HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063566Generated: October 25, 2026
Ethylenediaminetetraacetic Acid → 2-anilino-6-fluoro-7-methyl-1-phenyl-1,8-naphthyridin-4(1H)-one
https://huagongshe.com/reaction/1063566
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylenediaminetetraacetic Acid | HCID 6049 | — |
| Reactant | 2-anilino-7-chloro-6-fluoro-1-phenyl-1,8-naphthyridin-4(1H)-one | HCID 21948186 | — |
| Reactant | HCID 178477797 | HCID 178477797 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-anilino-6-fluoro-7-methyl-1-phenyl-1,8-naphthyridin-4(1H)-one | HCID 21948176 | 89% |
Reaction Steps
To 2-anilino-7-chloro-6-fluoro-1-phenyl-1,8-naphthyridin-4(1H)-one (100 mg, 0.273 mmol) in THF (5 mL) was added Pd(PPh3)4 (13 mg, 0.001 mmol) and methyl zinc chloride (2M, 0.819 mL, 1.64 mmol) and the reaction was heated to 75° C. for 18 h. The reaction was then cooled to room temperature and poured into a solution of EDTA in water (2.5 g/20 mL) and extracted with Et2O. The organic layer was washed with brine and concentrated in vacuo. The residue was then taken up in MeOH and filtered. The filtrate was concentrated in vacuo to give 2-anilino-6-fluoro-7-methyl-1-phenyl-1,8-naphthyridin-4(1H)-one (83.0 mg, 89%): LCMS RT: 2.43 min, MH+: 346.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06964971B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-17a85a5bf31b43e88fcae07a9774e844 |
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| Source note | uspto-grants-2005_11 |
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