Réaction #51720

ord-b6a0b864235042f99a35593d3de787e0

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe title compound was prepared
  2. 2
    LavageChromatography of the residue, eluting with 3:1 hexane

Mode opératoire

The title compound was prepared as described in General Method 1 using 1.4 g (11.0 mmol) of 4-methyl-5-thiazolecarbaldehyde (Example A-12), 6.2 g (13.1 mmol) of (3-methyl-2-oxobutyl)triphenylarsonium bromide, 1.8 g (13.1 mmol) of potassium carbonate, 75 mL of acetonitrile, and 0.75 mL of H2O. Chromatography of the residue, eluting with 3:1 hexane:EtOAc gave the title compound.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06852711B2uspto-grants-2005_02