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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 333959생성일: 2026년 10월 26일

Diisopropylethylamine → (E)-4-Ethyl-1-[4-[2-methyl-7-(trifluoromethyl)-4-quinolyl]piperazin-1-yl]hex-2-en-1-one

https://huagongshe.com/reaction/333959

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물(E)-4-Ethylhex-2-enoic acidHCID 6437410—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물2-Methyl-4-piperazin-1-yl-7-(trifluoromethyl)quinolineHCID 66835798—
용매DimethylformamideHCID 6228—
생성물(E)-4-Ethyl-1-[4-[2-methyl-7-(trifluoromethyl)-4-quinolyl]piperazin-1-yl]hex-2-en-1-oneHCID 56949204320%

반응 단계

(E)-4-Ethyl-hex-2-enoic acid (21.3 mg, 0.15 mmol) was dissolved in DMF (350 μl), diisopropylethylamine was added (26 μl, 0.15 mmol) followed by HATU (57 mg, 0.15 mmol dissolved in 0.25 ml DMF). The mixture was stirred at room temperature for 15 minutes, then 2-methyl-4-piperazin-1-yl-7-(trifluoromethyl)quinoline (44 mg, 0.15 mmol, dissolved in 1 ml DMF) was added and stirring was continued overnight. The mixture was evaporated under reduced pressure, the residue was dissolved in dichloromethane, the solution was washed with 5% sodium bicarbonate solution and water, evaporated to dryness under reduced pressure. The residue was purified by preparative HPLC (gradient of water containing 0.1% NH3 and acetonitrile) to yield 20.3 mg (0.48 mmol, 32.3%) of a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883791B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-23d9052b54ca46bc91e6c5c92c1738e0
출처 메모uspto-grants-2014_11