Reacción #90514

ord-5de892651a514d5ca22c4e338408d1f5

Condiciones de reacción

Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadowashed with water (3×25 mL)
  2. 2
    SecadoThe organic layer was dried over sodium sulphate
  3. 3
    Concentraciónconcentrated
  4. 4
    Otroto get the crude material, which
  5. 5
    Otrowas purified through flash chromatography
  6. 6
    LavadoEluting at 30% ethyl acetate in hexane

Procedimiento

To a solution of 13 (150 mg, 0.607 mmol) in toluene 15 mL was added 1-benzylpiperidine-4-carbaldehyde 21 (123.4 mg, 0.607 mmol). p-Toluene sulphonic acid (PTSA) (230.9 mg, 1.214 mmol) was added to the reaction mixture, and stirred at 120° C. for 6 h. The reaction mass was diluted with ethyl acetate and washed with water (3×25 mL). The organic layer was dried over sodium sulphate and concentrated to get the crude material, which was purified through flash chromatography using 100-200 mesh silica gel. Eluting at 30% ethyl acetate in hexane gave yellow coloured solid (E)-2-((1-benzylpiperidin-4-yl)methylene)-6-methoxy-5-morpholino-2, 3-dihydro-1H-inden-1-one 22.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09446047B2uspto-grants-2016_09