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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79113생성일: 2026년 10월 23일

N-Cyclohexylaniline → (5-Bromo-2-chloro-pyrimidin-4-yl)-cyclohexyl-phenyl-amine

https://huagongshe.com/ko/reaction/79113

반응식

참여 물질

역할이름HCID투입량
반응물N-CyclohexylanilineHCID 74567—
반응물5-Bromo-2,4-dichloropyrimidineHCID 289973—
용매Ethyl AcetateHCID 8857—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물(5-Bromo-2-chloro-pyrimidin-4-yl)-cyclohexyl-phenyl-amineHCID 5829958924%

반응 조건

온도120 °C

반응 단계

5-Bromo-2,4-dichloro-pyrimidine (2.17 ml, 17.14 mmol) and cyclohexyl-phenyl-amine (2.0 g, 11.43 mmol) were dissolved in N-methylpyrrolidone (NMP) (25 ml), and this reaction was heated to 120° C. for 24 hours. The reaction was cooled to room temperature and diluted with ethyl acetate, washed with water and brine. The organic phase was dried using sodium sulfate and concentrated. Purification by flash chromatography (ethyl acetate/hexane) gave compound 37 as a yellow solid (855 mg, 24%). 1H NMR (500 MHz, DMSO-d6) δ ppm 8.27 (1 H, s), 7.41 (3 H, m), 7.21 (2 H, m), 4.62 (1 H, m), 1.93 (2 H, d, J=10 Hz), 1.75 (2 H, d, J=10 Hz), 1.58 (1 H, d, J=10 Hz), 1.34 (2 H, m), 1.15 (2 H, m), 0.91 (1 H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841312B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-6e09e02edeb2407fa29c35bb3c7b1f63
출처 메모uspto-grants-2014_09