Réaction #2487389

ord-c5f94b46f945434eba5fab96760098c3

Équation de réaction

Cc1cccc(-c2nccn2CCCCCCN2C(=O)c3ccccc3C2=O)n1
2-(6-methyl-2-pyridyl)-1-(6-(phthalimido)hexyl)imidazole
NN.O
hydrazine hydrate
Cc1cccc(-c2nccn2CCCCCCN)n1
crude product
Cc1cccc(-c2nccn2CCCCCCN)n1
1-(6-Aminohexyl)-2-(6-methyl-2-pyridyl)imidazole

Solvants

Conditions de réaction

Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe solution was cooled to room temperature
  2. 2
    Filtrationsuction filtered
  3. 3
    Autreto remove the precipitate
  4. 4
    AutreThe filtrate was evaporated

Mode opératoire

To a solution of 2-(6-methyl-2-pyridyl)-1-(6-(phthalimido)hexyl)imidazole (4.2 g) in 50 mL EtOH was added 1.5 mL hydrazine hydrate. The resulting solution was stirred at 80° C. overnight. The solution was cooled to room temperature and suction filtered to remove the precipitate. The filtrate was evaporated to give the crude product, which was purified by a silica gel column using 5% conc. NH3H2O/CH3CN as the eluent. Yield: about 2.5 g.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08795490B2uspto-grants-2014_08