反应 #1435728

ord-f483e3bf53794d85b2583432dbceba08

反应方程式

CCOC(=O)C(C(=O)OCC)c1c(F)cccc1Cl
diethyl (2-chloro-6-fluorophenyl)malonate
Cl.Nc1ncc[nH]1
aminoimidazole hydrochloride
C1CN=C2CCCN2C1
1,5-diazabicyclo[4.3.0]-5-nonene
C1CN=C2CCCN2C1.Oc1nc2nccn2c(O)c1-c1c(F)cccc1Cl
5,7-dihydroxy-6-(2-chloro-6-fluorophenyl)imidazo[1,2-a]pyrimidine DBN
收率 44.5%

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filtered the precipitate
  3. 3
    其他dried

实验过程

A mixture of 2.89 g of diethyl (2-chloro-6-fluorophenyl)malonate, 1.20 g of aminoimidazole hydrochloride, 2.48 g of 1,5-diazabicyclo[4.3.0]-5-nonene (DBN) and 10 ml of N,N-dimethylformamide (DMF) was heated at 100° C. for 4 hours. The reaction mixture was allowed to cool, filtered the precipitate and dried to give 1.80 g of 5,7-dihydroxy-6-(2-chloro-6-fluorophenyl)imidazo[1,2-a]pyrimidine DBN salt.

来源

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