Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 2-[4-(2-Furylcarbonyl)-1-piperazinyl]-4-methoxypyrimidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1-(2-Furoyl)piperazine | HCID 550206 | — |
| 반응물 | 2-Chloro-4-methoxypyrimidine | HCID 588935 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 생성물 | 2-[4-(2-Furylcarbonyl)-1-piperazinyl]-4-methoxypyrimidine | HCID 6919147 | 70.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06372746B1 |
| 출처 데이터셋 | uspto-grants-2002_04 |
| ORD ID | ord-823576c4dea949db9a3d27153e6f60b3 |
| 출처 메모 | uspto-grants-2002_04 |