HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → N-(4-benzyloxy-5-fluoro-2-nitrophenyl)pyrazinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | N-(4-benzyloxy-3-fluorophenyl)pyrazinecarboxamide | HCID 23145734 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(4-benzyloxy-5-fluoro-2-nitrophenyl)pyrazinecarboxamide | HCID 23145743 | — |
Reaction Steps
40 ml of trifluoroacetic acid and 1.99 g of potassium nitrate were added to a chloroform (40 ml) suspension of 5.80 g of N-(4-benzyloxy-3-fluorophenyl)pyrazinecarboxamide, with cooling with ice, and the reaction liquid was stirred overnight at room temperature. The solvent was evaporated away under reduced pressure, and aqueous saturated sodium bicarbonate was added to it. The resulting solid was washed with a mixed solvent of ethyl acetate and hexane to obtain the entitled compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728025B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-ca3065c4765142768db3178da2f15c3d |
| Source note | uspto-grants-2010_06 |