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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1896114생성일: 2026년 10월 27일

Triethylamine → 2-(4-(Tert-butoxycarbonyl)-1-(4,5-dichloro-2-nitrophenyl)piperazin-2-yl)acetic acid

https://huagongshe.com/reaction/1896114

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1,2-Dichloro-4-fluoro-5-nitrobenzeneHCID 533951—
반응물2-(4-(tert-Butoxycarbonyl)piperazin-2-yl)acetic acidHCID 44607724—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-(4-(Tert-butoxycarbonyl)-1-(4,5-dichloro-2-nitrophenyl)piperazin-2-yl)acetic acidHCID 67249390—

반응 조건

온도50 °C

반응 단계

1,2-Dichloro-4-fluoro-5-nitrobenzene (0.125 mL, 0.952 mmol) and 2-(4-(tert-butoxycarbonyl)piperazin-2-yl)acetic acid (256 mg, 1.048 mmol) were dissolved in N,N-dimethylformamide (2 mL) and water (1 mL). Triethylamine (0.398 mL, 2.86 mmol) was slowly added. The resulting mixture was heated at 50° C. overnight. The mixture was concentrated and ethyl acetate was added. 1 N HCl was then added slowly until the pH=6. The water layer was separated and washed multiple times with ethyl acetate. The organic layers were then combined and concentrated. The crude material was purified by silica gel chromatography eluting with a gradient of 10% to 50% of ethyl acetate in hexane to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 12.32 (br, 1 H), 8.17 (s, 1 H), 7.69 (s, 1 H), 3.36-3.90 (m, 4 H), 2.97-3.29 (m, 2 H), 2.88 (dd, J=8.92, 3.37 Hz, 1 H), 2.18-2.47 (m, 2 H), 1.41 (s, 9 H); MS (DCI+) m/z 434.1 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08518933B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-4b42ad2e1a994449a5da30417fb9d65c
출처 메모uspto-grants-2013_08