Réaction #2329003
ord-472d4c255d49435e873579756197c59b
Équation de réaction
4-Aminoresorcinol hydrochloride
triethylamine
6-Methoxynicotinaldehyde
→
4-{[(6-methoxypyridin-3-yl)methylene]amino}benzene-1,3-diol
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1AutreThe solvents were removed under reduced pressure
- 2workup.ADDITIONthe mixture diluted with EtOAc
- 3Lavagewashed with brine (2×)
- 4Séchagedried (Na2SO4)
- 5Filtrationfiltered
- 6Autreevaporated
- 7Autreto give 1.31 g as a dark solid
- 8AutreThe crude product was taken to the next step without further purification
Mode opératoire
4-Aminoresorcinol hydrochloride (3.09 mmol) and triethylamine (3.25 mmol) were dissolved in dry methanol (20 mL). 6-Methoxynicotinaldehyde (3.09) was added and the mixture was stirred overnight. The solvents were removed under reduced pressure, the mixture diluted with EtOAc, washed with brine (2×), dried (Na2SO4), filtered and evaporated to give 1.31 g as a dark solid. The crude product was taken to the next step without further purification. MS m/z (M+H) 245.