Potassium Hydroxide → 2-[(4-Bromophenyl)(pyridin-4-yl)methoxy]-4-methylpentanoic acid potassium salt
反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:19]2[CH:24]=[CH:23][N:22]=[CH:21][CH: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:7]=[CH:6][C:5]([CH:8]([C:19]2[CH:20]=[CH:21][N:22]=[CH:23][CH:24]=2)[O:9][CH:10]([CH2:15][CH:16]([CH3:18])[CH3:17])[C:11]([O-:13])=[O:12])=[CH:4][CH:3]=1参加物
3
実験手順
Using the same protocol as described in example 17, step 5, methyl 2-[(4-bromophenyl)(pyridin-4-yl)methoxy]-4-methylpentanoate from step 2 (293 mg, 0.75 mmol) was hydrolysed with potassium hydroxide. The solid residue obtained was used as such in the next step.
後処理
- customThe solid residue obtained
出典と根拠
- ORDレコード
- ord-b72668f28caa4aedb32fa74b63afb640
- 出典データセット
- uspto-grants-2007_10
- 特許番号
- US07279478B2
反応ノート
読み込み中…