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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2193794생성일: 2026년 10월 27일

4-Bromopyridin-1-ium-1-olate → 2-(7-(2-Fluoro-4-(3-oxo-3-(phenylamino)propanamido)phenoxy)thieno[3,2-b]pyridin-2-yl)pyridine 1-oxide

https://huagongshe.com/reaction/2193794

반응식

참여 물질

역할이름HCID투입량
반응물4-Bromopyridin-1-ium-1-olateHCID 139708—
반응물N1-(3-Fluoro-4-(2-iodothieno[3,2-b]pyridin-7-yloxy)phenyl)-N3-phenylmalonamideHCID 58790317—
촉매HCID 178418397HCID 178418397—
용매1,4-DioxaneHCID 31275—
생성물2-(7-(2-Fluoro-4-(3-oxo-3-(phenylamino)propanamido)phenoxy)thieno[3,2-b]pyridin-2-yl)pyridine 1-oxideHCID 5879036727%

반응 단계

A solution of 411 (45 mg, 0.08 mmol), 4-bromopyridine N-oxide (250 mg, 1.43 mmol), bistrimethyltin (26 μL, 40 mg, 0.12 mmol) and Pd(PPh3)4 (10 mg, 0.01 mmol) in dioxane (1 mL) was heated to reflux for 4 hrs. The reaction mixture was cooled, concentrated and the residue was purified by flash chromatography using the gradient 5-10% MeOH in DCM as an eluent, to afford 409 (11 mg, 27% yield). 1H NMR 6 (400 MHz, CD3OD): 8.71 (d, 1H, J=5.4 Hz), 8.6 (m, 3H), 8.04 (dd, 1H, J=2.5 Hz, J=12.3 Hz), 7.85 (t, 1H, J=8.4 Hz), 7.78 (m, 2H), 7.65 (m, 1H), 7.62 (m, 1H), 7.53 (m, 3H), 7.32 (t, 1H, J=7.4 Hz), 6.81 (d, 1H, J=5.5 Hz), 3.75 (s, 2H). MS (m/z): (M+1) 515.0 (100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08329726B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-e8034baefef941918487e2e58176aa0d
출처 메모uspto-grants-2012_12