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HRID 845413作成日:2026年10月24日

Chloroform → 4-amino-6,7-dimethoxy-2-[4-(N-phenylcarbamoyl)piperazin-1-yl]quinoline dihydrochloride

https://huagongshe.com/ja/reaction/845413

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroformHCID 6212—
反応物Phenyl isocyanateHCID 7672—
反応物4-Amino-6,7-dimethoxy-2-(piperazin-1-yl)quinolineHCID 14068998—
生成物4-amino-6,7-dimethoxy-2-[4-(N-phenylcarbamoyl)piperazin-1-yl]quinoline dihydrochlorideHCID 20131131—

反応手順

Phenylisocyanate (1.1 g) was added to a stirred suspension of 4-amino-6,7-dimethoxy-2-(piperazin-1-yl)quinoline (0.72 g) in chloroform (25 ml) a room temperature and the reaction mixture was stirred for 4 hours. The mixture was evaporated in vacuo, the residue taken up in methanol-chloroform and treated with ethereal hydrogen chloride. The crude product was purified by chromatography on silica gel eluting with methylene chloride followed by chloroform/methanol and then recrystallised from methanol/ether to give 4-amino-6,7-dimethoxy-2-[4-(N-phenylcarbamoyl)piperazin-1-yl]quinoline dihydrochloride (0.18 g), m.p. 235°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04758568
出典データセットuspto-grants-1988_07
ORD IDord-7c57e5701076476490997332b4bee357
出典メモuspto-grants-1988_07