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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1035277생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1035277

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, 1H), 8.17 (s, 1H), 7.69 (s, 1H), 3.36-3.90 (m, 4H), 2.97-3.29 (m, 2H), 2.88 (dd, J=8.92, 3.37 Hz, 1H), 2.18-2.47 (m, 2H), 1.41 (s, 9H); MS (DCI+) m/z 434.1 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08546377B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-8f16ccf92fca4fb8ace579f73593c7be
출처 메모uspto-grants-2013_10