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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280109Generated: October 29, 2026

Triphenylphosphine → Isoxazolo(4,5-c)quinolin-3(2H)-one, 8-fluoro-2-phenyl-

https://huagongshe.com/reaction/280109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-ethoxycarbonyliminocarbamateHCID 86599450—
ReactantN,4-dihydroxy-6-fluoro-N-phenyl-3-quinoline carboxamideHCID 178519810—
SolventDimethylformamideHCID 6228—
ProductIsoxazolo(4,5-c)quinolin-3(2H)-one, 8-fluoro-2-phenyl-HCID 1366923714.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a mixture of 8.81 g of triphenylphosphine and 50 ml of dimethylformamide, 5.58 g of ethyl azodicarboxylate were poured at 10°-15° C. and after continued stirring for 15 minutes, 6.68 g of the product of Step A were added in small fractions. Stirring was maintained for 2 hours at 0° C. and for 16 hours at ambient temperature and the crystallized product was separated. The filtrate was poured into iced water, and extracted with dichloromethane. The organic phase was washed with water, dried and the solvent was eliminated. The residue was chromatographed on silica and eluted with a methylene chloride-ethyl acetate mixture (9-1) to obtain 0.92 g of 8-fluoro-2-phenylisoxazolo(4,5-c)quinolin-3-(2H)-one melting at 174° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04588731
Source datasetuspto-grants-1986_05
ORD IDord-9301a79aaf864eb5867b3fa139b9f8bc
Source noteuspto-grants-1986_05