Réaction #42465

ord-6c64bd91ce79480595b00e36b5437384

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureat reflux for 1.5 h
  2. 2
    Concentrationthe resulting solution was concentrated under reduced pressure
  3. 3
    LavageThe residue was washed with hexanes
  4. 4
    Filtrationfiltered
  5. 5
    Concentrationthe filtrate was concentrated under reduced pressure
  6. 6
    AutrePurification by flash column chromatography (silica, 10% ethyl acetate/hexanes)

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07727997B2uspto-grants-2010_06