Preparation method of dextromethorphan hydrobromide N-oxide impurity
A technology of dextromethorphan hydrobromide and sodium hydroxide, applied in the direction of organic chemistry and the like, can solve the problem of not finding the preparation documents of nitrogen oxides, etc., and achieve the effects of high stability, mild and controllable reaction conditions, and high purity
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Embodiment 1
[0032]
[0033] Take 3.7g (1.0eq) of dextromethorphan hydrobromide, dissolve it in 150ml of water, add 5ml of 5N aqueous sodium hydroxide solution, stir for 3-5 minutes, add 100ml of dichloromethane for extraction, and dry the organic phase with anhydrous sodium sulfate , and concentrated the solvent under reduced pressure to obtain dextromethorphan (free state). Add 50ml of absolute ethanol to dextromethorphan, then add dropwise 1.7g (1.5eq) of 30% hydrogen peroxide, and keep stirring at 10-20°C for 16h after the addition is complete. Post-processing: the reaction solution was concentrated under reduced pressure, purified and separated by silica gel column chromatography, the eluent was DCM / MeOH=20 / 1-10 / 1, and concentrated to obtain 2.5 g of the product with a yield of 87%.
[0034] MS(m / z):288.1[M+H] + , 576.2[2M+H] + .
[0035] 1 HNMR (400MHz, CDCl 3 )δ:0.97-0.98(m,1H),1.22-1.26(m,2H),1.42-1.64(m,5H),2.32(d,1H),2.49(d,1H),2.84(d,1H) , 2.98-3.03 (m, 4H), 3.06 (s, 3H...
Embodiment 2
[0037]
[0038] Take 1.85g (1.0eq) of dextromethorphan hydrobromide, dissolve it in 75ml of water, add 3ml of 5N aqueous sodium hydroxide solution, stir for 3-5 minutes, add 50ml of dichloromethane for extraction, and dry the organic phase with anhydrous sodium sulfate , and concentrated the solvent under reduced pressure to obtain dextromethorphan (free state). Add 25ml of methanol to dextromethorphan, then dropwise add 0.85g (1.5eq) of 30% hydrogen peroxide, and keep stirring at 20-30°C for 16h after the addition is complete. Post-processing: the reaction solution was concentrated under reduced pressure, purified and separated by silica gel column chromatography, the eluent was DCM / MeOH=20 / 1-10 / 1, and concentrated to obtain 1.09 g of the product, with a yield of 76%.
Embodiment 3
[0040]
[0041] Take 7.4g (1.0eq) of dextromethorphan hydrobromide, dissolve it in 300ml of water, add 10ml of 5N aqueous sodium hydroxide solution, stir for 3-5 minutes, add 150ml of dichloromethane for extraction, and dry the organic phase with anhydrous sodium sulfate , and concentrated the solvent under reduced pressure to obtain dextromethorphan (free state). Add 100ml of absolute ethanol to dextromethorphan, then add 8.12g (2.0eq) of 85% m-chloroperoxybenzoic acid, and keep stirring at 0-10°C for 16h after the addition is complete. Post-processing: the reaction solution was concentrated under reduced pressure, purified and separated by silica gel column chromatography, the eluent was DCM / MeOH=20 / 1-10 / 1, and concentrated to obtain 4.6 g of the product with a yield of 80%.
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