Methane → HCID 69197192, compound

Participants

Reaction Conditions

Reaction Steps

To a solution of 4-bromo-2-nitro-1-[(phenylmethyl)oxy]benzene (7.0 g, 22.7 mmol) in dioxane (120 ml) was added cis-2,6-dimethylpiperazine (7.8 g, 67.4 mmol) followed by cesium carbonate (11.0 g, 33.8 mmol), rac-2,2′-bis(diphenylphosphino)-1,1′-binapthyl (2.1 g, 3.4 mmol) and palladium acetate (516 mg, 2.3 mmol). The resulting mixture was heated at 100° C. under an atmosphere of argon overnight. The mixture was allowed to cool, charcoal was added and the mixture stirred at room temperature for 30 minutes. The solids were then removed by filtration through celite and the residue washed with ethyl acetate. The filtrate was then reduced in vacuo and the residue dissolved in 2M aqueous hydrochloric acid and ethyl acetate added. A yellow solid formed that was immiscible in both phases so the mixture was filtered and the solid washed with ethyl acetate. The biphasic filtrate was then separated and the aqueous layer washed with more ethyl acetate. The aqueous was then basified with 0.880 ammonia and the yellow solid collected by filtration added. The resulting basified aqueous solution was then extracted with dichloromethane (×2) and the combined dichloromethane layers dried over anhydrous magnesium sulfate, filtered and reduced in vacuo. The residue was then purified by chromatography on silica gel (gradient 0 to 15% methanol in dichloromethane) to afford the title product. MS (ES+) m/e 342 [M+H]+.

Provenance & Evidence