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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12665생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/12665

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물tert-Butyl(4-iodobutoxy)dimethylsilaneHCID 4250746—
반응물5-(3-Methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dioneHCID 14914592—
용매DimethylformamideHCID 6228—
생성물1-[4-(tert-Butyl-dimethyl-silanyloxy)-butyl]-5-(3-methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dioneHCID 6913498823.2%

반응 조건

온도70 °C

반응 단계

To a solution of 5-(3-methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dione (Prep 26, 250 mg, 1.2 mmol) in DMF (10 mL), 60% NaH (58 mg, 1.44 mmol) was added portionwise. The reaction was then heated to 70° C. and this temperature was maintained for 1.5 hour. After cooling to room temperature, (4-iodo-butoxy)-tert-butyl-dimethyl-silane (452 mg, 1.44 mmol) was then added dropwise and the reaction was stirred for 24 hours. Water (30 mL) was added and the product was extracted with Et2O. The organic phase was dried (Na2SO4) and evaporated. The crude was purified by flash chromatography with ethyl acetate-petroleum ether (15-85) followed by DCM/MeOH (70:30) to give the title compound as a yellow oil (110 mg, 23% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727988B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f8276ed10f254d9d97d0a20aa58f09dd
출처 메모uspto-grants-2010_06