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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2384513Generated: October 30, 2026

Acetonitrile → 4-(Phenylsulfanyl)-6-ethyl-5-fluoropyrimidine

https://huagongshe.com/reaction/2384513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantThiophenolHCID 7969—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Chloro-6-ethyl-5-fluoropyrimidineHCID 16743445—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-(Phenylsulfanyl)-6-ethyl-5-fluoropyrimidineHCID 6754210195%

Reaction Steps

40 g of 4-chloro-6-ethyl-5-fluoropyrimidine was added to 400 ml of acetonitrile, and 28 ml of thiophenol was added thereto, followed by lowering the temperature to 10° C. 43.39 ml of diisopropylethylamine was added to the resulting solution, and reacted for 2 hours while maintaining the temperature at room temperature. 65 ml of dichloromethane and 200 ml of water were added to the resulting mixture to separate layer, and the resulting aqueous mixture was extracted with 200 ml of dichloromethane. The organic layer was dried over magnesium sulfate and concentrated under a reduced pressure to obtain the title compound as an oil (63.6 g, yield: 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263769B2
Source datasetuspto-grants-2012_09
ORD IDord-52519844df134ab7b07fa71a8309cc65
Source noteuspto-grants-2012_09