HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561046Generated: November 1, 2026
4-Fluorophenylboronic acid → 7-Chloro-3-(4-chloro-benzenesulfonyl)-4-(4-fluoro-phenyl)-quinoline
https://huagongshe.com/reaction/561046
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Reactant | 4-Bromo-7-chloro-3-(4-chloro-benzenesulfonyl)-quinoline | HCID 67000154 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 7-Chloro-3-(4-chloro-benzenesulfonyl)-4-(4-fluoro-phenyl)-quinoline | HCID 25168521 | 67.1% |
Reaction Steps
A mixture of 4-bromo-7-chloro-3-(4-chloro-benzenesulfonyl)-quinoline (0.42 g, 1 mmol), 4-fluorophenylboronic acid (0.21 g, 1.5 mmol) and tetrakis-(triphenylphosphin)palladium(0) (0.08 g, 0.07 mmol) in 30 ml 1,2-dimethoxyethane and 8 ml of 2M aqueous sodium carbonate solution was stirred for 2 hours at 70° C. After cooling the mixture was concentrated in vacuo. The crude residue was purified by column chromatography on silica gel (Kieselgel 60, eluent: chloroform) and crystallized from methanol to obtain 0.29 g of the title compound in 67% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063220B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-0a25ebb70ce944ccb556e2193e04c014 |
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| Source note | uspto-grants-2011_11 |
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