Reaction #63611

ord-381c5c99556c4f848281c9ccb2896c0f

Conditions

Temperature
70°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    TemperatureAfter cooling overnight to room temperature
  2. 2
    Otherthe reaction mixture was evaporated
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in trichloromethane
  4. 4
    WashThe solution was washed with water
  5. 5
    Otherdried
  6. 6
    Filtrationfiltered
  7. 7
    Otherevaporated

Procedure

A mixture of 6.6 parts of 2-chloro-N-(5-fluoro-2-methylphenyl)acetamide, 5 parts of hexahydro-3,3-dimethyl-3H-oxazolo[3,4-a]pyrazine, 6.1 parts of N,N-diethylethanamine and 67.5 parts of N,N-dimethylformamide was stirred and heated for 8 hours at about 70° C. After cooling overnight to room temperature, the reaction mixture was evaporated. The residue was dissolved in trichloromethane. The solution was washed with water, dried, filtered and evaporated, yielding 8.5 parts of N-(5-fluoro-2-methylphenyl)-tetrahydro-3,3-dimethyl-3H-oxazolo[3,4-a]pyrazine-7(8H)-acetamide as an oily residue (intermediate 121).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04766125uspto-grants-1988_08