Reacción #1171

ord-aad08f27e18e4070affc2570d3f9689b

Ecuación de reacción

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

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadowashed with 1N aq. HCl, 5N aq. NaOH
  2. 2
    Secadodried over MgSO4
  3. 3
    Concentraciónconcentrated

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723490uspto-grants-1998_03