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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115756Generated: October 30, 2026

6-Bromo-1-fluoronaphthalen-2-OL → 2-(6,7-Dimethoxy-4-quinolyloxy)-6-bromo-1-fluoronaphthalene

https://huagongshe.com/reaction/2115756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-1-fluoronaphthalen-2-OLHCID 11241940—
Reactantn-[6-(6,7-Dimethoxy(4-quinolyloxy))(2-naphthyl)](phenylmethoxy)carboxamideHCID 59813732—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product2-(6,7-Dimethoxy-4-quinolyloxy)-6-bromo-1-fluoronaphthaleneHCID 67520564—

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 4-chloro-6,7-dimethoxy-quinoline (prepared as in Example 1, Step b)(371 mg, 1.66 mmol), 6-bromo-1-fluoro-naphthalen-2-ol (Step a, 400 mg, 1.66 mmol) and DMAP (203 mg, 1.66 Aldrich) in toluene (in a microwave tube) was heated in a microwave oven (Personal Chemistry, Emrys Optimizer) at 180° C. for 2 h. The mixture was cooled to RT and diluted with 30 mL of EtOAc. The solution was washed with 10 mL of brine twice, dried over Na2SO4 and concentrated in vacuo. The residue was further purified with silica gel column chromatography (40-100% EtOAc in hexanes) to give title compound as a white solid. MS (ESI, pos. ion) m/z: 428.0 (M+1). Mass Calc'd for C21H15BrFNO3: 427.02.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435823B2
Source datasetuspto-grants-2008_10
ORD IDord-638c3b58742840c5844a6a214bd7b097
Source noteuspto-grants-2008_10