反应详情

3-(1-Methyl-1,2,3,6-tetrahydro-pyridin-4-yl)-5-nitro-1H-indole (2.7 g, Step A) was dissolved in MeOH (50 mL), the mixture was bubbled with H2 for 10 min. 10% Pd/C (150 mg) was added and the mixture was stirred under H2 overnight. The mixture was filtered through Celite® and concentrated in vacuo to afford 3-(1-methyl-4-piperidyl)indole-5-ylamine as a yellow oil. MS: 230 (M+1). Calc'd. for C14H19N3−229.32.

1. customthe mixture was bubbled with H2 for 10 min
2. addition10% Pd/C (150 mg) was added
3. filtrationThe mixture was filtered through Celite®
4. concentrationconcentrated in vacuo