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HRID 639465作成日:2026年10月26日

2,4-Difluorobenzoic acid → t-Butyl 4-(2,4-difluorobenzoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/639465

反応式

関与物質

役割名称HCID仕込み量
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—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
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 EDCl 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-difluorobenzoyi)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US07691869B2
出典データセットuspto-grants-2010_04
ORD IDord-82a25cea578d45319caaf2457edebde3
出典メモuspto-grants-2010_04