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5-Fluorouracil → 1(2H)-Pyrimidinecarboxamide, N-butyl-5-fluoro-3,4-dihydro-2,4-dioxo-

HRID 1834766
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HRID 1834766 반응식
[F:1][C:2]1[C:3](=[O:9])[NH:4][C:5](=[O:8])[NH:6][CH:7]=1.[CH2:10]([N:14]=[C:15]=[O:16])[CH2:11][CH2:12][CH3:13]>CN(C)C=O>[CH2:10]([NH:14][C:15]([N:6]1[CH:7]=[C:2]([F:1])[C:3](=[O:9])[NH:4][C:5]1=[O:8])=[O:16])[CH2:11][CH2:12][CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 33855-FluorouracilHCID 8110Butyl isocyanate

생성물 1

HCID 1165421(2H)-Pyrimidinecarboxamide, N-butyl-5-fluoro-3,4-dihydro-2,4-dioxo-수율 72.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

13.0g (0.10 mole) of 5-fluorouracil was dissolved in 70 ml of dimethyl formamide, then 11.9g (0.12 mole) of n-butyl isocyanate was added thereto at room temperature and stirred at the same temperature for 24 hours. The reaction mixture was concentrated to 40ml by removing dimethyl formamide and excess n-butyl isocyanate under reduced pressure. The residue was poured into 300ml of water and resultant precipitate was filtered off. The precipitate was washed and dried and 16.6g (72.3% yield) of 1-(n-butylcarbamoyl)-5-fluorouracil was obtained

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후처리

  1. concentrationThe reaction mixture was concentrated to 40ml
  2. customby removing dimethyl formamide and excess n-butyl isocyanate under reduced pressure
  3. additionThe residue was poured into 300ml of water and resultant precipitate
  4. filtrationwas filtered off
  5. washThe precipitate was washed
  6. customdried

출처 및 근거

ORD 기록
ord-d9b1029cb8e94d3ca81e29df96f4a0d7
출처 데이터셋
uspto-grants-1978_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04071519

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