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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466012Generated: October 26, 2026

Dimethylamine → 3-(2-Oxo-1,2-dihydropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/466012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant1-(Carbamoylmethyl)pyridinium ChlorideHCID 2756440—
Reactant3-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)acrylaldehydeHCID 53819832—
SolventMethanolHCID 887—
Product3-(2-Oxo-1,2-dihydropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridineHCID 1515811224.8%

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)acrylaldehyde (cis and trans mixture) (1.15 g) and 1-carbamoylmethylpyridinium chloride (0.80 g), 50% aqueous dimethylamine (0.44 g) and methanol (10 ml) was refluxed for 3 hours. The reaction mixture was evaporated in vacuo and the residue was heated for 10 minutes at 200° C. The resulting mixture was chromatographed on silica gel (80 g) with a mixture of chloroform and methanol (100:1). The fractions containing the object compound were combined and evaporated in vacuo and recrystallized from ethanol to give 3-(2-oxo-1,2-dihydropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine (0.33 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155114
Source datasetuspto-grants-1992_10
ORD IDord-39ff9bbc27a5468db683fa52ee1ed7be
Source noteuspto-grants-1992_10