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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 639465생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/639465

반응식

참여 물질

역할이름HCID투입량
반응물2,4-Difluorobenzoic acidHCID 74102—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물t-Butyl 4-(2,4-difluorobenzoyl)piperazine-1-carboxylateHCID 68414338—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07691869B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-82a25cea578d45319caaf2457edebde3
출처 메모uspto-grants-2010_04