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Preparing method of edaravone

A technology for edaravone and phenylhydrazine, which is applied in the field of preparation of heterocyclic compounds, can solve the problems of high content, difficult removal of phenylhydrazine and its derivatives, and the like, achieves low impurity content, and reduces phenylhydrazine residues and derivatives thereof. The content of impurities, the effect of short synthesis route

Inactive Publication Date: 2019-04-12
HENAN RUNHONG PHARMA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

The preparation method of this Edaravone has simple process, low reaction temperature and high product purity, but because the solubility of phenylhydrazine and its derivatives in ethanol is very large, it is difficult to remove phenylhydrazine and its derivatives in the product. Higher levels in daravone products

Method used

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preparation example Construction

[0020] The preparation method of edaravone provided by the present invention includes the following steps:

[0021] 1) Reaction of phenylhydrazine and ethyl acetoacetate with a molar ratio of 1:1.019 to 1.080 in an organic solvent at 25 to 30°C for 1 to 4 hours, and then removing the solvent to obtain an oil;

[0022] 2) Mix the oil obtained in step 1) uniformly with acetic acid, perform reflux reaction at 75-77°C for 6-10 hours, then remove the unreacted acetic acid, add alcohol solvent to mix uniformly, and separate solid-liquid to obtain.

[0023] The chemical reaction involved in the preparation method of edaravone of the present invention is:

[0024]

[0025] Through process research, it is found that when there is too much ethyl acetoacetate, more impurities are produced. When the feeding ratio of phenylhydrazine to ethyl acetoacetate is 1:1.019~1.080, there are fewer impurities and it also meets the requirements of economic production.

[0026] Preferably, an inert gas is used t...

Embodiment 1

[0056] The preparation method of edaravone of this embodiment includes the following steps:

[0057] 1) Add anhydrous ethanol to a 500L reactor, add 70kg of phenylhydrazine (about 647mol) while continuously stirring the anhydrous ethanol, pass nitrogen protection, and stir to make it completely dissolved. Cool the circulating water, add 88.5kg ethyl acetoacetate (approximately 680mol) dropwise, keep the temperature not higher than 40℃, after the dropwise addition, keep the temperature at 25℃ and react for 4h, monitor the reaction by TLC; concentrate and distill the ethanol under reduced pressure to obtain oily Thing

[0058] 2) Add 147 kg of acetic acid to the oily substance obtained by concentrating, stir, pass nitrogen protection, heat up to 105° C. to reflux, reflux for 10 hours, monitor the reaction by TLC, and distill off the acetic acid under reduced pressure to obtain an oily substance.

[0059] 120kg of ethanol was added to the obtained oily substance and stirred at room tem...

Embodiment 2

[0066] The preparation method of edaravone of this embodiment includes the following steps:

[0067] 1) Add anhydrous ethanol to a 500L reactor, add 70kg of phenylhydrazine (about 647mol) while continuously stirring the anhydrous ethanol, pass nitrogen protection, and stir to make it completely dissolved. Cool the circulating water, add 85.9kg ethyl acetoacetate (approximately 660mol) dropwise, keep the temperature not higher than 40°C, after the dropwise addition, keep the temperature at 25°C and react for 4h, monitor the reaction by TLC; concentrate under reduced pressure and distill the ethanol to obtain an oily Thing

[0068] 2) Add 147 kg of acetic acid to the oily substance obtained by concentrating, stir, pass nitrogen protection, heat up to 110° C. to reflux, reflux for 6 hours, monitor the reaction by TLC, and evaporate the acetic acid under reduced pressure to obtain an oily substance.

[0069] Add 160 kg of ethanol to the obtained oil, and stir at room temperature. After ...

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Abstract

The invention relates to a preparing method of edaravone, and belongs to the technical field of preparation of heterocyclic compounds. The preparing method of edaravone comprises the steps of carryingout a reaction between phenylhydrazine and ethyl acetoacetate at 25-30 DEG C for 1-4 h in an organic solvent, and then removing the solvent to obtain an oily substance, wherein the mole ratio of phenylhydrazine to ethyl acetoacetate is 1:(1.019-1.080); uniformly mixing the obtained oily substance with acetic acid, carrying out a reflux reaction at 105-115 DEG C for 6-10 h, then removing unreactedacetic acid, then adding an alcohol solvent for uniform mixing, and conducting soil-liquid separation to obtain edaravone. According to the preparing method of edaravone, by controlling the reactioncondition, stepwise reactions are carried out, the reaction process is more easily controlled, the content of impurities in the product is also greatly reduced, particularly, the contents of residualphenylhydrazine and derivative impurities thereof can be reduced, the genotoxicity of the product is greatly lowered, and the safety of using edaravone is improved.

Description

Technical field [0001] The invention relates to a preparation method of edaravone and belongs to the technical field of preparation of heterocyclic compounds. Background technique [0002] Edaravone, whose chemical name is 3-methyl-1-phenyl-2-pyrazoline-5-one, has the following structural formula: [0003] [0004] Edaravone is a brain protective agent developed by Japan's Mitsubishi Pharmaceutical Company. It can scavenge free radicals and inhibit lipid peroxidation, thereby inhibiting the oxidative damage of brain cells, vascular endothelial cells and nerve cells. Therefore, it is mainly used clinically to improve neurological symptoms, activities of daily living and dysfunction caused by acute cerebral infarction. [0005] At present, edaravone is mainly synthesized through the reaction of phenylhydrazine and ethyl acetoacetate. Although the process is simple, the residual phenylhydrazine and the by-product phenylhydrazine derivatives in the product can still cause damage to the...

Claims

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Application Information

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IPC IPC(8): C07D231/26
CPCC07D231/26
Inventor 崔海龙王晓雪马莉艳石勇志杨婷张炜何燕闫浩利
Owner HENAN RUNHONG PHARMA
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