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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386653Generated: October 31, 2026

6-Aminoquinoline → 5-Bromoquinolin-6-amine

https://huagongshe.com/reaction/386653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-AminoquinolineHCID 11373—
ReactantSodium ThiosulfateHCID 24477—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product5-Bromoquinolin-6-amineHCID 1274123232%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372865B2
Source datasetuspto-grants-2013_02
ORD IDord-baedc0ae213d4078870c0f88eb117d14
Source noteuspto-grants-2013_02