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HRID 522936作成日:2026年10月26日

1,5-Dichloroanthraquinone → 1,5-Bis((2-(dimethylamino)ethyl)(methyl)amino)anthracene-9,10-dione

https://huagongshe.com/reaction/522936

反応式

関与物質

役割名称HCID仕込み量
反応物1,5-DichloroanthraquinoneHCID 6711—
反応物1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
溶媒WaterHCID 962—
生成物1,5-Bis((2-(dimethylamino)ethyl)(methyl)amino)anthracene-9,10-dioneHCID 59229118—

反応手順

A mixture of 1,5-dichloroanthraquinone (5.5 g, 20 mmol) and N,N,N′-trimethylethylenediamine (40 ml) was refluxed for 18 h. The mixture was cooled to room temperature, diluted with water (400 mL) and extracted with chloroform (2×200 mL). The combined organic layer was washed with water, brine, dried over MgSO4 and evaporated to dryness. The residue thus obtained was purified by silica gel flash chromatography [CHCl3/MeOH/Et3N (44:5:1)] to provide Compound 9. Abs (max, PBS pH 7.4)=508 nm. The structure of Compound 9 is given below:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09334281B2
出典データセットuspto-grants-2016_05
ORD IDord-e3151e542a2f4975a8558c2400efa07e
出典メモuspto-grants-2016_05