HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Nitrate → 5-Fluoro-4-(6-ethanesulfonyl-pyridin-3-yloxy)-2-nitro-phenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 3-Fluoro-4-(6-ethanesulfonyl-pyridin-3-yloxy)-phenylamine | HCID 23145605 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 5-Fluoro-4-(6-ethanesulfonyl-pyridin-3-yloxy)-2-nitro-phenylamine | HCID 23145095 | — |
Reaction Steps
3.8 g of potassium nitrate was added to a trifluoroacetic acid (100 ml) solution of 10.5 g of 3-fluoro-4-(6-ethanesulfonyl-pyridin-3-yloxy)-phenylamine, and the reaction liquid was stirred for 1 hour at room temperature, and the solvent was evaporated away under reduced pressure. The residue was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=1/2) to obtain the entitled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728025B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-37e3c2824ee24e1991bba8bd626a02a6 |
| Source note | uspto-grants-2010_06 |