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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348449Generated: October 26, 2026

Dimethyl Ether → [5-(4-Fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid

https://huagongshe.com/reaction/348449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl EtherHCID 8254—
ReactantSodium HydroxideHCID 14798—
ReactantDCM MeOH AcOHHCID 21877243—
Reactant[5-(4-Fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid methyl esterHCID 69522849—
SolventMeOH tetrahydrofuranHCID 21899815—
Product[5-(4-Fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acidHCID 2108735616.3%

Reaction Steps

To a solution of [5-(4-fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid methyl ester (prepared above, 82 mg, 0.269 mmol) in THF/methanol (6 mL/0.3 mL) was added 1 N NaOH (0.3 mL, 0.3 mmol). Additional 1 N NaOH aliquots were added after 5 min (0.15 mL), 25 min (0.25 mL), and 2 h (1.0 mL). By thin layer chromatography (15/84/1 methanol/dichloromethane/acetic acid) it appeared that the starting material never disappeared, but LC/MS showed the presence of mostly methyl ether, with some desired acid and no starting material. The reaction mass was extracted with ethyl acetate. The combined organic layers were washed 1× with water, then 2× with 5% NaHCO3. The aqueous layers were combined, acidified to pH 1 with 3% HCl and extracted with dichloromethane. The organic layers were combined, washed with brine, dried and concentrated in vacuo to afford 12.8 mg (16% yield) of the titled carboxylic acid as a white solid. ESI-MS m/z 292 (MH+), 290 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176310B1
Source datasetuspto-grants-2007_02
ORD IDord-dd9c924abb3f41efa2bd2e05fc07d16b
Source noteuspto-grants-2007_02