反応式
[CH3:1][CH2:2][N:3]([CH2:6][CH2:7][NH:8][C:9]([C:11]1[C:12]([CH3:29])=[C:13](/[CH:17]=[C:18]2/[C:19]3[CH:20]=[C:21]([F:28])[CH:22]=[CH:23][C:24]=3[NH:25][C:26]/2=[O:27])[NH:14][C:15]=1[CH3:16])=[O:10])[CH2:4][CH3:5].Cl.[OH-].[Na+]>O>[CH3:1][CH2:2][N:3]([CH2:6][CH2:7][NH:8][C:9]([C:11]1[C:12]([CH3:29])=[C:13](/[CH:17]=[C:18]2/[C:19]3[CH:20]=[C:21]([F:28])[CH:22]=[CH:23][C:24]=3[NH:25][C:26]/2=[O:27])[NH:14][C:15]=1[CH3:16])=[O:10])[CH2:4][CH3:5]参加物
4
反応条件
- 温度
- 90 °C
実験手順
Sunitinib hydrochloride (1.0 g) and H2O (60 mL) was added into a flask in r.t. and heated to 90° C., the mixture turned clear, pH of the mixture was adjusted to 8˜9 with 1N NaOH and cooled r.t. stirred over night, filtered, washed, dried in vacuo to give 0.67 g of crude sunitinib with 99.0% purity by HPLC analysis in 78.3% yield.
後処理
- temperaturecooled r.t.
- filtrationfiltered
- washwashed
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-ec7d05eb1cef40c8b6783229183d3fe6
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08846953B2
関連ノート
読み込み中…