反应详情

温度

80 °C

Following a procedure from JOC 1998, p. 8224, 2-iodo-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one (100 mg, 0.32 mmol), sodium cyanide (31 mg, 0.64 mmol), palladium tetrakis(triphenylphosphine) (19 mg, 0.05 mmol), and copper(I) iodide were combined in a schlenk tube. The vessel was evacuated and refilled with argon gas three times. Degassed propionitrile (2 mL) was added, and the reaction was stirred at 80° C. under an argon atmosphere for 15 h. The reaction mixture was partitioned between water and 25% iPrOH/CHCl3. The layers were separated and the aqueous layer extracted thrice with 25% iPrOH/CHCl3. The combined organic layers were dried (MgSO4) and concentrated in vacuo. The yellow solid was recrystallized from CH2Cl2/MeOH/hexanes to yield 6-oxo-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indole-2-carbonitrile, 38 mg (56%) as a pale yellow solid: m.p. 315° C. (dec); 1H NMR (300 MHz, d6-DMSO) δ3.04 (m, 2H), 3.47 (m, 2H), 7.46 (t, J=7.5 Hz, 1H), 7.64 (dd, J=8.1, 0.9 Hz, 1H), 7.81 (dd, J=7.2, 0.9 Hz, 1H), 8.24 (br t, 1H), 12.44 (br s, 1H). MS (electrospray, [M+Na]+): 234. Anal. (C12H9N3O) C, H, N.

1. customThe vessel was evacuated
2. additionrefilled with argon gas three times
3. additionDegassed propionitrile (2 mL) was added
4. customThe reaction mixture was partitioned between water and 25% iPrOH/CHCl3
5. customThe layers were separated
6. extractionthe aqueous layer extracted thrice with 25% iPrOH/CHCl3
7. dry with materialThe combined organic layers were dried (MgSO4)
8. concentrationconcentrated in vacuo
9. customThe yellow solid was recrystallized from CH2Cl2/MeOH/hexanes