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HRID 456715作成日:2026年10月25日

2-Amino-3-benzyloxypyridine → 8-(Benzyloxy)-2-(4-fluorophenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/456715

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-3-benzyloxypyridineHCID 90334—
反応物2-Bromo-1-(4-fluorophenyl)ethan-1-oneHCID 96749—
溶媒EthanolHCID 702—
生成物8-(Benzyloxy)-2-(4-fluorophenyl)imidazo[1,2-a]pyridineHCID 1843671425%

反応手順

3-(Benzyloxy)pyridin-2-amine (2.52 g, 13 mmol) and 2-bromo-1-(4-fluorophenyl)ethanone (2.73 g, 13 mmol) in ethanol (30 mL) were heated at 75° C. for 16 hours. The mixture was concentrated and the residue was purified by silica gel chromatography, eluting with dichloromethane and then 10% methanol in dichloromethane to yield 1.03 g (25%) of 8-(benzyloxy)-2-(4-fluorophenyl)imidazo[1,2-a]pyridine. 1H NMR (CDCl3): δ 8.01 (dd, 2H), 7.82 (s, 1H), 7.78 (d, 1H), 7.55 (d, 2H), 7.41 (m, 3H), 7.14 (t, 2H), 6.65 (t, 1H), 6.48 (d, 1H), 5.44 (s, 2H); MS m/z 319 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07186714B2
出典データセットuspto-grants-2007_03
ORD IDord-03c940d437dd4037a5e45c29490526e4
出典メモuspto-grants-2007_03