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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618793Generated: November 1, 2026

2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl → HCID 67285789, compound

https://huagongshe.com/reaction/1618793

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
ReactantSodium t-butoxideHCID 23676156—
Reactant4-Chloro-7-fluoro-3-methyl-2-(pyridin-2-yl)quinolineHCID 59631075—
ReactantHCID 67284959HCID 67284959—
Catalyst2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
SolventTolueneHCID 1140—
ProductHCID 67285789HCID 67285789—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a microwave vial was added sodium tert-butoxide (0.035 g, 0.37 mmol), ruphos (8.6 mg, 0.018 mmol), 4-chloro-7-fluoro-3-methyl-2-(pyridin-2-yl)-quinoline (0.053 g, 0.19 mmol), 2,2-dimethyl-6′-morpholinospiro[[1,3]dioxane-5,3′-indoline] (0.056 g, 0.18 mmol), and XPhos pre-catalyst (0.014 g, 0.018 mmol) in toluene (1.2 mL). The suspension was deoxygenated with argon for 5 min and stirred at 100° C. for 90 min under microwave irradiation. Purification by column chromatography (eluting with a gradient of 10-60% EtOAc in hexanes) gave 1′-(7-fluoro-3-methyl-2-(pyridin-2-yl)quinolin-4-yl)-2,2-dimethyl-6′-morpholinospiro[[1,3]dioxane-5,3′-indoline] as a yellow solid. Mass Spectrum (ESI) m/e=541.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765940B2
Source datasetuspto-grants-2014_07
ORD IDord-7a42c9cf74934b40819d438aed102e3b
Source noteuspto-grants-2014_07