Reaction #55509

ord-a2f5cb5990274416bd3a02dbb45350bb

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    TemperatureThe mixture is cooled for 2 hours
  2. 2
    workup.STIRRINGstirred at room temperature for 16 hours
  3. 3
    workup.DISTILLATIONThe solvent is distilled off at 25° C. in a high vacuum
  4. 4
    OtherThe precipitate obtained
  5. 5
    Filtrationis filtered off
  6. 6
    Washwashed with methylene chloride, methanol and water
  7. 7
    WashThe filtrate is washed with water
  8. 8
    Dryingdried over sodium sulfate
  9. 9
    ConcentrationBy concentrating the solvent

Procedure

5 G. of 2,4-diamino-6-chloropyrimidine-3-oxide are suspended in 50 ml. of dimethylformamide and 5 ml. of triethylamine and cooled to 0° C. while stirring. 4.3 G. of chloroformic acid 2-methoxyethyl ester are added dropwise to the cold suspension in the course of 15 minutes. The mixture is cooled for 2 hours and then stirred at room temperature for 16 hours. The solvent is distilled off at 25° C. in a high vacuum and the residue is digested with methylene chloride. The precipitate obtained is filtered off and washed with methylene chloride, methanol and water. The filtrate is washed with water and dried over sodium sulfate. By concentrating the solvent, there is obtained pure 2-methoxyethyl 2-amino-6-chloro-4-pyrimidinecarbamate-3-oxide having a melting point of 176°-178° C. Additional material is obtained by subjecting the mother liquor to chromatographical separation on silica gel.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04220772uspto-grants-1980_09