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Anisole → 7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine

HRID 1783385
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1783385
O[C:2]1[N:3]=[CH:4][C:5]([O:11][CH3:12])=[C:6]2[C:10]=1[NH:9][CH:8]=[CH:7]2.C1(OC)C=CC=CC=1.P(Br)(Br)([Br:23])=O>>[Br:23][C:2]1[N:3]=[CH:4][C:5]([O:11][CH3:12])=[C:6]2[C:10]=1[NH:9][CH:8]=[CH:7]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 7519AnisoleHCID 24613Phosphorus oxybromideHCID 178493790HCID 178493790, Verbindung

Produkt 1

HCID 207912447-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridineAusbeute 27,4 %

Reaktionsbedingungen

Temperatur
160 °C

Versuchsvorschrift

To a flask containing 7-hydroxy-4-methoxy-6-azaindole (0.200 g, 1.22 mmol) was added anisole (3 mL) and then POBr3 (1.57 g, 6.09 mmol). The system was purged with Ar and then it was heated at 160° C. (oil bath temperature) for 1 h. The reaction mixture was then allowed to cool to room temperature, quenched with 2M HBr (5 mL) and extracted with methyl t-butyl ether. The aqueous phase was separated and the pH was adjusted to 6-7, after which it was extracted with EtOAc. The resulting organic phase was dried (MgSO4) and evaporated to give a solid residue which was chromatographed (SiO2/5% MeOH-DCM) to afford the title compound (0.076 g, 27%) as a white solid:

Aufarbeitung

  1. customThe system was purged with Ar
  2. temperatureto cool to room temperature
  3. customquenched with 2M HBr (5 mL)
  4. extractionextracted with methyl t-butyl ether
  5. customThe aqueous phase was separated
  6. extractionafter which it was extracted with EtOAc
  7. dry with materialThe resulting organic phase was dried (MgSO4)
  8. customevaporated
  9. customto give a solid residue which
  10. customwas chromatographed (SiO2/5% MeOH-DCM)

Quellen und Nachweise

ORD-Eintrag
ord-0c85563ae20744998fe7eb3cad8fa76e
Quelldatensatz
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07501419B2

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