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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839241Generated: November 1, 2026

2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline → HCID 69827563, compound

https://huagongshe.com/reaction/1839241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
ReactantHCID 69827790HCID 69827790—
SolventMethanolHCID 887—
ProductHCID 69827563HCID 6982756375.1%

Reaction Steps

A mixture of (3aS,4S,6R,6aR)-6-(6-isopropylamino-purin-9-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole-4-carboxylic acid (4.82 g) and 2-ethoxy-N-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ, 3.36 g) in methanol (150 ml) was heated under reflux for 60 h. After cooling to room temperature, the solution was concentrated in vacuo and the resulting residue partitioned between ethyl acetate (100 ml) and citric acid solution (0.5M, 75 ml). The aqueous layer was extracted with ethyl acetate (4×25 ml) and the combined organic extracts were washed with water (50 ml) and brine (75 ml), dried (MgSO4), filtered and concentrated in vacuo. The resulting residue was purified by flash chromatography on silica gel, eluting with ethyl acetate: cyclohexane (1:1) to afford the title compound as a white solid (3.76 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677316B2
Source datasetuspto-grants-2004_01
ORD IDord-cf1275365dd140acb940194159b919a3
Source noteuspto-grants-2004_01