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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297656Generated: October 28, 2026

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

https://huagongshe.com/reaction/2297656

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 numberUS06492348B1
Source datasetuspto-grants-2002_12
ORD IDord-1c79b1b391664077994dc9cc90bc3af8
Source noteuspto-grants-2002_12