Reacción #1379886

ord-5e4504704ed9444f96b6857ac121ab98

Ecuación de reacción

COc1ccc([N+](=O)[O-])c(Cl)n1
2-chloro-3-nitro-6-methoxypyridine
CNCC(O)CO
3-methylamino-1,2-dihydroxypropane
COc1ccc([N+](=O)[O-])c(CNCC(O)CO)n1
yellow powder
Rendimiento 87.1%
COc1ccc([N+](=O)[O-])c(CNCC(O)CO)n1
3-[(6-methoxy-3-nitro-2-pyridyl)methylamino]propane-1,2-diol
Rendimiento 87.1%

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

4 g (0.0219 mol) of the product 2-chloro-3-nitro-6-methoxypyridine, 50 ml of ethanol and 4.15 ml (0.0438 mol) of 3-methylamino-1,2-dihydroxypropane 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. 4.74 g of yellow powder are obtained, ie a yield of 87.1%.

Fuente

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