反应详情

A mixture of (±)-cis-4,5,6a,7,8,9,10,10a-octahydropyrido[4.3-b]pyrrolo[3,2,1-hi]indole (2.8 g, 14 mmol), 4-chloro-4′-fluorobutyrophenone (4.21 g, 21 mmol), triethylamine (3 mL), KI (3.48 g, 21 mmol), dioxane (25 mL), and toluene (25 mL) was stirred and refluxed for 15 h under an atmosphere of nitrogen and then evaporated under reduced pressure to remove the volatiles. The residue was triturated with a small volume of dichloromethane and decanted from the insoluble material. The process was repeated two more times and the combined dichloromethane solution was added to 0.5N solution of hydrogen chloride in ether(200 mL). The salt that separated was filtered off, washed with ether, dissolved immediately in a minimum quantity of water and the solution extracted with ether. The ether extract was discarded and aqueous layer basified with 10% aqueous sodium hydroxide. The resulting mixture was extracted with dichloro-methane (2×) and the extract dried over magnesium sulfate and stripped of the solvent under reduced pressure to yield the title compound (3.3 g, 65%) as a highly viscous light brown liquid. 1H NMR (CDCl3, 300 MHz) δ1.70-1.80 (m, 2H), 1.80-2.02 (m, 2H), 2.19 (t, J=10.9 Hz, 1H), 2.30-2.52 (m, 3H), 2.62-2.72 (m, 1H), 2.72-2.85 (m, 1H), 2.99 (t, J=7.0 Hz, 2H), 3.02-3.20 (m, 2H), 3.25-3.42 (m, 2H), 3.59-3.65 (m, 1H), 6.85 (s, 1H), 6.90 (s, 1H0, 7.01 (t, J=7.0 Hz, 2H), 7.98-8.03 (m, 2H) ppm. MS (CI): 365 (M+H+).

1. temperaturerefluxed for 15 h under an atmosphere of nitrogen
2. customevaporated under reduced pressure
3. customto remove the volatiles
4. customThe residue was triturated with a small volume of dichloromethane
5. customdecanted from the insoluble material
6. additionthe combined dichloromethane solution was added to 0.5N solution of hydrogen chloride in ether(200 mL)
7. customThe salt that separated
8. filtrationwas filtered off
9. washwashed with ether
10. dissolutiondissolved immediately in a minimum quantity of water
11. extractionthe solution extracted with ether
12. extractionThe ether extract
13. extractionThe resulting mixture was extracted with dichloro-methane (2×)
14. dry with materialthe extract dried over magnesium sulfate