Hydrochloric Acid → 2-(4-((4-chloropyrimidin-2-yl)amino)-1H-pyrazol-1-yl)-2-methylpropan-1-ol

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Reaction Steps

To a solution of calcium chloride (540 mg) in a mixed solvent of tetrahydrofuran-ethanol (v/v=1/1, 5.0 mL) was added sodium borohydride (240 mg), and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added a solution of ethyl 2-(4-((4-chloropyrimidin-2-yl)amino)-1H-pyrazol-1-yl)-2-methylpropanoate (1.0 g) obtained in Step D of Example 347 in a mixed solvent of tetrahydrofuran-ethanol (v/v=1/1, 5.0 mL) in an ice bath, and the mixture was stirred overnight while it was allowed to be gradually warmed to room temperature. To the reaction mixture was added 1 M hydrochloric acid in an ice bath, and the mixture was stirred at the same temperature for 10 min. 1 M Aqueous sodium hydroxide solution was added thereto, and the solvent was evaporated under reduced pressure. To the residue was added water, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (700 mg).

Provenance & Evidence