Reacción #1102147

ord-83487f6e43bd4f7092c5b7de08e125ae

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe methanol removed under reduced pressure
  2. 2
    TemperaturaAfter cooling the resulting precipitate
  3. 3
    Filtraciónwas filtered
  4. 4
    Lavadowashed with water

Procedimiento

A solution of 2-{3-[1-((2-chloro)phenoxycarbanoyl)piperidin-4-yl]propyn-1-yl}adenosine (0.720 g, 1.326 mmol) in methanol (25 mL) and 1.0 M HCl (2.50 mL) was stirred at 90° C. in a pressure apparatus for 22 h. The pH was adjusted to 5 with 1.0 M NaOH and the methanol removed under reduced pressure. After cooling the resulting precipitate was filtered and washed with water to afford the pure product as a white solid: yield 1.481 g, 88%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07985754B2uspto-grants-2011_07