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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1479803생성일: 2026년 10월 26일

Diethyl Pyrocarbonate → 2-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[2-[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]prop-2-enamide

https://huagongshe.com/reaction/1479803

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl PyrocarbonateHCID 3051—
반응물[2-(4-Trifluoromethyl-phenyl)-pyridin-4-yl]methylamineHCID 68758847—
반응물2-[Ethyl-(4-fluorophenyl)sulfonyl-amino]prop-2-enoic acidHCID 90384201—
용매TetrahydrofuranHCID 8028—
생성물2-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[2-[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]prop-2-enamideHCID 7832460119.7%

반응 단계

Acid 4B (273.28 mg, 1 mmol) was dissolved in 10 ml of THF and at rt DEPC (1.1 equiv, 0.15 ml) and [2-[4-(trifluoromethyl)phenyl]-4-pyridyl]methanamine 21A (1.1 equiv., 277.5 mg) were added to the solution. The mixture was stirred at rt overnight then evaporated. The residue was dissolved in AcOEt (30 ml) and washed with water (1×20 ml) and brine. The organic phase was dried over sodium sulfate and concentrated under vacuum. The purification of the crude by chromatographic column (EtOAc 1/petroleum ether 1) afforded 100 mg of a white solid. Yield=19% 1HNMR (DMSO, 400 MHz) δ 1.09 (3H, t, J=7.2 Hz), 3.39 (2H, q, J=6.8 Hz), 4.48 (2H, d, J=6 Hz), 5.15 (1H, s), 6.14 (1H, s), 7.36 (1H, dd, J=4.8 Hz, J′=1.2 Hz), 7.47 (2H, t, J=8.8 Hz), 7.84 (4H, m), 8.01 (1H, s), 8.30 (2H, d, J=8 Hz), 8.64 (1H, dd, J=5.2 Hz, J′=0.8 Hz), 8.89 (1H, bt) [M+1] 508.7 (C24H21F4N3O3S requires 507.50).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09409864B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-6138cc1de4934b42858f387fb8a57c70
출처 메모uspto-grants-2016_08