反应 #684966

ord-9961c8484dcc4be4b00da7c8305d5882

反应方程式

C#Cc1ccc2ccnc(Cc3ccc(CCCC)cc3)c2c1
compound
C#Cc1ccc2ccnc(Cc3ccc(CCCC)cc3)c2c1
1-(4-Butylbenzyl)-7-(1-ethynyl)isoquinoline
CCCCc1ccc(Cc2nccc3ccc(CC)cc23)cc1
title compound
收率 10.4%
CCCCc1ccc(Cc2nccc3ccc(CC)cc23)cc1
1-(4-Butylbenzyl)-7-ethylisoquinoline
收率 10.4%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The catalyst was removed by filtration
  2. 2
    浓缩the filtrate was concentrated
  3. 3
    其他The residue was purified by silica gel column chromatography

实验过程

Palladium-carbon (10%, 5.0 mg) was added to a solution of the compound of Example B158 (2.0 mg) in tetrahydrofuran (2.0 ml), and the mixture was stirred at room temperature under nitrogen atmosphere (1 atm) for 1 hour. The catalyst was removed by filtration, and the filtrate was concentrated. The residue was purified by silica gel column chromatography to give the title compound (0.21 mg).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07897387B2uspto-grants-2011_03