戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 722118作成日:2026年10月27日

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

https://huagongshe.com/reaction/722118

反応式

関与物質

役割名称HCID仕込み量
反応物HydroxylamineHCID 787—
反応物Sodium hydrideHCID 24758—
反応物4-Fluorobenzyl bromideHCID 68021—
反応物Ethyl Beta-Carboline-3-CarboxylateHCID 105078—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物9-(4-Fluorobenzyl)-N-Hydroxy-9h-Beta-Carboline-3-CarboxamideHCID 301345939%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07138408B2
出典データセットuspto-grants-2006_11
ORD IDord-ab202bdd67744da588d578813329d47f
出典メモuspto-grants-2006_11