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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431477Generated: November 4, 2026

2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl → HCID 59631343, compound

https://huagongshe.com/reaction/1431477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantSodium t-butoxideHCID 23676156—
Reactant2,5-Dimorpholinopyridin-3-amineHCID 59631046—
ReactantHCID 59631278HCID 59631278—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 59631343HCID 59631343—

Reaction Steps

The Buchwald coupled product was prepared according to Procedure H using dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (0.022 g, 0.045 mmol), 2,5-dimorpholinopyridin-3-amine (0.090 g, 0.34 mmol), 4-chloro-2-(3,4-dimethylphenyl)-5,7-difluoro-3-methylquinoline (0.090 g, 0.283 mmol), Pd2dba3 (0.010 g, 0.011 mmol) and sodium tert-butoxide (0.068 g, 0.71 mmol) in toluene (2.8 mL) at 120° C. for 1 h. The crude product was purified by column chromatography on basic alumina (0 to 50% hexanes/EtOAc) to give the desired product 2-(3,4-dimethylphenyl)-N-(2,5-dimorpholinopyridin-3-yl)-5,7-difluoro-3-methylquinolin-4-amine. 1H NMR (400 MHz, CDCl3) δ ppm 7.71-7.68 (1H, br d, J=10.0 Hz), 7.63 (2H, m), 7.37 (1H, br s), 7.28 (2H, m), 6.98 (1H, ddd, J=13.3, 8.6, 2.5 Hz), 6.36 (1H, d, J=2.2 Hz), 3.92 (4H, m), 3.83 (4H, app t, J=4.3 Hz), 3.25 (4H, br. s), 3.06 (4H, app t, J=4.3 Hz), 2.36 (6H, s), 2.15 (3H, s). Mass Spectrum (ESI) m/e=546.3 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-3fe01bdeb620459abbf5e7626b30d90c
Source noteuspto-grants-2015_01