Reacción #160205

ord-802daad4cb2646d09d67cbdd6ffa03e9

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe reaction mixture was filtered
  2. 2
    Otropartitioned between sat. aq. sodium bicarbonate/ethyl acetate
  3. 3
    ExtracciónThe aqueous layer was extracted further with ethyl acetate (3×50 mL)
  4. 4
    Lavadowashed with sat. aq. sodium bicarbonate (50 mL)
  5. 5
    Secadodried over MgSO4
  6. 6
    Filtraciónfiltered
  7. 7
    Concentraciónconcentrated in vacuo

Procedimiento

To a solution of [8-benzyl-10-(1,2-dihydroxyethyl)-11-oxa-3,8-diazaspiro[5.5]undecan-3-yl]-(4-isopropoxy-3-methyl-phenyl)methanone (417 mg, 0.86 mmol) in THF (10 mL) was added NaIO4 (468 mg, 2.19 mmol) and H2O (4 mL). The reaction mixture was stirred at room temperature for 2 hours. The reaction mixture was filtered and partitioned between sat. aq. sodium bicarbonate/ethyl acetate. The aqueous layer was extracted further with ethyl acetate (3×50 mL). The organics were combined, washed with sat. aq. sodium bicarbonate (50 mL), dried over MgSO4, filtered and concentrated in vacuo to yield 8-benzyl-3-(4-isopropoxy-3-methyl-benzoyl)-11-oxa-3,8-diazaspiro[5.5]undecane-10-carbaldehyde (384 mg, 99%) as a white solid. ESI-MS m/z calc. 450.3. Found 451.3 (M+1)+; Retention time: 1.33 minutes (3 min run).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08828996B2uspto-grants-2014_09