Реакция #1171

ord-aad08f27e18e4070affc2570d3f9689b

Уравнение реакции

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

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаwashed with 1N aq. HCl, 5N aq. NaOH
  2. 2
    Сушкаdried over MgSO4
  3. 3
    Концентрированиеconcentrated

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05723490uspto-grants-1998_03