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HRID 723661作成日:2026年10月27日

Tetrahydrofuran → 4-Fluoro-N-[2-(5-methyl-2-furanyl)ethyl]benzamide

https://huagongshe.com/reaction/723661

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物TriethylamineHCID 8471—
反応物4-Fluorophenylacetyl chlorideHCID 3744988—
反応物2-(5-Methylfuran-2-yl)ethan-1-amineHCID 14933778—
生成物4-Fluoro-N-[2-(5-methyl-2-furanyl)ethyl]benzamideHCID 2187484695%

反応手順

4-Fluorophenylacetyl chloride (0.290 mL, 2.44 mmol) was added dropwise to a solution of β-(5-methyl-2-furanyl)ethanamine (300 mg, 2.44 mmol, made according to the procedure of Yur'ev et al. J. Gen. Chem. USSR (Engl. Transl.) 33, 3444–8 (1963)) in THF (2.5 mL) at rt, followed by the dropwise addition of Et3N (0.340 mL, 2.44 mmol). Once the starting material was consumed, as was evident by HPLC, the reaction was quenched with H2O and extracted with CH2Cl2. The combined organic layers were dried over MgSO4 and concentrated under reduced pressure. Purification by flash chromatography on silica gel eluting with a gradient of 0–50% EtOAc/hexane gave 523 mg (95%) of compound 237A as a white solid. HPLC: 99% at 2.84 min (retention time) (Phenomenex-prime S5-C18 column 4.6×50 mm eluting with 1090% aqueous methanol over 4 minutes containing 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm). MS (ES): m/z 248.15 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07141578B2
出典データセットuspto-grants-2006_11
ORD IDord-2dca0ba2cdac47c0a7d8c908db8f5311
出典メモuspto-grants-2006_11