Reacción #42465

ord-6c64bd91ce79480595b00e36b5437384

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaat reflux for 1.5 h
  2. 2
    Concentraciónthe resulting solution was concentrated under reduced pressure
  3. 3
    LavadoThe residue was washed with hexanes
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónthe filtrate was concentrated under reduced pressure
  6. 6
    OtroPurification by flash column chromatography (silica, 10% ethyl acetate/hexanes)

Procedimiento

A solution of Methyl 4-butyl-8-iodo-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate (680 mg) and 9-BBN (900 mg) in tetrahydrofuran (30 mL) was heated at reflux for 1.5 h. The mixture was cooled to room temperature, ethanolamine (0.22 mL) was added, and the resulting solution was concentrated under reduced pressure. The residue was washed with hexanes, filtered, and the filtrate was concentrated under reduced pressure. Purification by flash column chromatography (silica, 10% ethyl acetate/hexanes) afforded 600 mg of the title compound: 1H NMR (300 MHz, CDCl3) δ 7.75, 7.28, 4.34, 3.86, 3.36, 3.28, 1.58, 1.40, 0.96.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07727997B2uspto-grants-2010_06