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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1035270생성일: 2026년 10월 25일

Potassium Carbonate → 2-(1-(5-Bromo-2-nitrophenyl)-4-(tert-butoxycarbonyl)piperazin-2-yl)acetic acid

https://huagongshe.com/reaction/1035270

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-Bromo-2-fluoro-1-nitrobenzeneHCID 2783362—
반응물2-(4-(tert-Butoxycarbonyl)piperazin-2-yl)acetic acidHCID 44607724—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물2-(1-(5-Bromo-2-nitrophenyl)-4-(tert-butoxycarbonyl)piperazin-2-yl)acetic acidHCID 67248179—

반응 조건

온도70 °C

반응 단계

4-Bromo-2-fluoro-1-nitrobenzene (5.3 g, 24.1 mmol) was dissolved in acetonitrile (70 mL) and water (10 mL). To this mixture, potassium carbonate (10 g, 72.3 mmol) and 2-(4-(tert-butoxycarbonyl)piperazin-2-yl)acetic acid (7.1 g, 28.9 mmol) were added. The resulting mixture was heated at 70° C. for 2 days. The mixture thus obtained was concentrated and ethyl acetate was added. 1 N HCl was then added slowly to the reaction solution until pH=6. The water layer was separated and washed multiple times with ethyl acetate. The organic layers thus obtained were combined and concentrated. The crude material thus obtained was purified by silica gel chromatography eluting with a gradient of 0% to 10% of methanol in dichloromethane to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 12.28 (br s), 7.71-7.83 (m, 1H), 7.56-7.66 (m, 1H), 7.30-7.40 (m, 1H), 3.56-3.82 (m, 3H), 3.33-3.44 (m, 1H), 2.99-3.24 (m, 2H), 2.87 (m, 1H), 2.32-2.47 (m, 1H), 2.17-2.29 (m, 1H), 1.32-1.51 (s, 9H); MS (DCI+) m/z 444.1 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08546377B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-53c9427b942044f38f12349787042f79
출처 메모uspto-grants-2013_10