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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582981Generated: November 2, 2026

HCID 12988027, compound → HCID 12988028, compound

https://huagongshe.com/reaction/1582981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12988027HCID 12988027—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 12988028HCID 12988028—

Reaction Conditions

Temperature100 °C

Reaction Steps

A 720 mg portion of ethyl N-[4-(3-chlorophenyl)-1-ethyl-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]carbamate was stirred in 40 ml of an ethanol-3M sodium hydroxide aqueous solution (1:1) under heating at an oil bath temperature of 100° C. for 4 hours. After cooling to room temperature, the reaction mixture was diluted with water and then extracted with ethyl acetate. The organic layer was washed with saturated brine and the solvent was evaporated. The resulting residue was purified by a silica gel column chromatography (toluene-ethyl acetate) and then recrystallized from diisopropyl ether-ethyl acetate to obtain 298 mg of 3-amino-4-(3-chlorophenyl)-1-ethyl-7-methyl-1,8-naphthyridin-2(1H)-one as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06740662B1
Source datasetuspto-grants-2004_05
ORD IDord-e5007139015e4fbbb332ea1ad38b84d3
Source noteuspto-grants-2004_05