反応 #2069959

ord-3ee3960ca37f4080b9dbcbad8ff00152

反応方程式

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
収率 10.4%
CCCCc1ccc(Cc2nccc3ccc(CC)cc23)cc1
1-(4-Butylbenzyl)-7-ethylisoquinoline
収率 10.4%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The catalyst was removed by filtration
  2. 2
    濃縮the filtrate was concentrated
  3. 3
    その他The residue was purified by silica gel column chromatography

実験手順

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).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07541332B2uspto-grants-2009_06