Реакция #5529
ord-824f8a15b5d240dc96f33facfa1f2b99
Уравнение реакции
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Температураat reflux for 3 hours
- 2ПромывкаThe reaction solution was washed with an aqueous 3N-sodium hydroxide solution
- 3Сушкаdried over anhydrous magnesium sulfate
- 4workup.DISTILLATIONAfter the solvent was distilled off
- 5Другоеthe residue was purified by column chromatography (eluent: methanol/chloroform=1:10)
Методика
A solution of 5-[2-(methylsulfonyloxy)ethylthio]imidazo[1,2-a]pyridine (2.18 g, 8 mmoles), triethylamine (2.24 ml, 16 mmoles) and a 40% methylamine-methanol solution (20 ml) in chloroform (20 ml) was heated at reflux for 3 hours. The reaction solution was washed with an aqueous 3N-sodium hydroxide solution and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: methanol/chloroform=1:10) to obtain 781 mg of the desired product (47.1%, light brown oily product).