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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3155생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylethylenediamineHCID 66053—
반응물6-chloro-3-fluoro-7H-indeno[2,1-c]quinoline-7-onHCID 19356100—
생성물6-(((dimethylamino)ethyl)amino)-3-fluoro-7H-indeno[2,1-c]quinoline-7-on dihydrochlorideHCID 1935611568.6%

반응 조건

온도90 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733918
출처 데이터셋uspto-grants-1998_03
ORD IDord-afb2bac37106446f80150be5390395af
출처 메모uspto-grants-1998_03