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Phosphorus oxychloride → HCID 19967110, Verbindung

HRID 326272
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 326272
[N:1]1([CH2:6][C:7]2[CH:8]=[C:9]3[C:14](=[CH:15][CH:16]=2)[NH:13][C:12](=O)[CH:11]=[C:10]3[CH3:18])[CH:5]=[CH:4][N:3]=[CH:2]1.P(Cl)(Cl)([Cl:21])=O>>[Cl:21][C:12]1[CH:11]=[C:10]([CH3:18])[C:9]2[C:14](=[CH:15][CH:16]=[C:7]([CH2:6][N:1]3[CH:5]=[CH:4][N:3]=[CH:2]3)[CH:8]=2)[N:13]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 19967123HCID 19967123, Verbindung

Produkt 1

HCID 19967110HCID 19967110, VerbindungAusbeute 12,5 %

Versuchsvorschrift

A solution of 13 parts of 6-(1H-imidazol-1-ylmethyl)-4-methyl-2(1H)-quinolinone in 55 parts of phosphoryl chloride was stirred for 1 hour at room temperature. After evaporation, the residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of acetonitrile and 2,2'-oxybispropane. The product was filtered off and dried, yielding 1.75 parts (12.5%) of 2-chloro-6-(1H-imidazol-1-ylmethyl)-4-methylquinoline; mp. 120.6° C. (compound 34).

Aufarbeitung

  1. customAfter evaporation
  2. custom
the residue was purified by column chromatography over silica gel using
  • additiona mixture of trichloromethane and methanol (95:5 by volume) as eluent
  • customThe pure fractions were collected
  • customthe eluent was evaporated
  • customThe residue was crystallized from a mixture of acetonitrile and 2,2'-oxybispropane
  • filtrationThe product was filtered off
  • customdried
  • Quellen und Nachweise

    ORD-Eintrag
    ord-931164969d174a59af27fafc6cd74178
    Quelldatensatz
    uspto-grants-1993_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US05268380

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