HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884978Generated: October 25, 2026
Triethylamine → 3-chloro-N-[2-hydroxy-5-(trifluoromethoxy)phenyl]isonicotinamide
https://huagongshe.com/reaction/884978
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | 3-Chloropyridine-4-carboxylic acid | HCID 2735816 | — |
| Reactant | 2-Amino-4-(trifluoromethoxy)phenol | HCID 2737729 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-chloro-N-[2-hydroxy-5-(trifluoromethoxy)phenyl]isonicotinamide | HCID 66880033 | 71.3% |
Reaction Steps
A mixture of 0.35 g of 2-amino-4-trifluoromethoxy phenol, 0.29 g of 3-chloroisonicotinic acid, 1.04 g of (benzotriazole-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (hereinafter, referred to as a BOP reagent), 0.24 g of triethylamine and 5 ml of DMF was stirred at room temperature for two hours. Water was added to the reaction mixture, precipitated solid was collected by filtration. The resultant solid was dissolved in ethyl acetate. Then, the organic layer was washed with a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.43 g of 3-chloro-N-[2-hydroxy-5-(trifluoromethoxy)phenyl]isonicotinamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08242133B2 |
|---|
| Source dataset | uspto-grants-2012_08 |
|---|
| ORD ID | ord-6b396ef73cef4d3fab5bf1f3fc422a28 |
|---|
| Source note | uspto-grants-2012_08 |
|---|