Réaction #61173

ord-bd1616501d4f4ef8b89253b1c1924ab7

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreas prepared in the previous step)

Mode opératoire

Using a procedure similar to Example 3, step (c), dimethyl-(4-nitro-3-piperidin-1-yl-phenyl)-amine (100 mg, 0.4 mmol, as prepared in the previous step) was stirred with 80 mg 5% Pd—C in 5 mL MeOH under H2 to afford 89 mg (100%) of the title compound as an oil, which was used immediately without further purification. Mass spectrum (ESI, m/z) calcd. for C13H21N3, 220.1 (M+H), found 220.1.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07427683B2uspto-grants-2008_09