Reacción #47842

ord-73ba5e45096c471f9ddaf531198c004b

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

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

Procedimiento

1-Bromo-6-methoxy-3-phenyl-1H-indene-2-carboxylic acid ethyl ester (10 mg, 0.40 mmol) obtained in Example 18 was dissolved in THF (15 mL), and morpholine (175.01 mg, 0.18 mL, 2.01 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 126 mg of the titled compound (yield: 83%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07745439B2uspto-grants-2010_06