Novel isopentenyl flavonoid compound and preparation method and application thereof
A technology of prenyl flavonoids and compounds, which is applied in the field of novel prenyl flavonoids and their preparation, and achieves the effects of clear transformation mechanism, simple transformation method and convenient preparation method
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Embodiment 1
[0027] (1) Preparation of compounds
[0028] Take 100 g of dried epimedium, pulverize it, and ultrasonically extract it with 80% ethanol aqueous solution for 3 times, each time for 2 hours, filter, combine the extracts, recover the solvent under reduced pressure, and obtain the extract. After the extract was dissolved in 1L of water, put it on a D101 resin column (200g packing). After loading, gradient elution was carried out. Each gradient is a component. After the 30:70 water-ethanol eluted component is concentrated, the concentrated solution is separated by ODS column gradient elution, and the eluents used are 50:50, 45:55, 40 :60, 35:55, 30:70 water-methanol, concentrate the water-methanol 30:70 eluent components, and then use high-efficiency preparative liquid phase purification after concentration, using octadecyl bonded silica gel chromatography column to Water-acetonitrile 30:70 (V / V) is the mobile phase, the detection wave is 254nm, Capcell pak AQ column (250×10mm, 5...
Embodiment 2
[0038] Weigh 10 mg of 6"'-deoxy-4"'-carbonyl-2"'-β-D-allosyl icariin sample, add 10 mL of ethanol solution with a volume fraction of 50% to dissolve, add 10 μL of molar concentration It is a 1mol / L hydrogen chloride aqueous solution, stirred at 50°C for 20 minutes, after the reaction is completed, separated and purified by semi-preparative liquid phase, and lyophilized with a lyophilizer to obtain 6.0 mg of icariin.
Embodiment 3
[0040] Weigh 10 mg of 6"'-deoxy-4"'-carbonyl-2"'-β-D-allosyl icariin sample, add 10 mL of ethanol solution with a volume fraction of 10% to dissolve, and add to a pressurized tank In the tank, when the temperature in the tank reaches 140°C, it is treated for 2 hours. After the reaction is completed, it is separated and purified by semi-preparative liquid phase, and lyophilized with a lyophilizer to obtain 5.7 mg of icariin.
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