Sodium hydride → (1R*,2S*)-2-(1H-indazol-6-yl)spiro[cyclopropane-1,3'-indolin]-2'-one

Participants

Reaction Steps

To a solution of trimethylsulfoxonium iodide (264 mg, 1.2 mmol) in anhydrous DMF (40 mL) was added sodium hydride (60% dispersion in oil) (140 mg, 3.48 mmol) at 0° C. The mixture was stirred for 15 min after which time (E)-3-((1H-indazol-6-yl)methylene)indolin-2-one (151 mg, 0.58 mmol) was added. The solution was stirred overnight at rt. The reaction was quenched with sat. NH4Cl solution (10 mL), extracted with EtOAc (4×50 mL), dried over MgSO4 and concentrated to dryness. The major diastereomer was isolated by silica gel chromatography (50% EtOAc in hexane) as a beige solid (44 mg, 28%). 1H NMR (400 MHz, d6-DMSO) δ 13.01 (s, 1H), 10.61 (d, J=8.3 Hz, 1H), 8.01 (s, 1H), 7.63 (d, J=8.3 Hz, 1H), 7.44 (s, 1H), 6.99 (t, J=7.5 Hz, 1H), 6.92 (d, J=8.0 Hz, 1H), 6.84 (d, J=8.0 Hz, 1H), 6.51 (t, J=7.0 Hz, 1H), 5.98 (d, 8.0 Hz, 1H), 3.20-3.17 (m, 1H), 2.30-2.26 (m, 1H), 2.00-1.95 (m, 1H); MS ESI 276.1 [M+H]+, calcd for [C17H13N3O+H]+ 276.3.

Provenance & Evidence