Reaktion #2146702

Reaktionsgleichung

2-bromo-4′-hydroxyacetophenone

2-amino-5-bromopyridine

→

6-bromo-2-(4′-hydroxyphenyl)imidazo[1,2-a]pyridine

Ausbeute 83.2%

Lösungsmittel

acetonitrile

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeAfter the completion of the reaction
2. 2
   Temperaturthe reaction solution was cooled down to room temperature
3. 3
   Sonstigeprecipitates
4. 4
   Filtrationwere filtered
5. 5
   Sonstigerecovered
6. 6
   WaschenThe precipitates were washed with acetonitrile
7. 7
   Sonstigedried under reduced pressure
8. 8
   Sonstigesonicated for 5 minutes
9. 9
   SonstigePrecipitates
10. 10
    Filtrationwere filtered
11. 11
    Sonstigerecovered from the resulting mixture
12. 12
    Waschensufficiently washed with water
13. 13
    Sonstigedried under reduced pressure

Vorschrift

2.15 g (corresponding to 10.0 mmol) of 2-bromo-4′-hydroxyacetophenone and 1.74 g (corresponding to 10.0 mmol) of 2-amino-5-bromopyridine were dissolved in 50 mL of acetonitrile. The resulting solution was refluxed in an oil bath at 105° C. for 6 hours. After the completion of the reaction, the reaction solution was cooled down to room temperature, and precipitates were filtered and recovered. The precipitates were washed with acetonitrile, and dried under reduced pressure. The resulting crude crystals were suspended in a mixed solution of 20 mL of water and 20 mL of methanol, and then supplemented with about 25 mL of a saturated sodium hydrogencarbonate solution and sonicated for 5 minutes using an ultrasonic washing machine. Precipitates were filtered and recovered from the resulting mixture, sufficiently washed with water, and dried under reduced pressure, to obtain 2.41 g (corresponding to 8.32 mmol) of 6-bromo-2-(4′-hydroxyphenyl)imidazo[1,2-a]pyridine (FIG. 8, Step 2).

Quelle