Preparation method of huperzine A
A technology of huperzine A and exchange resin, which is applied in nervous system diseases, organic chemistry, drug combination, etc., can solve the problems of high production cost, serious pollution, and low product yield
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Embodiment 1
[0016] Take 10Kg of dry coarse powder of Melaleuca Tower, add 2 times the amount of 1% tartaric acid solution for ultrasonic extraction, power 100W, extract for 10 minutes, filter, pass through 201 × 2 type anion exchange resin, extract the medicinal solution with chloroform, combine the chloroform layers, reduce Chloroform was recovered under pressure and concentrated, added to AB-8 macroporous adsorption resin column, washed with water to remove impurities, eluted with 50% ethanol, collected eluate, recovered ethanol under reduced pressure, added acetone-chloroform (1:1) to crystallize , washed and dried to obtain 1.6 g of huperzine A, which was detected by HPLC with a purity of 95.2%.
Embodiment 2
[0018] Take 10Kg of dry coarse powder of Melaleuca Tower, add 30 times the amount of 1% hydrochloric acid solution for ultrasonic extraction, power 2000W, extract for 30 minutes, filter, pass through 201×4 type anion exchange resin, extract the medicinal solution with chloroform, combine the chloroform layers, and reduce Chloroform was recovered under pressure and concentrated, added to H-103 macroporous adsorption resin column, washed with water to remove impurities, eluted with 90% ethanol, collected eluate, recovered ethanol under reduced pressure, added acetone-chloroform (1:1) to crystallize , washed and dried to obtain 3.4 g of huperzine A, which was detected by HPLC with a purity of 94.4%.
Embodiment 3
[0020] Get 10Kg of dry coarse powder of Melaleuca Tower, add 20 times the amount of 1% tartaric acid solution for ultrasonic extraction, power 600W, extract for 20 minutes, filter, pass through 201×7 type anion exchange resin, extract the medicinal solution with chloroform, combine the chloroform layers, and reduce Chloroform was recovered under pressure and concentrated, added to D-101 macroporous adsorption resin column, washed with water to remove impurities, eluted with 70% ethanol, collected eluate, recovered ethanol under reduced pressure, added acetone-chloroform (1:1) to crystallize , washed and dried to obtain 2.4 g of huperzine A, which was detected by HPLC with a purity of 98.6%.
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