反应 #1435725
ord-3548f248f23c401e85b4ee7b9c5386b4
反应方程式
diethyl (2,4,6-trifluorophenyl)malonate
2-aminoimidazole hydrochloride
DBU
N,N-dimethylformamide
→
5,7-dihydroxy-6-(2,4,6-trifluorophenyl)imidazo[1,2-a]pyrimidine
收率 78.3%
反应条件
温度
100°CELSIUS
详细条件
See reaction.notes.procedure_details.
后处理
- 1温度to cool to room temperature
- 2浓缩The separated water layer was concentrated
- 3workup.ADDITIONthe residue was diluted with water and conc. hydrochloric acid
- 4workup.ADDITIONwas added
- 5温度under ice-cooling
- 6其他The precipitation
- 7过滤was filtered
- 8其他dried
实验过程
A mixture of 2.90 g of diethyl (2,4,6-trifluorophenyl)malonate, 2.39 g of 2-aminoimidazole hydrochloride, 4.57 g of DBU and 10 ml of N,N-dimethylformamide was heated at 100° C. for 6 hours. After allowing the reaction mixture to cool to room temperature, chloroform and water were added thereto. The separated water layer was concentrated, the residue was diluted with water and conc. hydrochloric acid was added thereto under ice-cooling. The precipitation was filtered and dried to give 2.2 g of 5,7-dihydroxy-6-(2,4,6-trifluorophenyl)imidazo[1,2-a]pyrimidine.