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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1479876생성일: 2026년 10월 25일

Diethyl Pyrocarbonate → 2-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[2-isopropoxy-6-[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]prop-2-enamide

https://huagongshe.com/reaction/1479876

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl PyrocarbonateHCID 3051—
반응물2-[Ethyl-(4-fluorophenyl)sulfonyl-amino]prop-2-enoic acidHCID 90384201—
반응물[2-Isopropoxy-6-[4-(trifluoromethyl)phenyl]-4-pyridyl]methanamineHCID 90390965—
용매TetrahydrofuranHCID 8028—
생성물2-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[2-isopropoxy-6-[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]prop-2-enamideHCID 9039053718%

반응 단계

A solution of acid 4B (300 g, 1.09 mmol) in THF (15 mL) was added with DEPC (0.21 mL, 1.3 mol eq) and the mixture was stirred at room temperature several minutes. Then [2-isopropoxy-6-[4-(trifluoromethyl)phenyl]-4-pyridyl]methanamine 27M (370 mg, 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 was added to the residue that is extracted with EtOAc (3×30 mL) and washed with brine (1×40 mL). The separated organic phase was dried over Na2SO4, evaporated to dryness and the residue was purified by flash chromatography (3/7 EtOAc/Petroleum ether) to afford a white solid (100 mg) after crystallization from ethyl ether. Yield=18%. 1HNMR (DMSO, 400 MHz) δ 1.08 (t, 3H, J=7.4), 1.26 (d, 6H, J=6.2), 3.39 (q, 2H), 4.40 (d, 2H, J=7.9), 5.13 (s, 1H), 5.39 (m, 1H), 6.12 (s, 1H), 6.65 (s, 1H), 7.42 (t, 3H, J=4), 7.56 (s, 1H), 7.86 (m, 4H), 8.23 (d, 2H, J=8), 8.79 (t, 1H). [M+1] 565.02 (C27H27F4N3O4S requires 565.58).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09409864B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-f2cfd55aeb1849d29f5f7546b6a647f3
출처 메모uspto-grants-2016_08