Реакция #1340595
ord-7162bd3ad69d4fe6aa23a6a99c06240a
Уравнение реакции
amine
(S,E)-tert-butyl 4-(4-(methylsulfonyl)-2-(tritylamino)but-3-en-1-yl)benzylcarbamate
TFA DCM
HCl
→
(S,E)-tert-butyl 4-(4-(methylsulfonyl)-2-aminobut-3-en-1-yl)benzylcarbamate
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Другоеresulted in a colourless suspension
- 2ДругоеDCM was removed under reduced pressure
- 3ЭкстракцияThe aqueous layer was extracted with Et2O (3×)
- 4Экстракцияafter which it was extracted with DCM (3×)
- 5СушкаThe latter combined organic layers were dried over MgSO4
- 6Концентрированиеconcentrated under reduced pressure
- 7Другоеwas subjected to the next step without further purification
Методика
Trityl protected amine 17 (0.54 g, 0.90 mmol) was treated with 1% v/v TFA/DCM (15 mL) at room temperature. To this yellow solution was added H2O (1 mL) which resulted in a colourless suspension. After stirring the mixture for 30 minutes, 10 mM aq. HCl (20 mL) was added and DCM was removed under reduced pressure. The aqueous layer was extracted with Et2O (3×) and basified with NaHCO3 until pH 9, after which it was extracted with DCM (3×). The latter combined organic layers were dried over MgSO4 and concentrated under reduced pressure. The resulting deprotected amine proved to be pure on LC-MS analysis and was subjected to the next step without further purification.