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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Tri-n-butylstannyl)thiophene | HCID 2779373 | — |
| Reactant | HCID 22711951 | HCID 22711951 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 22711977 | HCID 22711977 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06747032B2 |
|---|
| Source dataset | uspto-grants-2004_06 |
|---|
| ORD ID | ord-78052a060bde4bb0948e77ac98cf46e4 |
|---|
| Source note | uspto-grants-2004_06 |
|---|