Réaction #531883

ord-6a46019ecc1548ddb00deee41cfeafca

Équation de réaction

CC(C)N
isopropylamine
CC(N/C(=C(/C#N)C(=O)O)c1sccc1Br)c1nccs1
(2Z)-3-(3-bromo-2-thienyl)-2-cyano-3-{[1-(1,3-thiazol-2-yl)ethyl]amino}acrylic acid
Oc1cccc2[nH]nnc12
hydroxybenzotriazole
CCN(C(C)C)C(C)C
diisopropylethylamine
C(=NC1CCCCC1)=NC1CCCCC1
dicyclohexylcarbodiimide
CC(C)NC(=O)C(C#N)=C(NC(C)c1nccs1)c1sccc1Br
3-(3-bromo-2-thienyl)-2-cyano-N-isopropyl-3-{[1-(1,3-thiazol-2-yl)ethyl]amino}acrylamide
Rendement 45.2%

Solvants

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe solid formed
  2. 2
    Autreremoved by filtration
  3. 3
    AutreThe solvent was removed under reduced pressure

Mode opératoire

To a solution of (2Z)-3-(3-bromo-2-thienyl)-2-cyano-3-{[1-(1,3-thiazol-2-yl)ethyl]amino}acrylic acid (0.18 g, 0.468 mmol, 1 eq.) in 5 ml of DCM (CH2Cl2) were added isopropylamine (0.083 g, 1.40 mmol, 3 eq.), hydroxybenzotriazole (HOBT) (0.066 g, 0.49 mmol, 1.05 eq.) and diisopropylethylamine (DIPEA) (0.090 g, 0.70 mmol, 1.5 eq.). The reaction was cooled to 0° C. and dicyclohexylcarbodiimide (DCC) (0.101 g, 0.49 mmol, 1.05 eq.) was added. Stirring was allowed overnight and the solid formed removed by filtration. The solvent was removed under reduced pressure and the residual oil submitted to chromatography on silica gel to give 2Z)-3-(3-bromo-2-thienyl)-2-cyano-N-isopropyl-3-{[1-(1,3-thiazol-2-yl)ethyl]amino}acrylamide (0.090 g, 43% yield) as a white solid and a mixture of atropoisomers.

Source

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