Hydrochloric Acid → HCID 22678317, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:8]([CH2:9][N:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH:11]2[CH2:16][C:17]([O:19]CC)=[O:18])=[CH:7][CH:6]=[CH:5][N:4]=1.[OH-].[Na+].Cl>CO>[CH3:1][O:2][C:3]1[C:8]([CH2:9][N:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH:11]2[CH2:16][C:17]([OH:19])=[O:18])=[CH:7][CH:6]=[CH:5][N:4]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2.8 g of ethyl 2-[1-[(2-methoxy-3-pyridyl)methyl]-2-piperidyl]acetate, 20 ml of a 2N aqueous sodium hydroxide and 20 ml of methanol were stirred at 70° C. for 1.5 hours. 8 ml of a 5N aqueous hydrochloric acid was added thereto, and the solvent was evaporated. Ethanol was added to the residue and sodium chloride was filtered off. Ethanol was evaporated, to give 2.9 g of a colorless oil.
Workup
- customthe solvent was evaporated
- additionEthanol was added to the residue and sodium chloride
- filtrationwas filtered off
- customEthanol was evaporated
Sources & evidence
- ORD record
- ord-c4d4e6c2cd904111996c3897d4e4d6a1
- Source dataset
- uspto-grants-2004_08
- Patent number
- US06784192B2
Reaction notes
Loading…