HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus oxychloride → N-(5-chloropyridin-2-yl)-5-fluoro-2-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-Amino-5-chloropyridine | HCID 66174 | — |
| Reactant | 5-Fluoro-2-nitrobenzoic acid | HCID 2737420 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(5-chloropyridin-2-yl)-5-fluoro-2-nitrobenzamide | HCID 21906257 | 72% |
Reaction Steps
A solution of 5-fluoro-2-nitrobenzoic acid (10.0 g, 54 mmol, 1.0 equiv.), 2-amino-5-chloropyridine (9.02 g, 1.3 equiv.), in 80 mL of pyridine was treated with phosphorous oxychloride (25.3 g, 3.0 equiv.) for 30 minutes. The volatile was evaporated and the residue was redissolved into EtOAc, washed with 1N HCl, saturated aqueous NaHCO3 and saturated aqueous NaCl. The organic layer was dried over Na2SO4, filtered, and evaporated. The product was triturated with diethyl ether to give N-(5-chloro-2-pyridinyl)-(2-nitro)-5-fluorophenylcarboxamide (11.5 g, 72%). MS found for C12H7ClFN3O'(M+H)+: 296, (M+2+H): 298.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07022695B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-14264308875c496eb5454edb75c702cc |
| Source note | uspto-grants-2006_04 |