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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756004Generated: October 27, 2026

Water → Ethyl 4-(2-(4-butylthiophenyl)ethylamino)-6-ethylpyrimidine-5-carboxylate

https://huagongshe.com/reaction/1756004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-5-ethoxycarbonyl-6-ethylpyrimidineHCID 18357824—
Reactant4-ButylthiophenethylamineHCID 22407595—
SolventTolueneHCID 1140—
ProductEthyl 4-(2-(4-butylthiophenyl)ethylamino)-6-ethylpyrimidine-5-carboxylateHCID 5452212255.5%

Reaction Steps

Triethylamine (0.19 g, 1.88 mmol) was added to a solution of ethyl 4-chloro-6-ethylpyrimidine-5-carboxylate (0.20 g, 0.93 mmol) in toluene (4 ml). The mixture was stirred at room temperature. Then, 4-butylthiophenethylamine (0.20 g, 0.96 mmol) was added. After stirring for 3 hours, water (20 ml) was added to the reaction mixture. The mixture was extracted with ethyl acetate and dried over magnesium sulfate. After evaporation of the solvent, the residue was purified by column chromatography on silica gel eluting with n-hexane/ethyl acetate (=8/2) to give the desired ethyl 4-(2-(4-butylthiophenyl)ethylamino)-6-ethylpyrimidine-5-carboxylate (0.20 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05439911
Source datasetuspto-grants-1995_08
ORD IDord-072a39327bba4ebdbe07661de135886a
Source noteuspto-grants-1995_08