Tripropylamine → 4-Chloro-2-phenoxymethylquinazoline

HRID 7604

Reaktionsgleichung

Reaktionsgleichung von HRID 7604
O[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH2:12][O:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[N:3]=1.C(N(CCC)CCC)CC.P(Cl)(Cl)([Cl:32])=O>>[Cl:32][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH2:12][O:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[N:3]=1

Komponenten

4

Edukt 3

HCID 7616TripropylamineHCID 24813Phosphorus oxychlorideHCID 178418749HCID 178418749, Verbindung

Produkt 1

HCID 219910934-Chloro-2-phenoxymethylquinazoline

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

To a solution of 4-hydroxy-2-phenoxymethylquinazoline (2 g, 7.93 mmol) in phosphorus oxychloride (10 mL) is added tripropylamine (3.02 mL, 15.8 mmol) and the reaction mixture is heated for 30 minutes at 110° C. The excess phosphorus oxychloride is evaporated in vacuo, the residue is poured, on ice cold aqueous NaHCO3 and extracted with ethyl acetate. The organic layer is washed with brine, dried, filtered and evaporated. The resulting residue is purified on flash chromatography (SiO2, hexane/AcOEt gradient) to give 4-chloro-2-phenoxymethylquinazoline.

Aufarbeitung

  1. customThe excess phosphorus oxychloride is evaporated in vacuo
  2. additionthe residue is poured, on ice cold aqueous NaHCO3
  3. extractionextracted with ethyl acetate
  4. washThe organic layer is washed with brine
  5. customdried
  6. filtrationfiltered
  7. customevaporated
  8. customThe resulting residue is purified on flash chromatography (SiO2, hexane/AcOEt gradient)

Quellen und Nachweise

ORD-Eintrag
ord-69a15a6fb04248a0af12b6034489a596
Quelldatensatz
uspto-grants-2006_08
Patentnummer
US07087603B2

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