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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742285Generated: October 30, 2026

Ethyl bromoacetate → HCID 54051188, compound

https://huagongshe.com/reaction/1742285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantTriethylamineHCID 8471—
ReactantHCID 19008993HCID 19008993—
SolventDimethylformamideHCID 6228—
ProductHCID 54051188HCID 54051188—

Reaction Steps

To an ice-cooled solution of 3-[2-(2-aminoethyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine (1.5 g), triethylamine (1.5 ml), and N,N-dimethylformamide (15 ml) was added ethyl 2-bromoacetate (0.60 ml), and the mixture was stirred for 1 hour at room temperature. The reaction mixture was concentrated, and the residue was partitioned between chloroform and water. The organic layer was separated, washed with sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, and concentrated. Purification of the residue by column chromatography on silica gel (gradient elution, using 50:1 and 25:1 mixture of chloroform and methanol) gave 3-[2-{2-(ethoxycarbonylmethylamino)ethyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine (0.90 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05338743
Source datasetuspto-grants-1994_08
ORD IDord-c688cb6bc6de441281536e7b975de3cf
Source noteuspto-grants-1994_08