Reaktion #6237

ord-cc46162356544f669d9d762c2d76ff4b

Reaktionsgleichung

NCCCOc1ccncc1
4-(3-aminopropyloxy)pyridine
CCN(CC)CC
triethylamine
CC(C)(C)C(=O)Cl
pivaloyl chloride
CC(C)(C)C(=O)NCCCOc1ccncc1
desired compound
Ausbeute 77.3%
CC(C)(C)C(=O)NCCCOc1ccncc1
4-(3-pivaloylaminopropyloxy) pyridine
Ausbeute 77.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooling
  2. 2
    workup.STIRRINGThe mixture was stirred at room temperature for 1.5 hours
  3. 3
    WaschenThe reaction mixture was washed successively with a saturated aqueous solution of sodium bicarbonate and brine
  4. 4
    Trocknendried over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONthe solvent was distilled off
  6. 6
    SonstigeThe residue was purified by column chromatography (eluent: ethyl acetate)

Vorschrift

To a solution of 700 mg (4.60 mmol) of 4-(3-aminopropyloxy)pyridine and 0.77 ml (5.52 mmol) of triethylamine in 30 ml of methylene chloride, 0.57 ml (4.63 mmol) of pivaloyl chloride was added under ice-cooling with stirring. The mixture was stirred at room temperature for 1.5 hours. The reaction mixture was washed successively with a saturated aqueous solution of sodium bicarbonate and brine and dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 840 mg of the desired compound (yield: 77.3%, colorless crystals).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05246948uspto-grants-1993_09