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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | tert-Butyl(4-iodobutoxy)dimethylsilane | HCID 4250746 | — |
| 반응물 | 5-(3-Methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dione | HCID 14914592 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-[4-(tert-Butyl-dimethyl-silanyloxy)-butyl]-5-(3-methyl-thiophen-2-yl)-1H-pyrimidine-2,4-dione | HCID 69134988 | 23.2% |
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
| 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-f8276ed10f254d9d97d0a20aa58f09dd |
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| 출처 메모 | uspto-grants-2010_06 |
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