反应 #684966
ord-9961c8484dcc4be4b00da7c8305d5882
反应方程式
compound
1-(4-Butylbenzyl)-7-(1-ethynyl)isoquinoline
→
title compound
收率 10.4%
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其他The catalyst was removed by filtration
- 2浓缩the filtrate was concentrated
- 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).