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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7036생성일: 2026년 10월 24일

1-(Bromomethyl)-4-(trifluoromethoxy)benzene → cis-2-[(4-Chlorobenzenesulfonyl)-(4-trifluoromethoxy-benzyl)-amino]-cyclohexanecarboxylic acid amide

https://huagongshe.com/ko/reaction/7036

반응식

참여 물질

역할이름HCID투입량
반응물1-(Bromomethyl)-4-(trifluoromethoxy)benzeneHCID 142785—
반응물cis-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amideHCID 69655699—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물cis-2-[(4-Chlorobenzenesulfonyl)-(4-trifluoromethoxy-benzyl)-amino]-cyclohexanecarboxylic acid amideHCID 6965558267%

반응 단계

cis-2-(4-Chloro-benzenesulfonylamino)-cyclohexanecarboxylic acid amide (200 mg, 0.63 mmol), CsCO3 (250 mg, 0.76 mmol), and 1-bromomethyl-4-trifluoromethoxy-benzene (155 mg, 0.69 mmol) was stirred in acetonitrile (15 mL) at room temperature for 18 h. The reaction was then diluted with EtOAc (150 mL) and washed with H2O, brine, dried over Na2SO4 and concentrated to give a crude white wax. Further purification by flash chromatography (silica gel, 0.5%–1% MeOH/CHCl3) afforded the titled compound (205 mg) as a white solid in 67% yield: 1H NMR (DMSO-d6) δ 7.75 (d, 2 H, J=8.0 Hz), 7.59 (d, 2 H, J=8.0 Hz), 7.36 (m, 3 H), 7.21 (d, 2 H, J=8.0 Hz), 6.69 (s br, 1 H), 4.58 (AB2, 2 H, Δv=17, Jab=64 Hz), 3.89 (m, 1 H), 2.79 (s, 1 H), 2.44 (m, 1 H), 1.78 (m, 1 H), 1.66 (m, 2 H), 1.31 (m, 3 H), 0.98 (m, 1 H); MS m/e 491.03 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084178B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-ed10b2c70d2b47c3a62ee8f7be7d71c0
출처 메모uspto-grants-2006_08