戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2239791作成日:2026年10月26日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → t-Butyl 4-(2,4-difluorobenzoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2239791

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物2,4-Difluorobenzoic acidHCID 74102—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物DiisopropylethylamineHCID 81531—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物t-Butyl 4-(2,4-difluorobenzoyl)piperazine-1-carboxylateHCID 68414338—

反応手順

To a solution of 3.0 g (19 mmol) of 2,4-difluorobenzoic acid and 4 mL of DIEA (1.2 equiv.) in 40 mL of dry DCM is added 3.08 g (1.2 equiv) of HOBt and 4.2 g (22.55 mmol) of t-butyl piperazine-1-carboxylate, and the mixture was stirred at RT for 30 min. 4.4 g (11 equiv.) of EDCI are added and the reaction mixture is stirred overnight at RT. Water is added and the resulting mixture is extracted with DCM. The organic layer is dried over anhydrous MgSO4, filtered and concentrated in vacuo to obtain t-butyl 4-(2,4-difluorobenzoyl)piperazine-1-carboxylate as a yellow oil: 1H NMR (CDCl3, 400 MHz) δ 1.47 (s, 9H), 3.30 (m, 2H), 3.41 (m, 2H), 3.53 (m, 2H), 3.76 (m, 2H), 6.86 (dt, 1H, J=8.8 Hz and 0.8 Hz), 6.97 (dt, 1H, J=8.8 Hz and 0.8 Hz), 7.41 (dd, 1H, J=14.4 Hz and 7.2 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07723343B2
出典データセットuspto-grants-2010_05
ORD IDord-679f271b197c495091710f823684a374
出典メモuspto-grants-2010_05