Réaction #8525

ord-d9b0bffd894b426d850fcbbf6660c959

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreIn accordance with the process of Example 2, a condensation reaction

Mode opératoire

In accordance with the process of Example 2, a condensation reaction was performed by using 2,3,4-trifluoroaniline (100 mg), potassium carbonate (188 mg), methyl (2R)-2-[(methanesulfonyl)oxy]propionate (78 mg) and tetrahexylammonium chloride (40 mg) to give the title compound as an oily substance. As the result of the analysis by reversed phase HPLC with the use of the compound of Example 1 as a specimen, the product corresponded to 38 mg (24%) of the title compound.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07087778B2uspto-grants-2006_08