Reacción #40458

ord-dbeb848e8fc94ab2bca7c131609a2899

Disolventes

Condiciones de reacción

Temperatura
80°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe pyridine was then removed by rotary evaporation and 5% Na2CO3 solution
  2. 2
    workup.ADDITIONwas added
  3. 3
    OtroThe resulting solid that precipitated out
  4. 4
    Filtraciónwas collected by filtration
  5. 5
    OtroChromatographic purification

Procedimiento

6-chloro-7-methoxy-9H-β-carbolin-8-ylamine (100 mg, 0.4 mmol), EDCI (125 mg, 0.64 mmol) and 2-methyl nicotinic acid (66 mg, 0.48 mmol) were taken in a round-bottom flask and suspended in pyridine (2 ml). The resulting mixture was heated at 80° C. overnight. The pyridine was then removed by rotary evaporation and 5% Na2CO3 solution was added. The resulting solid that precipitated out was collected by filtration. Chromatographic purification gave the desired product in 50-70% yield.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07727985B2uspto-grants-2010_06