Réaction #531887

ord-1c51fc11b8234b18ba30d39a2625396c

Équation de réaction

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
Rendement 57.3%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08476197B2uspto-grants-2013_07