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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600610Generated: October 30, 2026

Toluene → ethyl 2,3-dihydro-2-oxo-1H-pyrrolo[1,2,3-de]quinoxaline-5-carboxylate

https://huagongshe.com/reaction/1600610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium MethoxideHCID 10942334—
Reactantethyl 1-ethoxycarbonylmethyl-7-nitro-1H-indole-2-carboxylateHCID 21714275—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuranHCID 8028—
Productethyl 2,3-dihydro-2-oxo-1H-pyrrolo[1,2,3-de]quinoxaline-5-carboxylateHCID 1543279985.7%

Reaction Steps

Ethyl 1-ethoxycarbonylmethyl-7-nitro-1H-indole-2-carboxylate (2.11 g, 6.59 mmol) was subjected to catalytic reduction in the presence of 10% palladium-carbon (0.20 g) in tetrahydrofuran (70 ml) at ordinary temperature and atmospheric pressure. After completion of the reaction, the catalyst was filtered off and the filtrate was concentrated under reduced pressure. Toluene (100 ml) and sodium methoxide (0.35 g, 6.48 mmol) were added to the residue, and the resulting mixture was heated under reflux for 2 hours. Then, the solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: ethyl acetate/n-hexane=2/8) to obtain ethyl 2,3-dihydro-2-oxo-1H-pyrrolo[1,2,3-de]quinoxaline-5-carboxylate (1.38 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977100
Source datasetuspto-grants-1999_11
ORD IDord-edbc0afe0577484c8098514331d3a7c1
Source noteuspto-grants-1999_11