Hydrochloric Acid → HCID 178517769, compound

Participants

Reaction Conditions

Reaction Steps

To a suspension of N-benzyl-2-chloro-5-fluoro-N-methylpyrimidin-4-amine (0.075 g, 0.30 mmol) in dioxane/H2O (1:1, 2 mL total volume) was added potassium hydroxide (KOH; 0.17 g, 3.0 mmol). The mixture was warmed to 100° C. and stirred for 72 h. The reaction mixture was diluted with H2O (5 mL), and the pH was adjusted to 7 with 2 N HCl. The resulting white precipitate was collected by vacuum filtration, but the majority of the product remained in the aqueous phase. The solid and filtrate were combined and the solvent was removed by azeotropic distillation with CH3CN in vacuo. The residue was dissolved/suspended in CH2Cl2 (25 mL), adsorbed onto Celite (3.0 g) and purified by normal phase chromatography (24 g SiO2; gradient, MeOH/CH2Cl2) to give 4-(benzylmethylamino)-5-fluoropyrimidin-2-ol (0.016 g, 23%) as a white solid: mp 122.8-123.6° C.; 1H NMR (300 MHz, CDCl3) δ 12.72 (s, 1H), 7.42-7.14 (m, 6H), 4.88 (s, 2H), 3.20 (d, J=3.2, 3H); ESIMS m/z 235 (M+2)+, 232 (M−H)−.

Provenance & Evidence