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Phosphorus oxychloride → HCID 70454969, Verbindung

HRID 364234
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 364234
[C:1]([NH:4][CH2:5][C:6]1[NH:7][C:8](=[O:13])[NH:9][C:10](=O)[CH:11]=1)(=O)[CH3:2].P(Cl)(Cl)([Cl:16])=O>>[Cl:16][C:10]1[CH:11]=[C:6]2[CH:5]=[N:4][CH:1]([CH3:2])[N:7]2[C:8](=[O:13])[N:9]=1
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Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 21793940N-[(2,6-Dioxo-1,2,3,6-tetrahydropyrimidin-4-yl)methyl]acetamide

Produkt 1

HCID 70454969HCID 70454969, Verbindung

Versuchsvorschrift

A suspension of 6.63 g (36.2 mmole) of 4-acetylaminomethylpyrimidine-2,6-dione in 250 ml of phosphorous oxychloride was heated at reflux for 20 hours, and was then cooled and evaporated. The residue was added to about 700 ml of cold saturated sodium bicarbonate solution. To the resulting mixture was added 200 ml of chloroform and sufficient solid sodium bicarbonate to neutralize the mixture. The solid was separated by filtration, and the filtrate was saved for Part B. The solid was washed with water and ethanol, and was then recrystallized from ethanol to provide yellow solid 7-chloro-3-methylimidazo[1,5-c]pyrimidin-5-one, m.p. 239° C. (dec.). Analysis: Calculated for C7H6ClN3O; %C, 45.8; %H, 3.3; %N, 22.9; Found: %C, 45.8; %H, 3.1; %N, 22.8.

Aufarbeitung

  • temperaturewas heated
  • temperatureat reflux for 20 hours
  • temperaturewas then cooled
  • customevaporated
  • additionThe residue was added to about 700 ml of cold saturated sodium bicarbonate solution
  • additionTo the resulting mixture was added 200 ml of chloroform and sufficient solid sodium bicarbonate
  • customThe solid was separated by filtration
  • washThe solid was washed with water and ethanol
  • customwas then recrystallized from ethanol
  • Quellen und Nachweise

    ORD-Eintrag
    ord-bd9e6669139c44ec8a1e095395181cc3
    Quelldatensatz
    uspto-grants-1986_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US04604466

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