Method for preparing pantoprazole sodium sulfone-nitrogen oxidized impurity
A technology for pantoprazole sodium and oxidized impurities, which is applied in the field of medicine, can solve problems such as being difficult to remove, and achieve the effects of cheap raw materials, simple and easy-to-obtain raw materials, and simple preparation methods
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Embodiment 1
[0030] (1) Add 10g2-chloromethyl-3,4-dimethoxypyridine hydrochloride (compound 1), 10g5-difluoromethoxy-2-mercapto-1H-benzimidazole (compound 2), 100ml of dichloromethane, stirring, dropwise adding 130g of sodium hydroxide solution with a concentration of 10%, stirring at 20-30°C for 2h, standing for stratification, washing the dichloromethane layer twice with 30ml of water each time, and then reducing Pressure distillation obtains yellow oil 16.6g (intermediate 3);
[0031] (2) Dissolve the yellow oil in step (1) with 40ml of acetic acid, add 15.8g of 50% hydrogen peroxide, 0.68g of methyl rhenium trioxide (MTO), heat up to 95°C, and react for 6h; after the reaction is completed, pour the reaction solution into 100ml of water was used to adjust the pH to neutral with 10% sodium hydroxide solution, and the aqueous layer was extracted three times with 50ml (each dosage) of dichloromethane, and the dichloromethane was distilled under reduced pressure to obtain a yellow oil. Dis...
Embodiment 2
[0034] (1) Dissolve the yellow oil in step (1) of Example 1 with 45ml of acetic acid, add 18.2g of 50% hydrogen peroxide, 0.88g of methyl rhenium trioxide (MTO), heat up to 95°C, and react for 7h; after the reaction is completed, The reaction solution was poured into 100ml of water, and the pH was adjusted to be neutral with 10% sodium hydroxide solution. The aqueous layer was extracted three times with 50ml (each dosage) of dichloromethane, and the dichloromethane was distilled under reduced pressure to obtain a yellow oil. Dissolve the oil in 23ml of toluene, add 175ml of methyl tert-butyl ether, stir for 1h, and filter with suction to obtain 14.1g of a light yellow solid (Intermediate 4), with a purity of 97.5% and a molar yield of 76.0%;
[0035] (2) Dissolve 14.1g of intermediate 4 in 23ml of acetone, add 8.5g of 20% sodium hydroxide solution, cool to 0°C and stir for 30min, then suction filter to obtain 13.2g of white solid with a purity of 98.4% and a molar yield of 88.9...
Embodiment 3
[0036] (1) The yellow oily matter of step (1) of Example 1 is dissolved with 50ml acetic acid, add 22.0g50% hydrogen peroxide, 1.0g methyl rhenium trioxide (MTO), heat up to 95°C, react for 8h; after the reaction is completed, The reaction solution was poured into 100ml of water, and the pH was adjusted to be neutral with 10% sodium hydroxide solution. The aqueous layer was extracted three times with 50ml (each dosage) of dichloromethane, and the dichloromethane was distilled under reduced pressure to obtain a yellow oil. Dissolve the oil in 25ml of toluene, add 180ml of methyl tert-butyl ether, stir for 1h, and filter with suction to obtain 14.6g of a light yellow solid (Intermediate 4), with a purity of 97.8% and a molar yield of 78.6%;
[0037] (2) Dissolve 14.6g of intermediate 4 in 25ml of acetone, add 8.8g of 20% sodium hydroxide solution, cool down to 0°C and stir for 30min, and suction filter to obtain 13.8g of white solid with a purity of 98.7% and a molar yield of 89....
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