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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889586Generated: October 31, 2026

(Aminooxy)acetic acid → ({[2-[6-ethyl-2,4-dioxo-1-{[2'-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-1,4-dihydrothieno[2,3-d]pyrimidin-3(2H)-yl]-1-(4-fluorophenyl)ethylidene]amino}oxy)acetic acid

https://huagongshe.com/reaction/1889586

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Aminooxy)acetic acidHCID 286—
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant6-ethyl-3-[2-(4-fluorophenyl)-2-oxoethyl]-1-{[2'-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}thieno[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 136052318—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product({[2-[6-ethyl-2,4-dioxo-1-{[2'-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-1,4-dihydrothieno[2,3-d]pyrimidin-3(2H)-yl]-1-(4-fluorophenyl)ethylidene]amino}oxy)acetic acidHCID 136052314—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 6-ethyl-3-[2-(4-fluorophenyl)-2-oxoethyl]-1-{[2′-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (0.2 g), (aminooxy)acetic acid (0.053 g), NaHCO3 (1.0 g) and ethanol (20 mL) was stirred at 80° C. for 16 hr. To the reaction mixture were added chloroform and water, and the mixture was adjusted to pH 4 with 1N hydrochloric acid. The chloroform layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as a stereoisomer mixture (0.062 g, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501750B2
Source datasetuspto-grants-2013_08
ORD IDord-19e88e8348bc4c12a5b00c8b4e43d47c
Source noteuspto-grants-2013_08