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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469251Generated: October 30, 2026

Ammonium Chloride → HCID 66636981, compound

https://huagongshe.com/reaction/469251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Methylpropan-2-olateHCID 4574913—
ReactantPotassiumHCID 5462222—
Reactant(3-Benzyloxypropyl)triphenylphosphonium bromideHCID 10929077—
ReactantHCID 86633064HCID 86633064—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66636981HCID 6663698199.6%

Reaction Steps

To a 20 ml THF suspension of 1081 mg of (3-benzyloxypropyl)triphenylphosphonium bromide was added 258 mg of potassium, tert-butoxide followed by stirring for 1.5 hours. A 10 ml THF solution of 358 mg of 7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde was added thereto, followed by stirring for 1 hour. To the reaction mixture was added aqueous saturated ammonium chloride, followed by extraction with ethyl acetate and washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate and subsequent concentration under a reduced pressure, the residue was purified by silica gel column chromatography to obtain 488 mg of 3-[4-(benzyloxy)but-1-en-1-yl]-7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoroquinolin-4(1H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629126B2
Source datasetuspto-grants-2014_01
ORD IDord-f386f690384a4225b083ba4e5a95032f
Source noteuspto-grants-2014_01