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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 333967생성일: 2026년 10월 25일

Triethylamine → (E)-1-[4-(2-methyl-4-quinolyl)piperazin-1-yl]oct-2-en-1-one

https://huagongshe.com/reaction/333967

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물2-Methyl-4-(piperazin-1-yl)quinolineHCID 702318—
반응물trans-2-Octenoic acidHCID 5282714—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물(E)-1-[4-(2-methyl-4-quinolyl)piperazin-1-yl]oct-2-en-1-oneHCID 5694920577%

반응 단계

(E)-Oct-2-enoic acid (71.1 mg, 0.5 mmol) was dissolved in dichloromethane (1 ml) and a 2M solution of oxalyl chloride in dichloromethane was added (0.3 ml, 0.6 mmol). The solution was stirred at room temperature for one hour after which a drop of DMF was added. Stirring was continued for another hour, the mixture was evaporated to dryness under reduced pressure. The residue was dissolved in dichloromethane (1 ml), the resulting solution was added to a solution of 2-methyl-4-piperazin-1-yl-quinoline (103 mg, 0.45 mmol) and triethylamine (90 μl, 0.64 mmol) in dichloromethane (1 ml). The resulting mixture was stirred at room temperature overnight, diluted with dichloromethane (1 ml), washed with water and 2M NaOH (2 ml each) and evaporated to dryness under reduced pressure. The residue was purified by preparative HPLC (gradient of water containing 0.1% ammonia and acetonitrile) to yield 121.3 mg of a solid (0.34 mmol, 77%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883791B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-1305db22f8584012a435e8e4486283d0
출처 메모uspto-grants-2014_11