Reacción #86546

ord-f2b7c86a945d41dca73116df1a92a05c

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadothe mixture was washed with water
  2. 2
    Secadodried over Na2SO4
  3. 3
    Concentraciónconcentrated
  4. 4
    Otropurified on silica gel (0-60% ethyl acetate/hexanes)

Procedimiento

A mixture of 6-bromo-7-(1-bromoethyl)-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one (3.7 g, 11 mmol) and sodium azide (1.4 g, 22 mmol) in N,N-dimethylformamide (30 mL) was stirred at room temperature for 1.5 hour. After diluted with ethyl acetate, the mixture was washed with water, dried over Na2SO4, concentrated and purified on silica gel (0-60% ethyl acetate/hexanes) to give the desired product (2.16 g). LCMS calculated for C8H7BrN5OS (M+H)+: m/z=300.0. Found: 300.0.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09434746B2uspto-grants-2016_09