Réaction #531880

ord-ba6fcd13e4a14af2b8cadfafb7e4f3b0

Équation de réaction

CCN(CC)CC
triethylamine
CCOC(=O)C(C#N)=C(Cl)c1cccnc1Cl
ethyl 3-chlor-3-(2-chloropyridin-3-yl)-2-cyanoacrylate
CC(N)c1ccc(Cl)nc1
1-(6-chloropyridin-3-yl)ethanamine
CCOC(=O)/C(C#N)=C(\NC(C)c1ccc(Cl)nc1)c1cccnc1Cl
ethyl (2Z)-3-(2-chloropyridin-3-yl)-3-{[1-(6-chloropyridin-3-yl)ethyl]amino}-2-cyanoacrylate
Rendement 73.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe reaction was microwaved
  2. 2
    Autre(130° C., 600 s, fixed hold, high absorption)
  3. 3
    Autrethe solvent evaporated

Mode opératoire

To a solution of ethyl 3-chlor-3-(2-chloropyridin-3-yl)-2-cyanoacrylate (0.150 g, 0.55 mmol, 1 eq.) in 3 ml of acetonitrile was added 1-(6-chloropyridin-3-yl)ethanamine (0.103 g, 0.66 mmol, 1.2 eq.) followed by triethylamine (TEA) (0.167 g, 1.66 mmol, 3 eq.). The reaction was microwaved (130° C., 600 s, fixed hold, high absorption) and the solvent evaporated. The residual oil was subjected to column chromatography to give ethyl (2Z)-3-(2-chloropyridin-3-yl)-3-{[1-(6-chloropyridin-3-yl)ethyl]amino}-2-cyanoacrylate (0.157 g, 68% yield) as a mixture of 2 atropoisomers.

Source

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