反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
The reaction solution of dimethyl 5,5′-[N-({6-amino-5-[(3-aminophenyl)ethynyl]pyridin-3-yl}carbonyl)sulfonimidoyl]dipentanoate (140 mg, 0.265 mmol, 1.0 equiv.) and 2-fluoro-5-methylphenyl isocyanate (38.8 μL, 0.292 mmol, 1.1 equiv.) in DMF (3 mL) was stirred at room temperature for 3 hours. It was then diluted with EtOAc, washed with sat. aq. NaHCO3, aq. NH4Cl, and brine, and finally dried with anhydrous Na2SO4. The solution was decanted, concentrated, and the oily residue was subject to a gradient column chromatography (from EtOAc-Hex 1:5 to 5:1) yielding the title compound as clear oil (169 mg). 1H NMR (DMSO-d6) δ: 9.14-9.15 (m, 1H), 8.56 (d, J=2.3 Hz, 1H), 8.54 (d, J=2.3 Hz, 1H), 8.04 (d, J=2.1 Hz, 1H), 7.99 (dd, J=7.9, 1.8 Hz, 1H), 7.81 (t, J=−1.8 Hz, 1H), 7.40 (dt, J=7.7, 1.9 Hz, 1H), 7.30-7.35 (m, 2H), 7.11 (dd, J=11.3, 8.4 Hz, 1H), 7.00 (br. s., 2H), 6.79-6.83 (m, 1H), 3.52-3.64 (m, 10H), 2.39 (t, J=7.3 Hz, 4H), 2.27 (s, 3H), 1.72-1.85 (m, 4H), 1.65-1.71 (m, 4H)
WORKUP
后处理
- washwashed with sat. aq. NaHCO3, aq. NH4Cl, and brine
- dry with materialfinally dried with anhydrous Na2SO4
- customThe solution was decanted
- concentrationconcentrated