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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747842Generated: October 31, 2026

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

https://huagongshe.com/reaction/747842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
ReactantTetrahydrofuranHCID 8028—
Reactant1-Benzylpiperazin-2-oneHCID 1514303—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTolueneHCID 1140—
ProductEthyl 2-benzyl-8-hydroxy-1-oxo-3,4-dihydropyrrolo[1,2-a]pyrazine-7-carboxylateHCID 3011066—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-benzylpiperazin-2-one (0.29 g, 1.54 mmol) and diethyl ethoxymethylenemalonate (0.35 g, 1.63 mmol) in toluene 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 (10 mL), cooled to 0° C. under an atmosphere of nitrogen, and treated with a solution of lithium bis(trimethylsilyl)amide in THF (1 M, 2.0 mL, 2.0 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-9d06fdaff6b5497284b2ecdf306e8cb8
Source noteuspto-grants-2008_07