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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 730301생성일: 2026년 10월 24일

Iodine → (2,3-Dihydro-benzo[1,4]dioxin-6-yl)-(4-iodo-pyridin-2-yl)-amine

https://huagongshe.com/ko/reaction/730301

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Potassium IodideHCID 4875—
반응물N2-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-pyridine-2,4-diamineHCID 57808069—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매1,2-DimethoxyethaneHCID 8071—
생성물(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-(4-iodo-pyridin-2-yl)-amineHCID 57808271—

반응 조건

온도62.5 °C

반응 단계

Isopentyl nitrile (Aldrich Chemical Company) (3.9 mL, 29 mmol) was added to a mixture of N2-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-pyridine-2,4-diamine (Example 2(a), 2.4 g, 9.8 mmol), potassium iodide (Aldrich Chemical Company) (1.6 g, 9.8 mmol), iodine (Aldrich Chemical Company) (1.2 g, 4.9 mmol) and copper (I) iodide (Aldrich Chemical Company) (1.9 g, 9.8 mmol) in 1,2-dimethoxyethane (60 mL). The reaction mixture was heated at 60-65° C. for 1 hr. After cooling to room temperature, the insoluble materials were removed by filtration and the filtrate was diluted with EtOAc, washed with 25% aqueous NH4OH, 5% aqueous sodium bisulfite and then brine. The organic layer was separated, dried over Na2SO4 and concentrated in vacuo. The residue was purified on a Biotage 40 M column (2.5:1 hexane:EtOAc) to give the title compound as an off-white solid. MS (ESI, pos. ion) m/z: 355 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582657B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-c79233cb225e4a3db5c6eaf432d4190d
출처 메모uspto-grants-2009_09