反応式
[CH2:1]([NH:3][C:4](=[O:12])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[Cl:11])[CH3:2].[CH:13]([Si:15](Cl)([CH3:17])[CH3:16])=[CH2:14]>>[CH2:1]([NH:3][C:4](=[O:12])[C:5]1[C:10]([Si:15]([CH:13]=[CH2:14])([CH3:17])[CH3:16])=[CH:9][CH:8]=[CH:7][C:6]=1[Cl:11])[CH3:2]参加物
3
実験手順
The title compound was prepared from the compound of Example f and 1.5 eq vinyldimethylsilyl chloride according to General Method C. Purification by HPLC with 1:4 ethyl acetate/hexanes gave 630 mg of the desired product as a white solid, a 9% yield. m.p. 86°-89° C.
後処理
- customPurification by HPLC with 1:4 ethyl acetate/hexanes
出典と根拠
- ORDレコード
- ord-ad201deba8f94feb8c7087a4d4f949a3
- 出典データセット
- uspto-grants-1998_01
- 特許番号
- US05705513
関連ノート
読み込み中…