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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277746Generated: November 3, 2026

Hydrochloric Acid → 4-[2-(Benzyloxy)-4-fluorophenyl]-5-fluoro-N-{3-[(methylsulfanyl)methyl]phenyl}pyrimidin-2-amine

https://huagongshe.com/reaction/2277746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
Reactant3-[(Methylsulfanyl)methyl]anilineHCID 39733359—
Reactant4-[2-(Benzyloxy)-4-fluorophenyl]-2-chloro-5-fluoropyrimidineHCID 86729610—
Solvent1-ButanolHCID 263—
SolventEthyl AcetateHCID 8857—
Product4-[2-(Benzyloxy)-4-fluorophenyl]-5-fluoro-N-{3-[(methylsulfanyl)methyl]phenyl}pyrimidin-2-amineHCID 8944460127.4%

Reaction Conditions

Temperature140 °C

Reaction Steps

A 4N solution of hydrogen chloride in dioxane (0.34 mL; 1.35 mmol) was added to a stirred solution of 4-[2-(benzyloxy)-4-fluorophenyl]-2-chloro-5-fluoropyrimidine (450 mg; 1.35 mmol) and 3-[(methylsulfanyl)methyl]aniline (311 mg; 2.03 mmol) in 1-butanol (3.00 mL). The batch was stirred at 140° C. for 16 hours. After cooling the batch was diluted with ethyl acetate and washed with aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution. The organic phase was filtered using a Whatman filter and concentrated. The residue was purified by preparative HPLC to give the desired product (167 mg; 0.37 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133171B2
Source datasetuspto-grants-2015_09
ORD IDord-0aa02245816d45029a87cae39a12e80c
Source noteuspto-grants-2015_09