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

HRID 2354487Notes

Reaction equation

HRID 2354487 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][CH:8]2[C:13](=O)[CH:12]3[CH2:15][CH2:16][N:9]2[CH2:10][CH2:11]3)[CH:2]=1.CN.[C:19]([BH3-])#[N:20].[Na+].[OH-].[K+]>[Cl-].[Zn+2].[Cl-].CO>[NH2:20][CH2:19][CH:13]1[CH:12]2[CH2:15][CH2:16][N:9]([CH2:10][CH2:11]2)[CH:8]1[CH2:7][C:3]1[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=1

Participants

7

Reactant 4

HCID 6329MethylamineHCID 14797Potassium HydroxideHCID 5003444Sodium cyanoborohydrideHCID 102200302-(Pyridin-3-ylmethyl)quinuclidin-3-one

Product 1

HCID 223113793-Aminomethyl-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octaneYield 83%

Reagents, catalysts & solvents 2

HCID 3007855ZincchlorideCatalystHCID 887MethanolSolvent

Procedure

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.

Workup

  1. stirringthe mixture stirred at room temperature for 48 h
  2. customthe solvent was removed by rotary evaporation
  3. extractionThe residue was extracted with chloroform (3×50 mL)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated by rotary evaporation

Sources & evidence

ORD record
ord-14f8e3dfe0224a7b800408b857287a07
Source dataset
uspto-grants-2010_07
Patent number
US07754189B2

Reaction notes

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