反应详情

HG-6 was also synthesized using the following alternative method: tetrabenazine (317 mg, 1 mmol) was dissolved in ethanol (EtOH, 10 ml) and hydroxylamine hydrochloride (70 mg, 1 mmol) was added, followed by the addition of pyridine (1 ml). The reaction was refluxed for 2 hours. After removing solvent, the residue was redissolved in methanol (MeOH, 10 ml). To this solution, MoO3 (80 mg) and sodium borohydride (80 mg) were slowly added. The reaction was stirred at room temperature for 24 hours and quenched with water. The aqueous solution was extracted with methylene chloride (10 ml) twice. The combined organic phase was washed with brine and dried with sodium sulfate. After removing solvent, the residue was purified by chromatography. Two hundred and fifty milligrams of HG-6 (3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinolin-2-amine) was obtained as white solid (yield: 78%).

1. customHG-6 was also synthesized
2. temperatureThe reaction was refluxed for 2 hours
3. customAfter removing solvent
4. dissolutionthe residue was redissolved in methanol (MeOH, 10 ml)
5. additionTo this solution, MoO3 (80 mg) and sodium borohydride (80 mg) were slowly added
6. customquenched with water
7. extractionThe aqueous solution was extracted with methylene chloride (10 ml) twice
8. washThe combined organic phase was washed with brine
9. dry with materialdried with sodium sulfate
10. customAfter removing solvent
11. customthe residue was purified by chromatography