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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878454Generated: November 3, 2026

Potassium Carbonate → 6-(oxazol-5-yl)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide

https://huagongshe.com/reaction/1878454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTosylmethyl isocyanideHCID 161915—
Reactant6-formyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 24771615—
SolventMethanolHCID 887—
Product6-(oxazol-5-yl)-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 4413776734.9%

Reaction Steps

To a suspension of 200 mg of 6-formyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide (Intermediate 8) in 10 mL of methanol are added 104 mg of potassium carbonate and 147 mg of para-toluenesulfonylmethylisonitrile (TOSMIC). The reaction mixture is refluxed for 2 hours and then evaporated to dryness under reduced pressure, taken up in 300 mL of dichloromethane and washed with water. The organic phase is dried and concentrated to dryness on silica and then chromatographed on a silica cartridge, eluting with a gradient of from 0 to 20% of methanol in dichloromethane. The fractions containing the expected product are concentrated to dryness and the solid obtained is triturated with a small amount of dichloromethane, filtered off and dried to give 80 mg of 6-(oxazol-5-yl)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314109B2
Source datasetuspto-grants-2012_11
ORD IDord-1eb4f777fc8441b89b3f037614ce0b07
Source noteuspto-grants-2012_11