反応式
[C:1]1([CH3:22])[CH:6]=[CH:5][C:4]([N:7]2[CH2:12][CH2:11][N:10]([CH2:13][C:14]3[C:15]([NH2:21])=[N:16][C:17]([NH2:20])=[N:18][CH:19]=3)[CH2:9][CH2:8]2)=[CH:3][CH:2]=1.[ClH:23]>CO>[ClH:23].[ClH:23].[C:1]1([CH3:22])[CH:2]=[CH:3][C:4]([N:7]2[CH2:8][CH2:9][N:10]([CH2:13][C:14]3[C:15]([NH2:21])=[N:16][C:17]([NH2:20])=[N:18][CH:19]=3)[CH2:11][CH2:12]2)=[CH:5][CH:6]=1参加物
4
実験手順
0.23 g (0.00077 mol) of 5-(4-p-tolyl-piperazin-1-ylmethyl)-pyrimidine-2,4-diamine was dissolved in 220 ml of hot methanol. The solution was treated at room temperature with 0.44 ml (0.00154 mol) of 3.5N ethanolic hydrochloric acid. The solution was completely freed from the solvents and the residue was recrystallized from ethanol/diethyl ether. 0.22 g (77%) of 5-(4-p-tolyl-piperazin-1-ylmethyl)-pyrimidine-2,4-diamine dihydrochloride was obtained as whited crystals; m.p. 220°-222°.
後処理
- customthe residue was recrystallized from ethanol/diethyl ether
出典と根拠
- ORDレコード
- ord-60f3192f14224afc936563c5caeac9ae
- 出典データセット
- uspto-grants-1997_11
- 特許番号
- US05688798
関連ノート
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