Preparation method for cannflavin compounds
AssigneeDeyi Pharmaceuticall Ltd.
InventorsJunlu LUO, Hongtao MOU, Yesong DU, Xin TAN, Shubin WANG, Pingping ZHANG, Lan LAN
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AssigneeDeyi Pharmaceuticall Ltd.
InventorsJunlu LUO, Hongtao MOU, Yesong DU, Xin TAN, Shubin WANG, Pingping ZHANG, Lan LAN
Estimating the term…
Disclosed in the present invention is a preparation method for cannflavin compounds. The preparation method has advantages such as cheap and easily available raw materials, few reaction steps, short production period, and easy operation. The method comprises: first, condensing 4′-hydroxy-3′-methoxyacetophenone and diethyl carbonate (DEC) under an alkaline condition to obtain ethyl 4′-hydroxy-3′-methoxybenzoylacetate, next, reacting 1,3,5-trihydroxybenzene with geraniol to obtain (E)-2-(3,7-dimethyloct-2,6-dien-1-yl)benzene-1,3,5-triphenol; and finally, condensing ethyl 4′-hydroxy-3′-methoxybenzoylacetate and (E)-2-(3,7-dimethyloct-2,6-dien-1-yl)benzene-1,3,5-triphenol at high temperature to produce cannflavin A and/or cannflavin C, and then carrying out separation and purification to obtain pure cannflavin A and cannflavin C.
A preparation method for a cannflavin compound, comprising the following steps:
Use of ethyl 4′-hydroxy-3′-methoxybenzoylacetate in preparing a compound, wherein the compound is a cannflavin compound.
Dependencies are inferred from the claim text.