反应详情

A 1N solution of bis(trimethylsilyl)amide in THF (2.78 mL, 2.80 mmol) was added dropwise to a solution of 5-(4-piperidin-1-ylmethyl-phenyl)-2-fluoro-[3,4]bipyridinyl-3′-ylamine (101 mg, 0.278 mmol) in THF (5.0 mL) at ambient temperature. The mixture was stirred for 1 h at ambient temperature and then treated with water. The resultant brown solution was partitioned between DCM and water, the layers separated, and the aqueous phase extracted into 20% methanol in DCM. The combined organic phase was concentrated in vacuo. The resultant residue was absorbed onto silica gel, and purified by flash chromatography (silica, 1-20% methanol in DCM) to provide a light orange-yellow solid (39.9 mg, 42%). 1H NMR. (DMSO-D6, 500 MHz): 12.24 (s, 1H), 8.99 (d, J=1.8 Hz, 1H), 8.93 (s, 1H), 8.92 (d, J=1.8 Hz, 1H), 8.45 (d, J=5.2 Hz, 1H), 8.22 (d, J=5.2 Hz, 1H), 7.77 (d, J=7.5 Hz, 2H), 7.45 (d, J=7.5 Hz, 2H), 3.49 (s, 2H), 2.36 (m, 4H), 1.52 (m 4H), 1.41 (m, 2H). LCMS (Method D): RT=4.64 min, M+H+=343.

1. customThe resultant brown solution was partitioned between DCM and water
2. customthe layers separated
3. extractionthe aqueous phase extracted into 20% methanol in DCM
4. concentrationThe combined organic phase was concentrated in vacuo
5. customThe resultant residue was absorbed onto silica gel
6. custompurified by flash chromatography (silica, 1-20% methanol in DCM)