Sodium hydride → HCID 86619736, Verbindung

HRID 1675780Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1675780
[H-].[Na+].Br[CH2:4][C:5]([O:7][C:8]([CH3:11])([CH3:10])[CH3:9])=[O:6].[S:12]1[CH2:17][CH2:16][CH:15]([N:18]2[C:22]3[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=3[NH:20][C:19]2=[O:27])[CH2:14][CH2:13]1>CN(C=O)C>[O:27]=[C:19]1[N:20]([CH2:4][C:5]([O:7][C:8]([CH3:11])([CH3:10])[CH3:9])=[O:6])[C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=2[N:18]1[CH:15]1[CH2:16][CH2:17][S:12][CH2:13][CH2:14]1

Komponenten

5

Edukt 3

HCID 24758Sodium hydrideHCID 79177tert-Butyl bromoacetateHCID 67336664HCID 67336664, Verbindung

Produkt 1

HCID 86619736HCID 86619736, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

Sodium hydride (68.3 mg of a 60% dispersion in mineral oil, 1.71 mmol) followed by tert-butyl bromoacetate (0.189 mL, 1.28 mmol) was added to a solution of 1-tetrahydro-2H-thiopyran-4-yl-1,3-dihydro-2H-benzimidazol-2-one from Step B (200 mg, 0.854 mmol) in DMF (5 mL). After 1 h, the reaction was quenched with H2O (10 mL) and extracted with CH2Cl2 (10 mL). The organic layer was washed with saturated NaHCO3 (5 mL), dried over MgSO4, filtered, and concentrated in vacuo. Purification by silica gel chromatography, eluting with a gradient of hexane:EtOAc-100:0 to 50:50, gave the title compound. MS: m/z=349 (M+1).

Aufarbeitung

  1. customthe reaction was quenched with H2O (10 mL)
  2. extractionextracted with CH2Cl2 (10 mL)
  3. washThe organic layer was washed with saturated NaHCO3 (5 mL)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customPurification by silica gel chromatography
  8. washeluting with a gradient of hexane

Quellen und Nachweise

ORD-Eintrag
ord-4a7e26ac4cc74110abc7a26ee37587ba
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US08003792B2

Notizen zur Reaktion

Wird geladen…