참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Bromopropane | HCID 6358 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 4,6-Dimethoxypyrimidine-5-carbaldehyde | HCID 4436645 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 반응물 | HCID 178418365 | HCID 178418365 | — |
| 생성물 | 1-(4,6-Dimethoxy pyrimidin-5-yl)-3-methylbutan-2-ol | HCID 22648760 | 54% |
반응 단계
0.81 g (33 mmol) of magnesium was added to 30 ml of tetrahydrofuran, and 4.1 g (33 mmol) of 2-bromopropane was added to prepare a tetrahydrofuran solution of isopropyl magnesium bromide. 2.8 g (17 mmol) of 4,6-dimethoxypyrimidine-5-carboaldehyde was dissolved in 50 ml of tetrahydrofuran, and the solution was added to the above tetrahydrofuran solution at room temperature and reacted overnight. The reaction solution was poured into an aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with an aqueous citric acid solution, water and an aqueous sodium chloride solution in this order, dried and concentrated, and the obtained oily product was purified by column chromatography (ethyl acetate:n-hexane=1:4) to obtain 1.9 g (yield: 54%) of 1-(4,6-dimethoxy pyrimidin-5-yl)-3-methylbutan-2-ol as slightly yellow crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06806230B1 |
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| 출처 데이터셋 | uspto-grants-2004_10 |
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| ORD ID | ord-d022aedc6a5e46c7be25577186f30d77 |
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| 출처 메모 | uspto-grants-2004_10 |
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