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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841913Generated: October 24, 2026

Triethylamine → 2-[4-(2-Furylcarbonyl)-1-piperazinyl]-4-methoxypyrimidine

https://huagongshe.com/en/reaction/841913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(2-Furoyl)piperazineHCID 550206—
Reactant2-Chloro-4-methoxypyrimidineHCID 588935—
Solvent1-ButanolHCID 263—
Product2-[4-(2-Furylcarbonyl)-1-piperazinyl]-4-methoxypyrimidineHCID 691914770.2%

Reaction Steps

A solution of 1.0 g (6.92 mmol) of 2-chloro-4-methoxypyrimidine, 1.49 g (8,30 mmol) of 1-(2-furylcarbonyl)piperazine and 1.39 g (13.84 mmol) of triethylamine in 20 mL of n-butanol is maintained under gentle reflux conditions overnight. The solvent is evaporated off under reduced pressure and the crude residue is diluted in chloroform and washed in water. The organic phase is dried over NaSO4 and evaporated to dryness to give a crude product which is purified using silica-gel chromatography eluting with ethyl acetate/petroleum ether 70:30 to yield an oil which solidifies when left to stand. The solid is suspended in petroleum ether to yield 1.4 g (4.86 mmol) of 2-[4-(2-furylcarbonyl)-1-piperazinyl]-4-methoxypyrimidine. m.p.=85-86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372746B1
Source datasetuspto-grants-2002_04
ORD IDord-823576c4dea949db9a3d27153e6f60b3
Source noteuspto-grants-2002_04