crystallization. Suction filtration, the filter cake was washed with isopropyl ether and sucked dry. The solid was dried at 45°C under reduced pressure (-0.09MPa) to obta...

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Abstract

The invention belongs to the field of medicinal chemistry, and specifically to an esomeprazole sodium polymorph, a preparation method and an application thereof. The present invention discloses an esomeprazole sodium polymorph having good stability and excellent solubility, wherein a preparation process of the esomeprazole sodium polymorph is easily industrialized, quality reproducibility is good, and product purity is easy to control.

Description

technical field [0001] The invention belongs to the field of medicinal chemistry, in particular to 5-methoxy-2-((S)-((4-methoxy-3,5-dimethyl-2-pyridyl)methyl)sulfinic acid Acyl-1H-benzimidazole sodium is esomeprazole sodium polymorph and its preparation method and application. Background technique [0002] Common name for 5-methoxy-2-((S)-((4-methoxy-3,5-dimethyl-2-pyridyl)methyl)sulfinyl-1H-benzimidazole sodium Esomeprazole sodium (Esomeprazole sodium), the left-handed isomer of omeprazole sodium, is the world's first single-isomer proton pump inhibitor (PPI) developed by AstraZeneca, Sweden. Sexually inhibit the proton pump of gastric parietal cells to reduce gastric acid secretion. Esomeprazole sodium for injection was approved by the US FDA on March 31, 2005, and is used as a prescription drug for the treatment of short-term gastroesophageal reflux disease (GERD). Its chemical structure is as follows: [0003] [0004] For polymorphic forms of drugs, different polym...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D401/12A61K31/4439A61P1/04
Inventor 赵俊陈祥峰王易杜有国
Owner JIANGSU AOSAIKANG PHARMA CO LTD
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