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
CONDITIONS
反应条件
- 温度
- 80 °C
PROCEDURE
实验过程
To a stirred solution of methyl 3-bromo-4,6-dichloropyridine-2-carboxylate (600 mg, 2.1 mmol) in DMF (5 ml) was added TEA (587 μl, 4.21 mmol) followed by N-methyloxan-4-amine (240 mg, 2.1 mmol) and the reaction mixture was heated at 80° C. for 20 h. The reaction mixture was then cooled to room temperature and poured onto water (100 ml), followed by extraction of the product into EtOAc (3×100 ml), washing of the combined organics with brine (50 ml), drying with Na2SO4 and evaporation. The crude product was then purified over a 10 g silica Isolute column eluting with a gradient of 0% to 100% EtOAc in heptane to afford the title compound as a white solid (110 mg, 14%). LC-MS 100%, 1.94 min (3.5 minute LC-MS method), m/z=362.8/365.2/346.8, 1H NMR (250 MHz, Chloroform-d) δ 6.87 (s, 1H), 4.17-3.99 (m, 2H), 3.98 (s, 3H), 3.93-3.70 (m, 1H), 3.41 (t, J=10.9 Hz, 2H), 2.81 (s, 3H), 1.93 (dd, J=11.9, 4.6 Hz, 2H), 1.71 (d, J=10.3 Hz, 2H).
WORKUP
后处理
- temperatureThe reaction mixture was then cooled to room temperature
- additionpoured onto water (100 ml)
- extractionfollowed by extraction of the product into EtOAc (3×100 ml)
- washwashing of the combined organics with brine (50 ml)
- dry with materialdrying with Na2SO4 and evaporation
- customThe crude product was then purified over a 10 g silica Isolute column
- washeluting with a gradient of 0% to 100% EtOAc in heptane