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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1775087생성일: 2026년 10월 27일

N-Iodosuccinimide → 2-Fluoro-6-iodopyridin-3-amine

https://huagongshe.com/reaction/1775087

반응식

참여 물질

역할이름HCID투입량
반응물N-IodosuccinimideHCID 120273—
반응물2-Fluoropyridin-3-amineHCID 2762816—
용매DimethylformamideHCID 6228—
생성물2-Fluoro-6-iodopyridin-3-amineHCID 71743077—

반응 단계

To a solution of 2-fluoropyridin-3-amine (5.00 g, 44.60 mmol) in DMF (100 mL) was added N-iodosuccinimide (11.04 g, 49.06 mmol). The resulting mixture was stirred overnight. The reaction mixture was partitioned between EtOAc and water. The organic layer was dried with MgSO4 and concentrated. The residue was purified on silica eluted 0 to 50% EtOAc in Heptane. 2-fluoro-6-iodopyridin-3-amine was obtained as a dark tan solid (8.8674 g, 83%). To an ice cooled mixture of tert-Butyl nitrite (356.8 uL, 3.000 mmol) and Copper(II) bromide (536.0 mg, 2.400 mmol) in Acetonitrile (5 mL) was added 2-fluoro-6-iodopyridin-3-amine was obtained as a dark tan solid (476.0 mg, 2.000 mmol). The resulting mixture was stirred overnight allowing warming to room temperature. The mixture was filtered through Celite. The filtrated was concentrated. The residue was partitioned between Et2O and saturated NH4Cl. The organic layer was dried with MgSO4, and then concentrated. The residue was purified on silica eluted with 0 to 20% EtOAc in Heptane. 3-Bromo-2-fluoro-6-iodopyridine was obtained as a yellow solid (407.1 mg, 57%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09260425B2
출처 데이터셋uspto-grants-2016_02
ORD IDord-e03edef362924da6a93d64eb4ff4694e
출처 메모uspto-grants-2016_02