Реакция #216148
ord-7641f74449164c8abd217465b8feedc0
Уравнение реакции
product
3-(1-Methyl-1,2,3,6-tetrahydro-4-pyridyl)-1H-indole-5-carbaldehyde
hydantoin
ammonium acetate
→
desired product
Выход 76.0%
5-[3-(1-Methyl-1,2,3,6-tetrahydro-4-pyridyl)-1H-indol-5-ylmethylene]-2,4-imidazolidinedione
Выход 76.0%
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ТемператураThe mixture was cooled
- 2Фильтрацияthe resulting precipitate filtered off
- 3Другоеdried
Методика
A mixture of the product from step (b) (2.4 g), hydantoin (Aldrich, 0.98 g) and ammonium acetate (0.74 g) in glac. acetic acid (2.4 ml) was heated at 120° C. for 4 hours. The mixture was cooled and the resulting precipitate filtered off and dried to give the desired product as a yellow solid (2.4 g).