Reaktion #68668

ord-960ea339c49649c9aae6f33a7baa0486

Lösungsmittel

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas quenched with 40 mL of satd
  2. 2
    workup.ADDITIONThe mixture was diluted with 60 mL of EtOAc
  3. 3
    SonstigeThe organic phase was separated
  4. 4
    Waschenwashed with brine
  5. 5
    Trocknendried over Na2SO4
  6. 6
    Einengenconcentrated in vacuo
  7. 7
    Sonstigeto give red solid
  8. 8
    SonstigeThe residue was purified by a silica gel column chromatography (5% EtOAc/Hex to EtOAC)
  9. 9
    Sonstigeto provide a red solid

Vorschrift

To a solution of 6-bromo-3-methylquinazolin-4(3H)-one (0.485 g, 2.0 mmol), tris(dibenzylideneacetone)dipalladium (0) (0.19 g, 0.20 mmol) and Q-phos (0.20 g) in 40 mL of THF was added 2-tert-butoxy-2-oxoethylzinc chloride 0.5 M in diethyl ether (8.1 ml, 4.1 mmol). The reaction was heated at 50° C. for 16 hours and was quenched with 40 mL of satd. NH4Cl. The mixture was diluted with 60 mL of EtOAc. The organic phase was separated, washed with brine, dried over Na2SO4 and concentrated in vacuo to give red solid. The residue was purified by a silica gel column chromatography (5% EtOAc/Hex to EtOAC) to provide a red solid. MS (ESI pos. ion) m/z: 275 (MH+). Calc'd exact mass for C15H18N2O3:

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08524900B2uspto-grants-2013_09