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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416545Generated: November 1, 2026

N-Methyl dicyclohexylamine → HCID 69922546, compound

https://huagongshe.com/reaction/2416545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl dicyclohexylamineHCID 24210—
Reactant1,4-DioxaneHCID 31275—
ReactantEthyl trans-crotonateHCID 429065—
Reactant4-(Pyrimidin-2-yl)bromobenzeneHCID 22287544—
CatalystTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
ProductHCID 69922546HCID 6992254670%

Reaction Steps

Dioxane (2 mL) was added to a mixture of 2-(4-bromophenyl)pyrimidine (0.59 g, 2.51 mmol, prepared as described in U.S. Pat. No. 5,780,473), tri-t-butylphosphonium tetrafluoroborate (36 mg, 0.12 mmol), and tris(dibenzylideneacetone)dipalladium(0) (57 mg, 0.062 mmol). N-Methyldicyclohexylamine (0.64 mL, 2.99 mmol) and ethyl crotonate (0.62 mL, 4.99 mmol) were added and the mixture was stirred for 18 h at room temperature. The mixture was diluted with ethyl acetate, filtered through a small plug of silica gel which was washed with additional ethyl acetate, and the combined filtrates were concentrated. Purification by chromatography (SiO2, 5:1 hexane/ethyl acetate) provided 0.47 g (70%) of the title compound as an off-white solid. MS 269 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825170B2
Source datasetuspto-grants-2004_11
ORD IDord-1d8cf2c969e04f8c849c3abb06db7d3e
Source noteuspto-grants-2004_11