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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491522Generated: October 27, 2026

Hydrochloric Acid → Ethyl 1,4-dihydro-8-fluoro-6-iodo-1-[2-(tert-butyldimethylsilyloxy)ethyl]-4-oxo-3-quinolinecarboxylate

https://huagongshe.com/reaction/491522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178472040HCID 178472040—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 1,4-dihydro-8-fluoro-6-iodo-1-[2-(tert-butyldimethylsilyloxy)ethyl]-4-oxo-3-quinolinecarboxylateHCID 2308397492%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2-(2,3-difluoro-5-iodobenzoyl)-3-[2-(tert-butyldimethylsilyloxy)ethylamino]acrylate (2.3 g, 4.3 mmol) obtained in Step 3 was dissolved in THF (25 ml), sodium hydride (256 mg, 6.4 mmol) was added under ice-cooling and the mixture was stirred at 0° C. for 1 hr. 1N Hydrochloric acid (6.4 ml, 6.4 mmol) was added to neutralize the reaction mixture. Water was further added and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (ethyl acetate:hexane=1:2 to ethyl acetate:hexane=2:1) to give the object product (2.0 g, yield 92%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531554B2
Source datasetuspto-grants-2009_05
ORD IDord-52e0a1b389724202bd1b485b08524b62
Source noteuspto-grants-2009_05