Mitoxantrone → HCID 12888484、化合物
反応式
[OH:1][CH2:2][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][CH2:31][OH:32])=[CH:10][CH:9]=1.[F:33][C:34]([F:41])([F:40])[C:35]([O:37]CC)=O>CO>[OH:1][CH2:2][CH2:3][N: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][N:29]([CH2:30][CH2:31][OH:32])[C:35](=[O:37])[C:34]([F:33])([F:40])[F:41])=[CH:10][CH:9]=1)[C:35](=[O:37])[C:34]([F:41])([F:40])[F:33]参加物
4
実験手順
A suspension of 1.50 g. of 1,4-bis[2-(2-hydroxyethylamino)ethylamino]-5,8-dihydroxyanthraquinone in 75 ml. of ethyl triflouroacetate and 75 ml. of methanol is stirred for 10 minutes. Evaporation of the resulting solution in vacuo at 30° C. leaves a residue which is washed and macerated with methylene chloride, giving 2.11 g. of blue-black solid, m.p. 162° C.
後処理
- additionA suspension of 1.50 g