Preparation method of parecoxib sodium synthesis technology impurities
A technology of parecoxib sodium and synthesis process, applied in the field of preparation of process impurity 4-benzenesulfonic acid ethyl ester, can solve the problems such as no impurity synthesis literature report and the like, achieve the effect of simple operation and control of finished product quality
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Embodiment 1
[0037] Example 1: A method for preparing parecoxib sodium synthesis process impurity 4-(5-methyl-3-phenyl-isoxazolyl) ethyl benzenesulfonate
[0038] Add 8.0 g of 5-methyl-3,4-diphenylisoxazole and 40 g of dichloromethane into the reaction flask, cool down to -5°C in an ice bath, start adding 32 g of chlorosulfonic acid dropwise, and control the internal temperature of the reaction solution to < 5 ℃. After the addition of chlorosulfonic acid was completed, the temperature was slowly raised to 35° C., and the reaction was kept for 10 hours. The reaction solution was monitored by TLC until the spot of the raw material 5-methyl-3,4-diphenylisoxazole disappeared (the developer was ethyl acetate:petroleum ether=1:6, v:v), and the reaction was stopped. Add 100 g of crushed ice to the reaction flask, stir for 1 h, pour into a separatory funnel and let stand to separate layers, and separate the lower aqueous phase. Add 5 g of anhydrous sodium sulfate to the upper organic phase, dry ...
Embodiment 2
[0044] Embodiment 2: A kind of synthetic method of parecoxib sodium process impurity 4-(5-methyl-3-phenyl-isoxazolyl) ethyl benzenesulfonate
[0045] Add 8.0 g of 5-methyl-3,4-diphenylisoxazole and 40 g of dichloromethane into the reaction flask, cool down to -5°C in an ice bath, start adding 40 g of chlorosulfonic acid dropwise, and control the internal temperature of the reaction solution to <5 ℃. After the addition of chlorosulfonic acid was completed, the temperature was slowly raised to 35° C., and the reaction was kept for 10 hours. The reaction solution was monitored by TLC until the spot of the raw material 5-methyl-3,4-diphenylisoxazole disappeared (the developer was ethyl acetate:petroleum ether=1:6, v:v), and the reaction was stopped. Add 100 g of crushed ice to the reaction flask, stir for 1 h, pour into a separatory funnel and let stand to separate layers, and separate the lower aqueous phase. Add 5 g of anhydrous sodium sulfate to the upper organic phase, dry i...
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