Reacción #1946561

ord-75850a36f1a24abb9732c11e16c87418

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ExtracciónThe oily precipitate was extracted with methylene chloride
  2. 2
    Lavadothe extract was washed with water
  3. 3
    Secadodried over magnesium sulfate
  4. 4
    Concentraciónconcentrated
  5. 5
    Otrowas used without further purification

Procedimiento

To a solution of 100.8 g (316.5 mmol) of crude 2-di-n-butylamino-4-(3-methoxyphenyl)thiazole (compound 2-12) and 630 ml of DMF was added, over about 30 mins, a solution of 55.81 g (364 mmol) of phosphorus oxychloride in 188 ml of DMF. The mixture was stirred overnight and poured into a solution of 158.1 g of sodium carbonate in 3.5 l of water. The oily precipitate was extracted with methylene chloride, and the extract was washed with water, dried over magnesium sulfate, and concentrated. The yield of brown oil was 88.77 g and was used without further purification. Anal. Calcd. For C19H26N2O2S: C, 65.9; H, 7.6; N, 8.1; S, 9.3. Found: C, 66.20; H, 7.85; N, 8.60; S, 7.93.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06528223B1uspto-grants-2003_03