Reaktion #531887

ord-1c51fc11b8234b18ba30d39a2625396c

Reaktionsgleichung

CCN(CC)CC
triethylamine
N#CC=C(Cl)c1cccnc1Cl
3-chloro-3-(2-chloropyridin-3-yl)acrylonitrile
CCC1CC1N.Cl
2-ethylcyclopropanamine hydrochloride
CCC1CC1NC(=CC#N)c1cccnc1Cl
3-(2-chloropyridin-3-yl)-3-[(2-ethylcyclopropyl)amino]acrylonitrile
Ausbeute 57.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction was microwaved
  2. 2
    Sonstige(130° C., 2000 s, fixed hold, high absorption)
  3. 3
    Sonstigethe solvent evaporated
  4. 4
    SonstigeThe residual oil was triturated in ethyl acetate
  5. 5
    Sonstigethe white solid removed by filtration
  6. 6
    EinengenAfter 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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08476197B2uspto-grants-2013_07