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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1041903생성일: 2026년 10월 25일

Potassium Carbonate → 6-Bromo-3-[3-(2-morpholin-4-yl-ethoxy)-phenyl]-[1,2,4]-triazolo[4,3-a]pyridine

https://huagongshe.com/reaction/1041903

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-(2-Bromoethyl)morpholine hydrochlorideHCID 12955540—
반응물3-(6-Bromo-[1,2,4]triazolo[4,3-a]pyridin-3-yl)phenolHCID 66977718—
용매DimethylformamideHCID 6228—
생성물6-Bromo-3-[3-(2-morpholin-4-yl-ethoxy)-phenyl]-[1,2,4]-triazolo[4,3-a]pyridineHCID 6697758398%

반응 단계

A mixture of Example 10 step a (250 mg, 1.21 mmol), N-(2-bromoethyl)morpholine hydrochloride (306 mg, 1.32 mmol) and K2CO3 (500 mg, 3.62 mmol) in DMF (20 mL) was heated at 50° C. for 24 h. The reaction was then allowed to cool to RT and concentrated in vacuo. The residue was purified by FCC (DCM:MeOH, 1:0 to 9:1) to afford the title compound (479 mg, 98%) as a yellow oil. 1H NMR (300 MHz, CDCl3): δ 8.44 (1 H, dd, J 1.7, 1), 7.74-7.69 (1 H, m), 7.50 (1 H, t, J 7.9), 7.39-7.35 (2 H, m), 7.35-7.30 (1 H, m), 7.14-7.08 (1 H, m), 4.21 (2 H, t, J 5.6), 3.74 (4 H, t, J 4.6), 2.85 (2 H, t, J 5.6), 2.63-2.56 (4 H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08557797B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-e82fa9190dbc4272a5485489d96209ee
출처 메모uspto-grants-2013_10