Réaction #72943

Équation de réaction

potassium hydroxide

2-((3-Pyridinyl)methyl)-1-azabicyclo[2.2.2]octan-3-one

methylamine

sodium cyanoborohydride

→

amine

Rendement 83.0%

3-Aminomethyl-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane

Rendement 83.0%

Solvants

methanol

Conditions de réaction

Traitement

1. 1
   workup.STIRRINGthe mixture stirred at room temperature for 48 h
2. 2
   Autrethe solvent was removed by rotary evaporation
3. 3
   ExtractionThe residue was extracted with chloroform (3×50 mL)
4. 4
   Séchagedried (MgSO4)
5. 5
   Filtrationfiltered
6. 6
   Concentrationconcentrated by rotary evaporation

Mode opératoire

2-((3-Pyridinyl)methyl)-1-azabicyclo[2.2.2]octan-3-one (2.16 g, 0.01 mol), methylamine (25 mL, 0.05 mol) and zinc chloride (5 mL, 0.005 mol) were added to dry methanol (30 mL) and stirred at room temperature for 30 min. Then, sodium cyanoborohydride (30 mL, 1.0M in THF) was added carefully and the mixture stirred at room temperature for 48 h. The mixture was adjusted to pH 10 using 2N potassium hydroxide and then the solvent was removed by rotary evaporation. The residue was extracted with chloroform (3×50 mL), dried (MgSO4), filtered and concentrated by rotary evaporation to yield the crude desired amine as a light yellow oil (2.40 g, 83% yield). The product was taken on to the next step without further purification.

Source