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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672200Generated: October 30, 2026

2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl → HCID 59405022, compound

https://huagongshe.com/reaction/1672200

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3-Bromo-5-chloro-2-(trifluoromethyl)pyridineHCID 53417468—
ReactantHCID 59405023HCID 59405023—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59405022HCID 5940502212%

Reaction Steps

A mixture of 2-amino-9-(trifluoromethyl)-5,7-dihydro-6H-pyrimido[5,4-d][1]benzazepin-6-one (0.42 g, 1.44 mmol), 3-bromo-5-chloro-2-(trifluoromethyl)pyridine (0.37 g, 1.44 mmol), Xphos (0.054 g, 0.115 mmol), and tris(dibenzylideneacetone)dipalladium(0) (0.052 g, 0.057 mmol) in a sealed microwave tube was evacuated and purged with argon 3 times. To the vial were added tert-butyl alcohol (5.3 mL) and 1.00 M of t-BuOK in tert-butyl alcohol (2.0 mL, 2.0 mol) via syringe. The mixture was allowed to stir to mix well, then was subjected to microwave irradiation at 150° C. for 1200 sec. The mixture was allowed to cool to rt and THF (6 mL) was added. The mixture was filtered and the solid was washed with THF. The organic solutions were combined and concentrated. The residue was purified by column chromatography to give 2-{[5-chloro-2-(trifluoromethyl)pyridin-3-yl]amino}-9-(trifluoromethyl)-5,7-dihydro-6H-pyrimido[5,4-d][1]benzazepin-6-one (0.081g, 12%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998952B2
Source datasetuspto-grants-2011_08
ORD IDord-8642ea942fbd493c8d16b6c84e8cb681
Source noteuspto-grants-2011_08