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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1665601생성일: 2026년 10월 25일

1-Hydroxybenzotriazole → N-Biphenyl-4-yl-3-oxo-3-[4-(3,4,5-trifluoro-benzoyl)-piperazin-1-yl]-propionamide

https://huagongshe.com/reaction/1665601

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물3,4,5-Trifluorobenzoic acidHCID 853154—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물N-Biphenyl-4-yl-3-oxo-3-piperazin-1-yl-propionamide hydrochlorideHCID 66625265—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-Biphenyl-4-yl-3-oxo-3-[4-(3,4,5-trifluoro-benzoyl)-piperazin-1-yl]-propionamideHCID 5787579543.6%

반응 조건

온도10 °C

반응 단계

HOBt (34 mg, 0.25 mmol) and DIPEA (67.9 mg, 0.51 mmol) were added to a stirred solution of 3,4,5-trifluorobenzoic acid (37 mg, 0.21 mmol) in DMF (2 mL). The reaction mixture was cooled to 10° C. and EDCI.HCl (48 mg, 0.25 mmol) followed by N-biphenyl-4-yl-3-oxo-3-piperazin-1-yl-propionamide hydrochloride (75 mg, 0.2 mmol) were added. The reaction mixture was stirred at room temperature overnight then diluted with water. The resulting precipitate was filtered and purified by column chromatography using silica gel 60-120 mesh (40% ethyl acetate in hexane) to afford 42 mg (42%) of N-Biphenyl-4-yl-3-oxo-3-[4-(3,4,5-trifluoro-benzoyl)-piperazin-1-yl]-propionamide. LCMS: 482.16 (M+1)+ 94.2%, 1H NMR: (CDCl3): δ 9.5 (s, 1H), 7.58 (m, 6H), 7.43 (t, 2H), 7.34 (m, 1H), 7.08 (t, 2H), 3.7 (bs, 8H), 3.54 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08039463B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-5d802727d5a049ffabbb331bfcdc6970
출처 메모uspto-grants-2011_10