反応式
[CH2:1]([N:3]([CH2:13][CH3:14])[C:4](=[O:12])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[Cl:11])[CH3:2].[Cl:15][CH2:16][Si:17](Cl)([CH3:19])[CH3:18]>>[CH2:13]([N:3]([CH2:1][CH3:2])[C:4](=[O:12])[C:5]1[C:10]([Si:17]([CH2:16][Cl:15])([CH3:19])[CH3:18])=[CH:9][CH:8]=[CH:7][C:6]=1[Cl:11])[CH3:14]参加物
3
実験手順
The title compound was prepared according to General Method A from the compound of Example e and 1.5 eq (chloromethyl)dimethylsilyl chloride. Purification by HPLC using 1:9 ethyl acetate/hexanes gave 5.4 g of the desired compound as a yellow oil, an 85% yield.
後処理
- customThe title compound was prepared
- customPurification by HPLC
出典と根拠
- ORDレコード
- ord-50db707cf0e149059d1bd51e3d57c7ab
- 出典データセット
- uspto-grants-2000_10
- 特許番号
- US06133252
関連ノート
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