反应 #1171

ord-aad08f27e18e4070affc2570d3f9689b

反应方程式

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

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    洗涤washed with 1N aq. HCl, 5N aq. NaOH
  2. 2
    干燥dried over MgSO4
  3. 3
    浓缩concentrated

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05723490uspto-grants-1998_03