Réaction #9561

Équation de réaction

Butyryl chloride

7-bromo-N4-(2-methylpropyl)quinoline-3,4-diamine

→

7-bromo-1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinoline

Solvants

pyridine

Conditions de réaction

Traitement

1. 1
   AutreA pale yellow precipitate formed
2. 2
   TempératureThe reaction mixture was heated
3. 3
   Températureat reflux for eight hours
4. 4
   Concentrationwas concentrated under reduced pressure
5. 5
   workup.DISSOLUTIONThe residue was dissolved in 1 N hydrochloric acid
6. 6
   workup.ADDITIONadjusted to pH 14 with the addition of 10% aqueous sodium hydroxide
7. 7
   AutreA precipitate formed
8. 8
   Autrewas isolated by filtration
9. 9
   Lavagewashed with water (3×100 mL)
10. 10
    Autredried overnight on the filter funnel

Mode opératoire

Butyryl chloride (1.1 equivalent) was slowly added to a stirred solution of 7-bromo-N4-(2-methylpropyl)quinoline-3,4-diamine (52.9 g, 0.18 mol.) in pyridine (700 mL) at room temperature. A pale yellow precipitate formed and then went into solution. The reaction mixture was heated at reflux for eight hours, and then allowed to slowly cool to room temperature over the weekend. The dark gold, turbid reaction mixture was concentrated under reduced pressure. The residue was dissolved in 1 N hydrochloric acid and then adjusted to pH 14 with the addition of 10% aqueous sodium hydroxide. A precipitate formed, was isolated by filtration, washed with water (3×100 mL), and dried overnight on the filter funnel to provide 7-bromo-1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinoline as an off-white solid.

Source