戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1984416作成日:2026年10月27日

Sodium Iodide → 2-ethyl-1-[4-(4-pyridin-2-ylpiperazin-1-yl)butyl]-2H-pyrazolo[3,4-c]quinolin-4-amine monohydrate

https://huagongshe.com/reaction/1984416

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Potassium CarbonateHCID 11430—
反応物1-(2-Pyridyl)piperazineHCID 94459—
反応物1-(4-chlorobutyl)-2-ethyl-2H-pyrazolo[3,4-c]quinolin-4-amineHCID 57717514—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-ethyl-1-[4-(4-pyridin-2-ylpiperazin-1-yl)butyl]-2H-pyrazolo[3,4-c]quinolin-4-amine monohydrateHCID 6695856294.8%

反応条件

温度60 °C

反応手順

A mixture of 1-(4-chlorobutyl)-2-ethyl-2H-pyrazolo[3,4-c]quinoline-4-amine (prepared as described in Example 19, 1.0 g, 3.3 mmol), 1-(2-pyridyl)piperazine (0.752 mL, 4.95 mmol), potassium carbonate (1.8 g, 13.2 mmol), and sodium iodide (123 mg, 0.825 mmol) in DMF (6 mL) was heated at 60° C. for 1 hour, then at 90° C. for 2 hours. The reaction was allowed to cool to ambient temperature and white solid formed. Water (100 mL) was added to the mixture. The mixture was stirred for 30 min and the solid was isolated by filtration and dried to yield 1.4 g of 2-ethyl-1-[4-(4-pyridin-2-ylpiperazin-1-yl)butyl]-2H-pyrazolo[3,4-c]quinolin-4-amine monohydrate as a white solid, mp 183-184° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07544697B2
出典データセットuspto-grants-2009_06
ORD IDord-5eae0d2446d24be28b3e211cd9403b5b
出典メモuspto-grants-2009_06