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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341230생성일: 2026년 10월 26일

Water → 7-(4-Fluoro-phenyl)-3-iodo-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/341230

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물N-IodosuccinimideHCID 120273—
반응물7-(4-Fluoro-phenyl)-imidazo[1,2-a]pyridineHCID 59320799—
용매DimethylformamideHCID 6228—
생성물7-(4-Fluoro-phenyl)-3-iodo-imidazo[1,2-a]pyridineHCID 5932077629%

반응 단계

To a solution of 7-(4-fluoro-phenyl)-imidazo[1,2-a]pyridine (13.0 g, 61.3 mmol) in N,N-dimethylformamide (100 mL) stirring under a nitrogen atmosphere at ambient was added N-iodosuccinimide (14.5 g, 64.4 mmol). The reaction mixture was stirred for 2 h and then poured into water (1 L) and stirred for a further 30 min. The solid obtained was collected by filtration, washed with water and air dried on the filter. The solid was triturated with ether, collected by filtration and dried under vacuum at 50° C. The solid obtained was partitioned between water and EtOAc. The organic layer was washed with brine, dried (MgSO4), filtered and concentrated under reduced pressure. The solid thus obtained was partitioned between aqueous sodium thiosulphate solution and EtOAc. The organic layer was washed with brine, dried (MgSO4) and concentrated under reduced pressure. The product was triturated with EtOAc, collected by filtration and air-dried to afford 6.0 g (29%) of the title compound. 1H NMR (400 MHz, CDCl3) δ 8.23 (1H, d), 7.91 (1H, s), 7.78 (1H, s), 7.67 (2H, dd), 7.28 (1H, d), 7.22 (2H, t). A further crop of product (11.0 g) containing minor impurities was obtained by evaporating the filtrates under reduced pressure, triturating with petrol/EtOAc and collection by filtration.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895745B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-28ddd69c586946899a8a3707ac18036e
출처 메모uspto-grants-2014_11