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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244596Generated: October 30, 2026

Hydrochloric Acid → 3-Quinolinecarboxylic acid, 6-bromo-4-(((2S)-2-methoxypropyl)amino)-

https://huagongshe.com/reaction/244596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactantethyl 6-bromo-4-[[(2S)-2-methoxypropyl]amino]quinoline-3-carboxylateHCID 68108432—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Quinolinecarboxylic acid, 6-bromo-4-(((2S)-2-methoxypropyl)amino)-HCID 6810756286%

Reaction Conditions

Temperature50 °C

Reaction Steps

Add a solution of sodium hydroxide (296.7 g, 7.42 mol, 6 eq.) in water (454 mL) to a solution of ethyl 6-bromo-4[[(2S)-2-methoxypropyl]amino]quinoline-3-carboxylate (454 g, 1.24 mol) in tetrahydrofuran (4.54 L) at room temperature. Heat the mixture at 50° C. overnight. After 18 hours, cool the reaction to 0° C., add 37% aq. HCl dropwise over 30 minutes until pH=6 (ca. 450 mL) with the temperature under 23° C. Filter the precipitate formed with filter paper and wash it with water (2 L), acetone (2 L) and methyl tert-butyl ether (2 L) subsequently. Dry the white solid to give the titled compound (359 g, 86%). MS (ESI) m/z (M+H)+ 338.9, 340.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658668B2
Source datasetuspto-grants-2014_02
ORD IDord-62cf9a8b6aa940fc8d45db2d2f168719
Source noteuspto-grants-2014_02