Sodium Hydroxide → 2-[3-Ethyl-4-(quinolin-2-yl-methoxy)phenyl]acetic acid
Reaction equation
[CH2:1]([C:3]1[CH:4]=[C:5]([CH2:21][C:22]([O:24]C)=[O:23])[CH:6]=[CH:7][C:8]=1[O:9][CH2:10][C:11]1[CH:20]=[CH:19][C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[N:12]=1)[CH3:2].[OH-].[Na+]>>[CH2:1]([C:3]1[CH:4]=[C:5]([CH2:21][C:22]([OH:24])=[O:23])[CH:6]=[CH:7][C:8]=1[O:9][CH2:10][C:11]1[CH:20]=[CH:19][C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[N:12]=1)[CH3:2]Participants
3
Procedure
The title compound is prepared from 1.5 g (4.48 mmol) of the compound from Example XXXIV and 10 ml (10 mmol) of 1N sodium hydroxide solution analogously to the procedure of Example V.
Sources & evidence
- ORD record
- ord-1ffabec3f635496da78864f9126656ca
- Source dataset
- uspto-grants-1994_04
- Patent number
- US05304563
Reaction notes
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