HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-Hydroxyquinoline-7-carboxylic Acid → HCID 178522603, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-Hydroxyquinoline-7-carboxylic Acid | HCID 231363 | — |
| Reactant | 2-Amino-5-(4-chlorophenyl)-4-thiazolol | HCID 18372726 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178522603 | HCID 178522603 | 40.1% |
Reaction Steps
A solution of 8-hydroxyquinoline-7-carboxylic acid (0.280 g) of Preparation 1 and 2-amino-5-(4-chlorophenyl)-4-hydroxy-1,3-thiazole (0.340 g) in 50 mL xylenes is heated to reflux. To this is added dropwise PCl8 (0.103 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 triturated with HOAc to yield 0.236 g of the title product as a gold solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06252080B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-8f21d5ce278a42a0a72eb404b93a8eb5 |
| Source note | uspto-grants-2001_06 |