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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703969Generated: October 25, 2026

Ethyl chloroformate → 3-(3-Methylpyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/703969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant3-MethylpyridazineHCID 74208—
Reactant2-Phenylpyrazolo[1,5-a]pyridineHCID 15620342—
SolventDichloromethaneHCID 6344—
Product3-(3-Methylpyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridineHCID 1515810832%

Reaction Steps

To a mixture of 2-phenylpyrazolo[1,5-a]pyridine (5.00 g), 3-methylpyridazine (2.90 g) and methylene chloride (20 ml), was added a solution of ethyl chloroformate (5.57 g) in methylene chloride for 17 minutes under ice-cooling and stirred for an hour at the same temperature and then for 6 hours and 40 minutes at room temperature. To the reaction mixture was added methylene chloride (20 ml), and washed with a solution of potassium carbonate (10 ml) and a saturated aqueous solution of sodium chloride (10 ml) and dried over magnesium sulfate. The solvent was removed and chromatographed on silica gel (70 g) with a mixture of n-hexane and ethyl acetate (2:1). The fractions containing the object compound were combined and evaporated in vacuo and recrystallized from a mixture of ethyl acetate and n-hexane to give 3-(3-methylpyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine (2.36 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985444
Source datasetuspto-grants-1991_01
ORD IDord-1b8fad8c32fd46e18cdac9cda1d9d6a2
Source noteuspto-grants-1991_01