A kind of preparation method of prednisolone sodium phosphate intermediate
A technology of prednisolone sodium phosphate and prednisolone phosphate, which is applied in the field of medicinal chemistry, can solve problems such as serious environmental pollution, failure to meet energy conservation and environmental protection, and unfavorable quality of raw materials, and achieve more guaranteed quality and yield , to avoid impurities, to avoid the effect of damage
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Embodiment 1
[0017] A. In the reaction bottle, add 50g of prednisolone and 500ml of MTHP under the protection of nitrogen, stir and cool down to -55~-60℃, slowly add 40ml of pyrophosphoryl chloride dropwise within 40min, after the addition is completed, keep warm for 1h, and detect by TLC No raw material points;
[0018] B. Add 100ml of purified water to quench the reaction, let it stand for 2 hours, and separate the layers;
[0019] C. The organic phase was extracted twice with 150ml of purified water each time, and then 2.5g of activated carbon was added to the organic phase for decolorization at 30°C for 1 hour;
[0020] D. Filter, concentrate under reduced pressure at 60°C to a paste, cool to below 0°C and discharge, vacuum-dry at 60°C to constant weight, HPLC99.5%, maximum simplex 0.2%, yield 115.2%.
Embodiment 2
[0022] A. In the reaction bottle, add 100g of prednisolone and 1000ml of MTHP under the protection of nitrogen, stir and cool down to -55~-60℃, slowly add 80ml of pyrophosphoryl chloride dropwise within 1 hour, after the addition is completed, keep it warm for 80min, and detect it by TLC No raw material points;
[0023] B. Add 200ml of purified water to quench the reaction, let it stand for 3 hours, and separate the layers;
[0024] C. The organic phase was extracted twice with 300ml of purified water each time, and then 5g of activated carbon was added to the organic phase for decolorization at 40°C for 1.5h;
[0025] D. Filtrate, concentrate under reduced pressure at 60°C to a paste, cool to below 0°C and discharge, vacuum-dry at 70°C to constant weight, HPLC99.4%, maximum simplex 0.25%, yield 116.3%, of which MTHP800ml was recovered.
Embodiment 3
[0027] A. In the reaction bottle, add 50g of prednisolone under the protection of nitrogen, recover 500ml of MTHP, stir and lower the temperature to -55~-60℃, slowly add 50ml of pyrophosphoryl chloride dropwise within 45min, after the addition is completed, keep warm for 1h, TLC Detect no raw material point;
[0028] B. Add 75ml of purified water to quench the reaction, let it stand for 3 hours, and separate the layers;
[0029] C. The organic phase was extracted twice with 200ml of purified water each time, and then 3g of activated carbon was added to the organic phase for decolorization at 40°C for 1.5h;
[0030] D. Filtrate, concentrate under reduced pressure at 60°C to a paste, cool to below 0°C and discharge, vacuum-dry at 60°C to constant weight, HPLC99.5%, maximum simplex 0.21%, yield 116.5%.
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