Diethylamine → 3,6-Bis(4-diethylaminobutoxy)acridine trihydrochloride
反応式
[ClH:1].[Cl:2][CH2:3][CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:9]=[CH:10][C:11]2[C:20]([CH:21]=1)=[N:19][C:18]1[C:13](=[CH:14][CH:15]=[C:16]([O:22][CH2:23][CH2:24][CH2:25][CH2:26]Cl)[CH:17]=1)[CH:12]=2.[CH2:28]([NH:30][CH2:31][CH3:32])[CH3:29]>>[ClH:2].[ClH:1].[ClH:2].[CH2:28]([N:30]([CH2:31][CH3:32])[CH2:3][CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:9]=[CH:10][C:11]2[C:20]([CH:21]=1)=[N:19][C:18]1[C:13](=[CH:14][CH:15]=[C:16]([O:22][CH2:23][CH2:24][CH2:25][CH2:26][N:19]([CH2:20][CH3:11])[CH2:18][CH3:17])[CH:17]=1)[CH:12]=2)[CH3:29]参加物
3
実験手順
A mixture of 2.0 g. of 3,6-bis(4-chlorobutoxy) acridine hydrochloride and 150 ml. of diethylamine is heated in a steel bomb at 100° C. for 24 hours. The excess diethylamine is removed under reduced pressure. The residue is dissolved in 150 ml. of chloroform and this chloroform solution is washed with two 30 ml. portions of saturated aqueous sodium bicarbonate, then dried over sodium sulfate and filtered. The chlorofrom is evaporated and the residue is dissolved in 50 ml. of absolute ethanol. A 10 ml. portion of 6 N hydrochloric acid in isopropanol is added giving the desired product as yellow crystals.
後処理
- additionA mixture of 2.0 g
- customThe excess diethylamine is removed under reduced pressure
- dissolutionThe residue is dissolved in 150 ml
- washof chloroform and this chloroform solution is washed with two 30 ml
- dry with materialportions of saturated aqueous sodium bicarbonate, then dried over sodium sulfate
- filtrationfiltered
- customThe chlorofrom is evaporated
- dissolutionthe residue is dissolved in 50 ml
- additionportion of 6 N hydrochloric acid in isopropanol is added
出典と根拠
- ORDレコード
- ord-a85676bb159f43a2a4936ca80286b5a0
- 出典データセット
- uspto-grants-1982_02
- 特許番号
- US04314061
反応ノート
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