Réaction #710482
ord-90bae05e2b3541eb987dc28d6e2c1646
Équation de réaction
2-chloro-5-chloromethyl pyridine
2-aminopyridine
→
1-[(6-chloropyridin-3-yl)methyl]pyridin-2(1H)-imine hydrochloride
Rendement 86.9%
Réactifs
Aucun
Solvants
Conditions de réaction
Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1workup.DISTILLATIONDMF was distilled off under reduced pressure, acetonitrile
- 2workup.ADDITIONwas added
- 3Autreto precipitate a solid
- 4Autrethe solid was collected
- 5Lavagewashed well with acetonitrile
- 6Autredried
Mode opératoire
3.00 g (18.6 mmol) of 2-chloro-5-chloromethyl pyridine was dissolved in 20 ml of anhydrous DMF, 1.75 g (18.6 mmol) of 2-aminopyridine was added thereto, and the resulting mixture was stirred at 80° C. for 8 hours and at room temperature for 5 hours. After the reaction was completed, DMF was distilled off under reduced pressure, acetonitrile was added thereto to precipitate a solid, and the solid was collected, washed well with acetonitrile and then dried to obtain 2.07 g (yield 44%) of 1-[(6-chloropyridin-3-yl)methyl]pyridin-2(1H)-imine hydrochloride.