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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284795Generated: October 31, 2026

Ethyl Acetate → 5-ethynyl-N2-(3-fluorophenyl)-N4-propylpyrimidine-2,4-diamine

https://huagongshe.com/reaction/2284795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
ReactantN2-(3-fluorophenyl)-N4-propyl-5-((trimethylsilyl)ethynyl)pyrimidine-2,4-diamineHCID 123868172—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product5-ethynyl-N2-(3-fluorophenyl)-N4-propylpyrimidine-2,4-diamineHCID 9005251256.3%

Reaction Steps

To a solution of N2-(3-fluorophenyl)-N4-propyl-5-((trimethylsilyl)ethynyl)pyrimidine-2,4-diamine (S1, 509 mg) in methanol (10 mL) and tetrahydrofuran (10 mL), potassium carbonate (246 mg) was added at room temperature, and the mixture was stirred at the same temperature for 30 minutes. To the reaction mixture, ethyl acetate and saturated aqueous ammonium chloride were added. The organic layer was separated, washed successively with saturated aqueous ammonium chloride and saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent, 94 to 60% hexane in ethyl acetate) to obtain 5-ethynyl-N2-(3-fluorophenyl)-N4-propylpyrimidine-2,4-diamine (S2, 226 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-45475adcce404cc4b6715489532c7d5a
Source noteuspto-grants-2015_09