反応式
[OH:1][CH:2]([CH3:34])[CH2:3][NH:4][CH2:5][CH2:6][NH:7][C:8]1[C:21]2[C:20](=[O:22])[C:19]3[C:14](=[C:15]([OH:24])[CH:16]=[CH:17][C:18]=3[OH:23])[C:13](=[O:25])[C:12]=2[C:11]([NH:26][CH2:27][CH2:28][NH:29][CH2:30][CH:31]([OH:33])[CH3:32])=[CH:10][CH:9]=1.[C:35]([OH:40])(=[O:39])[CH:36]([CH3:38])[OH:37].C(O)C>CC(C)=O>[C:35]([OH:40])(=[O:39])[CH:36]([CH3:38])[OH:37].[C:35]([OH:40])(=[O:39])[CH:36]([CH3:38])[OH:37].[OH:1][CH:2]([CH3:34])[CH2:3][NH:4][CH2:5][CH2:6][NH:7][C:8]1[C:21]2[C:20](=[O:22])[C:19]3[C:14](=[C:15]([OH:24])[CH:16]=[CH:17][C:18]=3[OH:23])[C:13](=[O:25])[C:12]=2[C:11]([NH:26][CH2:27][CH2:28][NH:29][CH2:30][CH:31]([OH:33])[CH3:32])=[CH:10][CH:9]=1参加物
5
実験手順
A mixture of 228 mg. of 1,4-bis[2-(2- hydroxypropylamino)ethylamino]-5,8-dihydroxyanthraquinone, 120 mg. of 80% DL-lactic acid, and 10 ml. of ethanol is heated on a steam bath for 10 minutes, cooled, treated with 50 ml. of acetone and cooled to obtain the title compound.
後処理
- additionA mixture of 228 mg
- temperaturecooled
- additiontreated with 50 ml
出典と根拠
- ORDレコード
- ord-9c4bb4e21d134267b17ad23616663b7f
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04614618
関連ノート
読み込み中…