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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971621Generated: October 30, 2026

Pyridine → HCID 25196652, compound

https://huagongshe.com/reaction/1971621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Fluorophenylacetyl chlorideHCID 3744988—
ReactantHCID 57607467HCID 57607467—
SolventTetrahydrofuranHCID 8028—
ProductHCID 25196652HCID 25196652—

Reaction Conditions

Temperature0 °C

Reaction Steps

6-fluoro-3-phenylimidazo[1,2-a]pyridin-2-amine (compound l, 0.075 g, 0.00033 mol) was dissolved in tetrahydrofuran (5.0 mL) and pyridine (29 uL, 0.00036 mol) was added. Rxn cooled to 0° C. and 4-fluorophenylacetyl chloride (48 uL, 0.00036 mol) was added. The reaction was stirred at 0° C. for 30 minutes. The solvent was removed and the crude product was partioned between water (25 mL) and EtOAc (25 mL). The layers were separated and the organic layer was washed 3×20 mL with water. The organic layer was dried (magnesium sulfate) then chromatographed on silica (70% ethyl acetate/hexanes) to give N-(6-fluoro-3-phenylimidazo[1,2-a]pyridin-2-yl)-2-(4-fluorophenyl)acetamide Rf 0.37, 70% ethyl acetate/hexanes; MS m/z 364 (M+H). SH-SY5Y_EC50 (μM): 0.7321.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431608B2
Source datasetuspto-grants-2013_04
ORD IDord-578b6dc5a47140e5987b95c64281f387
Source noteuspto-grants-2013_04