Sodium hydride → 1-(2-(4-(Benzo[b]thiophen-2-yl)-5-bromopyrimidin-2-yloxy)ethyl)imidazolidin-2-one

HRID 507678Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 507678
[OH:1][CH2:2][CH2:3][N:4]1[CH2:8][CH2:7][NH:6][C:5]1=[O:9].[H-].[Na+].[S:12]1[C:16]([C:17]2[C:22]([Br:23])=[CH:21][N:20]=[C:19](Cl)[N:18]=2)=[CH:15][C:14]2[CH:25]=[CH:26][CH:27]=[CH:28][C:13]1=2>C1COCC1.C(OCC)(=O)C.C(=O)(O)[O-].[Na+]>[S:12]1[C:16]([C:17]2[C:22]([Br:23])=[CH:21][N:20]=[C:19]([O:1][CH2:2][CH2:3][N:4]3[CH2:8][CH2:7][NH:6][C:5]3=[O:9])[N:18]=2)=[CH:15][C:14]2[CH:25]=[CH:26][CH:27]=[CH:28][C:13]1=2

Komponenten

7

Edukt 3

HCID 24758Sodium hydrideHCID 77290Hydroxyethyl imidazolidinoneHCID 574288214-(Benzo[b]thiophen-2-yl)-5-bromo-2-chloropyrimidine

Produkt 1

HCID 602046301-(2-(4-(Benzo[b]thiophen-2-yl)-5-bromopyrimidin-2-yloxy)ethyl)imidazolidin-2-one

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 8028TetrahydrofuranLösungsmittel3×HCID 8857Ethyl AcetateLösungsmittelHCID 516892Sodium BicarbonateLösungsmittel

Versuchsvorschrift

1-(2-Hydroxyethyl)imidazolidin-2-one (0.6 g, 4.6 mmol) was taken up in anhydrous THF (5 mL) and added dropwise to a reaction flask containing a suspension of sodium hydride (0.147 g (60% in oil), 3.68mmol) in anhydrous THF (10 mL) at 0° C. The ice bath was removed and the reaction allowed to warm up to room temperature over a 2 h period. 4-(benzo[b]thiophen-2-yl)-5-bromo-2-chloropyrimidine (0.3 g, 9.2 mmol), dissolved in THF was added dropwise. The reaction was stirred overnight. The reaction was then diluted with ethyl acetate and saturated sodium bicarbonate. The organic layer was then washed with water and brine. The organic portion was dried with sodium sulfate and then purified by flash chromatography on silica gel using a gradient of 0 to 10% methanol in dichloromethane to give a white solid. Yield=0.085 g. MS (M+H)+ 420.

Aufarbeitung

  1. additionadded dropwise to a reaction flask
  2. additioncontaining
  3. customThe ice bath was removed
  4. additionwas added dropwise
  5. washThe organic layer was then washed with water and brine
  6. dry with materialThe organic portion was dried with sodium sulfate
  7. custompurified by flash chromatography on silica gel using a gradient of 0 to 10% methanol in dichloromethane
  8. customto give a white solid

Quellen und Nachweise

ORD-Eintrag
ord-8979ffcb32d14b2cb853211be7a9a425
Quelldatensatz
uspto-grants-2010_08
Patentnummer
US07786132B2

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