HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922808Generated: October 31, 2026
Toluene → 7-Chloro-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carbonitrile
https://huagongshe.com/reaction/922808
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (2-Fluoro-4-methoxyphenyl)boronic acid | HCID 15789384 | — |
| Reactant | 4,7-Dichloroquinoline-2-carbonitrile | HCID 57437829 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Chloro-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carbonitrile | HCID 89543584 | 52.3% |
Reaction Steps
To a stirred solution of 4,7-dichloroquinoline-2-carbonitrile (6 g, 26.9 mmol), (2-fluoro-4-methoxyphenyl)boronic acid (5.03 g, 29.6 mmol), 2M sodium carbonate (29.6 ml, 59.2 mmol) in 10:1 toluene (48.9 ml) ethanol (4.89 ml) was added tetrakis(triphenylphosphine)palladium(0) (0.777 g, 0.672 mmol). The mixture was stirred at 75° C. under N2 for 18 hours. The reaction was allowed to cool to ambient temperature. The cooled reaction mixture was diluted with EtOAc and then washed with H2O, brine, dried (MgSO4) and concentrated. The residue was mostly dissolved in warm EtOAc (100 ml), added 100 ml of Et2O, allowed to stand at ambient temperature for 1 hour. The solid was collected and washed with cold Et2O (50 ml) to give 7-chloro-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carbonitrile (4.4 g, 14.07 mmol, 52.3% yield) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278960B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-043c0f46d0a242ee9fa78391287e62b8 |
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| Source note | uspto-grants-2016_03 |
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