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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606074Generated: October 26, 2026

Triethylamine → N-{[3-(4-fluorophenyl)isoxazol-5-yl]methyl}-3-nitro[1,5]naphthyridin-4-amine

https://huagongshe.com/reaction/606074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-fluoro-N-hydroxybenzenecarboximidoyl chlorideHCID 2756316—
Reactant3-nitro-N-prop-2-ynyl[1,5]naphthyridin-4-amineHCID 86247623—
SolventDichloromethaneHCID 6344—
ProductN-{[3-(4-fluorophenyl)isoxazol-5-yl]methyl}-3-nitro[1,5]naphthyridin-4-amineHCID 6704143731.9%

Reaction Conditions

Temperature40 °C

Reaction Steps

Under a nitrogen atmosphere, 4-fluoro-N-hydroxybenzenecarboximidoyl chloride (44.6 g, 257 mmol) was added to a mixture of 3-nitro-N-prop-2-ynyl[1,5]naphthyridin-4-amine (29.34 g, 129 mmol) and anhydrous triethylamine (39.5 mL, 283 mmol) in anhydrous dichloromethane (1 L). The reaction was stirred at 40° C. for 18 hours and then concentrated under reduced pressure. The residue was triturated with water; the resulting solid was isolated by filtration, washed sequentially with isopropanol and a small amount of diethyl ether, and then dried under vacuum to provide 15.02 g of N-{[3-(4-fluorophenyl)isoxazol-5-yl]methyl}-3-nitro[1,5]naphthyridin-4-amine as a brownish-green solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915281B2
Source datasetuspto-grants-2011_03
ORD IDord-949fc96ab45747949bd4864a7d0908bf
Source noteuspto-grants-2011_03