反应 #463502

ord-642cb24e823a4997b41d9ec7ebc93a14

反应方程式

COc1ccc2c(c1)-c1nc(-c3ccccc3C)cn1C(C)C2
9-methoxy-5-methyl-2-(2-methylphenyl)-5,6-dihydroimidazo[2,1-a]isoquinoline
ClC(Cl)Cl
chloroform
COc1ccc2cc(C)n3cc(-c4ccccc4C)nc3c2c1
title compound
收率 61.6%
COc1ccc2cc(C)n3cc(-c4ccccc4C)nc3c2c1
9-Methoxy-5-methyl-2-(2-methylphenyl)imidazo[2,1-a]isoquinoline
收率 61.6%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度the mixture was refluxed for 6 hours
  2. 2
    温度After being cooled
  3. 3
    过滤the mixture was filtered
  4. 4
    其他the filtrate was evaporated in vacuo
  5. 5
    其他The resultant residue was crystallized from a mixture of hexane and ethyl acetate(6:1)

实验过程

To a solution of 4.9 g of 9-methoxy-5-methyl-2-(2-methylphenyl)-5,6-dihydroimidazo[2,1-a]isoquinoline in 30 ml of decalin was added 0.97 g of palladium on activated carbon (Pd 10%) and the mixture was refluxed for 6 hours. After being cooled and an addition of 200 ml of chloroform, the mixture was filtered and the filtrate was evaporated in vacuo. The resultant residue was crystallized from a mixture of hexane and ethyl acetate(6:1) to give 3.0 g of the title compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06020342uspto-grants-2000_02