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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12662생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/12662

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물(3-Bromopropoxy)(tert-butyl)dimethylsilaneHCID 607486—
반응물5-(3-Methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dioneHCID 14914592—
용매DimethylformamideHCID 6228—
생성물1-[3-(tert-Butyl-dimethyl-silanyloxy)-propyl]-5-(3-methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dioneHCID 6869130037%

반응 조건

온도100 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727988B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-02bf8d507037412cb69175d867be4cb6
출처 메모uspto-grants-2010_06