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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213101Generated: October 31, 2026

Pyridinium, 1-amino-, iodide (1:1) → HCID 21956522, compound

https://huagongshe.com/reaction/2213101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridinium, 1-amino-, iodide (1:1)HCID 2733704—
ReactantHCID 21956511HCID 21956511—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 21956522HCID 21956522—

Reaction Steps

A solution of ethyl(2E)-3-(3-methoxy-4-pyridin-2-ylphenyl)prop-2-enoate (55 mg, 0.2 mmol) and 1-aminopyridinium iodide (86 mg, 0.4 mmol) in DMF (1 mL) was stirred at rt for 2 days open to the atmosphere. The deep purple reaction mixture was diluted with CH2Cl2 (25 mL) and washed with a saturated solution of sodium thiosulfate (25 mL) and brine (25 mL), then dried (MgSO4) and concentrated. The residue was purified by flash column chromatography on silica gel eluting with EtOAc:hexanes (1:9 to 3:2) to afford the desired ethyl 2-(3-methoxy-4-pyridin-2-ylphenyl)pyrazolo[1,5-a]pyridin-3-carboxylate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105533B2
Source datasetuspto-grants-2006_09
ORD IDord-5649251577844a0d8001551b1ae6c183
Source noteuspto-grants-2006_09