HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloropyridine-2-carboxamide → 4-(4-Amino-2,3-difluorophenoxy)pyridine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloropyridine-2-carboxamide | HCID 303543 | — |
| Reactant | 4-Amino-2,3-difluorophenol | HCID 2778766 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Amino-2,3-difluorophenoxy)pyridine-2-carboxamide | HCID 57470878 | 41.5% |
Reaction Steps
To a solution of 4-amino-2,3-difluorophenol (208 mg, 1.43 mmol) in DMF (4 mL) was added t-BuOK (257 mg, 2.29 mmol). The reaction was stirred at rt for 30 minutes, then 4-chloropicolinamide (249 mg, 1.59 mmol) was added. The mixture was microwaved at 120° C. for 3 hours, then cooled to rt and diluted with 25 mL of water. The resulted mixture was extracted with EtOAc (30 mL×3), and the combined organic phases were washed with brine (30 mL×3), dried over anhydrous Na2SO4, and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (v/v)=1/2) to give the title compound as an orange solid (110 mg, 41.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09326975B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-c93dea3067014e3bb73173238c7a25d0 |
| Source note | uspto-grants-2016_05 |