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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407209Generated: October 27, 2026

Hydrochloric Acid → 7-[4-({[(2-Fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]thieno[3,2-b]pyridine-2-carboxylic acid

https://huagongshe.com/reaction/2407209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantLithium hydroxide methanolHCID 23717829—
ReactantMethyl 7-[4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)-phenoxy]thieno[3,2-b]pyridine-2-carboxylateHCID 51041147—
SolventMethanolHCID 887—
Product7-[4-({[(2-Fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]thieno[3,2-b]pyridine-2-carboxylic acidHCID 50915125—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred suspension of methyl 7-[4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)-phenoxy]thieno[3,2-b]pyridine-2-carboxylate (50 mg, 0.11 mmol) in MeOH (3 ml), was added 0.4M LiOH/MeOH solution (10 ml, 4.0 mmol). The mixture was heated at 50° C. for 7 hours, and poured into 100 ml of water. 1M HCl was added until pH=4. The resulting precipitates were filtered, washed with water and dried in vacuo to give 7-[4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]thieno[3,2-b]pyridine-2-carboxylic acid as light grey solid. Yield: 40 mg, 83%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809534B2
Source datasetuspto-grants-2014_08
ORD IDord-3313b26a8f934b20afa2fe5182d46b30
Source noteuspto-grants-2014_08