A ratiometric fluorescent probe and its preparation method and application
A fluorescent probe, ratiometric technique
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0043] The present invention also provides a method for preparing a ratiometric fluorescent probe, comprising the following steps:
[0044] a) Mix triphenylbromoethylene and 3-formyl-4-hydroxyphenylboronic acid pinacol ester in the presence of toluene, potassium carbonate solution and tetrabutylammonium bromide, and then add a catalyst for the first reaction , compound A is obtained after the first separation and purification; the catalyst is tetrakis (triphenylphosphine) palladium (0);
[0045] The compound A has a structure shown in formula (II):
[0046]
[0047] b) The compound A obtained in step a) and 2-benzimidazole acetonitrile are reacted for the second time in the presence of ethanol and piperidine, and the ratiometric fluorescent probe is obtained after the second separation and purification;
[0048] The ratiometric fluorescent probe has a structure shown in formula (I):
[0049]
[0050] The present invention first mixes triphenylbromoethylene and 3-formyl...
Embodiment 1
[0079] (1) Dissolve 670mg of triphenylbromoethylene in 20mL of toluene, add 4mL of potassium carbonate solution and 50mg of tetrabutylammonium bromide under stirring, then add 500mg of 3-formyl-4-hydroxyphenylboronic acid pinacol ester, stirred at room temperature for 20 min, and finally added 10 mg of catalytic amount of tetrakis(triphenylphosphine) palladium (0), heated to 90 °C under nitrogen protection for 24 h, added ethyl acetate after cooling, washed with water 3 times, and organically The phase was dried over anhydrous sodium sulfate and concentrated, and the reaction crude product was purified by column chromatography to obtain 306 mg of light yellow compound A (yield 41%).
[0080] (2) Dissolve 188mg of compound A and 78.5mg of 2-benzimidazole acetonitrile in 7.5mL of ethanol, add 40μL of piperidine, heat to 80°C under nitrogen protection for 1h, filter after cooling to room temperature, and wash with ethanol for 3 times After vacuum drying, 190.5 mg of milky white p...
Embodiment 2
[0083] (1) Dissolve 670 mg of triphenylbromoethylene in 25 mL of toluene, add 6 mL of potassium carbonate solution and 70 mg of tetrabutylammonium bromide under stirring, and then add 600 mg of 3-formyl-4-hydroxyphenylboronic acid pinacol ester, stirred at room temperature for 30 min, and finally added 15 mg of catalytic amount of tetrakis(triphenylphosphine) palladium (0), heated to 95 °C for 22 h under nitrogen protection, added ethyl acetate after cooling, washed with water for 3 times, and organically The phase was dried and concentrated over anhydrous sodium sulfate, and the crude reaction product was purified by column chromatography to obtain 331 mg of pale yellow compound A (yield 44%).
[0084] (2) Dissolve 188mg of Compound A and 86.5mg of 2-benzimidazole acetonitrile in 9mL of ethanol, add 50μL of piperidine, heat to 82°C under nitrogen protection and reflux for 1.2h, cool to room temperature, filter, and wash with ethanol for 3 times After vacuum drying, 198.5 mg o...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


