HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431530Generated: November 2, 2026
2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl → HCID 59631540, compound
https://huagongshe.com/reaction/1431530
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 2,5-Dimorpholinopyridin-3-amine | HCID 59631046 | — |
| Reactant | HCID 59631233 | HCID 59631233 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59631540 | HCID 59631540 | — |
Reaction Steps
The Buchwald coupled product was prepared according to Procedure H using dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (0.019 g, 0.040 mmol), 2,5-dimorpholinopyridin-3-amine (0.080 g, 0.30 mmol), 4-chloro-5,7-difluoro-3-methyl-2-(4-vinylpyridin-2-yl)quinoline (0.08 g, 0.25 mmol), Pd2dba3 (0.009 g, 0.010 mmol) and sodium tert-butoxide (0.061 g, 0.63 mmol) in toluene (2.5 mL) at 100° C. for 4.5 h. The crude product was purified by column chromatography on silica gel (0 to 100% DCM/MeOH/ammonium hydroxide (90/9/1)) to give the desired product N-(2,5-dimorpholinopyridin-3-yl)-5,7-difluoro-3-methyl-2-(4-vinylpyridin-2-yl)quinolin-4-amine. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.54 (1H, br. s), 8.28 (1H, d, J=5.9 Hz), 7.83 (1H, d, J=2.7 Hz), 7.50-7.58 (2H, m), 7.28 (1H, d, J=2.7 Hz), 7.24 (1H, m), 7.08 (1H, d, J=2.2 Hz), 6.87 (1H, dd, J=5.7, 2.3 Hz), 5.76 (1H, m), 5.41 (1H, dd, 17.8, 1.6 Hz), 3.71-3.76 (4H, m), 3.55-3.60 (4H, m), 3.08 (4H, m), 3.02 (4H, m), 2.40 (3H, s). Mass Spectrum (ESI) m/e=545.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940724B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-903ee0b8211547e59b8e04aa83526dd4 |
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| Source note | uspto-grants-2015_01 |
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