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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1752053생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1752053

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Sodium hydrideHCID 24758—
반응물N-(4-iodophenyl)pyrimidin-2-amineHCID 57762548—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물N-(4-iodophenyl)-N-ethylpyrimidin-2-amineHCID 57762566—

반응 단계

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)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09162988B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-b243e64e209244ba96acac282bbdf298
출처 메모uspto-grants-2015_10