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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709646Generated: October 29, 2026

Hydrochloric Acid → N-(3-((6-(2,2-dimethylpropyl)-5-(2-fluoro-5-methoxyphenyl)pyridin-2-yl)methoxy)phenyl)-N-ethylglycine

https://huagongshe.com/reaction/709646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(ethyl(3-((5-(2-fluoro-5-methoxyphenyl)-6-neopentylpyridin-2-yl)methoxy)phenyl)amino)acetateHCID 117760074—
SolventEthanolHCID 702—
ProductN-(3-((6-(2,2-dimethylpropyl)-5-(2-fluoro-5-methoxyphenyl)pyridin-2-yl)methoxy)phenyl)-N-ethylglycineHCID 117759993—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of ethyl 2-(ethyl(3-((5-(2-fluoro-5-methoxyphenyl)-6-neopentylpyridin-2-yl)methoxy)phenyl)amino)acetate (entire amount) in ethanol (3.0 mL) was added 1N aqueous sodium hydroxide solution (2.0 mL), and the mixture was stirred at 50° C. for 1 hr. 1N Hydrochloric acid was added, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (90 mg) as pale-yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181186B2
Source datasetuspto-grants-2015_11
ORD IDord-0f0ddb9884214a06a4260d8a6de5cf05
Source noteuspto-grants-2015_11