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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-fluoro-N-hydroxybenzenecarboximidoyl chloride | HCID 2756316 | — |
| Reactant | 3-nitro-N-prop-2-ynyl[1,5]naphthyridin-4-amine | HCID 86247623 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-{[3-(4-fluorophenyl)isoxazol-5-yl]methyl}-3-nitro[1,5]naphthyridin-4-amine | HCID 67041437 | 31.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915281B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-949fc96ab45747949bd4864a7d0908bf |
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| Source note | uspto-grants-2011_03 |
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