Preparation method of antidepressant drug Vortioxetine
A vortioxetine and antidepressant technology, applied in the field of medicine and chemical industry, can solve problems such as long steps, and achieve the effect of simple operation
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Embodiment 2
[0037] 13.8 g (0.1 mol) of compound 2,4-dimethylthiophenol of formula (4), 28.3 g (0.1 mol) of 2-bromoiodobenzene, 10.3 g (0.12 mol) of piperazine, 16.8 g (0.3 mol) potassium hydroxide and 1.9 g (0.01 mol) cuprous iodide, 33.4 g (0.12 mol) tetrabutylammonium chloride, add 300 mL of water, stir and heat up to 85-90 ° C, react for 11 hours, After the reaction is complete, extract three times with dichloromethane, 300ml each time, combine the organic layers, wash the organic layer with saturated brine and pure water, collect the organic layer, dry, evaporate the dichloromethane, add 150 mL of acetone to the residue for recrystallization , 26.6 g of white solid was obtained, the yield was 89.3%, and the purity was 97.2%.
Embodiment 3
[0039] 13.8 g (0.1 mol) of compound 2,4-dimethylthiophenol of formula (4), 28.3 g (0.1 mol) of 2-bromoiodobenzene, 10.3 g (0.12 mol) of piperazine, Add 12.0 g (0.3 mol) sodium hydroxide and 1.9 g (0.01 mol) cuprous iodide, 48.3 g (0.15 mol) tetrabutylammonium bromide, add 300 mL of water, stir and raise the temperature to 85-90 ° C, react for 11 hours, After the reaction is complete, extract three times with dichloromethane, 300ml each time, combine the organic layers, wash the organic layer with saturated brine and pure water, collect the organic layer, dry, evaporate the dichloromethane, add 150 mL of acetone to the residue for recrystallization , 26.8 g of white solid was obtained, the yield was 89.3%, and the purity was 96.5%.
Embodiment 4
[0041]13.8 g (0.1 mol) of compound 2,4-dimethylthiophenol of formula (4), 28.3 g (0.1 mol) of 2-bromoiodobenzene, 10.3 g (0.12 mol) of piperazine, 12.0 g (0.3 mol) sodium hydroxide and 1.9 g (0.01 mol) cuprous iodide, 29.1 g (0.11 mol) 18-crown-6, add 300 mL of water, stir and heat up to 85-90 ° C, react for 10 h, After the reaction is complete, extract three times with dichloromethane, 300ml each time, combine the organic layers, wash the organic layer with saturated brine and pure water, collect the organic layer, dry, evaporate the dichloromethane, add 150 mL of acetone to the residue for recrystallization , 22.4 g of white solid was obtained, the yield was 75.2%, and the purity was 96.8%.
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