HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925245Generated: October 28, 2026
6-Bromo-1-fluoronaphthalen-2-OL → 2-(6,7-Dimethoxy-4-quinolyloxy)-6-bromo-1-fluoronaphthalene
https://huagongshe.com/reaction/1925245
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Bromo-1-fluoronaphthalen-2-OL | HCID 11241940 | — |
| Reactant | n-[6-(6,7-Dimethoxy(4-quinolyloxy))(2-naphthyl)](phenylmethoxy)carboxamide | HCID 59813732 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(6,7-Dimethoxy-4-quinolyloxy)-6-bromo-1-fluoronaphthalene | HCID 67520564 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178557B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-a425f14724fb463582e6e94f222ea4d7 |
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| Source note | uspto-grants-2012_05 |
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