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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247638Generated: October 27, 2026

Potassium Iodide → (+/-)-[1-(2,4-Dichloro-pyrimidin-5-yl)-ethyl]-(4-methoxy-phenyl)-amine

https://huagongshe.com/reaction/1247638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantP-AnisidineHCID 7732—
ReactantPotassium CarbonateHCID 11430—
Reactant(+/-)-2,4-Dichloro-5-(1-bromoethyl)-pyrimidineHCID 21908975—
SolventAcetonitrileHCID 6342—
Product(+/-)-[1-(2,4-Dichloro-pyrimidin-5-yl)-ethyl]-(4-methoxy-phenyl)-amineHCID 10086026—

Reaction Steps

(±)-2,4-Dichloro-5-(1-bromoethyl)-pyrimidine (1.97 g; 7.70 mmol) (from Example 1c supra) was dissolved in acetonitrile (21 mL). p-Anisidine (0.95 g; 7.70 mmol) (Aldrich), potassium carbonate (1.17 g; 8.48 mmol) and potassium iodide (0.32 g; 1.93 mmol) were added and the mixture was stirred at room temperature. After 16 hours, the mixture was partitioned between ethyl acetate and water. The organic phase was washed with water and brine, dried over anhydrous sodium sulfate, filtered and concentrated. Purification by flash chromatography (Biotage 40M, 20:80 to 25:75 ethyl acetate-hexanes gradient) gave (±)-[1-(2,4-dichloro-pyrimidin-5-yl)-ethyl]-(4-methoxy-phenyl)-amine. (Yield 1.82 g; 76.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129351B2
Source datasetuspto-grants-2006_10
ORD IDord-94082007b502404fad65d26aaae319ae
Source noteuspto-grants-2006_10