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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860440Generated: October 26, 2026

Ethyl Acetate → Ethyl 6-[7-ethyl-4-(4-fluorophenyl)-2-methylpyrrolo[1,2-b]pyridazin-3-yl]hexanoate

https://huagongshe.com/reaction/860440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantEthyl 7-(4-fluorobenzoyl)-8-oxononanoateHCID 57444527—
Reactant(1-amino-5-ethyl-1H-pyrrol-2-yl)(4-fluorophenyl)methanoneHCID 69311541—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductEthyl 6-[7-ethyl-4-(4-fluorophenyl)-2-methylpyrrolo[1,2-b]pyridazin-3-yl]hexanoateHCID 69308101—
ProductEthyl 6-[7-ethyl-2,4-bis(4-fluorophenyl)pyrrolo[1,2-b]pyridazin-3-yl]hexanoateHCID 69308766—

Reaction Steps

A mixture of ethyl 7-(4-fluorobenzoyl)-8-oxononanoate (300 mg), (1-amino-5-ethyl-1H-pyrrol-2-yl)(4-fluorophenyl)methanone (216 mg), and p-toluenesulfonic acid monohydrate (35.4 mg) in ethanol (6 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 6-[7-ethyl-2,4-bis(4-fluorophenyl)pyrrolo[1,2-b]pyridazin-3-yl]hexanoate (83 mg) and ethyl 6-[7-ethyl-4-(4-fluorophenyl)-2-methylpyrrolo[1,2-b]pyridazin-3-yl]hexanoate (40 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153854B2
Source datasetuspto-grants-2006_12
ORD IDord-a936da50096a4a398d4d232617be9aa1
Source noteuspto-grants-2006_12