Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1759381생성일: 2026년 10월 26일
5-fluoro-1-[(4R,6R)-6-(hydroxymethyl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]pyrimidine-2,4-dione → 5'-O-(5-morpholinopentanoyl)-5-fluorouridine
https://huagongshe.com/reaction/1759381
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 5-fluoro-1-[(4R,6R)-6-(hydroxymethyl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]pyrimidine-2,4-dione | HCID 200831 | — |
| 반응물 | 5-(Morpholin-4-yl)pentanoic acid hydrochloride | HCID 13137165 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 5'-O-(5-morpholinopentanoyl)-5-fluorouridine | HCID 22820979 | — |
반응 단계
To a solution of 2.96 g (13.2 m-mol) of 5-morpholinopentanoic acid hydrochloride in pyridine (30 ml) was added 4.2 g (13.9 m-mol) of TPS, and the mixture was stirred for 15 minutes at room temperature. To this solution was added 2.00 g (6.62 m-mol) of 2',3'-O-isopropylidene-5-fluorouridine, and the mixture was stirred for 18 hours at room temperature. The reaction liquid was concentrated under reduced pressure and the residue was distributed in chloroform (50 ml) and an 8% aqueous solution of potassium carbonate (50 ml). The aqueous phase was extracted with chloroform (50 ml ×5) and the extracts were combined with the chloroform phase previously obtained. The chloroform phase was dried with Na2SO4 and concentrated and the residue was subjected to a separation-purification treatment by way of silica gel column chromatography (column size: 5×8 cm, developing solvents: chloroform and chloroform containing 2% methanol) whereby 1.17 g of 5'-O-(5-morpholinopentanoyl)-2',3'-O-isopropylidene-5-fluorouridine was obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04340728 |
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| 출처 데이터셋 | uspto-grants-1982_07 |
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| ORD ID | ord-4dd768277ddc4bfaa84c3a27647af9c5 |
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| 출처 메모 | uspto-grants-1982_07 |
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