홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

5-Fluorouracil → HCID 12812862, 화합물

HRID 1702787
노트
인쇄 미리보기

반응식

HRID 1702787 반응식
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][N:8]=[C:9]=[O:10])=[CH:3][CH:2]=1.[F:11][C:12]1[C:13](=[O:19])[NH:14][C:15](=[O:18])[NH:16][CH:17]=1>>[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][NH:8][C:9]([N:16]2[CH:17]=[C:12]([F:11])[C:13](=[O:19])[NH:14][C:15]2=[O:18])=[O:10])=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 33855-FluorouracilHCID 204582734-(Isocyanatomethyl)pyridine

생성물 1

HCID 12812862HCID 12812862, 화합물

실험 절차

To the above solution of 4-pyridylmethyl isocyanate was added 5-fluorouracil (2.60 g.) at 80° C. and stirred for 4 hours at the same temperature. The resultant mixture was evaporated in vacuo. The residue was washed with diethyl ether (3 times) and crystallized. The crystals were filtered and washed with a small amount of ethanol. To the washed crystals a small amount of pyridine was added, and the mixture was warmed to be dissolved and cooled to be recrystallized. The crystals were washed successively with ethyl acetate and diethyl ether to give 1-[N-(4-pyridylmethyl)carbamoyl]-5-fluorouracil (1.75 g.)

후처리

  1. customThe resultant mixture was evaporated in vacuo
  2. washThe residue was washed with diethyl ether (3 times)
  3. customcrystallized
  4. filtrationThe crystals were filtered
  • washwashed with a small amount of ethanol
  • additionTo the washed crystals a small amount of pyridine was added
  • temperaturethe mixture was warmed
  • dissolutionto be dissolved
  • temperaturecooled
  • customto be recrystallized
  • washThe crystals were washed successively with ethyl acetate and diethyl ether
  • 출처 및 근거

    ORD 기록
    ord-f856788c31b34ea696eca4220a64e135
    출처 데이터셋
    uspto-grants-1982_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04349552

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트