Synthesis of 2,8-diaryl(amino) Chaoger base derivatives and their anti-hepg2 activity in human liver cancer

A synthetic method, technology of chaogle base, applied in the synthesis of 2,8-diaryl chaogle base derivatives, in the field of anti-human liver cancer HepG2 activity, can solve the problem of lack of Kang liver cancer drugs, and achieve green reaction , High practical application value, high yield effect

Active Publication Date: 2017-11-03
南京百鑫德诺生物科技有限公司
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] The purpose of the present invention is to provide a kind of synthetic method of 2,8-diaryl (amino) chaogel base derivative, introduce the segment that has physiological activity such as phenothiazine, carbazole into TB skeleton, hope to pass both Compounds with anti-liver cancer activity were screened out by the powerful combination of the company to solve the serious shortage of Kangkang liver cancer drugs

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
  • Synthesis of 2,8-diaryl(amino) Chaoger base derivatives and their anti-hepg2 activity in human liver cancer
  • Synthesis of 2,8-diaryl(amino) Chaoger base derivatives and their anti-hepg2 activity in human liver cancer
  • Synthesis of 2,8-diaryl(amino) Chaoger base derivatives and their anti-hepg2 activity in human liver cancer

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0046] Embodiment 1: 2,8-diaryl (amino) Chaoger base derivatives of the present invention include: 2,8-triarylpyridine (tripyridine) Chaoger base (TB) derivatives, 2,8- Diaryl Chaoger base (TB) derivatives and 2-aryl-8-amino Chaoger base (TB) derivatives;

[0047] 1. The synthetic method of 2,8-triarylpyridine (tripyridine) Chaoger base derivative, the substance structure of "2,8-triarylpyridine (tripyridine) Chaoger base (TB) derivative" is as follows:

[0048]

[0049] The method comprises the steps of:

[0050]

[0051] (a) trifluoroacetic acid, -15°C-0°C, 6d; (b) n-butyl lithium, trimethyl borate, -78°C-r.t.; (c) tetrakistriphenylphosphine palladium, potassium carbonate, toluene, 110°C;

[0052] 1) Synthesis of compound 1a, i.e. 2,8-dibromochauger base:

[0053] Add 60mmol of p-bromoaniline and 120mmol of paraformaldehyde into a 250mL dry three-neck round bottom flask at -15°C, and slowly drop 120mL of trifluoroacetic acid into it with a constant pressure funnel u...

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 synthesis method of 2,8-diaryl(amino) Troger's base derivatives, belonging to the synthesis method of the Troger's base derivatives. The 2,8-diaryl(amino) Troger's base derivatives comprise 2(8)-triarylpyridyl (tripyridyl) Troger's base (TB) derivative, 2,8-diaryl Troger's base (TB) derivative and 2-aryl-8-amino Troger's base (TB) derivative; the synthesis method adopts Suzuki reaction to respectively introduce triarylpyridyl, tripyridyl, phenyl, phenanthryl or anthryl fragment into the TB skeleton, and Ullmann reaction to introduce carbazole, diphenylamine or phenothiazine into the TB skeleton, to obtain the new 2,8-diaryl(amino) Troger's base (TB) derivatives. Four products with excellent human liver cancer HepG2 cell activity resistance are selected from all products with human liver cancer HepG2 cell activity resistance. The method introduces phenothiazine, carbazole and other fragments with physiological activities into the TB skeleton, to design and synthesize 2,8-diaryl(amino) Troger's base derivatives for the first time, so as to screen compounds with liver cancer activity resistance through the combination of both.

Description

technical field [0001] The present invention relates to the technical field of chemical synthesis, in particular to a synthesis method of a 2,8-diaryl (amino) Chaoger base derivative and its anti-human liver cancer HepG2 activity. Background technique [0002] Liver cancer is one of the most common malignant tumors. Current treatment methods include surgery, radiation therapy, and drug therapy. Surgical treatment can delay or even stop the proliferation of liver cancer cells, but it will cause serious secondary damage to the patient. Some patients died of wound infections after surgery to remove the cancerous lesions of their livers, as their bodies were already overwhelmed. Chemical drugs can reduce the patient's pain and prolong the survival time, so it is an ideal important means and treatment method. Therefore, in recent years, the research and development of new drugs against liver cancer has become a multi-disciplinary field of pharmacy, chemistry, pharmacology, and...

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): C07D487/08A61P35/00A61P1/16
CPCC07D487/08
Inventor 宛瑜邱峰黄树颖吴翚
Owner 南京百鑫德诺生物科技有限公司
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