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Phosphorus oxychloride → HCID 21104341, Verbindung

HRID 1010828
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1010828
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[NH:9][C:10](=O)[C:11]2[C:16]([CH3:17])=[N:15][N:14]([CH3:18])[C:12]=2[N:13]=1.P(Cl)(Cl)([Cl:22])=O>>[Cl:22][C:10]1[N:9]=[C:8]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[F:1])[N:13]=[C:12]2[N:14]([CH3:18])[N:15]=[C:16]([CH3:17])[C:11]=12
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 136008000HCID 136008000, Verbindung

Produkt 1

HCID 21104341HCID 21104341, VerbindungAusbeute 51 %

Versuchsvorschrift

6-(2-Fluoro-phenyl)-1,3-dimethyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one (2.0 g, 7.74 mmole) was treated with 40 ml phosphorous oxychloride and heated to reflux overnight. The excess phosphorous oxychloride was removed under vacuum and ice water was added to the residue. The product was extracted with ethyl acetate, washed with 10% sodium carbonate, water, dried over sodium sulfate (anh) and the solvent was removed to give crude product. Crude product was chromatographed on silica gel column eluting with chloroform to give 1.10 g of pure product (yield: 51%).

Aufarbeitung

  1. temperatureheated
  2. temperatureto reflux overnight
  • customThe excess phosphorous oxychloride was removed under vacuum and ice water
  • additionwas added to the residue
  • extractionThe product was extracted with ethyl acetate
  • washwashed with 10% sodium carbonate, water
  • dry with materialdried over sodium sulfate (anh)
  • customthe solvent was removed
  • customto give crude product
  • customCrude product was chromatographed on silica gel column
  • washeluting with chloroform
  • Quellen und Nachweise

    ORD-Eintrag
    ord-b8ea70571351437a813f036081da0b04
    Quelldatensatz
    uspto-grants-2011_07
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US07977342B2

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