A kind of preparation method of doxycycline hydrochloride
A technology of doxycycline hydrochloride and benzene mesylate, applied in the field of preparation of doxycycline hydrochloride, can solve the problems of many process steps, low overall yield of doxycycline hydrochloride, etc. The effect of improving selectivity and yield, simplifying the preparation process
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Embodiment 1
[0057] The preparation of embodiment 1 doxycycline sulfosalicylate
[0058] Add 150 ml of 50% ethanol aqueous solution into the hydrogenation kettle, add 2.5 g of palladium carbon (dried) under stirring, 0.05 g of methylthiouracil, 4.5 g of quinoline, 0.04 g of pyridine, and 0.15 g of sulfamethazine, and start Heat to 55°C and keep stirring for 30min. Add 50.0 g of 11a-chloro-6-methine oxytetracycline p-toluenesulfonate, nitrogen replacement 3 times, hydrogen replacement 3 times, hydrogen pressure 2kg / cm 2 , Stirring reaction 8 ~ 10h. After the reaction is complete, filter out the palladium carbon, cool to room temperature, add 45.0 g of sulfosalicylic acid, stir and crystallize at room temperature, filter, wash the filter cake with ethanol, and blow dry at 40-50 ° C to obtain 46.9 g of a yellow powdery solid , yield 92.0%.
Embodiment 2
[0059] The preparation of embodiment 2 doxycycline hydrochloride
[0060] Add 40.0 g of the α-6-deoxyoxytetracycline sulfosalicylate obtained above into 270 ml of 8% hydrogen chloride ethanol solution, heat and stir until dissolved, add 18 ml of purified water, stir and crystallize for 2 hours, and cool to room temperature , stirred for 16h. After filtering, the filter cake was washed with ethanol, and air-dried at 40-50° C. to obtain 27.8 g of a yellow powdery solid with a yield of 89.8% and a purity of 99.6%.
Embodiment 3
[0062] Add 150ml of 50% ethanol aqueous solution into the hydrogenation kettle, add 2.5g of palladium carbon (dried) under stirring, 4.5g of quinoline, 0.04g of pyridine, and 0.25g of sulfamethazine, start heating to 55°C, and keep stirring 30min. Add 50.0 g of 11a-chloro-6-methine oxytetracycline p-toluenesulfonate, nitrogen replacement 3 times, hydrogen replacement 3 times, hydrogen pressure 2kg / cm 2 , Stir the reaction for 8-10h. After the reaction is complete, filter out the palladium carbon, cool to room temperature, add 45.0 g of sulfosalicylic acid, stir and crystallize at room temperature, filter, wash the filter cake with ethanol, and blow dry at 40-50 ° C to obtain 37.3 g of a yellow powdery solid , yield 73.0%.
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