Reaktion #531887
ord-1c51fc11b8234b18ba30d39a2625396c
Reaktionsgleichung
triethylamine
3-chloro-3-(2-chloropyridin-3-yl)acrylonitrile
2-ethylcyclopropanamine hydrochloride
→
3-(2-chloropyridin-3-yl)-3-[(2-ethylcyclopropyl)amino]acrylonitrile
Ausbeute 57.3%
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1SonstigeThe reaction was microwaved
- 2Sonstige(130° C., 2000 s, fixed hold, high absorption)
- 3Sonstigethe solvent evaporated
- 4SonstigeThe residual oil was triturated in ethyl acetate
- 5Sonstigethe white solid removed by filtration
- 6EinengenAfter concentration under vacuum
Vorschrift
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).