Hydrochloric Acid → 1152111-05-1
Reaction equation
[CH3:1][N:2]([CH3:17])[CH:3]1[C:7]2([CH2:9][CH2:8]2)[CH2:6][N:5](CC2C=CC=CC=2)[CH2:4]1.[ClH:18]>CO.[Pd]>[ClH:18].[ClH:18].[CH3:1][N:2]([CH3:17])[CH:3]1[C:7]2([CH2:9][CH2:8]2)[CH2:6][NH:5][CH2:4]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of racemic N,N-dimethyl-5-(phenylmethyl)-5-azaspiro[2.4]heptan-7-amine (0.8015 g, 3.479 mmol) in MeOH (18 mL) was added 1 N aq. HCl (6.96 mL, 6.96 mmol) and 10% Pd/C (50% water, 160 mg). The mixture was hydrogenated under balloon pressure overnight and then filtered. The solution was concentrated in vacuo to give crude racemic N,N-dimethyl-5-azaspiro[2.4]heptan-7-amine dihydrochloride (0.8060 g, >100% crude yield). LCMS: (M+H)+: 141.1.
Workup
- customwas hydrogenated under balloon pressure overnight
- filtrationfiltered
- concentrationThe solution was concentrated in vacuo
Sources & evidence
- ORD record
- ord-64582a033838487fad6e45d315ce610c
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07893056B2
Reaction notes
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