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HRID 1365638作成日:2026年10月26日

Iodoethane → N-(4-iodophenyl)-N-ethylpyrimidin-2-amine

https://huagongshe.com/reaction/1365638

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Sodium hydrideHCID 24758—
反応物N-(4-iodophenyl)pyrimidin-2-amineHCID 57762548—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物N-(4-iodophenyl)-N-ethylpyrimidin-2-amineHCID 57762566—

反応手順

Under an argon atmosphere, a solution of N-(4-iodophenyl)pyrimidin-2-amine (255 mg) in anhydrous DMF (1 ml) was added dropwise to a suspension of sodium hydride (40 mg) in anhydrous DMF (1 ml), and the resulting mixture was stirred at room temperature for 75 minutes. Ethyl iodide (0.10 ml) was added dropwise to the reaction solution and the resulting mixture was stirred at room temperature overnight. Saturated brine was added thereto and the resulting mixture was extracted with chloroform. Organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by column chromatography (silica gel, eluent: cyclohexane/chloroform=1/10) to obtain N-(4-iodophenyl)-N-ethylpyrimidin-2-amine (264 mg). NMR (H1, CDCl3): δ 1.23 (3H, t, J=6.8 Hz), 4.01 (2H, q, J=6.8 Hz), 6.57 (1H, t, J=4.9 Hz), 7.03-7.06 (2H, m), 7.70-7.74 (2H, m), 8.32 (2H, d, J=4.9 Hz)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07893046B2
出典データセットuspto-grants-2011_02
ORD IDord-518ab98fab034534ac24799b9be2526f
出典メモuspto-grants-2011_02