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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | (3-Bromopropoxy)(tert-butyl)dimethylsilane | HCID 607486 | — |
| 반응물 | 5-(3-Methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dione | HCID 14914592 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-[3-(tert-Butyl-dimethyl-silanyloxy)-propyl]-5-(3-methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dione | HCID 68691300 | 37% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07727988B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-02bf8d507037412cb69175d867be4cb6 |
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| 출처 메모 | uspto-grants-2010_06 |
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