Preparation method of polaprezinc and polaprezinc preparation

A technology of polypurix zinc and reagents, which is applied in the preparation of polypurex zinc and the field of polypurex zinc preparations, can solve the problems of long filtration time and drying time, easy generation of impurities, serious environmental pollution, etc., and achieve prevention and treatment of digestion Sexual ulcer, no safety hazard, low preparation cost

Active Publication Date: 2020-05-26
皕达生物科技(上海)有限公司
View PDF14 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This method produces more impurities, poor product quality, and the production process produces toxic sulfides that seriously pollute the environment.
[0007] 3. Skoblik et al. and Zhang Guolin et al. used Boc-β-alanine or N-benzyloxycarbonyl-β-alanine as raw materials to react with succinyl hydroxylimide respectively to obtain the corresponding N-hydroxysuccinyl hydroxylimide Amino ester reacts with L-histidine to obtain dipeptide, and after deprotection group, obtains L-carnosine. The reaction steps of this method are long, and the production cost is too high, so it is not suitable for industrialized production
[0008] 4. Sifferd et al. synthesized N-benzyloxycarbonyl-β-alanine from β-alanine, then reacted with sodium nitrite to generate N-benzyloxycarbonyl azide, and then reacted with L-histidine methyl ester , and then obtain L-carnosine through hydrolysis and hydrogenolysis. The intermediate of this method involves explosive azide, and there are potential safety hazards in the preparation process, which is not suitable for industrial production
[0009] 5. In the KR2017023417 patent, L-carnosine is used as a raw material, and an alkali metal salt of self-made alcohol is added to the alcohol suspension of L-carnosine and zinc acetate to prepare polypre zinc, an...

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 polaprezinc and polaprezinc preparation
  • Preparation method of polaprezinc and polaprezinc preparation
  • Preparation method of polaprezinc and polaprezinc preparation

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0035] One embodiment of the present invention provides a kind of preparation method of polyprezinc, refer to figure 1 , figure 1 It is a flow chart of the preparation method of the polyprezinc of an embodiment of the present invention, and the preparation method of the polyprezinc comprises:

[0036]Step S1: Mix benzylamine, 3-haloacetone aldehyde, the first acidic reagent and the first organic solvent together, react for 20-30 minutes, add ammonium halide and polyoxymethylene to react for 8-12 hours, and obtain 1-benzyl -4-(halomethyl)-1 hydrogen-imidazole, wherein the reaction temperature is 60°C to 80°C;

[0037] Step S2: Dissolve 2-aminoacetonitrile and alkaline reagent in the second organic solvent, and after reacting for 20min to 30min, add 1-benzyl-4-(halomethyl)-1hydro-imidazole and 3-aminopropionic acid was reacted for 10h to 24h to obtain 3-amino-nitrogen-(2-(1-benzyl-1hydrogen-4-imidazole)-1-cyanoethyl)propionamide, wherein the reaction temperature was 60 ℃~80℃;...

Embodiment 1

[0052] The preparation method of the described polyprezinc of the present embodiment comprises the steps:

[0053] Step S1: Weigh 3.6g of benzylamine and 3.6g of 3-chloroacetoaldehyde, and weigh 0.3mL of hydrochloric acid and 130mL of methanol, mix them together and add them to a three-necked flask, heat up to 60°C, and react for 30 minutes, then transfer to the three-necked flask Add 1.8 g of ammonium chloride and 1.0 g of polyoxymethylene into the bottle, keep the reaction temperature at 60°C to 80°C, and continue the reaction for 8 hours. After the reaction was completed, the mixed solution was successively distilled under reduced pressure, washed with water, filtered and dried to obtain 5.7 g of 1-benzyl-4-(chloromethyl)-1 hydrogen-imidazole, and the calculated yield (in terms of benzyl Amine) was 83%.

[0054] Step S2: Weigh 1.5g of 2-aminoacetonitrile and 1.5g of potassium hydroxide, dissolve them in 130mL of tetrahydrofuran, add them to a three-necked flask, raise the ...

Embodiment 2

[0058] The preparation method of the described polyprezinc of the present embodiment comprises the steps:

[0059] Step S1: Weigh 3.6g of benzylamine and 5.1g of 3-bromoacetoglyoxal, and measure 0.2mL of phosphoric acid and 140mL of ethanol, mix them together and add them to a three-necked flask, raise the temperature to 70°C, and react for 30min. Add 3.3g of ammonium bromide and 1.0g of polyoxymethylene into the bottle, keep the reaction temperature at 70°C to 80°C, and continue the reaction for 10h. After the reaction was completed, the mixed solution was successively distilled under reduced pressure, washed with water, filtered and dried to obtain 6.3g of 1-benzyl-4-(bromomethyl)-1 hydrogen-imidazole, and the calculated yield (in terms of benzyl Amine) was 92%.

[0060] Step S2: Weigh 1.1g of 2-aminoacetonitrile and 1.1g of sodium methoxide, dissolve them in 140mL of tetrahydrofuran, add them to a three-necked flask, raise the temperature to 70°C, and react for 30 minutes, t...

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 provides a preparation method of polaprezinc and a polaprezinc preparation. The preparation method of polaprezinc comprises the steps that benzylamine, 3-halopyruvic aldehyde, a first acid reagent and a first organic solvent are mixed for a reaction, then ammonium halide and polyformaldehyde are added, and 1-phenylmethyl-4-(halomethyl)-1H-imidazole is obtained through a reaction; thematerial is added in a reaction mixture of 2-aminoacetonitrile, an alkaline reagent and a second organic solvent, and the materials are reacted to obtain 3-amino-nitrogen-(2-(1-phenylmethyl-1H-4-imidazole)-1-cyanoethyl) propanamide; the material is mixed with a reducing agent, a second acidic reagent and a third organic solvent, and the materials are reacted to obtain 3-amino-nitrogen-(1-carboxyl-2-(1hydrogen-4-imidazole) ethyl) propionamide; and the obtained product and zinc salt are dissolved in a fourth organic solvent, and a reaction is carried out to obtain the polaprezinc. According tothe technical scheme, almost no pollution is caused to the environment, no potential safety hazard exists in the preparation process, the steps are short, the conditions are simple, purification is easy, the yield is high, the preparation cost of the polaprezinc is low, and the polaprezinc is suitable for industrial production.

Description

technical field [0001] The invention relates to the technical field of pharmacy, in particular to a preparation method of polyprezinc and a polyprezinc preparation. Background technique [0002] The chemical name of polaprezinc is L-carnosine zinc, which is a new anti-ulcer drug jointly developed by Japan Hamari Chemical Co., Ltd. and Zeria Pharmaceutical Company. Among them, L-carnosine is a dipeptide composed of β-alanine and L-histidine, which belongs to an antioxidant, and zinc can promote wound healing, so polyprezinc can accelerate the healing of chronic gastric ulcer, And can stimulate the proliferation of epithelial cells. Clinical experimental data show that polyprezinc has the effect of anti-oxidation and membrane stabilization, so as to maintain the homeostasis of gastric mucosa and protect gastric mucosal cells; at the same time, polyprezinc can also promote wound healing and enhance defense factors role, to achieve the role of prevention and treatment of pepti...

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): C07K5/023C07K1/02A61K38/05A61P1/04
CPCC07K5/0202A61K38/05A61P1/04
Inventor 金国范戚雪勇廉云飞
Owner 皕达生物科技(上海)有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products