Реакция #157089
ord-cd8e2e88020b46ec997df1a4c964011f
Уравнение реакции
Реагенты
Нет
Растворители
Условия реакции
Температура
60°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Концентрированиеthen concentrated in vacuo
- 2workup.ADDITIONThe crude residue was diluted with EtOAc
- 3Промывкаwashed with 1.0 N NaOH
- 4Экстракцияextracted with CH2Cl2
- 5СушкаThe combined organic phases were dried over anhydrous MgSO4
- 6Фильтрацияfiltered
- 7Концентрированиеconcentrated 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+).