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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465997Generated: October 25, 2026

Pyridazine → 3-(1-Ethoxycarbonyl-1,4-dihydropyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/465997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridazineHCID 9259—
ReactantEthyl chloroformateHCID 10928—
Reactant2-Phenylpyrazolo[1,5-a]pyridineHCID 15620342—
SolventDichloromethaneHCID 6344—
Product3-(1-Ethoxycarbonyl-1,4-dihydropyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridineHCID 1179186053.4%

Reaction Conditions

Temperature10 °C

Reaction Steps

Ethyl chloroformate (3.38 g) was added dropwise with stirring to a solution of 2-phenylpyrazolo[1,5-a]pyridine (2.54 g) and pyridazine (5.00 g) in methylene chloride (5.0 ml) at 10° C. After being stirred at 10° C. for 1 hour and then at room temperature for 2 hours, the reaction mixture was poured onto ice-water (100 ml), and extracted with ethyl acetate. The combined extracts were washed with saturated sodium chloride aqueous solution (100 ml), dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel (150 g) with a mixture of chloroform and n-hexane (1:1) as an eluant. The fractions containing main-product [compound (A)] were combined and evaporated in vacuo to give 3-(1-ethoxycarbonyl-1,4-dihydropyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine (2.42 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155114
Source datasetuspto-grants-1992_10
ORD IDord-c7262b43437944ed8a03a8289694a8d5
Source noteuspto-grants-1992_10