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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352347Generated: October 30, 2026

2-(Tri-n-butylstannyl)thiophene → HCID 22711977, compound

https://huagongshe.com/reaction/352347

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tri-n-butylstannyl)thiopheneHCID 2779373—
ReactantHCID 22711951HCID 22711951—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 22711977HCID 22711977—

Reaction Conditions

Temperature130 °C

Reaction Steps

In a round-bottom flask under a current of argon, mix 5 g of 7-bromo-3-(2-hydroxyethyl)-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one, 6.2 ml of tributyl-thiophen-2-yl-stannane, 1 g of tetrakis(triphenylphosphine) palladium and 250 ml of N-methylpyrrolidone. Heat the solution at 130° C. for 2 hours and then evaporate off the solvent in vacuo; take up the residue in 200 ml of dichloromethane, wash the solution with 10% potassium fluoride solution, filter, separate off the organic phase and wash it with water. After drying over magnesium sulphate and evaporation, the residue obtained is purified by chromatography on silica gel using a mixture of dichloromethane/methanol: 95/5 as eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747032B2
Source datasetuspto-grants-2004_06
ORD IDord-78052a060bde4bb0948e77ac98cf46e4
Source noteuspto-grants-2004_06