Reacción #4699

ord-02572d7994bc44c39cdf4b16503d331d

Ecuación de reacción

COc1ccc(N)cc1
p-anisidine
CN(C)c1ccc(C(=O)Cl)cc1
4-dimethylamino-benzoic acid chloride
S=P12SP3(=S)SP(=S)(S1)SP(=S)(S2)S3
phosphorus pentasulfide
COc1ccc(NC(=S)c2ccc(N(C)C)cc2)cc1
4-dimethylamino-N-(4'-methoxyphenyl)-benzenecarbothiamide
Rendimiento 63.5%

Disolventes

Condiciones de reacción

Temperatura
30°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe mixture was refluxed for one hour
  2. 2
    Temperaturawas refluxed for 2 hours
  3. 3
    Filtraciónfiltered
  4. 4
    Lavadothe product was washed with 0.1N hydrochloric acid
  5. 5
    workup.ADDITIONA mixture of the product and 300 ml of N sodium hydroxide solution
  6. 6
    workup.STIRRINGwas stirred for one hour
  7. 7
    Filtraciónfiltered
  8. 8
    LavadoThe product was washed with water
  9. 9
    Otrodried

Procedimiento

13.6 g of p-anisidine were added to a solution of 22.2 g of 4-dimethylamino-benzoic acid chloride in 84 ml of anhydrous pyridine and the mixture was refluxed for one hour and cooled to 30° C. 33 g of phosphorus pentasulfide were added to the mixture which was refluxed for 2 hours and was then poured into an ice water-concentrated hydrochloric acid mixture. The mixture was stirred for one hour and was vacuum filtered and the product was washed with 0.1N hydrochloric acid. A mixture of the product and 300 ml of N sodium hydroxide solution was stirred for one hour and was vacuum filtered. The product was washed with water and dried to obtain 13.5 g of 4-dimethylamino-N-(4'-methoxyphenyl)-benzenecarbothiamide melting at 192° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04727084uspto-grants-1988_02