Reacción #5523

ord-39c6db17ee584deba9aaa702687d55e0

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ExtracciónThe CH2Cl2 solution was extracted with water and 1N HCl
  2. 2
    LavadoThe organic solution was washed with saturated NaHCO3 solution and with brine solution
  3. 3
    SecadoThe CH2Cl2 solution was dried (MgSO4)
  4. 4
    Concentraciónconcentrated in vacuo

Procedimiento

To a solution of (±)-6-acetyl-4-(di-n-propylamino)-1,2,2a,3,4,5-hexahydrobenz[cd]indole (2.3 g, 7.7 mmol) and triethylamine (1.1 ml, 8 mmol) in 90 ml CH2Cl2 under N2 was added dropwise a solution of 2,2,2-trichloroethyl chloroformate. The reaction mixture was stirred at RT for 1 hr. The CH2Cl2 solution was extracted with water and 1N HCl. The organic solution was washed with saturated NaHCO3 solution and with brine solution. The CH2Cl2 solution was dried (MgSO4) and concentrated in vacuo to give 3.3 g of the 1-carbamylindoline.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05244911uspto-grants-1993_09