A novel isopentenyl flavonoid compound and its preparation method and application
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 the dried Epimedium medicinal material, crush it, and extract it by ultrasonic with 80% ethanol aqueous solution for a total of 3 times, 2 hours each time, filter, combine the extracts, and recover the solvent under reduced pressure to obtain the extract. After the extract was dissolved in 1L of water, it was applied to a D101 resin column (200g filler). After the sample was loaded, gradient elution was carried out. Each gradient is one component. After concentrating the components eluted with 30:70 water-ethanol, the concentrated solution is separated by gradient elution of ODS column, and the eluents used are 50:50, 45:55, 40 : 60, 35:55, 30:70 water-methanol, the water-methanol 30:70 eluent fraction was concentrated, purified by high-efficiency preparative liquid phase after concentration, and an octadecyl-bonded silica gel chromatographic column was used. Water-acetonitrile 30:70 (V / V) is the mobile phase, the det...
Embodiment 2
[0038] Weigh 10 mg of 6"'-deoxy-4"'-carbonyl-2"'-β-D-allosyl icariin sample, add 10 mL of 50% ethanol aqueous solution to dissolve, and add 10 μL of molar concentration It is a 1 mol / L aqueous hydrogen chloride solution, stirred at 50 °C for 20 min, and after the reaction is completed, 6.0 mg of icariin can be obtained by semi-preparative liquid phase separation and purification, and lyophilized by a freeze dryer.
Embodiment 3
[0040] Weigh 10 mg of 6"'-deoxy-4"'-carbonyl-2"'-β-D-allosyl icariin sample, add 10 mL of 10% ethanol aqueous solution to dissolve, and add it to a pressurized tank Inside, when the temperature in the tank reaches 140° C., the treatment is carried out for 2 hours. After the reaction is completed, 5.7 mg of icariin can be obtained by semi-preparative liquid phase separation and purification, and lyophilized by a freeze dryer.
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