Реакция #5683

ord-95de830301e84a0d9f33eedda961e5bd

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGThe mixture is stirred at room temperature overnight
  2. 2
    workup.STIRRINGthe mixture is stirred at room temperature for two hours
  3. 3
    Экстракцияthe mixture is extracted with dichloromethane
  4. 4
    Сушкаthe extract is dried over magnesium sulfate
  5. 5
    workup.DISTILLATIONThe solvent is distilled off under reduced pressure
  6. 6
    Другоеthe resulting residue is purified by silica gel column chromatography (eluent; methyl acetate)
  7. 7
    workup.ADDITIONis added
  8. 8
    workup.ADDITIONa mixture of hydrochloric acid/methanol
  9. 9
    workup.STIRRINGThe mixture is stirred at room temperature for one hour

Методика

In a solution of 5-hydroxymethyl-7-chloro-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.4 g) in chloroform (10 ml) are dissolved with heating dimethylaminopyridine (0.41 g) and dimethylaminopyridine hydrochloride (0.35 g), and thereto is added N,N-dimethylglycine hydrochloride (0.15 g) at room temperature with stirring, and further added dicyclohexylcarbodiimide (0.46 g). The mixture is stirred at room temperature overnight. To the mixture are added methanol (1.3 ml) and acetic acid (0.4 ml), and the mixture is stirred at room temperature for two hours. Saturated aqueous sodium hydrogen carbonate solution is added to the reaction solution, and the mixture is extracted with dichloromethane, and the extract is dried over magnesium sulfate. The solvent is distilled off under reduced pressure, and the resulting residue is purified by silica gel column chromatography (eluent; methyl acetate), and thereto is added a mixture of hydrochloric acid/methanol. The mixture is stirred at room temperature for one hour to give 5-[(2-dimethylaminoacetyloxy)methyl]-7-chloro-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine hydrochloride (0.36 g) as colorless amorphous.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05244898uspto-grants-1993_09