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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469228Generated: October 30, 2026

Sodium Iodide → HCID 86633057, compound

https://huagongshe.com/reaction/469228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantChloromethyl pivalateHCID 87885—
ReactantHCID 66636857HCID 66636857—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventAcetonitrileHCID 6342—
ProductHCID 86633057HCID 86633057—

Reaction Conditions

Temperature80 °C

Reaction Steps

500 mg of {(E)-2-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]vinyl}phosphonic acid was dissolved in 10 ml of acetonitrile, and 86 mg of sodium iodide, 0.51 ml of 1,8-diazabicyclo[5.4.0]-7-undecene, 194 mg of tetrabutylammonium hydrogensulfate and 0.53 ml of chloromethyl pivalate were added in that order, followed by overnight stirring at 80° C. Aqueous saturated ammonium chloride was added to the reaction mixture, followed by extraction with chloroform. The organic layer was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate and then evaporated under a reduced pressure. By purifying the resulting residue by silica gel column chromatography, 400 mg of bis{[(2,2-dimethylpropanoyl)oxy]methyl}{(E)-2-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]vinyl}phosphonate (Example 25) and 190 mg of {[{(E)-2-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydro-3-quinolinyl]vinyl}(hydroxy)phosphoryl]oxy}methyl pivalate (Example 26) were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629126B2
Source datasetuspto-grants-2014_01
ORD IDord-f56b214053504496a521e5ba19e46efc
Source noteuspto-grants-2014_01