反应详情

To a solution of 1-[5-tert-butyl-2-(4-hydroxymethyl-phenyl)-2H-pyrazol-3-yl]-3-[2-fluoro-4-(2-methyl-pyridin-4-yloxy)-phenyl)-urea (170 mg, 0.35 mmol) in anhydrous THF was added K2CO3 (52 mg, 0.38 mmol) followed by methanesulfonyl chloride (30 μL, 0.38 mmol). The mixture was stirred at room temperature for one day, and then 2-methoxy-ethanol (213 mg, 3.5 mmol) was added. The mixture was stirred at room temperature overnight, then EtOAc was added followed by saturated Na2CO3. The organic layer was washed with saturated Na2CO3 and brine, dried over MgSO4 and evaporated at reduced pressure. Purification by HPLC (10% to 90% aq acetonitrile afforded pure product (10 mg, 5%). 1H-NMR (CD3OD) δ 8.17 (d, J=6.0 Hz, 1H), 8.01 (t, J=9.3 Hz, 1H), 7.48-7.37 (m, 4H), 6.93-6.69 (m, 4H), 6.36 (s, 1H), 4.54 (s, 2H), 3.58 (m, 2H), 3.50 (m, 2H), 3.28 (s, 3H), 2.37 (s, 3H), 1.25 (s, 9H); MS LC-MS [M+H]+=548.1, RT=2.69 min.

1. stirringThe mixture was stirred at room temperature overnight
2. washThe organic layer was washed with saturated Na2CO3 and brine
3. dry with materialdried over MgSO4
4. customevaporated at reduced pressure
5. customPurification by HPLC (10% to 90% aq acetonitrile afforded pure product (10 mg, 5%)