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Phosphorus oxychloride → HCID 70454969, Verbindung

HRID 2418681
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2418681
[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 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 enough solid sodium bicarbonate to neutralize the mixture. The solid was separated by filtration, washed with water and ethanol, and 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

  1. temperature
was heated
  • temperatureat reflux for 20 hours
  • temperaturewas 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 enough solid sodium bicarbonate
  • customThe solid was separated by filtration
  • washwashed with water and ethanol
  • customrecrystallized from ethanol
  • Quellen und Nachweise

    ORD-Eintrag
    ord-f1598504103e4ae78d30d391352fbc84
    Quelldatensatz
    uspto-grants-1984_09
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US04473570

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