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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494082Generated: October 30, 2026

Diethyl (ethoxymethylene)malonate → Ethyl 2-[(4-fluorophenyl)methyl]-8-hydroxy-1-oxo-3,4-dihydropyrrolo[1,2-a]pyrazine-7-carboxylate

https://huagongshe.com/reaction/494082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-(4-Fluorobenzyl)piperazin-2-oneHCID 18538638—
SolventTolueneHCID 1140—
ProductEthyl 2-[(4-fluorophenyl)methyl]-8-hydroxy-1-oxo-3,4-dihydropyrrolo[1,2-a]pyrazine-7-carboxylateHCID 3011068—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-(4-fluorobenzyl)piperazin-2-one (10.0 g, 48.0 mmol) and diethyl ethoxymethylenemalonate (10.9 g, 50.4 mmol) in toluene (250 mL) was heated in a sealed tube at 80° C. for 4 hours. The resultant mixture was concentrated under vacuum. The residue was dissolved in anhydrous DMF (350 mL), cooled to 0° C. under an atmosphere of nitrogen, and treated with a solution of lithium bis(trimethylsilyl)amide in THF (1 M, 57.4 mL, 57.4 mmol). The reaction mixture was stirred at room temperature overnight and concentrated under vacuum. The residue was partitioned between ethyl acetate and dilute aqueous HCl. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The residue was triturated with diethyl ether, and the solid precipitated was filtered to provide the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538112B2
Source datasetuspto-grants-2009_05
ORD IDord-fa1ec7bbb4644767a1f2ba9198566c11
Source noteuspto-grants-2009_05