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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 605881생성일: 2026년 10월 27일

2,4-Dichloro-5-fluoropyrimidine → 2-chloro-5-fluoro-N4-[4-(prop-2-ynyloxy)phenyl]-4-pyrimidineamine

https://huagongshe.com/reaction/605881

반응식

참여 물질

역할이름HCID투입량
반응물2,4-Dichloro-5-fluoropyrimidineHCID 250705—
반응물4-(Prop-2-yn-1-yloxy)anilineHCID 12668862—
용매Ethyl AcetateHCID 8857—
용매Methanol--water (1/1)HCID 22242641—
생성물2-chloro-5-fluoro-N4-[4-(prop-2-ynyloxy)phenyl]-4-pyrimidineamineHCID 57562899243.6%

반응 단계

Crude 4-(prop-2-ynyloxy)aniline (0.750 g, 5.10 mmol) and 2,4-dichloro-5-fluoropyrimidine (1.27 g, 0.760 mmol) were stirred in MeOH/water (4:1, 35 mL) at room temperature for 18 h. The reaction mixture was diluted with EtOAc (200 mL) and washed with 1N HCl (50 mL) and brine (50 mL). The organic layer was dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (silica gel, hexanes ramped to EtOAc:hexanes (1:10)) to provide 2-chloro-5-fluoro-N4-[4-(prop-2-ynyloxy)phenyl]-4-pyrimidineamine as a light brown solid (0.514 g). 1H NMR (CDCl3): δ 8.03 (d, J=2.7 Hz, 1H), 7.53 (d, J=8.7 Hz, 2H), 7.02 (d, J=8.7 Hz, 2H), 6.86 (s, 1H), 4.71 (d, J=2.4 Hz, 2H), 2.55 (t, J=2.4 Hz, 1H); LCMS: purity: 99%; MS (m/e): 279 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915273B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-ceb45e435ce34acd99ba8ed4e2c6a205
출처 메모uspto-grants-2011_03