Reaction #4001

ord-cb342278cc67421d861b38254858d7ca

Reaction equation

O=C1CC(Cl)(CCl)O1
4-chloro-4-chloromethyloxetan-2-one
Cl.N=C(N)N
guanidine hydrochloride
Cl
hydrogen chloride
Nc1nc(O)cc(CCl)n1
2-amino-4-chloromethyl-6-hydroxypyrimidine

Solvents

Conditions

Temperature
120°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperatureheated under nitrogen
  2. 2
    Otherpurge as the bath temperature
  3. 3
    Otherapproached 100° C.
  4. 4
    Otherreaction
  5. 5
    OtherWhen the initial reaction
  6. 6
    workup.WAITsubsided after a few minutes
  7. 7
    Temperaturethe bath temperature was raised to 130° C.
  8. 8
    Otheras indicated by cessation of gassing (about 1 hour)
  9. 9
    Temperatureto cool about 60° C.
  10. 10
    ExtractionThe solution was extracted with 500 parts of ethyl acetate
  11. 11
    workup.ADDITIONThe aqueous phase was treated with decolourising charcoal
  12. 12
    Filtrationfiltered
  13. 13
    workup.ADDITIONthe pH was adjusted to pH 8 by the addition of saturated aqueous sodium bicarbonate solution
  14. 14
    FiltrationThe precipitated solid was filtered
  15. 15
    Washwashed with water
  16. 16
    Otherdried to constant weight at 80° C. in a vacuum oven

Procedure

620 parts of 4-chloro-4-chloromethyloxetan-2-one and 440 parts of guanidine hydrochloride were charged to a reaction flask and the mixture was stirred and heated under nitrogen purge as the bath temperature was gradually raised to 120° C. When the bath temperature approached 100° C., reaction commenced accompanied by evolution of hydrogen chloride. When the initial reaction subsided after a few minutes the bath temperature was raised to 130° C. and held until the reaction ceased as indicated by cessation of gassing (about 1 hour). The reaction mixture was allowed to cool about 60° C. and 1750 parts of water was added to the syrup. The solution was extracted with 500 parts of ethyl acetate and the extract was discarded. The aqueous phase was treated with decolourising charcoal, filtered and the pH was adjusted to pH 8 by the addition of saturated aqueous sodium bicarbonate solution. The precipitated solid was filtered, washed with water and dried to constant weight at 80° C. in a vacuum oven to give 2-amino-4-chloromethyl-6-hydroxypyrimidine, m.p. 195°-197° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04723006uspto-grants-1988_02