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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469248Generated: October 27, 2026

Glycine ethyl ester, hydrochloride → HCID 131729495, compound

https://huagongshe.com/reaction/469248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
Reactant7-(Cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehydeHCID 86633051—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 131729495HCID 13172949547.5%

Reaction Steps

To a 5.0 ml ethanol solution of 500 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde was added 215 mg of ethyl aminoacetate hydrochloride, followed by stirring at room temperature for 2 hours. Next, 50 mg of palladium-carbon was added thereto, followed by stirring at room temperature for 4 hours in an atmosphere of hydrogen. The reaction mixture was filtered through celite and then evaporated under a reduced pressure. The resulting residue was purified by silica gel column chromatography. To a 3.6 ml dioxane solution of the resulting compound was added 4.0 ml of a 4 M hydrogen chloride dioxane solution, followed by overnight stirring at room temperature. The insoluble materials were collected by filtration to obtain 320 mg of ethyl({[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]methyl}amino)acetate hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629126B2
Source datasetuspto-grants-2014_01
ORD IDord-e8717cc79f984015b94a4d2ce9f2be55
Source noteuspto-grants-2014_01