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

Fluorescent probes for a class of tricyclic 2-aminopyridinium salts, preparation methods and applications thereof

An aminopyridinium salt, fluorescent probe technology, applied in the field of biomedical materials, can solve the problems of aggregation-induced luminescence quenching, reducing signal-to-noise ratio, reducing sensitivity, etc.

Active Publication Date: 2022-02-15
SOUTH CHINA UNIV OF TECH
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, due to its large π-conjugated system, traditional fluorescent materials have the problem of aggregation-induced luminescence quenching (ACQ) in the aggregated state; their high background fluorescence will also reduce the signal-to-noise ratio in the detection and diagnosis process. will greatly reduce the sensitivity of its detection

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
  • Fluorescent probes for a class of tricyclic 2-aminopyridinium salts, preparation methods and applications thereof
  • Fluorescent probes for a class of tricyclic 2-aminopyridinium salts, preparation methods and applications thereof
  • Fluorescent probes for a class of tricyclic 2-aminopyridinium salts, preparation methods and applications thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0078] Embodiment 1 Preparation of a fluorescent probe (BMTAPC-7)

[0079]

[0080] The synthetic route is as follows:

[0081]

[0082] 4-bromobenzoyl chloride (10mmol, 2.19g), 4-methoxyphenylacetylene (10mmol, 1.32g), PdCl 2 (PPh 3 ) 2 (0.2mmol, 144mg) and cuprous iodide (0.4mmol, 76mg) were added to a 250mL two-necked round-bottomed flask, then evacuated with a pump, replaced with nitrogen three times for 3 times; then added dry dichloromethane (100mL) . Triethylamine (11 mmol, 1.5 mL); the reaction was stirred at room temperature for 5 h (reaction progress was monitored by TLC). After the substrate reaction is complete, slowly add anhydrous AlCl to the reaction system 3 (1mmol, 133mg) and DBU (30mmol, 4.5mL), the reaction mixed solution was stirred at room temperature for 2h (TLC monitoring until the reaction was complete), the mixed reaction solution was filtered to remove the catalyst, the filtrate was concentrated, acidified with 20mL of 1M hydrochloric acid, ...

Embodiment 2

[0084] Embodiment 2 Preparation of a fluorescent probe (BMTAPC-5)

[0085]

[0086] The synthetic route is as follows:

[0087]

[0088] 4-bromobenzoyl chloride (10mmol, 2.19g), 4-methoxyphenylacetylene (10mmol, 1.32g), PdCl 2 (PPh 3 ) 2 (0.2mmol, 144mg) and cuprous iodide (0.4mmol, 76mg) were added to a 250mL two-necked round-bottomed flask, then evacuated with a pump, replaced with nitrogen three times for 3 times; then added dry dichloromethane (100mL) , triethylamine (11mmol, 1.5mL), the reaction was stirred at room temperature for 5h (reaction progress was monitored by TLC), and after the substrate had completely reacted, anhydrous AlCl was slowly added to the reaction system 3 (1 mmol, 133 mg) and DBN (30 mmol, 4.5 mL). The reaction mixed solution was stirred at room temperature for 2 h (TLC monitoring until the reaction was complete), the mixed reaction solution was filtered to remove the catalyst, the filtrate was concentrated, acidified with 20 mL of 1M hydroc...

Embodiment 3

[0090] Embodiment 3 Preparation of a fluorescent probe (BMTAP-7)

[0091]

[0092] The synthetic route is as follows:

[0093]

[0094] The solid BMTAPC-7 (1mmol, 485mg) synthesized in Example 1 was dissolved in acetone, an aqueous solution of potassium hexafluorophosphate (2mmol, 368mg) was added, stirred for 2h, the mixture was added with water and then filtered, and the filtered solid was washed with water to remove inorganic salts , dried to give 535 mg of yellow solid BMTAP-7 in 90% yield.

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 belongs to the technical field of fluorescent probes, and discloses a fluorescent probe of a tricyclic 2-aminopyridinium salt, a preparation method and an application thereof. The structure of the fluorescent probe of described tricyclic 2-aminopyridinium salt is formula I, wherein: R 1 , R 2 Independently aryl, heteroaryl, C 1‑18 Alkyl, C 3‑8 Electron-donating group of cycloalkyl or aromatic ring derivatives; X is a monovalent anion; m is any integer from 0 to 2; n is any integer from 0 to 1. The invention also discloses a preparation method of the fluorescent probe. The fluorescent probe of the present invention has aggregation-induced luminescent properties, can realize rapid staining and identification of microorganisms, and exhibits specific, efficient and sensitive characteristics. The fluorescent probe of the invention has excellent antibacterial effect. The fluorescent probe of the present invention is used to prepare reagents for specifically staining mitochondria and negatively charged microorganisms on the surface, and simultaneously used for preparing reagents and antibacterial agents for distinguishing dead and alive states of microorganisms. .

Description

technical field [0001] The invention belongs to the field of biomedical materials, and in particular relates to a fluorescent probe of a tricyclic 2-aminopyridine salt, a preparation method thereof, and an application in microbial marker recognition and bacteriostasis. Background technique [0002] Under normal conditions, microorganisms and humans are interdependent to maintain the balance of physiological metabolism; once the balance is broken, it is easy to cause diseases. Bacterial infection can cause a variety of diseases and seriously threaten human health. Diagnosis of the bacteria is the first step in the course of treatment. At present, the Gram staining method is mainly used, which is complicated to operate and cannot realize in situ monitoring of live bacteria. At the same time, in the process of treatment, due to the abuse of antibiotics, the emergence of drug-resistant bacteria makes the treatment more difficult. Therefore, it is very important to develop acc...

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): C07D471/16C09K11/06A61P31/04A61K31/55A61K31/519G01N21/64
CPCC07D471/16C09K11/06A61P31/04G01N21/6428C09K2211/1007C09K2211/1044G01N2021/6439
Inventor 唐本忠秦安军王柄楠胡蓉蓉赵祖金王志明
Owner SOUTH CHINA UNIV OF TECH
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