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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1512142생성일: 2026년 10월 27일

Morpholine → 4,4'-(6-Chloropyrimidine-2,4-diyl)dimorpholine

https://huagongshe.com/reaction/1512142

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물4-(4,6-Dichloropyrimidin-2-yl)morpholineHCID 2772068—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물4,4'-(6-Chloropyrimidine-2,4-diyl)dimorpholineHCID 68633493%

반응 조건

온도85 °C

반응 단계

To a slurry of 2-morpholino-4,6-dichloropyrimidine (prepared as in Method 22, 2.0 g, 8.54 mmol) in NMP (14 mL), triethylamine (1.43 mL, 10.25 mmol) was added. The heterogeneous mixture was stirred for 15 minutes, then treated with morpholine (0.75 mL, 8.54 mmol). Upon refluxing at 85° C. under argon for 2 hours, the solution was cooled, then added to EtOAc (160 mL). The organic solution was washed with 25 mL of NaHCO3(sat.) (2×), water (2×) and brine, dried over Na2SO4, filtered and concentrated. The crude material was dissolved in 200 mL EtOAc and filtered through a SiO2 pad, further eluting with EtOAc, yielding 2.2 g (93%) of 2,4-dimorpholino-6-chloropyrimidine as an off-white solid. LCMS (m/z): 285.0 (MH+), 1H NMR (CDCl3): δ 5.86 (s, 1H), 3.71-3.76 (m, 12H), 3.52-3.56 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08217035B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-70a4ae61e28048b5951c14898a2de0d4
출처 메모uspto-grants-2012_07