Phosphorus oxybromide → 4-Bromo-1,5-naphthyridine

HRID 1253510Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1253510
[N:1]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[C:4](O)=[CH:3][CH:2]=1.P(Br)(Br)([Br:14])=O>>[Br:14][C:4]1[C:5]2[C:10](=[CH:9][CH:8]=[CH:7][N:6]=2)[N:1]=[CH:2][CH:3]=1

Komponenten

3

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

A flask was charged with 1,5-naphthyridin-4-ol (1 g, 6.7 mmol) and phosphorousoxybromide (5 g, 17 mmol). The mixture was heated to 150° C., stirred for 1 hour, and then cooled to room temperature. The mixture was poured into ice-water and extracted with toluene. The combined organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated to give crude product, which was re-crystallized from petroleum ether to give 4-bromo-1,5-naphthyridine.

Aufarbeitung

  1. temperaturecooled to room temperature
  2. extractionextracted with toluene
  3. washThe combined organic extracts were washed with brine
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto give crude product, which
  8. customwas re-crystallized from petroleum ether

Quellen und Nachweise

ORD-Eintrag
ord-221d1e0d305a498c93b370d8baa12e97
Quelldatensatz
uspto-grants-2013_06
Patentnummer
US08455477B2

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