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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102419Generated: November 1, 2026

Acetone, oxime → HCID 86599612, compound

https://huagongshe.com/reaction/2102419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetone, oximeHCID 67180—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 66999313HCID 66999313—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86599612HCID 86599612—

Reaction Steps

To a solution of acetone oxime (2.20 equivalents) at room temperature is added t-BuOK (2.20 equivalents, 1.0 M solution in THF). After stirring for 30 minutes room temperature, the reaction mixture is cooled to 0° C. A solution 6-acetyl-5-chloro-4-fluoro-3-(2-fluorophenylamino)-pyridine-2-carboxylic acid methyl ester (1.00 equivalent) in THF is added. After stirring for 1 hour at 0-5° C., the reaction mixture is quenched with saturated aqueous NH4Cl and diluted with EtOAc. The organic layer is washed with brine, dried over MgSO4, concentrated in vacuo to give 6-acetyl-4-fluoro-3-(2-fluorophenylamino)-5-isopropylideneaminooxy-pyridine-2-carboxylic acid methyl ester that is used directly. A mixture of 6-acetyl-4-fluoro-3-(2-fluorophenylamino)-5-isopropylideneaminooxy-pyridine-2-carboxylic acid methyl ester in 5% aqueous MeOH is refluxed with stirring for 1 hour. The reaction mixture is diluted with EtOAc and washed with water. The organic layer is dried over MgSO4, filtered, and concentrated in vacuo to give the crude material that is purified by flash column chromatography to afford the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576072B2
Source datasetuspto-grants-2009_08
ORD IDord-4af073fe2d874bda8a5377f31cabb168
Source noteuspto-grants-2009_08