Preparation of quinoline-based derivative, and applications of quinoline-based derivative in anti-inflammation

A technology of derivatives and quinolines, applied in the field of preparation and application of quinoline derivatives, to achieve good inhibitory activity, strong inhibitory effect, and good correlation effects

Active Publication Date: 2017-04-26
GUANGDONG UNIV OF TECH
View PDF4 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, it has been found in clinical use that NSAIDs generally have adverse

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
  • Preparation of quinoline-based derivative, and applications of quinoline-based derivative in anti-inflammation
  • Preparation of quinoline-based derivative, and applications of quinoline-based derivative in anti-inflammation
  • Preparation of quinoline-based derivative, and applications of quinoline-based derivative in anti-inflammation

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] Embodiment 1: the synthesis of compound A2, B2, C2, D2, E2, F2, G2

[0035] 1:1.5 aniline and ethyl acetoacetate were catalyzed by polyphosphoric acid, and reacted at 130°C for 2h. After the reaction, cool to room temperature, add crushed ice, adjust the pH to 8 with sodium hydroxide, precipitate a solid, filter it with suction, dry it by infrared, and put it into the next step without purification.

[0036]

Embodiment 2

[0037] Embodiment 2: the synthesis of compound A3-A17

[0038]

[0039] 1:1 equivalent of benzyl bromide and A2 solution DMF, add 5 equivalents of potassium carbonate, react at room temperature for 8h. After the reaction, it was extracted with ethyl acetate and water, and the organic phase was collected and purified by a silica gel column to obtain a white solid with a yield of 87-93%.

Embodiment 3

[0040] Embodiment 3: the synthesis of compound A18-A32

[0041]

[0042] Dioxane was used as a solvent, 1:1.5 equivalents of A3-A17 were reacted with selenium dioxide at 65°C for 2 hours, filtered after the reaction, the filtrate was collected, purified by a silica gel column, and the yield was 71-85%.

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 present invention belongs to the field of pharmaceuticals and chemical industry, and discloses preparation of a quinoline-based derivative based on topoisomerase I inhibition, and uses of the quinoline-based derivative as an anti-inflammatory drug, wherein the structural formula of the quinoline-based derivative is represented by a formula (I), R1 is hydrogen, fluorine, chlorine, bromine, iodine, methoxy, methyl, trifluoromethyl, nitro and nitrile, R2 and R3 respectively are hydrogen, chlorine, bromine, iodine, methoxy, methyl, trifluoromethyl, nitro and nitrile, R4 is carboxyl, methyl, phenyl, cyano and hydrogen, n is 0, 1, 2 and 3, and X is CH or N. According to the present invention, the quinoline-based derivative can remarkably inhibit the activity of human DNA topoisomerase I, provides significant inhibition effects in inflammations, and has broad application space in the preparation of anti-inflammatory drugs. The formula (I) is defined in the specification.

Description

technical field [0001] The invention relates to the fields of medicine and chemical industry, and relates to the preparation and application of quinoline derivatives. Background technique [0002] Inflammation refers to the defense response of living tissue with vascular system to injury factors. The main symptoms of inflammation are fever, redness, and pain. The mechanism is quite complicated. It is generally believed that immune cells gather to the lesion under the action of chemokines and release a large number of inflammatory mediators, leading to inflammation. Bacteria, viruses, rickettsia, mycoplasma, fungi, spirochetes, and parasites are the most common causes of inflammation. [0003] There are two types of drugs for the treatment of inflammation: one is steroidal anti-inflammatory drugs, that is, the glucocorticoid hydrocortisone secreted by the adrenal cortex and its synthetic derivatives; the other is non-steroidal anti-inflammatory drugs (NSAIDs). , non-steroid...

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
IPC IPC(8): C07D417/06A61P29/00A61P43/00
Inventor 杜志云黎鹏辉招敏聪古曜豪周渭张琨
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
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap