反应 #545121

反应方程式

5-chloro-2-hydroxy-benzoyl chloride

triethylamine

4-bromo-2-fluorobenzylamine

dichloromethane

→

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

收率 53.0%

反应条件

后处理

1. 1
   洗涤the solution was washed successively with 2 N HCl and saturated aq NaCl
2. 2
   干燥The organic layer was dried over Na2SO4
3. 3
   过滤filtered
4. 4
   浓缩concentrated
5. 5
   其他Purification by MPLC (10–50% ethyl acetate in heptane, 23 mL/min, 70 min)

实验过程

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.

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