A kind of fluorescent probe and its preparation method and its application in the reversible detection of bisulfite/hydrogen peroxide in vivo
A bisulfite and fluorescent probe technology, applied in the field of fluorescent probes, can solve the problems of not being able to monitor redox balance at the same time, and fluorescent probes have not been reported, and achieve easy scale production, simple process, and easy control of conditions Effect
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[0039] The present invention provides a method for preparing a fluorescent probe described in the above scheme, comprising the following steps:
[0040] The raw material I and the raw material II are subjected to a nucleophilic addition-elimination reaction under the catalysis of piperidine to obtain a fluorescent probe having the structure shown in formula 1;
[0041] The structures of the raw material I and the raw material II are shown in formula 2 and formula 3 respectively:
[0042]
[0043] In formula 3, R is -CH 3 、-CH 2 CH 3 、-CH 2 CH 2 CH 3 、-CH 2 CH 2 CH 2 OH or
[0044] In the present invention, the molar ratio of the raw material I and the raw material II is preferably 1:1; the present invention has no special requirements on the source of the raw material I and the raw material II, and adopts commercially available products well known in the art or adopts The well-known preparation method can be prepared by oneself. In the present invention, the so...
Embodiment 1
[0054] (1) Synthesis of fluorescent probes
[0055] Each 1mol of the two raw materials shown in formula 2 and formula 3 (in formula 3, R=-CH 2 CH 3 ) was dissolved in 20 mL of dry methanol, and then 2 drops of piperidine were added to catalyze the reaction. The mixture was heated under reflux for 10 hours to stop the reaction, and the organic solvent was distilled off under reduced pressure. The crude product was purified by chromatographic silica gel column (developing solvent: dichloromethane / ethyl acetate v / v, 20:1) to obtain the blue-purple target product with a yield of 31%. The characterization data of the resulting product are as follows:
[0056] 1 H NMR (DMSO-d 6 ,600MHz),δ(ppm)8.49(s,1H),8.38(s,1H),8.25(s,1H),8.23(d,J=7.38Hz,1H),7.80(t,J=9.96Hz, 2H), 7.72(d, J=8.16Hz, 1H), 7.65(d, J=8.16Hz, 1H), 7.52(t, J=6.9Hz, 1H), 7.36(d, J=8.52Hz, 1H) ,7.28(t,J=6.84Hz,1H),7.21(s,1H),4.46(d,J=6.54Hz,2H),3.69(m,4H),3.09(m,2H),2.85(m, 2H), 1.90(m, 2H), 1.28(t, J=6.54Hz, 12H)...
Embodiment 2
[0081] Each 1mol of the two raw materials shown in formula 2 and formula 3 (in formula 3, R=-CH 3 ) was dissolved in 20 mL of dry methanol, and then 2 drops of piperidine were added to catalyze the reaction. The mixture was heated under reflux for 6 hours, the reaction was stopped, and the organic solvent was distilled off under reduced pressure. The crude product was purified by chromatographic silica gel column (developing solvent: dichloromethane / ethyl acetate v / v, 20:1) to obtain the blue-purple target product, which conforms to formula 1 (R=-CH 3 ), the fluorescent probe was successfully prepared.
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