Hydrochloric Acid → HCID 69432235, compound
Reaction equation
[ClH:1].C(OC([N:9]1[CH2:14][CH2:13][CH:12]([CH2:15][N:16]([CH3:23])[C:17]2[CH:22]=[CH:21][N:20]=[CH:19][CH:18]=2)[CH2:11][CH2:10]1)=O)(C)(C)C>CO>[ClH:1].[CH3:23][N:16]([CH2:15][CH:12]1[CH2:13][CH2:14][NH:9][CH2:10][CH2:11]1)[C:17]1[CH:22]=[CH:21][N:20]=[CH:19][CH:18]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Hydrogen chloride gas is passed through a methanol (500 mL) solution of 1-t-butoxycarbonyl-4-{[(methyl)(pyridin-4-yl)amino]methyl}piperidine maintaining <20° C., for 5 minutes. The mixture is kept at this temperature for 7 hours, then at 4° C. for 16 hours before it is concentrated in vacuo providing 4-{[(methyl)(pyridin-4-yl)amino]methyl}piperidine hydrochloride (4.85 g, >100%).
Workup
- concentrationat 4° C. for 16 hours before it is concentrated in vacuo
Sources & evidence
- ORD record
- ord-efe14952ecd74dd8b1f62c7f5d783114
- Source dataset
- uspto-grants-2007_11
- Patent number
- US07294627B2
Reaction notes
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