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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952207Generated: October 31, 2026

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

https://huagongshe.com/reaction/1952207

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—
SolventEthyl AcetateHCID 8857—
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 at 20° C. for 20 hours and then for a further 48 hours while adding, on 4 occasions, an additional 100 μl of osmium tetroxide and 80 mg of sodium periodate. The reaction mixture is poured into 50 ml of water and extraction is carried out twice with 50 ml of ethyl acetate. The combined organic phases are washed with a saturated aqueous sodium chloride solution, separated by settling, dried and concentrated to dryness under reduced pressure. The residue is chromatographed on silica, elution being carried out 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 numberUS08404848B2
Source datasetuspto-grants-2013_03
ORD IDord-db62c9ba5a374572b953d92a8caf996b
Source noteuspto-grants-2013_03