HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloroaniline → N-(4-Chlorophenyl)-8-hydroxy-7-quinolinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | 8-Hydroxyquinoline-7-carboxylic Acid | HCID 231363 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(4-Chlorophenyl)-8-hydroxy-7-quinolinecarboxamide | HCID 18372520 | 32.8% |
Reaction Steps
A solution of 8-hydroxyquinoline-7-carboxylic acid (3.78 g) of Preparation 1 and 4-chloroaniline (2.55 g) in 250 mL xylenes is heated to reflux. To this is added dropwise PCl3 (1.37 g). Refluxing is continued overnight. The reaction is then cooled and water is added to destroy excess PCl3. The resulting solid is collected, washed with water and dried. The crude product is recrystallized from EtOAc/hexanes to yield 1.96 g of the title product as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06310211B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-3dc46ab04c534ae0b46a7a1f71ba2db6 |
| Source note | uspto-grants-2001_10 |