反応式
[C:1]1([C:7]2[C:11]([C:12]([OH:14])=[O:13])=[C:10]([CH2:15][CH2:16]C3C=CC=CC=3)[O:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:23](Br)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>>[C:1]1([C:7]2[C:11]([C:12]([OH:14])=[O:13])=[C:10]([CH2:15][CH2:16][CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[O:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
3
実験手順
The title compound was prepared as described for Compound 28A but substituting 2-phenylethylbromide for benzyl bromide. The crude was purified by flash chromatography (ethyl acetate-petroleum ether-acetic acid 1:1:0.01 mL) to afford the title compound (72%).
後処理
- customThe title compound was prepared
- customThe crude was purified by flash chromatography (ethyl acetate-petroleum ether-acetic acid 1:1:0.01 mL)
出典と根拠
- ORDレコード
- ord-5384ec8b06e24c5a8f96afdfd5615e71
- 出典データセット
- uspto-grants-2002_04
- 特許番号
- US06365591B1
関連ノート
読み込み中…