Réaction #169605

Équation de réaction

ammonium formate

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

ether

sodium cyanoborohydride

→

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

Solvants

methanol

Conditions de réaction

Traitement

1. 1
   workup.STIRRINGAfter stirring another hour at ambient temperature
2. 2
   workup.STIRRINGThe reaction was then stirred at ambient temperature overnight
3. 3
   Autreterminated by addition of water (˜5 mL)
4. 4
   AutreThe quenched reaction
5. 5
   Autrewas partitioned between 5 M sodium hydroxide (10 mL) and chloroform (20 mL)
6. 6
   ExtractionThe aqueous layer was extracted with chloroform (20 mL)
7. 7
   Séchagewere dried (sodium sulfate)
8. 8
   Filtrationfiltered
9. 9
   Concentrationconcentrated
10. 10
    workup.ADDITIONa 1:9 mixture of the cis and trans amines

Mode opératoire

To a stirred solution of 2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octan-3-one (3.00 g, 13.9 mmol) in dry methanol (20 mL), under nitrogen, was added a 1 M solution of zinc chloride in ether (2.78 mL, 2.78 mmol). After stirring at ambient temperature for 30 min, this mixture was treated with solid ammonium formate (10.4 g, 167 mmol). After stirring another hour at ambient temperature, solid sodium cyanoborohydride (1.75 g, 27.8 mmol) was added in portions. The reaction was then stirred at ambient temperature overnight and terminated by addition of water (˜5 mL). The quenched reaction was partitioned between 5 M sodium hydroxide (10 mL) and chloroform (20 mL). The aqueous layer was extracted with chloroform (20 mL), and combined organic layers were dried (sodium sulfate), filtered and concentrated. This left 2.97 g of yellow gum. GCMS analysis indicated that the product was a 1:9 mixture of the cis and trans amines, along with a trace of the corresponding alcohol (98% total mass recovery).

Source