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

A kind of 3,3'-methylene-bisfluoroquinolone derivative containing ethyl quinoline ring and its preparation method and application

A technology of ethyl quinoline ring and bisfluoroquinolone, applied in the preparation of 3,3'-methylene-bisfluoroquinolone derivatives, in the field of 3,3'-methylene-bisfluoroquinolone derivatives, capable of Solve the problems of high toxicity of anti-tumor drugs, poor patient tolerance, and low cure rate of tumor diseases, and achieve the effect of increasing anti-tumor activity and reducing side effects

Inactive Publication Date: 2016-08-24
HENAN UNIVERSITY
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Due to the high toxicity of the current anti-tumor drugs and the poor tolerance of patients, the cure rate of tumor diseases is low. Therefore, it is increasingly urgent to develop anti-tumor drugs with new structures.
Although there are many ways to discover new drugs, the structural modification of existing drugs is still the most successful and economical strategy

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
  • A kind of 3,3'-methylene-bisfluoroquinolone derivative containing ethyl quinoline ring and its preparation method and application
  • A kind of 3,3'-methylene-bisfluoroquinolone derivative containing ethyl quinoline ring and its preparation method and application
  • A kind of 3,3'-methylene-bisfluoroquinolone derivative containing ethyl quinoline ring and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0044] The 3,3'-methylene-bisfluoroquinolone derivative containing an ethylquinoline ring in this example is 1-ethyl-6-fluoro-7-piperazin-1-yl-3-[1-ethyl Base-6-fluoro-7-piperazin-1-yl-2,3-dihydro-quinolin-4(1H)-one-3-ylidenemethyl]quinolin-4(1H)-one, its chemical The structural formula is:

[0045]

[0046] That is, R in formula (I) 1 is ethyl, R 2 , R 3 and R 4 are hydrogen atoms, and X is a hydrocarbon group.

[0047] The preparation method of the 3,3'-methylene-bisfluoroquinolone derivatives containing an ethylquinoline ring in this embodiment is: take 0.5g (1.8mmol) of 1-ethyl-6-fluoro-7-piper Azin-1-yl-2,3-dihydro-quinolin-4(1H)-one and 0.55g (1.8mmol) of 1-ethyl-6-fluoro-7-piperazin-1-yl-quinoline -4(1H)-keto-3-carbaldehyde, dissolved in 20ml of absolute ethanol, 0.5ml of piperidine was added dropwise, after reflux reaction for 24h, left overnight, the resulting solid was collected by filtration, and recrystallized with DMF-ethanol to obtain light Yellow cryst...

Embodiment 2

[0049]The 3,3'-methylene-bisfluoroquinolone derivative containing an ethylquinoline ring in this example is 1-ethyl-6-fluoro-7-piperazin-1-yl-3-[1-ethyl Base-6-fluoro-7-(4-methylpiperazin-1-yl)-2,3-dihydro-quinolin-4(1H)-one-3-ylidenemethyl]quinoline-4(1H )-ketone, its chemical structural formula is:

[0050]

[0051] That is, R in formula (I) 1 is ethyl, R 2 is a hydrogen atom, R 3 is methyl, R 4 is a hydrogen atom, and X is a hydrocarbon group.

[0052] The preparation method of the 3,3'-methylene-bisfluoroquinolone derivative containing ethylquinoline ring of the present embodiment is: get 0.52g (1.8mmol) of 1-ethyl-6-fluoro-7-( 4-methylpiperazin-1-yl)-2,3-dihydro-quinolin-4(1H)-one with 0.55g (1.8mmol) of 1-ethyl-6-fluoro-7-piperazine- 1-yl-quinolin-4(1H)-one-3-carbaldehyde, dissolved in 20ml of absolute ethanol, added dropwise with 0.5ml of piperidine, after reflux reaction for 24h, the resulting solid was collected by filtration and recrystallized with DMF-ethan...

Embodiment 3

[0054] The 3,3'-methylene-bisfluoroquinolone derivative containing ethylquinoline ring in this example is 1-ethyl-6-fluoro-7-piperazin-1-yl-3-[1-ring Propan-6-fluoro-7-piperazin-1-yl-2,3-dihydro-quinolin-4(1H)-one-3-ylidenemethyl]quinolin-4(1H)-one, its chemical The structural formula is:

[0055]

[0056] That is, R in formula (I) 1 is cyclopropyl, R 2 , R 3 and R 4 are hydrogen atoms, and X is a hydrocarbon group.

[0057] The preparation method of the 3,3'-methylene-bisfluoroquinolone derivatives containing ethylquinoline ring in this example is: take 0.52g (1.8mmol) of 1-cyclopropyl-6-fluoro-7- Piperazin-1-yl-2,3-dihydro-quinolin-4(1H)-one with 0.55 g (1.8 mmol) of 1-ethyl-6-fluoro-7-piperazin-1-yl-quinone Phenyl-4(1H)-one-3-carbaldehyde was dissolved in 20ml of absolute ethanol, 0.5ml of piperidine was added dropwise, after reflux reaction for 24h, left overnight, the resulting solid was collected by filtration, and recrystallized with DMF-ethanol to obtain Ligh...

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 discloses a 3,3'-methylene-bisfluoroquinolone derivative containing ethylquinoline rings as well as a preparation method and application thereof. The 3,3'-methylene-bisfluoroquinolone derivative containing ethylquinoline rings is a compound having the following structural general formula (I) as shown in the specification, wherein R1 is ethyl, cyclopropyl or fluoroethyl; R2 is H or methyl; R3 is H, methyl or ethyl; R4 is H or methyl; and X is CH, N, F-C or CH3O-C. The preparation method comprises the following steps of effectively combining fluoroquinolone pharmacophores and alpha, beta-unsaturated ketone pharmacophores and constructing two quinolone structural units into the 3,3'-methylene-bisfluoroquinolone derivative by virtue of condensation reaction, the anti-tumor activity is increased, the toxic and side effects to normal cells are decreased, the synergistic and toxicity-reducing effects are achieved and the 3,3'-methylene-bisfluoroquinolone derivative can be used as an anti-tumor active material to develop anticancer drugs having novel structures.

Description

technical field [0001] The invention belongs to the technical field of difluoroquinolone derivative compounds, in particular to a 3,3'-methylene-bisfluoroquinolone derivative containing an ethyl quinoline ring, and also to a 3'-difluoroquinolone derivative containing an ethyl quinoline ring. , Preparation method and application of 3'-methylene-bisfluoroquinolone derivatives. Background technique [0002] Tumor is one of the biggest diseases that threaten human life and health. Due to the high toxicity of the current anti-tumor drugs and the poor tolerance of patients, the cure rate of tumor diseases is low. Therefore, it is increasingly urgent to develop anti-tumor drugs with new structures. Although there are many ways to discover new drugs, the structural modification of existing drugs is still the most successful and economical strategy. Based on the similarity in sequence and function between the target enzyme of antibacterial fluoroquinolones—topoisomerase and the cor...

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): C07D215/38C07D519/00A61P35/00A61P35/02
CPCC07D215/38C07D471/04
Inventor 崔占军文曙光赵辉高留州谢玉锁李涛吴书敏倪礼礼闫强胡国强
Owner HENAN UNIVERSITY
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

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