反应详情

To a solution of 1,2,3,4-tetrahydroisoquinoline-7-carbonitrile (ABCR; 500 mg; 3.16 mmol) in MeOH (5 mL) at 0° C. was added acetaldehyde (0.51 mL, 8.91 mmol) and acetic acid (5 μL) and the resulting mixture was stirred for 1 hour. Sodium cyanoborohydride (218 mg; 3.47 mmol) was added and the mixture was stirred for 5 hours and diluted with DCM (100 mL) and water (20 mL). The aqueous layer was extracted with DCM (3×20 mL), the combined organics were dried (MgSO4) and the solvent was removed in vacuo. The residue was purified by flash chromatography on a Biotage 25+M column, eluting with petrol containing increasing amounts of EtOAc to give the title compound as a brown oil. 1H NMR: (CDCl3, 400 MHz) δ 7.39 (1H, d, J=8.0 Hz), 7.33 (1H, s), 7.19 (1H, d, J=8.0 Hz), 3.62 (2H, s), 2.99-2.90 (2H, m), 2.77-2.70 (2H, m), 2.66-2.54 (2H, m), 1.19 (3H, t, J=7.2 Hz).

1. stirringthe mixture was stirred for 5 hours
2. extractionThe aqueous layer was extracted with DCM (3×20 mL)
3. dry with materialthe combined organics were dried (MgSO4)
4. customthe solvent was removed in vacuo
5. customThe residue was purified by flash chromatography on a Biotage 25+M column
6. washeluting with petrol containing
7. temperatureincreasing amounts of EtOAc