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HRID 341230作成日:2026年10月26日

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

https://huagongshe.com/reaction/341230

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物N-IodosuccinimideHCID 120273—
反応物7-(4-Fluoro-phenyl)-imidazo[1,2-a]pyridineHCID 59320799—
溶媒DimethylformamideHCID 6228—
生成物7-(4-Fluoro-phenyl)-3-iodo-imidazo[1,2-a]pyridineHCID 5932077629%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895745B2
出典データセットuspto-grants-2014_11
ORD IDord-28ddd69c586946899a8a3707ac18036e
出典メモuspto-grants-2014_11