Reaktion #1171

ord-aad08f27e18e4070affc2570d3f9689b

Reaktionsgleichung

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

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with 1N aq. HCl, 5N aq. NaOH
  2. 2
    Trocknendried over MgSO4
  3. 3
    Einengenconcentrated

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723490uspto-grants-1998_03