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HRID 3155作成日:2026年10月23日

N,N-Dimethylethylenediamine → 6-(((dimethylamino)ethyl)amino)-3-fluoro-7H-indeno[2,1-c]quinoline-7-on dihydrochloride

https://huagongshe.com/ja/reaction/3155

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylethylenediamineHCID 66053—
反応物6-chloro-3-fluoro-7H-indeno[2,1-c]quinoline-7-onHCID 19356100—
生成物6-(((dimethylamino)ethyl)amino)-3-fluoro-7H-indeno[2,1-c]quinoline-7-on dihydrochlorideHCID 1935611568.6%

反応条件

温度90 °C

反応手順

To a suspension of 6-chloro-3-fluoro-7H-indeno[2,1-c]quinoline-7-on (860 mg, 3.0 mmol) in pyrydine (10 ml) was added N,N-dimethylethylenediamine (800 mg, 9.0 mmol), and the mixture was stirred with heat at 90° C. for 12 hours. The reaction mixture was distilled to dryness. To the residue was added water and chloroform for extraction. The chloroform layer was dried over magnesium sulfate and evaporated. The residue was purified by silica gel column chromatography (eluent; chloroform:ethanol=10:1(v/v)). The purified material was dissolved in 20 ml of tetrahydrofuran. To the the solution was added 4N-hydrochloride/dioxane (2 ml) and the mixture was concentrated under reduced pressure. The residue obtained was crystallized from diethylether to give 420 mg (yield 34.3%) of title compound. The physicochemical properties thereof are shown in table 1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733918
出典データセットuspto-grants-1998_03
ORD IDord-afb2bac37106446f80150be5390395af
出典メモuspto-grants-1998_03