Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl iodide | HCID 11166 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-fluoro-1,5-naphthyridin-2(1H)-one 5-oxide | HCID 68816493 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68816871 | HCID 68816871 | — |
Reaction Steps
Crude 7-fluoro-1,5-naphthyridin-2(1H)-one 5-oxide (0.995 g, 5.524 mmol) and potassium carbonate were stirred in anhydrous DMF (20 mL) under argon, and allyl iodide (1.5 mL, ca. 3 eq.) was added. The mixture was stirred at rt overnight. The solvent was removed under reduced pressure and the residue was partitioned between DCM (100 mL) and water (50 mL). The organic phase was separated using a hydrophobic frit and the aqueous phase was extracted with DCM (2×50 mL). The combined organic extracts were dried over anhydrous sodium sulphate, filtered and evaporated under reduced pressure to give the crude product as a brown gum. This was purified by column chromatography on silica gel eluted with 0-10% methanol in DCM. Appropriate fractions were combined and evaporated under reduced pressure to give 7-fluoro-1-(2-propen-1-yl)-1,5-naphthyridin-2(1H)-one 5-oxide (0.341 g) as a tan amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08071592B2 |
|---|
| Source dataset | uspto-grants-2011_12 |
|---|
| ORD ID | ord-cc1ad70fedf34e5c8a48f2bfc63117f2 |
|---|
| Source note | uspto-grants-2011_12 |
|---|