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HRID 230300作成日:2026年10月26日

Acetic Acid → N-(4-iodophenyl)pyrimidin-2-amine

https://huagongshe.com/reaction/230300

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物4-IodoanilineHCID 10893—
反応物2-ChloropyrimidineHCID 74404—
反応物Sodium BicarbonateHCID 516892—
溶媒1,4-DioxaneHCID 31275—
生成物N-(4-iodophenyl)pyrimidin-2-amineHCID 5776254854.7%

反応手順

Under an argon atmosphere, 2-chloropyrimidine (16.5 g) and acetic acid (11.7 ml) were added to a solution of 4-iodoaniline (30 g) in dioxane (500 ml), and the resulting mixture was stirred for 13 hours while heating the mixture to reflux. The reaction solution was cooled to room temperature and saturated aqueous sodium hydrogen carbonate solution was added thereto, followed by extracting the resulting mixture 4 times with ethyl acetate. Organic layers were washed 3 times 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/ethyl acetate=4/1). The product was recrystallized from dichloromethane/hexane mixed solvent to obtain N-(4-iodophenyl)pyrimidin-2-amine (22.27 g). NMR (H1, CDCl3): δ 6.73(1H, t, J=4.6 Hz), 7.18 (1H, brs), 7.40-7.42 (2H, m), 7.59-7.61 (2H, m), 8.41 (2H, d, J=4.6 Hz)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566724B2
出典データセットuspto-grants-2009_07
ORD IDord-3c1a4fad856f4545889429657a86ef75
出典メモuspto-grants-2009_07