반응 #5683

ord-95de830301e84a0d9f33eedda961e5bd

반응 방정식

C(=NC1CCCCC1)=NC1CCCCC1
dicyclohexylcarbodiimide
CN(C)c1ccccn1
dimethylaminopyridine
CN(C)c1ccccn1.Cl
dimethylaminopyridine hydrochloride
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2CCCC(CO)c3cc(Cl)ccc32)cc1
5-hydroxymethyl-7-chloro-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine
O=C([O-])O.[Na+]
sodium hydrogen carbonate
CN(C)CC(=O)O.Cl
N,N-dimethylglycine hydrochloride
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2CCCC(COC(=O)CN(C)C)c3cc(Cl)ccc32)cc1.Cl
5-[(2-dimethylaminoacetyloxy)methyl]-7-chloro-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine hydrochloride
수율 141.6%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  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
    추출the mixture is extracted with dichloromethane
  4. 4
    건조the extract is dried over magnesium sulfate
  5. 5
    workup.DISTILLATIONThe solvent is distilled off under reduced pressure
  6. 6
    기타the 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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05244898uspto-grants-1993_09