反应 #1435731

ord-7054545e715948659e3fcd2f805a7e49

反应方程式

Cl
hydrochloric acid
O
water
O
water
CCOC(=O)CC(=O)Cc1c(F)cccc1Cl
ethyl (2-chloro-6-fluorophenyl)acetoacetate
Cl.Nc1ncc[nH]1
aminoimidazole hydrochloride
C1CN=C2CCCN2C1
1,5-diazabicyclo[4.3.0]-5-nonene
Cc1nc2nccn2c(O)c1-c1c(F)cccc1Cl
5-hydroxy-6-(2-chloro-6-fluorophenyl)-7-methylimidazo[1,2-a]pyrimidine

反应条件

温度
100°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度to cool
  2. 2
    过滤the precipitate was filtered

实验过程

A mixture of 1.29 g of ethyl (2-chloro-6-fluorophenyl)acetoacetate, 0.60 g of aminoimidazole hydrochloride, 1.24 g of 1,5-diazabicyclo[4.3.0]-5-nonene (DBN) and 5 ml of N,N-dimethylformamide was heated at 100° C. for 14 hours. The reaction mixture was allowed to cool, and chloroform and water were added thereto. To the separated water layer, conc. hydrochloric acid was added and the precipitate was filtered, which was followed to subject to silica gel chromatography to give 0.16 g of 5-hydroxy-6-(2-chloro-6-fluorophenyl)-7-methylimidazo[1,2-a]pyrimidine.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07211545B2uspto-grants-2007_05