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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1499474생성일: 2026년 10월 25일

Potassium Iodide → 5-Iodo-1,2,3,4-tetrahydro-1,8-naphthyridine

https://huagongshe.com/reaction/1499474

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참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물Ammonium HydroxideHCID 14923—
반응물Ammonium AcetateHCID 517165—
반응물3-(3-Chloropropyl)-2-fluoro-4-iodopyridineHCID 23657233—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물5-Iodo-1,2,3,4-tetrahydro-1,8-naphthyridineHCID 5775625369%

반응 조건

온도60 °C

반응 단계

A mixture of 3-(3-chloropropyl)-2-fluoro-4-iodopyridine (5.0 g, 17 mmol), NH4OH (100 mL, 800 mmol), ammonium acetate (18 g, 230 mmol), potassium iodide (5.5 g, 33 mmol), potassium carbonate (12 g, 87 mmol) and DMF (26 mL) was heated at 60° C. for 8 h. The mixture allowed to cool, and diluted with EtOAc. The layers were separated and the organic layer was washed with brine, dried with MgSO4, then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using CombiFlash® apparatus, eluting with 0 to 50% EtOAc in hexanes, to give the sub-title compound (3.0 g, 69% yield). LCMS calc. for C8H10IN2(M+H)+: m/z=261.0. Found: 261.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09200004B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-78e87c30a9734fc689d5da3dea89c409
출처 메모uspto-grants-2015_12