참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 5-Fluorouracil | HCID 3385 | — |
| 반응물 | 2,3-Dihydrofuran | HCID 70934 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 1,3-Bis(tetrahydro-2-furanyl)-5-fluoro-2,4-pyrimidinedione | HCID 124956 | — |
반응 단계
In 20.8 ml of pyridine were dissolved 5.2 g (40 m mol) of 5-fluorouracil and 14 g (200 m mol) of 2,3-dihydrofuran. The solution were heated at about 150° C. in a closed tubular reactor under agitation for 6 hours. After the reaction, the reaction mixture was concentrated to dryness under reduced pressure. The residue was dissolved in chloroform and the solution was passed through a column of silica gel. The column was eluated with chloroform and the effluent was concentrated to dryness under reduced pressure. The residue was washed with a small amount of petroleum ether to give the above-mentioned compound as colorless crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04249006 |
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| 출처 데이터셋 | uspto-grants-1981_02 |
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| ORD ID | ord-2992a554a28e4ff7a9ce0121c7aa404d |
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| 출처 메모 | uspto-grants-1981_02 |
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