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

Method for preparing important midbody (1R,2S)-2-(3,4-difluorinated phenyl) cyclopropylamine of ticagrelor

A technology of difluorophenyl and ticagrelor, which is applied in the fields of organic synthesis and chemical medicine preparation, can solve the problems of poor reaction stereoselectivity, accidental environmental pollution, explosive and harmful reagents, etc. The effect of a short process route, reducing the risk of accidental injury

Active Publication Date: 2015-01-28
ZHEJIANG YONGTAI TECH CO LTD
View PDF4 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0011] Although the two synthetic routes reported above have been developed and improved for several years, they still have the disadvantages of long routes, poor reaction stereoselectivity, high production costs, explosive and harmful reagents, and accidental injuries and injuries in the production process. The shortcomings that are difficult to overcome, such as environmental pollution, are not conducive to large-scale industrial production

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
  • Method for preparing important midbody (1R,2S)-2-(3,4-difluorinated phenyl) cyclopropylamine of ticagrelor
  • Method for preparing important midbody (1R,2S)-2-(3,4-difluorinated phenyl) cyclopropylamine of ticagrelor
  • Method for preparing important midbody (1R,2S)-2-(3,4-difluorinated phenyl) cyclopropylamine of ticagrelor

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1-1

[0042] Add camphorsulfonium ylide I (24.4g, 0.06mol), THF (300mL) and acrylonitrile (2.65g, 0.05mol) successively into a 500mL three-neck flask, place at -10°C, add potassium tert-butoxide (16.8 g, 0.15mol), after the addition was completed, the reaction was continued at -10°C, and the reaction was monitored by TLC. After the reaction was completed for about 12 hours, the reaction mixture was first filtered, and the filtrate was concentrated under reduced pressure to remove the solvent. 7.6 g of product II as oily color. The yield was 85.0%.

Embodiment 1-2

[0043] Embodiment 1-2. (1R,2R)-2-(3,4-difluorophenyl) the synthesis of cyclopropyl nitrile compound II

[0044]Add camphorsulfonium ylide I (24.4g, 0.06mol), THF (200mL) and acrylonitrile (2.65g, 0.05mol) successively into a 500mL three-neck flask, place at -78°C, add potassium tert-butoxide (16.8 g, 0.15mol), after the addition was completed, the reaction was continued at -78°C, and the reaction was monitored by TLC. After the reaction was completed for 24 hours, the reaction mixture was first filtered, and the filtrate was concentrated under reduced pressure to remove the solvent. The obtained crude product was colorless after simple removal of impurities. Oily product II 7.3 g. The yield was 82.0%.

Embodiment 1-3

[0045] Embodiment 1-3. (1R,2R)-2-(3,4-difluorophenyl) the synthesis of cyclopropyl nitrile compound II

[0046] Add camphorsulfonium ylide I (20.3g, 0.05mol), methyltetrahydrofuran (200mL) and acrylonitrile (2.65g, 0.05mol) in sequence in a 500mL three-neck flask, place at -50°C, and add potassium tert-butoxide (16.8g, 0.15mol), after the addition was completed, the reaction was continued at -50°C, and the reaction was monitored by TLC. After the reaction was completed for 20 hours, the reaction mixture was first filtered, and the filtrate was concentrated under reduced pressure to remove the solvent. The obtained crude product was obtained by simple removal of impurities. Colorless oily product II 8.5g. The yield was 84%.

[0047] Then use the (1R,2R)-2-(3,4-difluorophenyl)cyclopropylnitrile compound II prepared in any of the above Examples 1-1~1-3 for the synthesis of (1R,2R)- 2-(3,4-difluorophenyl) cyclopropyl formamide III, specific examples are as follows:

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 a method for preparing important midbody (1R,2S)-2-(3,4-difluorinated phenyl) cyclopropylamine of ticagrelor. The method mainly comprises the following steps: performing cyclopropane reaction on camphor sulfonium ylide I and acrylonitrile, synthesizing (1R, 2S)-2-(3,4-difluorinated phenyl) cyclopropyl nitrile II in a stereoselectivity manner, and further performing hydrolysis and holfman degradation reaction, thereby obtaining a target product IV. The method has the characteristics of cheap initial materials, high yield, good stereoselectivity, high enantioselectivity, low production cost and the like, and has important significance in industrial production.

Description

technical field [0001] The invention belongs to the technical field of organic synthesis and chemical medicine preparation, and relates to a preparation method of (1R,2S)-2-(3,4-difluorophenyl)cyclopropylamine, in particular to a method for preparing anticoagulant The preparation method of the important intermediate (1R,2S)-2-(3,4-difluorophenyl)cyclopropylamine of the drug ticagrelor. technical background [0002] Ticagrelor is a novel, small molecule anticoagulant drug developed by AstraZeneca, and is the first reversibly binding, direct-acting, orally administered platelet adenosine diphosphate P2Y12 receptor antagonist. (1R,2S)-2-(3,4-difluorophenyl)cyclopropylamine as shown in formula IV is an important intermediate for the synthesis of anticoagulant drug ticagrelor, and its synthesis method research has been very active, There are many literature and patent reports. So far, there are two main synthetic routes of (1R,2S)-2-(3,4-difluorophenyl)cyclopropylamine reporte...

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): C07C211/40C07C209/56
Inventor 管月清周国斌
Owner ZHEJIANG YONGTAI TECH CO LTD
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