反应详情

温度

0 °C

(±)-cis-4,5,6a,7,8,9,10,10a-octahydropyrido[4,3-b]pyrrolo[3,2,1-hi]indole from Example 3 (0.050 g, 0.25 mmol) was dissolved in CH2Cl2 (5 mL) with Et3N (0.75 mL) and cooled to 0° C. The cyclopropanecarbonyl chloride (0.026 g, 0.26 mmol) was then added dropwise. The solution was stirred at 0° C. for 1 h and then warmed to room temperature and stirred for 1 h. The reaction mixture was partitioned between water and CHCl3(3×15 mL) and the layers separated. The aqueous layer was extracted with CHCl3. The combined organics were washed with brine, H2O and dried (Na2SO4) and evaporated affording a light yellow liquid which was further purified by preparatory silica gel TLC (5% MeOH/CH2Cl2). The title compound was isolated as a clear colorless liquid (0.042 g, 65%). 1H NMR (CD3OD, 300 MHz) δ 7.22–7.58 (m, 3H), 4.62–4.75 (m, 1H), 3.85–4.30 (m, 5H), 3.55–3.62 (m, 2H), 1.9–2.18 (m, 3H), 0.75–0.9 (m, 4H) ppm.

1. temperaturewarmed to room temperature
2. stirringstirred for 1 h
3. customThe reaction mixture was partitioned between water and CHCl3(3×15 mL)
4. customthe layers separated
5. extractionThe aqueous layer was extracted with CHCl3
6. washThe combined organics were washed with brine, H2O
7. dry with materialdried (Na2SO4)
8. customevaporated
9. customaffording a light yellow liquid which
10. customwas further purified by preparatory silica gel TLC (5% MeOH/CH2Cl2)