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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466027Generated: October 29, 2026

Sodium Hydroxide → 3-(2-Chloropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/466027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-(2-Oxo-1,2-dihydropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridineHCID 15158112—
Product3-(2-Chloropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridineHCID 15158142—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 3-(2-oxo-1,2-dihydropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine (0.6 g) and phosphorus oxychloride (1.8 ml) was stirred for 6 hours at 70° C. After cooling, the reaction mixture was poured onto ice (30 g) and made alkaline with 24% aqueous solution of sodium hydroxide (pH=10) and extracted with chloroform (18 ml). The combined extract was washed with water and sodium chloride aqueous solution and dried over magnesium sulfate. The solvent was removed in vacuo and the residue was chromatographed on silica gel (12 g) with chloroform as an eluent. The fractions containing the object compound were combined and evaporated in vacuo and recrystallized from a mixture of ethyl acetate and diisopropyl ether to give 3-(2-chloropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine (0.21 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155114
Source datasetuspto-grants-1992_10
ORD IDord-14eb3298a83749a8bc4fce3859f22e9e
Source noteuspto-grants-1992_10