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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466029Generated: October 30, 2026

Sodium Methoxide → 3-(3-Methoxypyridazin-6-yl)-2-phenylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/466029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant3-(3-Chloropyridazin-6-yl)-2-phenylpyrazolo[1,5-a]pyridineHCID 15158144—
SolventMethanolHCID 887—
Product3-(3-Methoxypyridazin-6-yl)-2-phenylpyrazolo[1,5-a]pyridineHCID 15158149—

Reaction Steps

A solution of sodium methoxide in methanol (28%, 411 mg) was added to a mixture of 3-(3-chloropyridazin-6-yl)-2-phenylpyrazolo[1,5-a]pyridine (436 mg) and methanol (4 ml) at room temperature. The reaction mixture was heated under reflux for 3 hours. After evaporating the solvent in vacuo, a saturated aqueous solution of sodium chloride (20 ml) was added to the residue and extracted with chloroform (20 ml×3). The combined extract was washed with a saturated aqueous solution of sodium chloride (20 ml), dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (10 g) using chloroform as an eluent and recrystallized from 95% EtOH to give 3-(3-methoxypyridazin-6-yl)-2-phenylpyrazolo[1,5-a]pyridine (165 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155114
Source datasetuspto-grants-1992_10
ORD IDord-d67a5835c85e41a485e8181b4f58e265
Source noteuspto-grants-1992_10