Potassium Hydroxide → HCID 69472579, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][N:20]=2)[O:9][CH:10]([CH2:15][CH:16]([CH3:18])[CH3:17])[C:11]([O:13]C)=[O:12])=[CH:4][CH:3]=1.[OH-].[K+:26]>>[K+:26].[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][N:20]=2)[O:9][CH:10]([CH2:15][CH:16]([CH3:18])[CH3:17])[C:11]([O-:13])=[O:12])=[CH:6][CH:7]=1Participants
3
Procedure
Using the same protocol as described in example 17, step 5, methyl 2-[(4-bromophenyl)(pyridin-2-yl)methoxy]-4-methylpentanoate from step 2 (623 mg, 1.59 mmol) was hydrolysed with potassium hydroxide. The solid residue obtained was used as such in the next step.
Workup
- customThe solid residue obtained
Sources & evidence
- ORD record
- ord-b46738a55dc445ac98279b252b12ae06
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07279478B2
Reaction notes
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