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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645368Generated: October 30, 2026

Piperidine → 6-ethynyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide

https://huagongshe.com/reaction/645368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 44135939—
CatalystHCID 178418476HCID 178418476—
SolventAmmonium ChlorideHCID 25517—
Product6-ethynyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 24771667—

Reaction Conditions

Temperature25 °C

Reaction Steps

0.2 g of 6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide, 156 μl of trimethylsilylacetylene, 20 mg of dichlorobis(triphenylphosphine)palladium and 2 ml of piperidine are charged to a 20 ml microwave tube. The mixture is heated for 15 minutes in the microwave device adjusted to 130° C. After cooling, the mixture is poured into 50 ml of a saturated aqueous ammonium chloride solution. Extraction is carried out twice with 70 ml of ethyl ether. The combined organic phases are separated by settling, dried and concentrated to dryness under reduced pressure. The residue is taken up in 4 ml of a 1M solution of tetrabutylammonium fluoride in THF and stirred at 25° C. for 16 hours. After evaporating the reaction medium to dryness, the residue is chromatographed on silica, elution being carried out with a mixture of cyclohexane and ethyl acetate (gradient from 0 to 35%), to give 30 mg of 6-ethynyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704989B2
Source datasetuspto-grants-2010_04
ORD IDord-808a29642e3c41ac9fa5ccc320c9c30b
Source noteuspto-grants-2010_04