HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tributylstannyl-5H-furan-2-one → HCID 22346469, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tributylstannyl-5H-furan-2-one | HCID 10915702 | — |
| Reactant | HCID 22346452 | HCID 22346452 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22346469 | HCID 22346469 | — |
Reaction Steps
The iodide from step 2 (4.37 g, 10.32 mmol) was dissolved in anhydrous toluene (40 ml) in an oven dried flask that was purged with nitrogen. Dichlorobis(triphenylphospine)palladium (II) (660 mgs., 0.94 mmol) and 4-(tributylstannyl)furan-2(5H)-one, (3.85 g, 10.32 mmol) (prepared as described by Gregory J. Hollingworth, Gemma Perkins, and Joseph Sweeney, J. Chem. Soc., Perkins 1. 1996, 1913) were then added to the reaction. After four hours at reflux the reaction was cooled and the solids that precipitated from the solution were collected by vacuum filtration. The product contained 17% of an impurity: N,N′-bis(4-fluorobenzyl)-8,8′-dihydroxy-5,5′-bi-1,6-naphthyridine-7,7′-dicarboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06921759B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-4fc55660dccf4039862341bf69191dfa |
| Source note | uspto-grants-2005_07 |