Реакция #216148

ord-7641f74449164c8abd217465b8feedc0

Уравнение реакции

CN1CC=C(c2c[nH]c3ccc(C=O)cc23)CC1
product
CN1CC=C(c2c[nH]c3ccc(C=O)cc23)CC1
3-(1-Methyl-1,2,3,6-tetrahydro-4-pyridyl)-1H-indole-5-carbaldehyde
O=C1CNC(=O)N1
hydantoin
CC(=O)[O-].[NH4+]
ammonium acetate
CN1CC=C(c2c[nH]c3ccc(C=C4NC(=O)NC4=O)cc23)CC1
desired product
Выход 76.0%
CN1CC=C(c2c[nH]c3ccc(C=C4NC(=O)NC4=O)cc23)CC1
5-[3-(1-Methyl-1,2,3,6-tetrahydro-4-pyridyl)-1H-indol-5-ylmethylene]-2,4-imidazolidinedione
Выход 76.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe mixture was cooled
  2. 2
    Фильтрацияthe resulting precipitate filtered off
  3. 3
    Другоеdried

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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05466699uspto-grants-1995_11