Dimethyl Sulfoxide → 1-ethyl-7-carboxy-N-(cyclohexylmethyl)-1H-pyrazolo[3,4-b]quinolin-4-amine
反応式
[CH2:1]([N:3]1[C:7]2=[N:8][C:9]3[C:14]([C:15](Cl)=[C:6]2[CH:5]=[N:4]1)=[CH:13][CH:12]=[C:11]([C:17]([OH:19])=[O:18])[CH:10]=3)[CH3:2].CS(C)=O.[CH:24]1([CH2:30][NH2:31])[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1.O>C(O)(=O)C>[CH2:1]([N:3]1[C:7]2=[N:8][C:9]3[C:14]([C:15]([NH:31][CH2:30][CH:24]4[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]4)=[C:6]2[CH:5]=[N:4]1)=[CH:13][CH:12]=[C:11]([C:17]([OH:19])=[O:18])[CH:10]=3)[CH3:2]参加物
6
実験手順
A mixture of 1-ethyl-4-chloro-7-carboxy-1H-pyrazolo[3,4-b]quinoline (0.9 g, 3.3 mmol), DMSO (9 ml) and cyclohexanemethyl amine (0.86 ml, 6.6 mmol) is heated at 120°-130° C. for 6 hours. The reaction mixture is poured into water, acidified with acetic acid and the solid which forms is collected by filtration, dissolved in 5% NaOH and extracted with CH2Cl2 (2×50 ml). The aqueous layer is acidified with acetic acid and the solid that forms is collected by filtration and washed with water. The solid is purified by column chromatography on silica gel eluting with 30% methanol/10% acetic acid/60% CH2Cl2 to afford 1-ethyl-7-carboxy-N-(cyclohexylmethyl)-1H-pyrazolo[3,4-b]quinolin-4-amine, as a yellow solid.
後処理
- temperatureis heated at 120°-130° C. for 6 hours
- filtrationthe solid which forms is collected by filtration
- dissolutiondissolved in 5% NaOH
- extractionextracted with CH2Cl2 (2×50 ml)
- filtrationthe solid that forms is collected by filtration
- washwashed with water
- customThe solid is purified by column chromatography on silica gel eluting with 30% methanol/10% acetic acid/60% CH2Cl2
出典と根拠
- ORDレコード
- ord-3ada8104b7874a67a64c83ef95b934e8
- 出典データセット
- uspto-grants-1999_08
- 特許番号
- US05942520
反応ノート
読み込み中…