HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386653Generated: October 31, 2026
6-Aminoquinoline → 5-Bromoquinolin-6-amine
https://huagongshe.com/reaction/386653
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Aminoquinoline | HCID 11373 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromoquinolin-6-amine | HCID 12741232 | 32% |
Reaction Steps
To a solution of quinolin-6-ylamine (503 mg, 3.49 mmol) in dichloromethane (17 mL) and methanol (8.6 mL) was added tetra-n-butylammonium tribromide (1.68 g, 3.49 mmol). The mixture was stirred at 25° C. for 90 minutes, and then 10 5 mL of aqueous sodium thiosulfate was added. The mixture was extracted with dichloromethane, and the combined extracts were washed with water, dried (Na2SO4), filtered and concentrated to dryness under reduced pressure. Purification by flash column (hexanes/ethylacetate gradient) gave 5-bromo-quinolin-6-ylamine (246 mg, 32%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372865B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-baedc0ae213d4078870c0f88eb117d14 |
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| Source note | uspto-grants-2013_02 |
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