Réaction #1171

ord-aad08f27e18e4070affc2570d3f9689b

Équation de réaction

NC(=O)C1CCNCC1
4-Piperidinecarboxamide
BrCc1ccccc1
benzyl bromide
O=C(NCc1ccccc1)C1CCNCC1
N-benzyl-4-piperidinecarboxamide
Rendement 35.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Lavagewashed with 1N aq. HCl, 5N aq. NaOH
  2. 2
    Séchagedried over MgSO4
  3. 3
    Concentrationconcentrated

Mode opératoire

4-Piperidinecarboxamide (10.2 g, 78.0 mmol) in DMSO (10 mL) was treated with benzyl bromide (20.0 mL, 168 mmol). The mixture was diluted with EtOAc and washed with 1N aq. HCl, 5N aq. NaOH, dried over MgSO4, and concentrated to give 5.90 g (35%) of N-benzyl-4-piperidinecarboxamide. [1H]-NMR(CDCl3) consistent with structure.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05723490uspto-grants-1998_03