Reacción #48920

ord-1f2b2ae8e5f1496aafb24688b567536b

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónconcentrated
  2. 2
    Otropurified by silica gel chromatography (7:3→1:4; hexanes:ethyl acetate)

Procedimiento

A mixture of 4-amino-8-(cyclopentyloxy)-7-methoxy-2H-chromen-2-one (100 mg, 0.36 mmol, Example 3, Step 1), Selectfluor (160 mg, 0.45 mmol), and acetonitrile (1.5 mL) were stirred vigorously for 18 h, concentrated, and then purified by silica gel chromatography (7:3→1:4; hexanes:ethyl acetate) to give 4-amino-8-(cyclopentyloxy)-3-fluoro-7-methoxy-2H-chromen-2-one: MS (ESI): 294.0.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07745646B2uspto-grants-2010_06