Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363728Generated: October 29, 2026

Water → 6-formyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide

https://huagongshe.com/reaction/2363728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-ButanolHCID 6386—
ReactantSodium periodateHCID 23667635—
ReactantN-phenyl-6-vinylimidazo[1,2-a]pyridine-2-carboxamideHCID 24771613—
CatalystOsmium TetroxideHCID 30318—
SolventTetrahydrofuranHCID 8028—
Product6-formyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 2477161566.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

A suspension of 150 mg of N-phenyl-6-vinylimidazo[1,2-a]pyridine-2-carboxamide, 232 μL of osmium tetroxide and 167.5 mg of sodium periodate in a mixture of 6 mL of THF, 3 mL of t-butanol and 3 mL of water is stirred for 20 hours at 20° C. and then for a further 48 hours while adding in four portions 100 μL of osmium tetroxide and 80 mg of sodium periodate. The reaction mixture is poured into 50 mL of water and the resulting mixture is extracted twice with 50 mL of ethyl acetate. The combined organic phases are washed with saturated aqueous sodium chloride solution, separated by settling, dried and concentrated to dryness under reduced pressure. The residue is chromatographed on silica, eluting with a mixture of cyclohexane and ethyl acetate (gradient from 0 to 50%) to give 100 mg of 6-formyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a white solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691990B2
Source datasetuspto-grants-2014_04
ORD IDord-6c51fd4a29d743ff8003153a00759f1b
Source noteuspto-grants-2014_04