Preparation method of palmatine hydrochloride
A technique for palmatine hydrochloride and berberine hydrochloride, which is applied in the field of synthesis of palmatine hydrochloride, can solve the problems of poor feasibility, unsuitability for large-scale production, and pending development of palmatine hydrochloride, and achieve easy operation and large scale Production and economical applicability, beneficial effect on the protection of natural resources and ecological environment
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Embodiment 1
[0018] (1) Weigh 200g of berberine hydrochloride, 1L of toluene and 500g of methanesulfonic acid into a 3L round-bottomed flask equipped with a reflux condenser, thermometer and stirring device. Keep the temperature of the reaction solution at 90°C and stir for about 12 hours. TLC monitors the disappearance of the raw materials, and the stirring is stopped. Add ethanol and stir at reflux for 2 hours. After cooling to room temperature and standing for crystallization, 151 g of 2,3-dihydroxyberberine methanesulfonate was obtained with a yield of 78%.
[0019] (2) Take 100g of the 2,3-dihydroxyberberine methanesulfonate obtained in the above steps and put it into a 3L round bottom flask, add 114g of methyl p-toluenesulfonate and 46g of potassium carbonate, and acetonitrile as the solvent and reflux for 5 hours. TLC monitors the disappearance of the raw materials, and the stirring is stopped. Reduce to room temperature, filter, and wash the filter cake with a small amount of water....
Embodiment 2
[0022] (1) Weigh 200g of berberine hydrochloride, 1L of toluene and 500g of methanesulfonic acid into a 3L round-bottomed flask equipped with reflux condenser, thermometer and stirring device. Keep the temperature of the reaction solution at 90℃. After about 12 hours, TLC Monitor the disappearance of the raw materials and stop stirring. Add ethanol and stir at reflux for 2 hours. After cooling to room temperature and standing for crystallization, 154 g of 2,3-dihydroxyberberine methanesulfonate was obtained with a yield of 80%.
[0023] (2) Take 100g of 2,3-dihydroxyberberine methanesulfonate obtained in the above steps and put it into a 3L round bottom flask, add 600ml of N,N-dimethylformamide to dissolve, add 100ml of dimethyl carbonate and cesium carbonate 109g, after addition, stirred at 140°C for 8 hours, TLC monitored the disappearance of the raw materials, and stopped stirring. It was cooled to room temperature, the solvent was removed, and the precipitated solid was col...
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