Gemfibrozil → Gemfibrozil Succinimide

HRID 1943981

Reaktionsgleichung

Reaktionsgleichung von HRID 1943981
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:18])=[C:6]([O:8][CH2:9][CH2:10][CH2:11][C:12]([C:15]([OH:17])=[O:16])([CH3:14])[CH3:13])[CH:7]=1.O[N:20]1[C:24](=[O:25])[CH2:23][CH2:22][C:21]1=[O:26].C1(N=C=NC2CCCCC2)CCCCC1>O1CCOCC1>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:18])=[C:6]([O:8][CH2:9][CH2:10][CH2:11][C:12]([C:15]([OH:17])=[O:16])([CH3:13])[CH3:14])[CH:7]=1.[C:21]1(=[O:26])[NH:20][C:24](=[O:25])[CH2:23][CH2:22]1

Komponenten

5

Reaktionsbedingungen

Temperatur
4 °C

Versuchsvorschrift

To Gemfibrozil (GEM) (5.0 g, 20.0 mmol) in 30 mL dioxane was added N-hydroxysuccinimide (2.3 g, 20.0 mmol) in 20 mL dioxane and dicyclohexylcarbodiimide (4.5 g, 22.0 mmol) in 50 mL dioxane. The reaction was stirred overnight and the insoluble dicyclohexylurea removed by filtration. The solvent was removed by rotary evaporation and the residue dissolved in 15-20 mL of CH2Cl2. Hexane was added dropwise until crystal formation was seen and the mixture was chilled to 4° C. overnight. Approximately 3 mL of additional n-hexane was added and the mixture chilled to −20° C. overnight. The activated ester formed small planer crystals and was harvested, washed with hexane and dried in vacuum (5.8 g, 80%).

Aufarbeitung

  1. customthe insoluble dicyclohexylurea removed by filtration
  2. customThe solvent was removed by rotary evaporation
  3. dissolutionthe residue dissolved in 15-20 mL of CH2Cl2
  4. additionHexane was added dropwise until crystal formation
  5. additionApproximately 3 mL of additional n-hexane was added
  6. temperaturethe mixture chilled to −20° C. overnight
  7. washwashed with hexane
  8. customdried in vacuum (5.8 g, 80%)

Quellen und Nachweise

ORD-Eintrag
ord-99aa1078cada41dbb1fb3818ba5879d7
Quelldatensatz
uspto-grants-2013_03
Patentnummer
US08394813B2

Verknüpfte Notizen

Wird geladen…