High-purity tauro ursodesoxy cholic acid and preparation method thereof

A technology of tauroursodeoxycholic acid and tauroursodeoxycholic acid, which can be used in pharmaceutical formulations, medical preparations containing active ingredients, steroids, etc., can solve the hidden safety hazards of tauroursodeoxycholic acid , can not effectively remove bezoar chenodeoxycholic acid and other problems, to achieve the effect of suitable for industrial production, low cost and environmental friendliness

Active Publication Date: 2012-05-30
CHENGDU GUOHONG PHARMA
View PDF4 Cites 22 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0011] Moreover, the tauroursodeoxycholic acid synthesis method in the prior art cannot effectively remove the tauroursodeoxycholic acid brought into the raw material, which brings certain potential safety hazards for the use of tauroursodeoxycholic acid

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
  • High-purity tauro ursodesoxy cholic acid and preparation method thereof
  • High-purity tauro ursodesoxy cholic acid and preparation method thereof
  • High-purity tauro ursodesoxy cholic acid and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0057] In this experiment, the liver toxicity of tauroursodeoxycholic acid samples containing different taurochenodeoxycholic acid impurities was studied.

[0058] 1. Materials and Methods

[0059] 1.1 Test drug: tauroursodeoxycholic acid containing 2% taurourchenodeoxycholic acid impurity (batch number: 100810), white powder, self-made; Sulfurursodeoxycholic acid (batch number: 100811), white powder, self-made; tauroursodeoxycholic acid (batch number: 100812), white powder, containing 0.7% taurodeoxycholic acid impurity; Tauroursodeoxycholic acid (batch number: 100813) with 0.5% impurity content of sulchenodeoxycholic acid, white powder, self-made; the above samples are all insoluble in water.

[0060] 1.2 Detection reagents: Liver function-related detection kits were purchased from Sichuan Mike Biotechnology Co., Ltd., mainly including: alanine aminotransferase (ALT) and aspartate aminotransferase (AST).

[0061] 1.3 Detection instrument: full-wavelength fluorescence and s...

Embodiment 2

[0077] The preparation of embodiment two high-purity tauroursodeoxycholic acid

[0078] a) The preparation of the crude product of tauroursodeoxycholic acid is carried out according to the following steps:

[0079] In the reaction kettle, add 4.0KG ursodeoxycholic acid, add 19KG acetone, add 1650ml triethylamine under stirring, turn on the jacket refrigeration, and lower the temperature of the mixture to -10°C. Add 1120ml of ethyl chloroformate, control the rate of addition of ethyl chloroformate, so that the temperature of the reaction solution is maintained between -5-0°C, the addition is completed in 30 minutes, continue to maintain the temperature and stir for 40 minutes to obtain ursodeoxy For the mixed anhydride of cholic acid and ethyl chloroformate, the above mixed anhydride reaction solution is filtered through a filter with nitrogen pressure to be equipped with 4.2KG purified water, 1.4KG taurine, and 0.4KG sodium hydroxide in a 50-liter reactor. The reaction was st...

Embodiment 3

[0084] The preparation method of embodiment three high-purity tauroursodeoxycholic acid

[0085] a) The preparation of the crude product of tauroursodeoxycholic acid is carried out according to the following steps:

[0086] In the reaction kettle, add 40.0KG of ursodeoxycholic acid, add 190KG of acetone, add 16.5L of triethylamine under stirring, turn on the jacket refrigeration, and lower the temperature of the mixture to -5°C. Add 11.2 L of ethyl chloroformate, control the rate of addition of ethyl chloroformate, so that the temperature of the reaction solution is maintained between 3-5 °C, the addition is completed in 30 minutes, and the temperature is continued to be stirred for 30 minutes to obtain ursodeoxy For the mixed acid anhydride of cholic acid and ethyl chloroformate, the above mixed anhydride reaction solution is filtered through a filter with nitrogen pressure into a 500-liter reactor equipped with 42KG purified water, 14KG taurine, and 4KG sodium hydroxide, and...

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 relates to high-purity tauro ursodesoxy cholic acid and a preparation method thereof. The content of taurochenodeoxycholic acid in the tauro ursodesoxy cholic acid is less than 0.7%. The tauro ursodesoxy cholic acid is safe and effective and does not have toxic and side effects in clinical application. The invention further provides a mixed anhydride reaction of ursodesoxycholic acid and ethyl chloroformate by taking acetone as a solvent. By means of control of a reaction condition and a reaction solvent, the tauro ursodesoxy cholic acid has the advantages of simple process, low cost, environmental friendlessness and industrial production; furthermore, the high-purity tauro ursodesoxy cholic acid can be obtained.

Description

technical field [0001] The present invention relates to a kind of raw medicine of medicine and its preparation method, in particular to a kind of high-purity tauroursodeoxycholic acid and its preparation method. technical background [0002] The chemical name of tauroursodeoxycholic acid is 2-[[(3α,5β,7β)-3,7-dihydroxy-24-oxocholestan-24-yl]amino]ethanesulfonic acid Dihydrate, discovered from bear bile in 1902, is the main bile acid in bear bile, and has antispasmodic, anticonvulsant, anti-inflammatory and gallstone-dissolving effects. Tauroursodeoxycholic acid can increase the secretion of bile acids, leading to changes in the composition of bile acids and increasing their content in bile. Tauroursodeoxycholic acid can also inhibit the synthesis of cholesterol in the liver, reduce the amount of cholesterol and cholesterol esters in bile and the saturation index of cholesterol, thereby facilitating the gradual dissolution of cholesterol in bile. [0003] Tauroursodeoxychol...

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): C07J9/00A61K31/575A61P1/16A61P31/14
Inventor 郭礼新徐开辉
Owner CHENGDU GUOHONG PHARMA
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