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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875056Generated: October 30, 2026

Imidazole → HCID 11642579, compound

https://huagongshe.com/reaction/875056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantEthyl 7-fluoro-1-[(2S)-1-hydroxy-3-methylbutan-2-yl]-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 58801740—
SolventDimethylformamideHCID 6228—
ProductHCID 11642579HCID 1164257992%

Reaction Steps

The compound (150 g, 335 mmol) obtained in Step 3 was dissolved in dimethylformamide (500 ml), imidazole (30 g, 0.436 mmol) and tert-butyldimethylsilyl chloride (56 g, 369 mmol) were added, and the mixture was stirred at room temperature for 1.5 hr. Water was added to the reaction mixture and extracted with ethyl acetate. The organic layer was washed successively with water, saturated aqueous ammonium chloride solution and saturated brine, and dried over sodium sulfate. The organic layer was filtered and the filtrate was concentrated under reduced pressure, and the obtained residue was purified by silica gel chromatography (ethyl acetate:hexane=1:3 to 1:2) to give 1-((S)-1-tert-butyldimethylsilyloxymethyl-2-methylpropyl)-7-fluoro-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylic acid ethyl ester (173 g, yield 92%) as a colorless amorphous form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981103B2
Source datasetuspto-grants-2015_03
ORD IDord-c10a48d70f8043229f3a2edf1000c5d2
Source noteuspto-grants-2015_03