참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 1-Butanol, 4-bromo-, 1-acetate | HCID 78491 | — |
| 반응물 | Lithium Bromide | HCID 82050 | — |
| 반응물 | 6-Amino-2-methoxy-3,4-dihydropyrimidin-4-one | HCID 135404214 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 6-Amino-2-methoxy-4-(4-acetoxybutyl)pyrimidine | HCID 23499088 | 16% |
반응 단계
Sodium hydride (60% dispersion in mineral oil, 8.2 g, 205 mmol) was added to a mixture of 6-amino-2-methoxy-4-pyrimidone (24.0 g, 170 mmol) in DMF at 0° C. After 0.5 hours, lithium bromide (19.2 g, 221 mmol) was added to the mixture and stirred for 0.5 hours at room temperature. The temperature was slowly increased to 70° C., and a solution of 4-bromobutyl acetate (50 g, 256 mmol) in DMF was added dropwise to the reaction mixture. The mixture was stirred at 70° C. for 3 hours. After cooling to room temperature, the solvent was removed in vacuo. The residue was purified by chromatography on silica gel using CHCl3/MeOH (1-5%) as eluent to give first 6.5 g (15%) of 6-amino-2-methoxy-4-(4-acetoxybutyl)pyrimidine as a white solid followed by 23.4 g (yield 54%) of 6-amino-2-methoxy-3-(4-acetoxybutyl)-4-pyrimidone as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06777420B2 |
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| 출처 데이터셋 | uspto-grants-2004_08 |
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| ORD ID | ord-f59ba468b9db4e56939ac0bf61cb8952 |
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| 출처 메모 | uspto-grants-2004_08 |
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