Sodium borohydride → Methyl N-{(4-bromophenyl)[4-(methylsulfonyl)phenyl]methyl}-L-leucinate
反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:19]2[CH:24]=[CH:23][C:22]([S:25]([CH3:28])(=[O:27])=[O:26])=[CH:21][CH:20]=2)=[N:9][C@H:10]([C:15]([O:17][CH3:18])=[O:16])[CH2:11][CH:12]([CH3:14])[CH3:13])=[CH:4][CH:3]=1.BrC1C=CC(C(C2C=CC(S(C)(=O)=O)=CC=2)=O)=CC=1.[BH4-].[Na+]>C(O)(=O)C.CO>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:19]2[CH:20]=[CH:21][C:22]([S:25]([CH3:28])(=[O:27])=[O:26])=[CH:23][CH:24]=2)[NH:9][C@H:10]([C:15]([O:17][CH3:18])=[O:16])[CH2:11][CH:12]([CH3:13])[CH3:14])=[CH:4][CH:3]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of a 1:1 mixture of methyl N-{(4-bromophenyl)[4-(methylsulfonyl)phenyl]methylene}leucinate and (4-bromophenyl)[4-(methylsulfonyl)phenyl]methanone from step 1 (185 mg, ˜0.2 mmol) in acetic acid/methanol (1:3, 4 mL) was added sodium borohydride (˜400 mg) by portions every 30 min over 2 days (addition was stopped during the night) using a solid addition funnel. The reaction mixture was partitioned between EtOAc and water, the organic layer was dried over Na2SO4 and concentrated. The resulting mixture was purified by chromatography using EtOAc and hexane as eluant. Methyl N-{(4-bromophenyl)[4-(methylsulfonyl)phenyl]methyl}-L-leucinate was obtained as a colorless gum and (4-bromophenyl){4-(methylsulfonyl)phenyl}methanol was obtained as a white solid.
後処理
- additionaddition
- additiona solid addition funnel
- customThe reaction mixture was partitioned between EtOAc and water
- dry with materialthe organic layer was dried over Na2SO4
- concentrationconcentrated
- customThe resulting mixture was purified by chromatography
出典と根拠
- ORDレコード
- ord-2d5ef937894a4dfe9838b58486594457
- 出典データセット
- uspto-grants-2012_11
- 特許番号
- US08318748B2
反応ノート
読み込み中…