Hydrochloric Acid → HCID 117966376, compound
Reaction equation
[CH3:1][N:2]([CH3:18])[C:3]([C@@H:5]1[CH2:10][CH2:9][CH2:8][N:7](C(OC(C)(C)C)=O)[CH2:6]1)=[O:4].[ClH:19]>CO>[ClH:19].[CH3:1][N:2]([CH3:18])[C:3]([C@@H:5]1[CH2:10][CH2:9][CH2:8][NH:7][CH2:6]1)=[O:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (R)-tert-butyl 3-(dimethylcarbamoyl)piperidine-1-carboxylate (9 g, 35.15 mmol) in methanol (20 mL) at 0° C. was added hydrogen chloride in methanol (50 mL). The reaction mixture was stirred at room temperature for 2 h. The solvent was evaporated in vacuo to afford (R)—N,N-dimethylpiperidine-3-carboxamide hydrochloride (7 g, 90%). MS (ES+APCI) [(M-2HCl)+H] 157.1; LCMS retention time: 6.36 min (Method F1).
Workup
- customThe solvent was evaporated in vacuo
Sources & evidence
- ORD record
- ord-d80a7d1d99814f7997951f41fdaeea4c
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09296745B2
Reaction notes
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