HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 4-Chloroquinolin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-Chloro-2-quinolinecarboxamide | HCID 22029287 | — |
| Reactant | HCID 67508184 | HCID 67508184 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 4-Chloroquinolin-2-amine | HCID 14067407 | — |
Reaction Steps
Bromine (2.32 mL) was dissolved in 5% aqueous potassium hydroxide solution (190 mL), and a solution of 4-chloroquinoline-2-carboxamide [product of Example 262 (1), 9.80 g] in tetrahydrofuran (190 mL) was dropwise added thereto. The mixture was stirred at room temperature for 30 min, and the mixture was stirred at 80° C. for 1 hr with heating. The reaction mixture was filtrated and the filtrate was added to water. The mixture was extracted with chloroform, and the extract was washed with brine and concentrated under reduced pressure. The residue was purified by silica gel chromatography to give 2-amino-4-chloroquinoline (1.98 g) as a pale-yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074794B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-ce7bfe590e3a4a64a00c07b68f3053f5 |
| Source note | uspto-grants-2006_07 |