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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294335Generated: October 27, 2026

Hydrochloric Acid → 2-[2-[[3-[(5-Methyl-2-phenyl-4-thiazolyl)methoxy]-5-isoxazolyl]methoxy]-3-pyridyl]acetic acid

https://huagongshe.com/reaction/1294335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant2-[2-[[3-[(5-Methyl-2-phenyl-4-thiazolyl)methoxy]-5-isoxazolyl]methoxy]-3-pyridyl]acetonitrileHCID 68887422—
Product2-[2-[[3-[(5-Methyl-2-phenyl-4-thiazolyl)methoxy]-5-isoxazolyl]methoxy]-3-pyridyl]acetic acidHCID 6888645681%

Reaction Steps

To a mixture of 2-[2-[[3-[(5-methyl-2-phenyl-4-thiazolyl)methoxy]-5-isoxazolyl]methoxy]-3-pyridyl]acetonitrile (0.35 g) and ethanol (10 mL) was added a 2N aqueous sodium hydroxide solution (10 mL) and the mixture was heated under reflux for 5 hrs. 1N Hydrochloric acid (20 mL) and water were added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated to give crystals (0.30 g, 81%) of 2-[2-[[3-[(5-methyl-2-phenyl-4-thiazolyl)methoxy]-5-isoxazolyl]methoxy]-3-pyridyl]acetic acid. Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 109-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238716B2
Source datasetuspto-grants-2007_07
ORD IDord-03975294f29a431eb297668d7a1bdf97
Source noteuspto-grants-2007_07