Reacción #1869214

ord-bdf2fce010bd419281858860233fc2c2

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction mixture was partitioned between ethyl acetate and H2O
  2. 2
    SecadoThe organic layer was dried over Na2SO4
  3. 3
    Filtraciónfiltered
  4. 4
    Concentraciónconcentrated
  5. 5
    OtroThe residue was purified by silica gel flash chromatography (0-100% ethyl acetate in petroleum spirit)

Procedimiento

A mixture of 2-(2-hydroxy-4-methoxyphenyl)-N-methylacetamide (15 mg, 0.076 mmol), (2S)-oxiran-2-ylmethyl 3-nitrobenzenesulfonate (20 mg, 0.076 mmol) and Cs2CO3 (30 mg, 0.091 mmol) in DMF (1.5 mL) was stirred at room temperature overnight. The reaction mixture was partitioned between ethyl acetate and H2O. The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel flash chromatography (0-100% ethyl acetate in petroleum spirit) to give the subtitled compound (18 mg).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07498338B2uspto-grants-2009_03