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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1479822생성일: 2026년 10월 25일

Diethyl Pyrocarbonate → 2-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[3-[4-(trifluoromethoxy)phenyl]phenyl]methyl]prop-2-enamide

https://huagongshe.com/reaction/1479822

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl PyrocarbonateHCID 3051—
반응물(4'-(Trifluoromethoxy)-[1,1'-biphenyl]-3-yl)methanamineHCID 61032752—
반응물2-[Ethyl-(4-fluorophenyl)sulfonyl-amino]prop-2-enoic acidHCID 90384201—
용매TetrahydrofuranHCID 8028—
생성물2-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[3-[4-(trifluoromethoxy)phenyl]phenyl]methyl]prop-2-enamideHCID 7832021824%

반응 단계

A solution of acid 4B (0.35 g, 1.28 mmol) in THF (25 mL) was added with DEPC (0.25 mL, 1.3 mol eq) and the mixture was stirred at room temperature for 10′. Then [3-[4-(trifluoromethoxy)phenyl]phenyl]methanamine 23B (0.376 g, 1.1 mol eq) and a catalytic amount of TEA were added, then the reaction mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure, water (40 mL) was added to the residue that is extracted with EtOAc (3×25 mL) and washed with brine (1×40 mL). The separated organic phase was anydrified over Na2SO4, evaporated to dryness and the residue was purified by flash chromatography (1:1 EtOAc:Petroleum ether) to afford a white solid (0.15 g) after recrystallization from ethyl ether. Yield=24%, 1HNMR (DMSO, 200 MHz) δ 1.08 (t, 3H, J=8), 3.37 (q, 2H, J=7.5), 4.44 (d, 2H, J06.1), 5.16 (s, 1H), 6.09 (s, 1H), 7.32 (d, 1H), 7.46 (m, 5H), 7.53 (d, 1H), 7.62 (s, 1H), 7.76 (dd, 2H), 7.86 (m, 2H), 8.78 (t, 1H); [M+1] 522.51 (C25H22F4N2O4S requires 522.12).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09409864B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-71898a139293460d905e0d816cdbf629
출처 메모uspto-grants-2016_08