Reacción #83615

ord-4759f96742e4405d80aa7044ee4bf327

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with water and 1N HCl
  2. 2
    LavadoThe organic solution was washed with a saturated NaHCO3 solution
  3. 3
    Secadoa saturated brine solution, dried over MgSO4
  4. 4
    Concentraciónconcentrated to dryness in vacuo

Procedimiento

To a solution of (+)(2aS,4R)-6-acetyl-4-(di-n-propylamino)-1,2,2a,3,4,5-hexahydrobenz[cd]indole (1.7 g, 5.7 mmol) and triethylamine (0.8 ml, 6 mmol) in 90 ml CH2Cl2 was added dropwise a solution of 2,2,2-trichloroethylchloroformate (1.3 g, 6 mmol) in 10 ml CH2Cl2. The reaction mixture was stirred at room temperature for one hour and then extracted with water and 1N HCl. The organic solution was washed with a saturated NaHCO3 solution, a saturated brine solution, dried over MgSO4 and then concentrated to dryness in vacuo to give 2.5 g of the 1-carbamylindoline.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05624944uspto-grants-1997_04