Réaction #3257

ord-3c865d11870445439885fc69ae3775bc

Solvants

Conditions de réaction

Température
5°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreA white precipitate formed
  2. 2
    workup.ADDITIONafter the addition
  3. 3
    FiltrationThe insoluble product was filtered
  4. 4
    Lavagewashed with cold water

Mode opératoire

To a cold (5° C.) solution of 5-cyano-2-hydrazino-4-methylamino-pyrimidine (21.7 g) from Example 4 in a mixture of water (260 mL) and concentrated HCl (26.5 mL) was added dropwise a solution of NaNO2 (10.03 g) in water (25 mL) with overhead mechanical stirring. A white precipitate formed and after the addition was completed, the reaction was stirred for an additional 20 minutes at 5° C. The insoluble product was filtered and washed with cold water to give 22.4 g of the title compound after drying at 23° C. under high vacuum overnight. Crystallization from ethanol provided an analytically pure sample of 2-azido-5-cyano-4-methylamino-pyrimidine; mp 225°-230° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05733914uspto-grants-1998_03