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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277755Generated: October 31, 2026

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

https://huagongshe.com/reaction/2277755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
Reactant2-Chloro-5-fluoro-4-(4-fluoro-2-methoxyphenyl)pyrimidineHCID 86729609—
Reactant3-Bromo-5-[(methylsulfanyl)methyl]anilineHCID 89444752—
Solvent1-ButanolHCID 263—
SolventEthyl AcetateHCID 8857—
ProductN-{3-Bromo-5-[(methylsulfanyl)methyl]phenyl}-5-fluoro-4-(4-fluoro-2-methoxyphenyl)pyrimidin-2-amineHCID 8944463146%

Reaction Conditions

Temperature140 °C

Reaction Steps

A 4N solution of hydrogen chloride in dioxane (0.54 mL; 2.15 mmol) was added to a stirred solution of 2-chloro-5-fluoro-4-(4-fluoro-2-methoxyphenyl)pyrimidine (553 mg; 2.15 mmol) and 3-bromo-5-[(methylsulfanyl)methyl]aniline (500 mg; 2.15 mmol) in 1-butanol (4.8 mL). The batch was stirred at 140° C. for 8 hours. After cooling the batch was diluted with ethyl acetate and washed with sodium bicarbonate 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 4:1) to give the desired product (450 mg; 0.99 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133171B2
Source datasetuspto-grants-2015_09
ORD IDord-3d69db03f8594a7e898c8ea8dfda43ef
Source noteuspto-grants-2015_09