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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440460Generated: October 27, 2026

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

https://huagongshe.com/reaction/440460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-5-ethoxycarbonyl-6-ethylpyrimidineHCID 18357824—
Reactant4-ButylaminophenethylamineHCID 22407607—
SolventTolueneHCID 1140—
ProductEthyl 4-(2-(4-butylaminophenyl)ethylamino)-6-ethylpyrimidine-5-carboxylateHCID 2240760058%

Reaction Steps

Triethylamine (0.28 g, 2.77 mmol) was added to a solution of ethyl 4-chloro-6-ethylpyrimidine-5-carboxylate (0.30 g, 1.40 mmol) in toluene (10 ml). The mixture was stirred at room temperature. Then, 4-butylaminophenethylamine (0.40 g 2.08 mmol) was added after stirring for 3 hours, water (20 ml) was added to the reaction mixture. The mixture was extracted with methylene chloride 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-butylaminophenyl)ethylamino)-6-ethylpyrimidine-5-carboxylate (0.30 g, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05519139
Source datasetuspto-grants-1996_05
ORD IDord-8f76ff00b3ea4fa7a201cce547be6cd4
Source noteuspto-grants-1996_05