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5-Fluorouracil → HCID 12812862, Verbindung

HRID 1702787
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1702787
[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
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 33855-FluorouracilHCID 204582734-(Isocyanatomethyl)pyridine

Produkt 1

HCID 12812862HCID 12812862, Verbindung

Versuchsvorschrift

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.)

Aufarbeitung

  1. customThe resultant mixture was evaporated in vacuo
  2. washThe residue was washed with diethyl ether (3 times)
  3. custom
crystallized
  • 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
  • Quellen und Nachweise

    ORD-Eintrag
    ord-f856788c31b34ea696eca4220a64e135
    Quelldatensatz
    uspto-grants-1982_09
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US04349552

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