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HRID 15783作成日:2026年10月27日

3-(2-[4-(2-Methyl-5-quinolinyl)-1-piperazinyl]ethyl}aniline → 3-{2-[4-(7-Chloro-2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}aniline

https://huagongshe.com/reaction/15783

反応式

関与物質

役割名称HCID仕込み量
反応物3-(2-[4-(2-Methyl-5-quinolinyl)-1-piperazinyl]ethyl}anilineHCID 49852105—
反応物7-Chloro-2-methyl-5-{4-[2-(3-nitrophenyl)ethyl]-1-piperazinyl}quinolineHCID 57444276—
生成物3-{2-[4-(7-Chloro-2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}anilineHCID 5744430992%

反応手順

The title compound was prepared in 92% yield using a similar procedure to description D6 starting from 7-Chloro-2-methyl-5-{4-[2-(3-nitrophenyl)ethyl]-1-piperazinyl}quinoline (D17).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732600B2
出典データセットuspto-grants-2010_06
ORD IDord-20c0a7ab65af41009b9addb9b4f0782f
出典メモuspto-grants-2010_06