Fluorescent dye with nitrobenzimidazole as RNA (ribonucleic acid) recognition group as well as preparation method and application of fluorescent dye
A nitrobenzimidazole and fluorescent dye technology, applied in the field of fluorescent dyes, can solve the problems of low phototoxicity, biological toxicity and photobleaching, poor photostability, high phototoxicity, etc., and achieve good cell membrane permeability, High selectivity and good specificity
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[0061] The preparation method of the fluorescent dye using nitrobenzimidazole as the RNA recognition group comprises the following steps: reacting the parent body of D with 6-nitrobenzimidazole in a molar ratio of 1:1-1:5, and reacting The temperature is 25-150°C, the reaction time is 6-48 hours, the reaction solvent is one or more of dichloromethane, ethanol and ethyl acetate, and the reaction is carried out in the presence of an organic base, with 4-dimethylamino Pyridine is the catalyst.
[0062] The fluorescent dye with nitrobenzimidazole as the RNA recognition group is a compound of general formula V, and the preparation method of the compound of general formula V comprises the following steps:
[0063]
[0064] (1), ethanolamine and concentrated hydrobromic acid according to the literature (AndrewF, DianaF, KarenLG.Drugs.1992.43 (4): 561:) to prepare the compound of general formula VIII
[0065]
[0066] (2), the preparation of the compound of general formula VI c...
Embodiment 1
[0090] Prepare fluorescent probe BIQ:
[0091]
[0092] (1) Synthesis of the compound of general formula VIII
[0093] Ethanolamine (122.2g, 120.8mL, 2.0mol) was added dropwise to concentrated hydrobromic acid (733mL, 5.4mol) under stirring at 10°C, and the temperature was controlled at 10-15°C. After dropping, continue stirring for 1h, and then add 400mL of xylene , warming up to reflux, and after separating about 515mL of water (containing a small amount of hydrobromic acid) with a water separator, the water pump decompresses to evaporate xylene and excess hydrobromic acid. Cool the solution to about 70%, add ice-cold (usually about 4°C) acetone (365mL), stir the mixture fully, so that the dark-colored solid is fully soaked, cool, suction filter, and cool (usually about 4°C) ) washed with acetone (150mL), sucked dry, and dried to obtain a white crystalline product of the compound of general formula VIII, weighing 358.8g, yield 87.6%, M.P.173-175°C.
[0094] (2) Synthesi...
Embodiment 2
[0136] Preparation of Fluorescent Probe IX
[0137]
[0138] (1) Synthesis of the compound of general formula X
[0139] 10mmol of p-fluorobenzaldehyde and 10mmol of 6-nitrobenzimidazole were dissolved in 20ml of dry DMF (dimethyl fumarate), each time adding a small amount of potassium carbonate (catalyst) to the mixed solution, carbonic acid The total amount of potassium was 12 mmol, and the addition was completed within 15 minutes. Reacted under stirring at 110°C for 10-12h. After the reaction was completed, the reaction system was cooled to room temperature, filtered with suction, and the filtrate was extracted with ethyl acetate. The organic phase was washed 3 times with water, dried over anhydrous sodium sulfate, and concentrated to obtain an oil. The product was separated by column chromatography.
[0140] (2) Synthesis of fluorescent dye (referred to as fluorescent probe IX) with nitrobenzimidazole as RNA recognition group
[0141] Put 0.85mmol of the intermedia...
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