Реакция #157089

ord-cd8e2e88020b46ec997df1a4c964011f

Растворители

Условия реакции

Температура
60°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Концентрированиеthen concentrated in vacuo
  2. 2
    workup.ADDITIONThe crude residue was diluted with EtOAc
  3. 3
    Промывкаwashed with 1.0 N NaOH
  4. 4
    Экстракцияextracted with CH2Cl2
  5. 5
    СушкаThe combined organic phases were dried over anhydrous MgSO4
  6. 6
    Фильтрацияfiltered
  7. 7
    Концентрированиеconcentrated in vacuo

Методика

4-chloro-3-nitropyridine (1.1 eq) was added to a solution of 3-methylpiperidine-3-carboxylic acid (1 eq) and DIEA (3 eq) in iPrOH (0.1 M). The reaction mixture was heated in a 60° C. oil bath for 3 h then concentrated in vacuo. The crude residue was diluted with EtOAc and washed with 1.0 N NaOH. The combined aqueous washes were acidified to pH=4 with 1.0 N HCl and extracted with CH2Cl2. The combined organic phases were dried over anhydrous MgSO4, filtered, and concentrated in vacuo to give 3-methyl-(3-nitropyridin-4-yl)piperidine-3-carboxylic acid. LC/MS (m/z): 266.2 (MH+).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08822497B2uspto-grants-2014_09