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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | (3-Bromopropoxy)(tert-butyl)dimethylsilane | HCID 607486 | — |
| Edukt | 5-(3-Methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dione | HCID 14914592 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-[3-(tert-Butyl-dimethyl-silanyloxy)-propyl]-5-(3-methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dione | HCID 68691300 | 37% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07727988B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-02bf8d507037412cb69175d867be4cb6 |
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| Quellennotiz | uspto-grants-2010_06 |
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