Réaction #684966

Équation de réaction

compound

1-(4-Butylbenzyl)-7-(1-ethynyl)isoquinoline

→

title compound

Rendement 10.4%

1-(4-Butylbenzyl)-7-ethylisoquinoline

Rendement 10.4%

Solvants

tetrahydrofuran

Conditions de réaction

Traitement

1. 1
   AutreThe catalyst was removed by filtration
2. 2
   Concentrationthe filtrate was concentrated
3. 3
   AutreThe residue was purified by silica gel column chromatography

Mode opératoire

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).

Source