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HRID 603164作成日:2026年10月27日

3-Chloro-4-(trifluoromethyl)aniline → N-[3-chloro-4-(trifluoromethyl)phenyl]-4-[(1-methylpiperidin-3-yl)methyl]piperazine-1-carboxamide

https://huagongshe.com/reaction/603164

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-4-(trifluoromethyl)anilineHCID 67962—
反応物Di-tert-butyl dicarbonateHCID 90495—
反応物1-[(1-Methylpiperidin-3-yl)methyl]piperazineHCID 2736940—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒ChloroformHCID 6212—
生成物N-[3-chloro-4-(trifluoromethyl)phenyl]-4-[(1-methylpiperidin-3-yl)methyl]piperazine-1-carboxamideHCID 115969126.7%

反応手順

To a solution of di-tert-butyl dicarbonate (114.6 mg) in chloroform (2 ml) was added 4-dimethylaminopyridine (6 mg). A solution of 4-amino-2-chlorobenzotrifluoride (98.1 mg) in chloroform (2 ml) was added and the reaction mixture stirred for 20 minutes at room temperature. A solution of 1-[(1-methylpiperidin-3-yl)methyl]piperazine (98.5 mg) in chloroform (2 ml) was added and the resulting solution was stirred at reflux for 18 hours. The reaction mixture was purified by column chromatography on silica gel (20 g) using a gradient of 100% dichloromethane through to 20% methanolic ammonia in dichloromethane to give the title compound (14 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07906645B2
出典データセットuspto-grants-2011_03
ORD IDord-756c6bebf35b4f39a1dcfd943e37587b
出典メモuspto-grants-2011_03