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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847373Generated: October 31, 2026

1,3-Dimethyl-2-imidazolidinone → DL-5 Chloro-6-ethyl-4-{alpha-ethyl-4-(4-cyano-2,3,5,6-tetrafluorophenoxy) benzylamino}pyrimidine

https://huagongshe.com/reaction/847373

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
ReactantPotassium CarbonateHCID 11430—
ReactantPentafluorobenzonitrileHCID 69882—
ReactantDL-5 Chloro-6-ethyl-4-(alphaethyl-4-hydroxybenzylamino)pyrimidineHCID 131716268—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductDL-5 Chloro-6-ethyl-4-{alpha-ethyl-4-(4-cyano-2,3,5,6-tetrafluorophenoxy) benzylamino}pyrimidineHCID 13171749782.6%

Reaction Steps

A mixture of 0.76 g of dl-5-chloro-6-ethyl-4-(αethyl-4-hydroxybenzylamino)pyrimidine, 0.5 g of pentafluorobenzonitrile, 0.4 g of anhydrous potassium carbonate and 20 ml of 1,3-dimethyl-2-imidazolidinone (DMI) was heated under stirring at 70 .C for 8 hours. After completion of the reaction, the reaction mixture was poured into water, and extracted with toluene. The extract was washed with water, dried over anhydrous sodium sulfate and then toluene was evaporated under reduced pressure. The oily product obtained was isolated by column chromatography (Wako gel C-200, eluted with toluene:ethyl acetate=10:1) to give 0.8 g of the desired product as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05141941
Source datasetuspto-grants-1992_08
ORD IDord-55c7dc7f75bb4437b862faf7e8a13ee0
Source noteuspto-grants-1992_08