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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375631Generated: November 2, 2026

Bromobenzene → [4-(5-Methyl-3-phenyl-isoxazol-4-yl)-pyrimidin-2-yl]-phenyl-amine

https://huagongshe.com/reaction/1375631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantBinap, (A+-)-HCID 634876—
Reactant4-(5-Methyl-3-phenylisoxazol-4-yl)pyrimidin-2-amineHCID 2745721—
ReactantSodium t-butoxideHCID 23676156—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product[4-(5-Methyl-3-phenyl-isoxazol-4-yl)-pyrimidin-2-yl]-phenyl-amineHCID 994933436.5%

Reaction Steps

To a solution of 50 mg (0.2 mmol) of 4-(5-methyl-3-phenyl-isoxazole-4-yl)-pyrimidin-2-ylamine in 1 mL of toluene was added successively 63 μL (0.6 mmol) of bromobenzene, 10 mg of tris(dibenzylideneacetone) dipalladium, 10 mg of BINAP and 39 mg (0.4 mmol) of sodium tert-butoxide. The mixture was heated at reflux for 16 h, diluted with ethyl acetate, filtered, washed successively with saturated aqueous sodium bicarbonate and brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography over silica gel eluted with ethyl acetate-hexanes 1:3, to afford 24 mg (36%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169798B2
Source datasetuspto-grants-2007_01
ORD IDord-c2d76d0e81494c2181d7679145ab6bc4
Source noteuspto-grants-2007_01