Réaction #47844

ord-fa352a66237a4e1da45c46fcb9bd6c19

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe solvent was removed under a reduced pressure
  2. 2
    AutreThe resulting residue was purified by flash chromatography

Mode opératoire

1-Bromo-6-methoxy-3-phenyl-1H-indene-2-carboxylic acid ethyl ester (100 mg, 0.27 mmol) obtained in Example 18 was dissolved in THF (10 mL), and cyclohexylamine (132.86 mg, 0.15 mL, 1.34 mmol) was added dropwise thereto. The mixture was stirred for 12 hrs at RT, and the solvent was removed under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 25 mg of the titled compound (yield: 24%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07745439B2uspto-grants-2010_06