反应 #2075728
ord-08bd5b1fcffc4e73b644031b84d9fd1c
反应方程式
4,6-Dichloro-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-methoxy-pyrimidine
water
ammonia
→
title compound
收率 88.0%
6-Chloro-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-methoxypyrimidin-4-ylamine
收率 88.0%
反应条件
温度
125°CELSIUS
详细条件
See reaction.notes.procedure_details.
后处理
- 1萃取extracted with ethyl acetate thrice
- 2洗涤The combined organic phases were washed once with brine
- 3其他dried
- 4其他evaporated
实验过程
4,6-Dichloro-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-methoxy-pyrimidine (500 mg, 1.5 mmol) was suspended in ammonia saturated ethanol (10 mL) and heated in a CEM microwave at 125° C. for 30 min. The mixture was poured into 15 mL water and extracted with ethyl acetate thrice. The combined organic phases were washed once with brine, dried and evaporated to give the title compound (420 mg, 88% yield: 1H NMR (DMSO-d6) δ 7.59 (dd, 1H), 7.45 (br s, 2H), 7.39 (dd, 1H), 3.91 (s, 3H), 3.76 (s, 3H).