Diisobutylaluminum hydride → (2-(4-Chlorophenylamino)pyrimidin-4-yl)methanol

Participants

Reaction Conditions

Reaction Steps

A suspension of 2-ethoxyethyl 2-((4-chlorophenyl)amino)pyrimidine-4-carboxylate (0.4 g, 1.243 mmol) in THF (12 mL) was cooled to −78° C. and a 1M solution of DIBAL-H (4.97 mL, 4.97 mmol) in toluene was added. The mixture was stirred for 1.5 h at room temperature. The reaction mixture was diluted with THF (20 mL) and quenched with Na2SO4.10H2O followed by a few drops of water. The mixture was stirred at room temperature for 18 h, then filtered through a pad of Celite topped with silica gel. The pad was washed with ethyl acetate and the filtrate was concentrated. The residue was purified by flash chromatography on silica gel using 75-100% ethyl acetate in hexanes. The desired fractions were concentrated to give (2-(4-chlorophenylamino)pyrimidin-4-yl)methanol as a pale yellow solid (0.224 g, 76%). 1H NMR (400 MHz, METHANOL-d4) δ ppm 8.41 (1H, d, J=5.02 Hz), 7.55-7.86 (2H, m), 7.19-7.40 (2H, m), 6.95 (1H, d, J=5.02 Hz), 4.57 (2H, s). LCMS: R.T.=3.10; [M+H]+=236.12.

Provenance & Evidence