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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 722118생성일: 2026년 10월 26일

Hydroxylamine → 9-(4-Fluorobenzyl)-N-Hydroxy-9h-Beta-Carboline-3-Carboxamide

https://huagongshe.com/reaction/722118

반응식

참여 물질

역할이름HCID투입량
반응물HydroxylamineHCID 787—
반응물Sodium hydrideHCID 24758—
반응물4-Fluorobenzyl bromideHCID 68021—
반응물Ethyl Beta-Carboline-3-CarboxylateHCID 105078—
용매MethanolHCID 887—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물9-(4-Fluorobenzyl)-N-Hydroxy-9h-Beta-Carboline-3-CarboxamideHCID 301345939%

반응 단계

To a stirred solution of ethyl 9H-β-carboline-3-carboxylate (368 mg, 1.53 mmol) in DMF (4 mL) under a nitrogen atmosphere was added NaH (61.2 mg, 60% in mineral oil, 1.53 mmol) portionwise, followed by 4-fluorobenzyl bromide (0.19 mL, 1.53 mmol). Stirring was continued for 24 hours at ambient temperature, water (10 mL) was then added to the mixture. The precipitate was filtered, washed with water and dried to give a solid that was dissolved in methanol (20 mL). To the resulting solution, H2NOH (20 mL, 50 wt. % solution in H2O, 0.30 mol) was added. The suspension was stirred for 5 days at ambient temperature. The mixture was then filtered, and the solid was boiled in methanol (40 mL). After filtration, the title product (0.20 g, 39%) was obtained. 1H NMR (300 MHz, DMSO-d6): δ 11.28 (1H, s), 9.02–9.08 (2H, m), 8.85 (1H, s), 8.48 (1H, d, J=9.0 Hz), 7.10–7.84 (7H, m), 5.85 (2H, s). HRMS (M+H)+ found: 336.1157. Calcd for C19H15N3O2F: 336.1148.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07138408B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-ab202bdd67744da588d578813329d47f
출처 메모uspto-grants-2006_11