Hydrochloric Acid → N-Benzyl-N-methylpiperidin-4-amine
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([N:14]([CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH3:15])[CH2:10][CH2:9]1)=O)(C)(C)C.CO.Cl>C(Cl)Cl.CCOCC>[CH2:16]([N:14]([CH3:15])[CH:11]1[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1)[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1Participants
6
Procedure
4-(Benzyl-methyl-amino)-piperidine-1-carboxylic acid tert-butyl ester was dissolved in DCM and methanol and 2.0M HCl in ether was added. After 3 hours the solvent was removed in vacuo and the residue was recrystallised from ethyl acetate/methanol to yield benzyl-methyl-piperidin-4-yl-amine (hydrochloride salt).
Workup
- customAfter 3 hours the solvent was removed in vacuo
- customthe residue was recrystallised from ethyl acetate/methanol
Sources & evidence
- ORD record
- ord-60a016d0fee6467898949490cb40ee42
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08993563B2
Reaction notes
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