Ammonia → 5-(Benzyloxy)pyridin-3-amine

HRID 1168946

Reaktionsgleichung

Reaktionsgleichung von HRID 1168946
Br[C:2]1[CH:3]=[C:4]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:5]=[N:6][CH:7]=1.[NH3:16]>O.O.O.O.O.S([O-])([O-])(=O)=O.[Cu+2]>[C:10]1([CH2:9][O:8][C:4]2[CH:3]=[C:2]([NH2:16])[CH:7]=[N:6][CH:5]=2)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
180 °C

Versuchsvorschrift

A thick-walled glass pressure tube was charged with copper(II) sulfate pentahydrate (1.96 g, 7.85 mmol), 5-bromo-3-(phenylmethoxy)pyridine (4.00 g, 15.15 mmol) and concentrated aqueous ammonia (29.7%, 14.8 M, 37 mL). The tube was sealed and the dark blue suspension was stirred and heated at ˜180° C. (oil bath temperature) for 24 h. The mixture was allowed to cool to ambient temperature. After further cooling in an ice-water bath, the mixture was concentrated on a rotary evaporator to a small volume (˜20 mL) of a dark-blue solution. The solution was diluted with water (40 mL) and saturated K2CO3 solution (40 mL) and extracted with CHCl3 (4×40 mL). The combined, turbid-brown CHCl3 extracts were washed with saturated NaCl solution (2×100 ml), dried (Na2SO4), filtered and concentrated (rotary evaporator). The resulting dark-brown oil, was briefly dried on the vacuum pump to give a dark-brown solid (2.06 g). The product was purified by column chromatography on silica gel (100 g) eluting with CHCl3—MeOH (3:1,v/v). Selected fractions, based on TLC (Rf 0.65) analysis, were combined and concentrated to give a 1.64 g(54.1%) of a tan-brown solid.

Aufarbeitung

  1. customThe tube was sealed
  2. temperatureto cool to ambient temperature
  3. temperatureAfter further cooling in an ice-water bath
  4. concentrationthe mixture was concentrated on a rotary evaporator to a small volume (˜20 mL) of a dark-blue solution
  5. additionThe solution was diluted with water (40 mL) and saturated K2CO3 solution (40 mL)
  6. extractionextracted with CHCl3 (4×40 mL)
  7. washturbid-brown CHCl3 extracts were washed with saturated NaCl solution (2×100 ml)
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated
  11. custom(rotary evaporator)
  12. customThe resulting dark-brown oil, was briefly dried on the vacuum pump

Quellen und Nachweise

ORD-Eintrag
ord-19c7fca597cb45329d889d6062cb0dd7
Quelldatensatz
uspto-grants-2003_09
Patentnummer
US06627648B1

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