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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434915Generated: November 3, 2026

Triphenylarsine → HCID 57936158, compound

https://huagongshe.com/reaction/1434915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylarsineHCID 11773—
Reactant2-(Methylthio)-4-(tributylstannyl)pyrimidineHCID 2763261—
ReactantHCID 64271090HCID 64271090—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 57936158HCID 57936158—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of (E)-4-(5-bromo-thiophen-2-yl)-but-3-en-2-one (1 g, 4.34 mmol), triphenylarsine (319 mg, 1.04 mmol), cuprous iodide (99 mg, 0.52 mmol) and Pd2(dba)3 (119 mg, 0.13 mmol) in 25 ml of NMP was heated to 80° C. To this hot solution 2-methylsulfanyl-4-tributylstannanyl-pyrimidine (1.8 g, 4.34 mmol) dissolved in 10 ml of NMP was added dropwise over a period of 10 minutes. Stirring was continued for 24 hours. The solvent was then removed in vacuo and the residue partitioned between water and EtOAc. The aqueous layer was separated and extracted once more with EtOAc. The combined organic extracts were washed with water and brine, dried over sodium sulfate and evaporated. The crude was purified by chromatography on silicagel (EtOAc/hexane:2/3) to give a yellow solid. Yield: 480 mg (40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615562B2
Source datasetuspto-grants-2009_11
ORD IDord-8d5868716fff41a29e0954415cc9657c
Source noteuspto-grants-2009_11