Reacción #43572

ord-1755bceb9bc04353b31a3fb470aae9cc

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe progress of the reaction by HPLC analysis
  2. 2
    OtroThe majority of the excess methylamine was removed under reduced pressure
  3. 3
    Temperaturathe remaining mixture cooled at 0° C. for 2 hours
  4. 4
    FiltraciónThe solid material was filtered off
  5. 5
    Lavadowashed with ice-cold 200 proof ethanol
  6. 6
    Otrodried under reduced pressure

Procedimiento

A mixture of ethyl 1-{9-[(4S,2R,3R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-aminopurin-2-yl}pyrazole-4-carboxylate (46.4 g) and methylamine (40% in water, 600 ml) was stirred at ambient temperature for about 4 hours, following the progress of the reaction by HPLC analysis. The majority of the excess methylamine was removed under reduced pressure, and the remaining mixture cooled at 0° C. for 2 hours. The solid material was filtered off, washed with ice-cold 200 proof ethanol, and dried under reduced pressure, to provide (1-{9-[(4S,2R,3R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-aminopurin-2-yl}pyrazol-4-yl)-N-methylcarboxamide as its monohydrate, 36.6 g, purity 99.6%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07732595B2uspto-grants-2010_06