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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421842Generated: November 1, 2026

Tetrahydrofuran → HCID 11993185, compound

https://huagongshe.com/reaction/421842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 136381720HCID 136381720—
SolventEthyl AcetateHCID 8857—
ProductHCID 11993185HCID 11993185—

Reaction Conditions

Temperature60 °C

Reaction Steps

1-{4-[Amino(hydroxyimino)methyl]pyrimidin-2-yl}-4-(4,4-dimethylpentanoyl)piperazine (186 mg) obtained in Example 64-1) was dissolved in tetrahydrofuran (3 mL), and oily sodium hydroxide (25 mg) was added thereto and stirred at 60° C. for 20 minutes. Then, ethyl acetate (0.082 ml) was added to it and heated under reflux for 1 hour. The reaction liquid was diluted with ethyl acetate, washed with water and saturated saline water, and dried with anhydrous sodium sulfate. The solvent was evaporated away, and the resulting residue was isolated and purified through thin-layer silica gel chromatography (chloroform/methanol=19/1) to obtain 53.4 mg of the entitled compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101618B2
Source datasetuspto-grants-2012_01
ORD IDord-314ddf6d0bf14b779fbecb6db79c4809
Source noteuspto-grants-2012_01