Réaction #531887
ord-1c51fc11b8234b18ba30d39a2625396c
Équation de réaction
triethylamine
3-chloro-3-(2-chloropyridin-3-yl)acrylonitrile
2-ethylcyclopropanamine hydrochloride
→
3-(2-chloropyridin-3-yl)-3-[(2-ethylcyclopropyl)amino]acrylonitrile
Rendement 57.3%
Réactifs
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1AutreThe reaction was microwaved
- 2Autre(130° C., 2000 s, fixed hold, high absorption)
- 3Autrethe solvent evaporated
- 4AutreThe residual oil was triturated in ethyl acetate
- 5Autrethe white solid removed by filtration
- 6ConcentrationAfter concentration under vacuum
Mode opératoire
To a solution of 3-chloro-3-(2-chloropyridin-3-yl)acrylonitrile (1.4 g, 7.03 mmol, 1 eq.) in 15 ml of acetonitrile was added 2-ethylcyclopropanamine hydrochloride (1.02 g, 8.44 mmol, 1.2 eq.) followed by triethylamine (TEA) (1.06 g, 10.55 mmol, 1.5 eq.). The reaction was microwaved (130° C., 2000 s, fixed hold, high absorption) and the solvent evaporated. The residual oil was triturated in ethyl acetate and the white solid removed by filtration. After concentration under vacuum, the residual oil was subjected to column chromatography to give 3-(2-chloropyridin-3-yl)-3-[(2-ethylcyclopropyl)amino]acrylonitrile (0.998 g, 51% yield).