Reacción #214616

ord-391e3988e0a84fcd9b479b48e55c37b0

Condiciones de reacción

Temperatura
10°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroprovided with an agitator
  2. 2
    Temperaturabeing maintained below 20° C
  3. 3
    OtroAfter agitation of the mixture, the crystals were dried off
  4. 4
    Lavadowashed with methylethylcetone
  5. 5
    Otrodried
  6. 6
    workup.DISSOLUTIONdissolved in water
  7. 7
    Otroreprecipitated by addition of 50 ml of 20% ammonia
  8. 8
    OtroThe crystals were dried off
  9. 9
    Lavadowashed with water
  10. 10
    Otrodried

Procedimiento

400 ml of methylethylacetone and 11 g of methylpiperazine were introduced into a balloon flask provided with an agitator and a thermometer. The mixture was cooled to 10° C. and then 41 g of 6,7-dibromo-8-nitro-1,4-benzodioxane-5-carbonyl chloride were added in portions with the temperature being maintained below 20° C. After agitation of the mixture, the crystals were dried off, washed with methylethylcetone and dried and then dissolved in water and reprecipitated by addition of 50 ml of 20% ammonia. The crystals were dried off, washed with water and dried. 33 g of 5-[(4-methyl-1-piperazinyl)-carbonyl]-6,7-dibromo-8-nitro-1,4-benzodioxane were obtained (M.P: 164° C.; yield: 69.6%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04255580uspto-grants-1981_03