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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228933Generated: November 1, 2026

Hydrochloric Acid → Ethyl 7-aminoquinoline-3-carboxylate

https://huagongshe.com/reaction/2228933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant7-(Benzhydrylidene-amino)-quinoline-3-carboxylic acid ethyl esterHCID 10287230—
SolventEthanolHCID 702—
ProductEthyl 7-aminoquinoline-3-carboxylateHCID 987780168.3%

Reaction Steps

Concentrated hydrochloric acid (1 mL, 2.5 volumes) was added to a solution of 7-(benzhydrylidene-amino)-quinoline-3-carboxylic acid ethyl ester (400 mg, 1.05 mmol, 1 equiv) in ethanol (4 mL, 10 volumes). The solution was stirred at room temperature for three hours and then concentrated. The residue was dissolved in ethyl acetate (20 mL, 50 volumes) and the organic layer was washed with 1 N hydrochloric acid (5×25 mL). The pH of the combined aqueous layer was then adjusted to about 8 with solid sodium hydroxide. The aqueous layer was then extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over sodium sulfate and concentrated to provide 7-amino-quinoline-3-carboxylic acid ethyl ester (155 mg, 68%) as a yellow solid. The crude solid can be further purified by flash column chromatography using silica gel (EM Science, Gibbstown, N.J., 230-400 mesh) in 60% ethyl acetate in hexanes if desired.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417367B1
Source datasetuspto-grants-2002_07
ORD IDord-f468ab9e614443f8b551d7a6fef60240
Source noteuspto-grants-2002_07