戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 912154作成日:2026年10月27日

(4-Ethylpiperazin-1-yl)-(4-methyl-3-nitrophenyl)methanone → 5-[(4-Ethylpiperazin-1-YL)carbonyl]-2-methylaniline

https://huagongshe.com/reaction/912154

反応式

関与物質

役割名称HCID仕込み量
反応物(4-Ethylpiperazin-1-yl)-(4-methyl-3-nitrophenyl)methanoneHCID 808340—
触媒HCID 178418390HCID 178418390—
溶媒MethanolHCID 887—
生成物5-[(4-Ethylpiperazin-1-YL)carbonyl]-2-methylanilineHCID 16788734105.8%

反応手順

(4-Ethyl-piperazin-1-yl)-(4-methyl-3-nitro-phenyl)-methanone (1.06 g, 3.82 mmol) obtained in Step A was stirred for 16 hours in methanol (20 ml) under a hydrogen atmosphere in the presence of 10% palladium carbon. After the reaction mixture was filtered, the filtrate was concentrated under reduced pressure, to obtain (4-ethyl-piperazin-1-yl)-(3-amino-4-methyl-phenyl)-methanone (1.0 g, quant.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08022205B2
出典データセットuspto-grants-2011_09
ORD IDord-9e2899b8544e4cc8836a451aa78a67ff
出典メモuspto-grants-2011_09