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HRID 457939생성일: 2026년 10월 23일

Dichloromethane → N-(4-bromo-2-fluoro-benzyl)-4-chloro-2-hydroxy-benzamide

https://huagongshe.com/ko/reaction/457939

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물TriethylamineHCID 8471—
반응물(4-Bromo-2-fluorophenyl)methanamineHCID 3770848—
반응물5-Chloro-2-hydroxybenzoyl chlorideHCID 12863233—
생성물N-(4-bromo-2-fluoro-benzyl)-4-chloro-2-hydroxy-benzamideHCID 1846819653%

반응 단계

A solution of 5-chloro-2-hydroxy-benzoyl chloride (4.00 g, 23.2 mmol) in dichloromethane (46 mL, 0.5 M) was treated with triethylamine (6.46 mL, 46.4 mmol) and 4-bromo-2-fluorobenzylamine (6.10 g, 30.1 mmol). After stirring at room temperature for 16 h, the solution was washed successively with 2 N HCl and saturated aq NaCl. The organic layer was dried over Na2SO4, filtered and concentrated. Purification by MPLC (10–50% ethyl acetate in heptane, 23 mL/min, 70 min) gave N-(4-bromo-2-fluoro-benzyl)-4-chloro-2-hydroxy-benzamide as a white crystalline solid (4.4 g, 53%): mp 159–161° C.; Rf 0.49 (30% ethyl acetate in heptane); 1H NMR (DMSO-d6, 300 MHz) δ 12.56 (br s, 1 H), 9.28 (br t, J=5.4 Hz, 1 H), 7.88 (d, J=6.0 Hz, 1 H), 7.50 (dd, J1=9.9 Hz, J2=1.8 Hz, 1 H), 7.37 (dd, J1=8.4 Hz, J2=1.8 Hz, 1 H), 7.33 (dd, J1=15.9 Hz, J2=8.1 Hz, 1 H), 6.99–6.93 (m, 2 H), 4.50–4.46 (m, 2 H). ESI-LC/MS m/z calcd for C14H10BrClFNO2: 358.6; found 360.0 (M+1)+. Anal. calcd for C14H10BrClFNO2: C, 46.89; H, 2.81; N, 3.91; Cl, 19.78. Found C, 46.89; H, 2.81; N, 3.90; Cl, 19.73.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07189749B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-3ee8918d40f64c448947756f401d90e5
출처 메모uspto-grants-2007_03