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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053084Generated: October 30, 2026

Ethyl Acetate → 2-Methylsulfanyl-6-(3-trifluoromethylphenyl)-pyrimidin-4-ylamine

https://huagongshe.com/reaction/2053084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Amino-6-chloro-2-methylthiopyrimidineHCID 70496—
Reactant3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2-Methylsulfanyl-6-(3-trifluoromethylphenyl)-pyrimidin-4-ylamineHCID 5851322860.7%

Reaction Steps

To a stirred solution of 4-amino-6-chloro-2-methylthiopyrimidine (3.5 g) in toluene (45 mL) under a nitrogen atmosphere was added, sequentially, 3-(trifluoromethyl)phenylboronic acid (4.15 g), potassium carbonate (25 mL, 2M) and tetrakis(triphenylphosphine)palladium(0) (1.16 g). The mixture was heated to reflux for ten hours. Ethyl acetate (150 mL) was added and the mixture washed with water (2×100 mL). Organic layer was separated, washed with saturated sodium chloride (100 mL), dried over sodium sulphate and solvent was evaporated under reduced pressure to yield crude product. Purification by flash chromatography yielded product 2-methylsulfanyl-6-(3-trifluoromethyl-phenyl)-pyrimidin-4-ylamine (3.45 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326715B2
Source datasetuspto-grants-2008_02
ORD IDord-a34b067471a64c818b8713335d50002e
Source noteuspto-grants-2008_02