Reacción #2467997

ord-9db21a052804466cab4b00ea945dfd76

Ecuación de reacción

O=c1[nH]c2cc(Cl)ccc2c(=O)c2sccc12
7-Chloro-9H-3-thia-9-aza-benzo[f]azulene-4,10-dione
Cc1ccccc1
toluene
O=P(Cl)(Cl)Cl
phosphorus oxychloride
COc1nc2cc(Cl)ccc2c(=O)c2sccc12
title compound
COc1nc2cc(Cl)ccc2c(=O)c2sccc12
7-Chloro-10-methoxy-3-thia-9-aza-benzo[f]azulen-4-one

Condiciones de reacción

Temperatura
108°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA 4-necked, round-bottomed flask, equipped with a mechanical stirrer
  2. 2
    workup.ADDITIONdigital thermometer, addition funnel and a condenser with nitrogen inlet-outlet
  3. 3
    OtroThe pipes are flushed with toluene (774 g)
  4. 4
    TemperaturaThen the mixture is cooled to −5° C.
  5. 5
    workup.ADDITIONa 30% solution of sodium methylate (1.43 kg) is added over 30 min at −5° C
  6. 6
    workup.ADDITIONAfter addition the mixture
  7. 7
    Temperaturais warmed to 40° C. over an hour
  8. 8
    workup.DISTILLATIONthe solvent is distilled at 20-45° C. under reduced pressure
  9. 9
    workup.ADDITIONTo the residue deionized water (6.7 kg) is added
  10. 10
    Concentraciónthe mixture is concentrated under reduced pressure to 7 L
  11. 11
    workup.ADDITIONThen heptane (3.06 kg) is added
  12. 12
    Temperaturathe temperature is raised to 70° C. over 1 hour
  13. 13
    workup.STIRRINGby additional stirring of 10 min
  14. 14
    TemperaturaThe suspension is then cooled to 0° C.
  15. 15
    Filtraciónthe solid is collected by filtration
  16. 16
    Lavadowashed with heptane (2×383 g) and deionized water (2×1.1 kg)
  17. 17
    Otrodried under vacuum at 65° C.

Procedimiento

A 4-necked, round-bottomed flask, equipped with a mechanical stirrer, digital thermometer, addition funnel and a condenser with nitrogen inlet-outlet is charged with 7-Chloro-9H-3-thia-9-aza-benzo[f]azulene-4,10-dione (559.6 g), toluene (6.8 kg) and dimethylformamide (100.73 g). To the stirred suspension phosphorus oxychloride (357.2 g) is added over 5 min at 20-25° C. The pipes are flushed with toluene (774 g), then the temperature is raised to 108° C. over 1 hour and stirring continued for about 5 hours. Then the mixture is cooled to −5° C. and a 30% solution of sodium methylate (1.43 kg) is added over 30 min at −5° C. After addition the mixture is warmed to 40° C. over an hour and the solvent is distilled at 20-45° C. under reduced pressure. To the residue deionized water (6.7 kg) is added and the mixture is concentrated under reduced pressure to 7 L. Then heptane (3.06 kg) is added and the temperature is raised to 70° C. over 1 hour, followed by additional stirring of 10 min. The suspension is then cooled to 0° C. and the solid is collected by filtration, washed with heptane (2×383 g) and deionized water (2×1.1 kg) and dried under vacuum at 65° C. to yield the title compound with a melting point of >195-197° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08258128B2uspto-grants-2012_09