1H,2H,3H,4H,5H,6H-azepino(4,5-b)indole → HCID 59075496、化合物
反応式
[CH2:1]1[C:14]2[C:13]3[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=3[NH:7][C:6]=2[CH2:5][CH2:4][NH:3][CH2:2]1>FC(F)(F)C(O)=O.CO>[CH2:1]1[C@@H:14]2[C@@H:6]([NH:7][C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:13]=32)[CH2:5][CH2:4][NH:3][CH2:2]1参加物
4
実験手順
A solution of 1,2,3,4,5,6-hexahydroazepino[4,5-b]indole (0.93 g, 5.0 mmol) in trifluoroacetic acid (17 mL) was cooled to 0° C., and treated with a freshly prepared solution of Na(CN)BH3 (1.57 g, 25 mmol) in MeOH (4 mL). The cooling bath was removed and the reaction mixture was stirred at room temperature for 1 h, then treated with water (75 mL), stirred for an additional 15 minutes before adjusting the pH to 14 with 45% KOH (aqueous). The resulting solution was extracted with EtOAc (3×40 mL), and the combined organic extracts were washed once with brine, dried over MgSO4, filtered, and concentrated in vacuo to give a yellow syrup. The crude product was purified by chromatography and using ethanol:ammonia:dichloromethane (15:1.5:83.5) and trituration of the resulting material gave the title compound (0.64g) as an off-white solid: mp 102-114° C.