Реакция #657284
ord-0bcef22479a64fc28b08471dcc3585bf
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Обработка
- 1Температураthe reaction mixture was heated
- 2Температураat reflux for 7 days
- 3ТемператураAfter cooling
- 4Концентрированиеthe mixture was concentrated
- 5workup.ADDITIONthe residue diluted with ice water and neutralised with aqueous sodium bicarbonate
- 6ЭкстракцияThe aqueous phase was extracted with ethyl acetate (4×)
- 7Промывкаthe combined organic layers washed with brine
- 8Сушкаdried over sodium sulfate
- 9Концентрированиеconcentrated
- 10ДругоеThe residue was purified by chromatography on silica gel (gradient ethyl acetate→ethyl acetate/methanol 20:1)
Методика
To a suspension of 1-methoxy-4-methylamino-piperidine-4-carboxylic acid hydrochloride salt (2.08 g, 9.26 mmol) in methanol (20 ml) at 0-5° C. was added thionyl chloride (2.41 ml, 3.97 g, 33.40 mmol) and the reaction mixture was heated at reflux for 7 days. After cooling, the mixture was concentrated, the residue diluted with ice water and neutralised with aqueous sodium bicarbonate. The aqueous phase was extracted with ethyl acetate (4×), the combined organic layers washed with brine, dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel (gradient ethyl acetate→ethyl acetate/methanol 20:1). Yield: 76 mg of 1-methoxy-4-methylamino-piperidine-4-carboxylic acid methyl ester (title compound P5.4) as an oil.