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

Synthetic method of azilsartan medoxomil or its salt and its intermediate

A technology for azilsartan medoxomil and intermediates, which is applied in the field of synthetic methods of azilsartan medoxomil or its salts and its intermediates, and can solve the problems of low yield and many by-products in the synthesis of azilsartan medoxomil, Achieve the effects of easy purification of finished products and increased reaction yield

Active Publication Date: 2015-12-30
ZHEJIANG YONGNING PHARMA
View PDF6 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] In order to solve the above problems, the present invention provides a new method for synthesizing Azilsartan Medoxomil or its salt, which solves the problems of low yield and many by-products in the synthesis of Azilsartan Medoxomil

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
  • Synthetic method of azilsartan medoxomil or its salt and its intermediate
  • Synthetic method of azilsartan medoxomil or its salt and its intermediate
  • Synthetic method of azilsartan medoxomil or its salt and its intermediate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0042] 1) Preparation of the compound of formula (4)

[0043]

[0044] Add 159g of methanol and 24.2g of the methyl ester compound of formula (5) into a 500mL reactor, stir for 10 minutes, add 10% sodium hydroxide solution dropwise, and heat to reflux for 2 hours. Cool down to room temperature, add 500g of water, adjust the pH value to neutral with 2N hydrochloric acid, precipitate a solid, filter, wash with water, and dry to obtain the compound of formula (4), with a yield of 95.6%.

[0045] 2) Preparation of the compound of formula (3)

[0046]

[0047] Add 16.2 g of the compound of formula (4) and 8.8 g of potassium carbonate into 200 mL of acetone, slowly add 6.0 g of the compound of formula (6) dropwise, and stir the reaction at room temperature for 10 hours after the addition. The insoluble matter was removed by filtration, and the mother liquor was concentrated to dryness to obtain the compound of formula (3), with a yield of 86.2%. HNMR (300MHz, DMSO-d 6 )δ: 1...

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 the field of medicines, in particular to a synthesis method for azilsartan medoxomil or salt thereof and an intermediate of the azilsartan medoxomil or the salt thereof. The invention provides a method for synthesizing the azilsartan medoxomil or the salt thereof and further provides a synthesis intermediate of the azilsartan medoxomil or the salt thereof and a preparation method for the synthesis intermediate. In a synthesis process, an alcohol fragment of the azilsartan medoxomil is introduced at first, so that a part of the azilsartan medoxomil is formed, and a cyclization structure fragment is synthesized; therefore, the problem that the yield is reduced because of side reaction caused by active hydrogen in a carbonyldimidazole structure of an azilsartan acid structure is solved in a reaction process; the reaction yield is greatly improved, so that a finished product is easier to purify; the synthesis method is particularly suitable for industrial production.

Description

technical field [0001] The invention relates to the field of medicine, in particular to a synthesis method of azilsartan medoxomil or a salt thereof and an intermediate thereof. Background technique [0002] Azilsartan medoxomil (INN, code TAK-491) is a selective angiotensin II receptor antagonist with antihypertensive and central nervous effects. It is the prodrug of Azilsartan. On April 28, 2010, the drug developed by Japan's Takeda Pharmaceutical Company (Takeda) completed the Phase III clinical trial. It was approved by the US FDA in 2011. The drug is a vascular tension drug. Candesartan receptor antagonists, which can be used alone or in combination with other antihypertensive drugs, are regarded as the next generation of candesartan cilexetil. [0003] In the prior art, for example, in patents CN1946717, CN102344415 and CN102731491, the preparation of azilsartan medoxomil is as shown in the following formula, firstly prepare azilsartan acid and then prepare the ester,...

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 Patents(China)
IPC IPC(8): C07D413/14C07D405/12
CPCC07D405/12C07D413/14
Inventor 叶凤起郁光亮张绩生马苏旺
Owner ZHEJIANG YONGNING 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