Water → 4-Chloro-5-methyl-1H-indole-2,3-dione
反応式
[Cl:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4](SC)[C:5](=[O:12])[NH:6]2.ClN1C(=[O:21])CCC1=O.C1COCC1.O>C(Cl)(Cl)(Cl)Cl>[Cl:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[C:7]2[C:3]=1[C:4](=[O:21])[C:5](=[O:12])[NH:6]2参加物
6
実験手順
This compound is prepared according to the procedure described in step B of Preparation 1.23, starting with 0.72 g of 4-chloro-5-methyl-3-methylthio-1,3-dihydro-2H-indol-2-one and 0.422 g of N-chloro-succinimide in 72 ml of carbon tetrachloride, and then 58 ml of THF and 14 ml of water. The product obtained is chromatographed on silica gel, eluting with DCM and then with a gradient of a DCM/EtOAc mixture up to (90/10; v/v). 0.5 g of the expected product is obtained.
後処理
- customThis compound is prepared
- customdescribed in step B of Preparation 1.23
- customThe product obtained
- customis chromatographed on silica gel
- washeluting with DCM
出典と根拠
- ORDレコード
- ord-f6d086a95a9645c9a0aaeb197e4a8f97
- 出典データセット
- uspto-grants-2005_03
- 特許番号
- US06864277B2
反応ノート
読み込み中…