Hydrochloric Acid → HCID 68782705, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:27])[CH2:4][O:5][C:6]1[CH:15]=[CH:14][C:13]([Cl:16])=[C:12]2[C:7]=1[C:8](Cl)=[C:9]([CH2:18][C:19]1[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][CH:20]=1)[C:10]([CH3:17])=[N:11]2.Cl>[Pd].C(O)C>[CH3:1][O:2][C:3](=[O:27])[CH2:4][O:5][C:6]1[CH:15]=[CH:14][C:13]([Cl:16])=[C:12]2[C:7]=1[CH:8]=[C:9]([CH2:18][C:19]1[CH:20]=[CH:21][C:22]([Cl:25])=[CH:23][CH:24]=1)[C:10]([CH3:17])=[N:11]2Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of [4,8-dichloro-3-(4-chlorobenzyl)-2-methylquinolin-5-yloxy]acetic acid methyl ester (0.12 g), palladium, 5 wt. % on activated carbon (0.010 g), ethanol, and 1.0 M aqueous hydrochloric acid (1.0 mL) was stirred at room temperature for 17 hours under an atmosphere of hydrogen. The mixture was filtered through hyflo, washing with ethanol and water and the solvent removed under reduced pressure to afford title compound, 0.11 g.
Workup
- filtrationThe mixture was filtered through hyflo
- washwashing with ethanol and water
- customthe solvent removed under reduced pressure
Sources & evidence
- ORD record
- ord-bc2b662135ca4b998f2245922ce77df4
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07858640B2
Reaction notes
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