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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456685Generated: October 29, 2026

Ammonium Chloride → 1-[8-Amino-2-(4-fluorophenyl)imidazo[1,2-a)pyridin-3-yl]ethanone

https://huagongshe.com/reaction/456685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-[2-(4-Fluorophenyl)-8-nitroimidazo[1,2-a]pyridin-3-yl]ethanoneHCID 69549302—
CatalystIronHCID 23925—
SolventMethanolHCID 887—
Product1-[8-Amino-2-(4-fluorophenyl)imidazo[1,2-a)pyridin-3-yl]ethanoneHCID 6954976670.9%

Reaction Steps

A solution of 1-[2-(4-fluorophenyl)-8-nitroimidazo[1,2-α]pyridin-3-yl]ethanone (100 mg, 0.33 mmol) in methanol (3 mL) was added to a suspension of iron (93 mg, 1.7 mmol) and ammonium chloride (149 mg, 2.8 mmol) in aqueous methanol. This reaction mixture was heated to reflux for 10 hours. The reaction mixture was filtered and the filtrate concentrated under reduced pressure to a solid. This solid was purified by silica gel chromatography (5% methanol in dichloromethane) to give 63 mg (70%) of 1-[8-amino-2-(4-fluorophenyl)imidazo[1,2-α]pyridin-3-yl]ethanone as a foam. 1H NMR (CDCl3): δ 9.21 (d, 1H), 7.61 (m, 2H), 7.25 (m, 2H), 6.94 (t, 1H) 6.72 (d, 1H), 4.63 (broad s, 2H), 2.19 (s, 3H); MS m/z 270 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186714B2
Source datasetuspto-grants-2007_03
ORD IDord-ae9679ebf79f4ee5b567661d24151925
Source noteuspto-grants-2007_03