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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250575Generated: October 25, 2026

Water → Ethyl 2-benzyl-4-(4-fluorophenyl)pyrrolo[1,2-b]pyridazine-3-carboxylate

https://huagongshe.com/reaction/2250575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant1-AminopyrroleHCID 136589—
ReactantEthyl 2-(4-fluorobenzoyl)-3-oxo-4-phenylbutanoateHCID 57444525—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventEthanolHCID 702—
ProductEthyl 2-benzyl-4-(4-fluorophenyl)pyrrolo[1,2-b]pyridazine-3-carboxylateHCID 6930825751.9%

Reaction Steps

A mixture of ethyl 2-(4-fluorobenzoyl)-3-oxo-4-phenylbutanoate (1.4 g), 1H-pyrrol-1-amine (350 mg), and p-toluenesulfonic acid monohydrate (41 mg) in ethanol (10 ml) was refluxed for 5 hours. The mixture was partioned between ethyl acetate and water. The organic layer was separated, washed with brine, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel eluting with a mixture of ethyl acetate and hexane (1:4) to give ethyl 2-benzyl-4-(4-fluorophenyl)pyrrolo[1,2-b]pyridazine-3-carboxylate (828 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317009B2
Source datasetuspto-grants-2008_01
ORD IDord-8766535b3e544727884c38e3c4b4d54c
Source noteuspto-grants-2008_01