Reacción #56600

ord-335a53d782364722a7b127312f3f5efa

Ecuación de reacción

O=C=O
dry ice
Cc1cn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]c1=O
thymidine
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CC(C)OC(=O)/N=N/C(=O)OC(C)C
diisopropylazodicarboxylate
Cc1cn2c(nc1=O)O[C@@H]1C[C@H]2O[C@@H]1CO
white solid
Rendimiento 83.0%
Cc1cn2c(nc1=O)O[C@@H]1C[C@H]2O[C@@H]1CO
Anhydrothymidine
Rendimiento 83.0%

Condiciones de reacción

Temperatura
20°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    Temperaturato warm to 10° C. over a period of 5 hours
  3. 3
    OtroThe reaction was then quenched with H2O (6 mL)
  4. 4
    Otroforming a white suspension
  5. 5
    workup.WAITto stand for 30 minutes
  6. 6
    Filtraciónwas filtered
  7. 7
    LavadoThe collected solid was washed with cold CH3CN
  8. 8
    Otrodried under vacuum

Procedimiento

To a dried round bottom flask containing thymidine(10.0 g, 41.6 mmol) was added triphenylphosphine (21.8 g, 82.2 mmol) and CH3CN (160 mL). The suspension was cooled to −20° C. ((40:60 iPrOH:H2O) and dry ice). To the reaction mixture was added diisopropylazodicarboxylate (16.8 g, 82.2 mmol) as CH3CN solution (60 mL) dropwise via an addition funnel, over a period of 1 hour. After the addition, the mixture was stirred for an additional 90 minutes at 20° C. The mixture was allowed to warm to 10° C. over a period of 5 hours. The reaction was then quenched with H2O (6 mL) forming a white suspension. The reaction was allowed to stand for 30 minutes and then was filtered. The collected solid was washed with cold CH3CN and dried under vacuum to afford 7.7 g (83% yield) of a white solid. If desired, the solid may be recrystallized in EtOH.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07419653B2uspto-grants-2008_09