Lithium Hydroxide → HCID 117622978, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:26]#[N:27])=[C:6]([C:8]2[C:13]([O:14][CH3:15])=[CH:12][N:11]([CH:16]([O:22][CH2:23][CH3:24])[C:17]([O:19]CC)=[O:18])[C:10](=[O:25])[CH:9]=2)[CH:7]=1.[OH-].[Li+]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:26]#[N:27])=[C:6]([C:8]2[C:13]([O:14][CH3:15])=[CH:12][N:11]([CH:16]([O:22][CH2:23][CH3:24])[C:17]([OH:19])=[O:18])[C:10](=[O:25])[CH:9]=2)[CH:7]=1Participants
3
Procedure
277 mg (0.69 mmol) of ethyl [4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl](ethoxy)acetate (racemate) were hydrolysed with lithium hydroxide according to General Method 6B. Yield: 180 mg (71% of theory)
Sources & evidence
- ORD record
- ord-1f6a8351003e4d6282fac9043ecc73b3
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09434690B2
Reaction notes
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