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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486915Generated: October 31, 2026

Sodium Hydroxide → 6-Bromo-4-(oxan-4-ylamino)quinoline-3-carboxylic acid

https://huagongshe.com/reaction/1486915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 6-bromo-4-(oxan-4-ylamino)quinoline-3-carboxylateHCID 118498649—
SolventEthanolHCID 702—
Product6-Bromo-4-(oxan-4-ylamino)quinoline-3-carboxylic acidHCID 118498620100.6%

Reaction Conditions

Temperature75 °C

Reaction Steps

On a larger scale, ethyl 6-bromo-4-(oxan-4-ylamino)quinoline-3-carboxylate (1925 g, 5.08 mol) was charged to the vessel with EtOH (12.5 L). 2M NaOH (12.5 L, 25.03 mol) was then added with an exotherm from 22-35° C. over the 20 minute addition. The batch was heated to 70-80° C. for 17 h at which point HPLC indicated 98.3% product and <1% starting material. The batch was concentrated in vacuo to remove EtOH and returned to the vessel. A 2M HCl solution (13 L) was then added until pH 5-6 was obtained maintaining a batch temperature below 50° C. An exotherm from 20-32° C. was observed over the 40 minute addition. A precipitate formed which was slurried at 20-25° C. for 1.5 h before filtration, washing with water until pH neutral (3×7 L). The collected solid was dried under vacuum at 70° C. to give 1794 g of desired material. Analytical data was consistent with that obtained from previous batches.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428503B2
Source datasetuspto-grants-2016_08
ORD IDord-5d835e1edd0742e980ff5ef913b25830
Source noteuspto-grants-2016_08