Reacción #156624

ord-66e9a8fd87d04aea8e26a46ce96c38f2

Condiciones de reacción

Temperatura
50°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    SecadoThe organic phase was dried over magnesium sulfate
  2. 2
    Concentraciónconcentrated
  3. 3
    OtroThe raw product was purified by preparative HPLC
  4. 4
    OtroIn this way the product was obtained with molecular weight 423.54 (C25H30FN3O2)

Procedimiento

A mixture of 2-[(S)-4-(2,7-diaza-spiro[4.4]non-2-yl)-phenyl]-6-hydroxy-3,4-dihydro-2H-isoquinolin-1-one (0.20 g), 1-bromo-3-fluoro-propane (76 mg), sodium hydrogencarbonate (10 mg) and NMP (5 mL) was heated at 50° C. for 15 hours. The reaction mixture was distributed between ethyl acetate and water. The organic phase was dried over magnesium sulfate and concentrated. The raw product was purified by preparative HPLC. In this way the product was obtained with molecular weight 423.54 (C25H30FN3O2); MS (ESI): 424 (M+H+).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08822495B2uspto-grants-2014_09