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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277749Generated: October 30, 2026

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

https://huagongshe.com/reaction/2277749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
Reactant3-[(Methylsulfanyl)methyl]anilineHCID 39733359—
Reactant2-Chloro-5-fluoro-4-(4-fluoro-2-methoxyphenyl)pyrimidineHCID 86729609—
Solvent1-ButanolHCID 263—
SolventEthyl AcetateHCID 8857—
Product5-Fluoro-4-(4-fluoro-2-methoxyphenyl)-N-{3-[(methylsulfanyl)methyl]phenyl}pyrimidin-2-amineHCID 8944439572.2%

Reaction Conditions

Temperature140 °C

Reaction Steps

A 4N solution of hydrogen chloride in dioxane (0.61 mL; 2.45 mmol) was added to a stirred solution of 2-chloro-5-fluoro-4-(4-fluoro-2-methoxyphenyl)pyrimidine (630 mg; 2.45 mmol) and 3-[(methyl-sulfanyl)methyl]aniline (564 mg; 3.68 mmol) in 1-butanol (5.4 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 chromatography (hexane/ethyl acetate 2:1) to give the desired product (662 mg; 1.77 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133171B2
Source datasetuspto-grants-2015_09
ORD IDord-57844259a38f41d4ad8be1906f9a8075
Source noteuspto-grants-2015_09