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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 841913생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-(2-Furoyl)piperazineHCID 550206—
반응물2-Chloro-4-methoxypyrimidineHCID 588935—
용매1-ButanolHCID 263—
생성물2-[4-(2-Furylcarbonyl)-1-piperazinyl]-4-methoxypyrimidineHCID 691914770.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06372746B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-823576c4dea949db9a3d27153e6f60b3
출처 메모uspto-grants-2002_04