Amido benzopyran cyanine fluorochrome and probe as well as synthetic method and application thereof

A technology of pyranocyanine and fluorescent dyes, which is applied in the fields of chemistry and biology, can solve the problems of difficult modification of cyanine dyes, poor stability, and influence on promotion, and achieve good light stability, reduce light damage, and enhance penetration ability Effect

Active Publication Date: 2019-01-01
HUNAN UNIV
View PDF0 Cites 16 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the current cyanine dyes have the disadvantages of poor stability, and are easily attacked by various biolo

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
  • Amido benzopyran cyanine fluorochrome and probe as well as synthetic method and application thereof
  • Amido benzopyran cyanine fluorochrome and probe as well as synthetic method and application thereof
  • Amido benzopyran cyanine fluorochrome and probe as well as synthetic method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0059] The preparation of embodiment 1 intermediate 5

[0060] The synthetic route of intermediate 5 is as follows, specifically comprises the following steps:

[0061]

[0062] Put 46mmol of compound 1 and 4.4mL of acetic anhydride in a round-bottomed flask, add 200mL of tetrahydrofuran to dissolve, then stir the reaction at room temperature for 2h, remove the tetrahydrofuran in the reaction solution after the reaction is complete, and obtain compound 2 after recrystallization;

[0063] Take 4mmol of compound 2, 4mmol of phthalic anhydride and 10mmol of aluminum trichloride in a round-bottomed flask, add 13mL of 1,1,2,2-tetrachloroethane under ice cooling until the reactants are completely dissolved, and react at room temperature for 2h. Then the reaction was heated to 100°C and stirred for 12 hours; after the reaction was completed, it was cooled to room temperature, poured into ice water to precipitate a solid, and compound 3 was obtained;

[0064] Take 1 mmol of compou...

Embodiment 2

[0066] Embodiment 2 Aminobenzopyranocyanine fluorescent dye NIR-NH of type I structural formula 2 Synthesis

[0067] 0.2mmol of intermediate 5 (prepared in Example 1) and 0.2mmol of X are C(CH 3 ) 2 , R 1 is methyl, L is hydrogen, and m is 0, compound 6-1 (structural formula is as follows) is placed in a round-bottomed flask, mixed in 4 mL of acetic anhydride solution, and stirred at room temperature for 1.5 h; The instrument was spin-dried under reduced pressure, and purified with a silica gel column to obtain intermediate 8-1 (structural formula is as follows).

[0068]

[0069] Intermediate 8-1 (0.11g, 0.2mmol) was dissolved in 6mL of acetic acid / concentrated hydrochloric acid (1:2, v / v) solution, stirred at 110°C for 2h, then cooled to room temperature, and the mixture was poured into ice water , basified with sodium hydroxide solution, stirred at room temperature for 0.5h, then extracted with dichloromethane, dried the organic phase with anhydrous sodium sulfate, t...

Embodiment 3

[0073] Example 3 Aminobenzopyranocyanine Fluorescent Dye Ben-NIR-NH of Type II Structural Formula 2 Synthesis

[0074] 0.2mmol of intermediate 5 (prepared in Example 1) and 0.2mmol of X are C(CH 3 ) 2 , R 1 is methyl, L is hydrogen, and m is 0, compound 7-1 (structural formula is as follows) is placed in a round-bottomed flask, mixed in 4 mL of acetic anhydride solution, and stirred at room temperature for 2 hours; after the reaction is complete, the reaction solution is It was spin-dried under reduced pressure and purified by a silica gel column to obtain intermediate 9-1 (structural formula is as follows).

[0075]

[0076] Intermediate 9-1 (0.138g, 0.2mmol) was dissolved in 6mL of acetic acid / concentrated hydrochloric acid (1:2, v / v) solution, stirred at 110°C for 2h. Then it was cooled to room temperature, the mixture was poured into ice water, basified with sodium hydroxide solution, stirred at room temperature for 0.5h, then extracted with dichloromethane, the org...

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 an amido benzopyran cyanine fluorochrome and a probe as well as a synthetic method and application thereof. The fluorochrome is any one kind in structural formulas I-II as shown in the description. According to near infrared fluorochromes I and II with an amido benzopyran cyanine structure provided by the invention, the fluorescence quantum yield is high, the light stability is good, the fluorescence-emission spectrum ranges from 650nm to 900nm and belongs to near infrared spectrum areas, the fluorescence imaging analysis in a living body level can be realized, meanwhile, the penetrating power of biological tissue samples is enhanced, the light damage is reduced, the fluorescence of biomolecules per se is relatively weak, and the biological system can be prevented from self-emitting fluorescent interference to obtain a relatively high signal-to-noise ratio, so that the sensitivity is improved.

Description

technical field [0001] The invention belongs to the field of chemistry and biotechnology, and in particular relates to an aminobenzopyranocyanine fluorescent dye and a probe as well as a synthesis method and application thereof. Background technique [0002] In recent years, with the development of fluorescence analysis and detection technology, fluorescent dyes have been widely used in various fields such as biomolecular labeling, enzyme analysis, environmental monitoring, cell staining, and clinical examination and diagnosis. The development of various functional fluorescent dye molecules with practical value has become a research hotspot that has attracted much attention. Molecular fluorescent probes based on organic fluorescent dyes have many advantages such as high sensitivity, easy operation, good reproducibility, good membrane permeability, and in situ detection. In addition, combined with fluorescence imaging technology, molecular fluorescent probes can be convenien...

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): C09K11/06C09B23/10G01N21/64
CPCC09B23/105C09K11/06C09K2211/1007C09K2211/1029C09K2211/1088G01N21/643G01N21/6486
Inventor 袁林程丹张晓兵吕芸柳东杰魏艳芬
Owner HUNAN UNIV
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