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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747845Generated: October 30, 2026

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

https://huagongshe.com/reaction/747845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-[(3-Chlorophenyl)methyl]piperazin-2-oneHCID 20099281—
SolventTolueneHCID 1140—
ProductEthyl 2-[(3-chlorophenyl)methyl]-8-hydroxy-1-oxo-3,4-dihydropyrrolo[1,2-a]pyrazine-7-carboxylateHCID 3011073—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-(3-chlorobenzyl)piperazin-2-one (3.97 g, 17.67 mmol) and diethyl ethoxymethylenemalonate (4.01 g, 18.55 mmol) in toluene (60 mL) was heated in a sealed tube at 80° C. overnight. The resultant mixture was concentrated under vacuum. The residue was dissolved in anhydrous DMF (200 mL), cooled to 0° C. under an atmosphere of nitrogen, and treated with a solution of lithium bis(trimethylsilyl)amide in THF (1 M, 21.2 mL, 21.2 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 title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399763B2
Source datasetuspto-grants-2008_07
ORD IDord-6202238b26b741f7b5527e19df42f912
Source noteuspto-grants-2008_07