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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232219Generated: October 30, 2026

2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline → 4-nitrobenzyl 2-[(4S)-4-phenylacetamido-3-oxo-2-isoxazolidinyl]-3-(2acetamidoethylthio)-5-oxo-2-tetrahydrofurancarboxylate

https://huagongshe.com/reaction/232219

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
Reactant(4S)-4-phenylacetamido-3-isoxazolidinoneHCID 56633768—
ReactantHCID 67901886HCID 67901886—
SolventDichloromethaneHCID 6344—
Product4-nitrobenzyl 2-[(4S)-4-phenylacetamido-3-oxo-2-isoxazolidinyl]-3-(2acetamidoethylthio)-5-oxo-2-tetrahydrofurancarboxylateHCID 6790227557.3%

Reaction Steps

In 5 ml of dichloromethane were suspended 48 mg of (4S)-4-phenylacetamido-3-isoxazolidinone and 95 mg of the Compound (70) obtained in Example 70. To the suspension was added 71 mg of 1-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline. The mixture was stirred for 5.5 hours at room temperature. The solvent was evaporated off, and the residue was subjected to a silica gel column chromatography, followed by elution with ethyl acetate to give 75 mg of the subject Compound (71) as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04851422
Source datasetuspto-grants-1989_07
ORD IDord-38b7c90d32a643a0bdcd277cb8efddfe
Source noteuspto-grants-1989_07