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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7042생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/7042

반응식

참여 물질

역할이름HCID투입량
반응물1-(Bromomethyl)-4-(trifluoromethyl)benzeneHCID 123062—
반응물trans-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amideHCID 69656245—
생성물trans-2-[(4-Chlorobenzenesulfonyl)-(4-trifluoromethyl-benzyl)-amino]-cyclohexanecarboxylic acid amideHCID 1143145345%

반응 단계

The titled compound (34 mg) was prepared in 45% yield from trans-2-(4-chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide and 1-bromomethyl-4-trifluoromethyl-benzene according to the N-alkylation procedure described in Example 11: 1H NMR (DMSO-d6) δ 7.77 (d, 2 H, J=8.0 Hz), 7.65 (d, 2 H, J=8.0 Hz), 7.57 (m, 3 H), 7.45 (d, 2 H, J=12.0 Hz), 7.35 (s, 1 H), 6.80 (s, 1H), 4.44 (AB2,2 H,ΔV=16,Jab=84 Hz), 4.01 (m, 1 H), 1.39 (m, 8 H); MS m/e 475.04 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084178B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-58448d7f5a0d42338e8645028949ddee
출처 메모uspto-grants-2006_08