反应 #2328986
ord-f78d0bd165cd4cf9825f747c0d83e1fb
反应方程式
5-(6-Methoxy-1,3-benzoxazol-2-yl)-N,N-dimethylpyridin-2-amine
hydrogen bromide
sodium bicarbonate
→
title compound
收率 19.6%
2-[6-(Dimethylamino)pyridin-3-yl]-1,3-benzoxazol-6-ol
收率 19.6%
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1其他the solid was collected
- 2workup.DISSOLUTIONThe solid was then dissolved in CH2Cl2/ethyl acetate
- 3干燥dried (MgSO4)
- 4过滤filtered
- 5其他evaporated in vacuo
实验过程
5-(6-Methoxy-1,3-benzoxazol-2-yl)-N,N-dimethylpyridin-2-amine (31 mg, 0.12 mmol) was mixed with hydrogen bromide (48% aq., 2 mL) and a crystal of tetrabutylammonium bromide was added. The reaction was run at 120° C. for 5 minutes in a microwave reactor. The reaction mixture was added to sodium bicarbonate (sat. aq.) and the solid was collected. The solid was then dissolved in CH2Cl2/ethyl acetate, dried (MgSO4), filtered and evaporated in vacuo, giving the title compound (6 mg) as a purple solid. 1H NMR (400 MHz, CD3OD) δ ppm 8.83 (d, 1H) 8.17 (dd, 1H) 7.44 (d, 1H) 7.02 (d, 1H) 6.75-6.88 (m, 2H) 3.19 (s, 6H); MS m/z (M+H) 256; (M−H) 254.