Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Device and method for rapidly constructing quinolone compound library

A technology for quinolones and compound libraries, which is applied in the field of devices for rapid construction of quinolones compound libraries. It can solve the problems of low yield, large pollution of three wastes, and long reaction time, and achieve simple reagent switching, accelerated research progress, and fast and efficient reactions. Effect

Pending Publication Date: 2022-06-24
GUANGDONG UNIV OF TECH
View PDF8 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although there are many synthesis methods for quinolones, most of them have disadvantages such as poor selectivity, low yield, long reaction time, large pollution of three wastes, and the need for multiple separation and purification in batch reactions.

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
  • Device and method for rapidly constructing quinolone compound library
  • Device and method for rapidly constructing quinolone compound library
  • Device and method for rapidly constructing quinolone compound library

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0062] Because the first feed pump, the second feed pump and the fourth feed pump in the synthesis process need to change different reaction reagents, a multi-channel electromagnetic selector valve is connected to these three pumps respectively, and all pre-prepared The reagents are respectively connected to different positions of the multi-channel electromagnetic selection valve, and the multi-channel electromagnetic selection valve is used to complete the switching of the reagents.

[0063] First, a series of primary amines (cyclopropylamine, ethylamine, 2,4-difluoro) were selected from ethyl 3-ethoxy-2-(2,4,5-trifluorobenzoyl)acrylate Aniline, etc.) and secondary amines (piperazine, N-methylpiperazine, 2-methylpiperazine, 2,6-dimethylpiperazine, 3-aminopyrrolidine, tetrahydropyrrole, piperidine, etc.) to construct A library of quinolones.

[0064] A total of 70 compounds are to be synthesized in this project, and 70 synthesis cycles are required. The operation process of ...

Embodiment 2

[0069] ethyl 3-ethoxy-2-(2,6-dichloro-5-fluoronicotinoyl)acrylate and 3-ethoxy-2-(2,4,5-trifluoro-3-chlorobenzene, respectively formyl) ethyl acrylate as the starting material, a series of primary amines (cyclopropylamine, ethylamine, 2,4-difluoroaniline, etc.) and secondary amines (piperazine, N-methylpiperazine, 2-methyl piperazine, 2,6-dimethylpiperazine, 3-aminopyrrolidine, tetrahydropyrrole, piperidine, etc.) to construct a library of quinolone compounds. According to the method of Example 1, a total of 140 quinolones were synthesized, and the automatically synthesized compounds were as follows:

[0070]

[0071]

Embodiment 3

[0073] Using 3-ethoxy-2-(2,3,4,5-tetrafluorobenzoyl) ethyl acrylate as the starting material and dimethyl sulfoxide as the solvent, S-(+)-2- Aminopropanol is a primary and a series of secondary amines (N-methylpiperazine, piperazine, piperidine, 1-[(3S)-3-pyrrolidine]-piperidine, cis-7-azabicyclo[ 3.3.0] octane, etc.) to construct a library of quinolone compounds. According to the method of Example 1, 9 quinolones including levofloxacin were synthesized, and the automatically synthesized compounds were as follows:

[0074]

[0075] The mass spectrometry characterization data of the compounds in the examples are as follows:

[0076]

[0077]

[0078]

[0079]

[0080]

[0081]

[0082]

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 device and a method for quickly constructing a quinolone compound library. According to the method, all the synthesis steps are continuously carried out in the reactor, and the intermediate does not need to be treated or separated, so that the required product is provided at a good yield. According to the method, the reaction is rapid and efficient, the reagent switching is simple, and hundreds of or more quinolone compounds with definite structures can be rapidly synthesized on a large scale. Knowledge technologies such as program design and automatic control are combined and integrated, drug molecules are continuously synthesized for researchers, and the research progress is accelerated. Various quinolone compound molecules can be obtained by adopting the quinolone compound library construction method disclosed by the invention, and can be directly applied to activity research.

Description

technical field [0001] The invention relates to a device and method for rapidly constructing a library of quinolone compounds. Background technique [0002] Continuous flow chemistry technology is a technology that uses pumps to provide power to carry out chemical reactions in microchannels in a continuous flow mode. Continuous flow chemistry technology has been transformed from a niche academic application research to a recognized industrial technology with broad application prospects in the pharmaceutical field. Several cases of rapid synthesis of multiple drugs or molecules have been reported based on continuous flow chemistry techniques. For example, in 2016, the research group of Jamison and Jensen of the Massachusetts Institute of Technology developed a continuous flow drug synthesis platform system with compact structure and flexible assembly configuration (Science, 2016, 352, 61-67.), which can be completed every day. Continuous synthesis of 1,000 doses of diphenhy...

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): B01J19/00B01J19/24B01F33/80B01F33/81C40B60/02C07D215/56C07D401/04
CPCB01J19/0093B01J19/242C40B60/02C07D215/56C07D401/04
Inventor 叶金星孙茂林梁超茗程瑞华
Owner GUANGDONG UNIV OF TECH
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
Eureka Blog
Learn More
PatSnap group products