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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266509Generated: November 2, 2026

Hydrochloric Acid → [8-chloro-3-(2-chloro-4-methanesulfonylbenzyl)-4-difluoromethoxy-2-methylquinolin-5-yloxy]acetic Acid

https://huagongshe.com/reaction/2266509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantLithium HydroxideHCID 3939—
Reactant[8-chloro-3-(2-chloro-4-methanesulfonylbenzyl)-4-difluoromethoxy-2-methylquinolin-5-yloxy]acetic Acid Methyl EsterHCID 68784446—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product[8-chloro-3-(2-chloro-4-methanesulfonylbenzyl)-4-difluoromethoxy-2-methylquinolin-5-yloxy]acetic AcidHCID 57742532—

Reaction Steps

A mixture of [8-chloro-3-(2-chloro-4-methanesulfonylbenzyl)-4-difluoromethoxy-2-methylquinolin-5-yloxy]acetic acid methyl ester (0.034 g), methanol (8.0 mL), tetrahydrofuran (8.0 mL), water (5.0 mL) and lithium hydroxide (0.027 μg) was stirred at room temperature for 1 hour. The solution was acidified by the addition of 1.0 M aqueous hydrochloric acid and extracted with ethyl acetate. The combined extracts were dried over magnesium sulfate and the solvent removed under reduced pressure. Purification of the residue by preparative reverse-phase HPLC using a gradient of acetonitrile in water gave title compound as a yellow solid, 0.09 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858640B2
Source datasetuspto-grants-2010_12
ORD IDord-a3d9cc9951df46a4836415361665137e
Source noteuspto-grants-2010_12