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HRID 1981517作成日:2026年10月25日

Floxacrine → S 82-5455

https://huagongshe.com/reaction/1981517

反応式

関与物質

役割名称HCID仕込み量
反応物FloxacrineHCID 68708—
反応物1-Amino-4-methylpiperazineHCID 81349—
溶媒EthanolHCID 702—
生成物S 82-5455HCID 3086317—

反応手順

40.75 g (0.1 mole) of 3-(4-trifluoromethylphenyl)-7-chloro-10-hydroxy-3,4-dihydroacridine-1,9(2H,10H)-dione are suspended in 500 ml of ethanol, 11.5 g (0.1 mole) of N-methyl-N'-aminopiperazine are added and the reaction mixture is heated to reflux for 30 minutes. A clear orange-red solution forms during this. After cooling down, the ethanol is distilled out in a rotary evaporator and the solid residue is recrystallized from toluene/cyclohexane (1:1). 43 g=85% of theory of the title compound is thus obtained in the form of orange-yellow crystals of melting point 213° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04593027
出典データセットuspto-grants-1986_06
ORD IDord-ddd22445b8dd44f5b8871cbe8470a71a
出典メモuspto-grants-1986_06