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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474474Generated: October 27, 2026

Acetic Anhydride → 4-((2-Fluoro-3-pyridinyl)methylene)-2-(2-thienyl)-5(4H)-oxazolone

https://huagongshe.com/reaction/1474474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium AcetateHCID 517045—
Reactant((2-Thienylcarbonyl)amino)acetic acidHCID 679227—
Reactant2-Fluoropyridine-3-carbaldehydeHCID 11434944—
SolventWaterHCID 962—
Product4-((2-Fluoro-3-pyridinyl)methylene)-2-(2-thienyl)-5(4H)-oxazoloneHCID 7523847564.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a screw-capped test tube, N-(2-thienylcarbonyl)glycine (56 mg, 0.3 mmol), 2-fluoropyridin-3-carboxaldehyde (41 mg, 0.3 mmol), sodium acetate (25 mg, 0.3 mmol) and acetic anhydride (0.3 mL) were added. The test tube was sealed, and it was then stirred at an external temperature of 90° C. Three hours later, the temperature of the reaction solution was returned to room temperature, and water (1.5 mL) was then added thereto. The obtained mixture was stirred at the same temperature as described above for 1.5 hours. Thereafter, the precipitated crystal was collected by filtration, and it was washed with water (5 mL) and was then dried under reduced pressure, so as to obtain 53 mg of the above-captioned compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018238B2
Source datasetuspto-grants-2015_04
ORD IDord-3e8eab59ba934e5cbb91518d333e02ad
Source noteuspto-grants-2015_04