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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1687209생성일: 2026년 10월 27일

Water → (2,5-Dichloro-pyrimidin-4-yl)-(3-morpholin-4-yl-phenyl)-amine

https://huagongshe.com/reaction/1687209

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물2,4,5-TrichloropyrimidineHCID 237259—
반응물3-(Morpholin-4-yl)anilineHCID 847768—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물(2,5-Dichloro-pyrimidin-4-yl)-(3-morpholin-4-yl-phenyl)-amineHCID 86633892—

반응 단계

2,4,5-Trichloropyrimidine (0.960 g, 5.2 mmol) was dissolved in tetrahydrofuran (20 mL). Potassium carbonate (1.20 g, 8.70 mmol) was added, followed by 3-morpholinoaniline (0.875 g, 4.90 mmol). After stirring overnight, water (30 mL) and dichloromethane (30 mL) were added, the phases separated and the aqueous layer extracted once with dichloromethane (30 mL). The combined organic fractions were dried over sodium sulfate, concentrated onto silica gel and chromatographed (120 g SiO2, 0-50% EA:Hex). (2,5-Dichloro-pyrimidin-4-yl)-(3-morpholin-4-yl-phenyl)-amine was isolated as an off-white solid (1.16 g, 73%). m.p.=142-145° C.; LCMS (m/e) 325 (M+1); 1H-NMR (CDCl3, 400 MHz) δ 8.20 (s, 1H), 7.38 (s, 1H), 7.28 (m, 1H), 7.21 (s, 1H), 7.01 (d, 1H, J=7.8 Hz), 6.75 (d, 1H, J=8.4 Hz), 3.88 (t, 4H, J=4.8 Hz), 3.21 (t, 4H, J=4.8 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08148391B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-cd86d93a7cc94ce381caa92fe7d30eed
출처 메모uspto-grants-2012_04