Reacción #1379884

ord-a405500cb4b54119b3ddd3d7e6735b7b

Ecuación de reacción

CCCCNCCO
2-butylaminoethanol
COc1ccc([N+](=O)[O-])c(Cl)n1
2-chloro-3-nitro-6-methoxypyridine
C1COCCO1
dioxane
CCCCN(CCO)c1nc(OC)ccc1[N+](=O)[O-]
yellow powder
Rendimiento 70.0%
CCCCN(CCO)c1nc(OC)ccc1[N+](=O)[O-]
2-[butyl-(6-methoxy-3-nitro-2-pyridyl)amino]ethanol
Rendimiento 70.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe mixture is refluxed for 2 hours
  2. 2
    workup.STIRRINGwith stirring
  3. 3
    OtroThe precipitate formed
  4. 4
    Filtraciónis filtered off by suction
  5. 5
    Otrodried under vacuum to constant weight

Procedimiento

1.9 g (0.01 mol) of the product 2-chloro-3-nitro-6-methoxypyridine, 30 ml of dioxane, 5 ml of water and 2.62 ml (0.02 mol) of 2-butylaminoethanol are placed in a fully equipped round-bottomed flask. The mixture is refluxed for 2 hours with stirring and is then poured onto an ice/water mixture with stirring. The precipitate formed is filtered off by suction and dried under vacuum to constant weight. 1.9 g of yellow powder are obtained, ie a yield of 70%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07238211B2uspto-grants-2007_07