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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12662Erstellt: 24. Oktober 2026

Sodium hydride → 1-[3-(tert-Butyl-dimethyl-silanyloxy)-propyl]-5-(3-methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dione

https://huagongshe.com/de/reaction/12662

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt(3-Bromopropoxy)(tert-butyl)dimethylsilaneHCID 607486—
Edukt5-(3-Methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dioneHCID 14914592—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-[3-(tert-Butyl-dimethyl-silanyloxy)-propyl]-5-(3-methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dioneHCID 6869130037%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a suspension of 5-(3-methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dione (Prep26, 110 mg, 0.52 mmol) in dry DMF (10 mL), 60% NaH (31 mg, 0.78 mmol) was added. The mixture was then heated at 100° C. for 1 hour. (3-bromo-propoxy)-tert-butyl-dimethyl-silane (180 μl, 0.7 mmol) was then added at room temperature and the reaction was stirred overnight. The solvent was evaporated and the crude was partitioned between NaHCO3 and Et2O. The organic phase was dried (Na2SO4) and evaporated. The crude was purified by flash chromatography with ethyl acetate-petroleum ether (2-8) to give the title compound as a white solid (73 mg, 37% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07727988B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-02bf8d507037412cb69175d867be4cb6
Quellennotizuspto-grants-2010_06