HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenol → 4-(4-Aminophenoxy)pyridine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | 4-Chloropyridine-2-carboxamide | HCID 303543 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 4-(4-Aminophenoxy)pyridine-2-carboxamide | HCID 23088338 | — |
Reaction Steps
Entry 14: 4-Chloropyridine-2-carbonyl chloride HCl salt was reacted with ammonia according to Method A2, Step 3b to form 4-chloro-2-pyridinecarboxamide. 4-Chloro-2-pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 using DMAC in place of DMF to give 4-(2-carbamoyl-4-pyridyloxy)aniline. According to Method C4,2-methoxy-5-(trifluoromethyl)aniline was reacted with phosgene followed by 4-(2-carbamoyl-4-pyridyloxy)aniline to afford the urea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897623B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-773ce1bd9e5f458e804aed7614fa7d6a |
| Source note | uspto-grants-2011_03 |