Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 2-(Tributylstannyl)furan | HCID 4393688 | — |
| Reactant | HCID 22494261 | HCID 22494261 | — |
| Product | HCID 22494108 | HCID 22494108 | — |
Reaction Steps
334 mg of ethyl 3-(3-[(tertiary butoxycarbonyl)amino]methyl-4-[(trifluoromethyl)sulfonyl]oxyphenyl)-2-isopropoxypropionate was dissolved in 4 ml dioxane. 280 mg of 2-tributylstannylfuran, 75 mg of tetrakistriphenylphosphine palladium and 83 mg of lithium chloride were added thereto, followed by stirring overnight at 80° C. in a nitrogen atmosphere. The reaction mixture was concentrated and the residue was purified by silica gel column chromatography, to give 180 mg of ethyl 3-(3-[(tertiary butoxycarbonyl)amino]methyl-4-[(trifluoromethyl)sulfonyl]oxyphenyl)-2-(2-furyl)propoxypropionate from fractions eluted with hexane-ethyl acetate (7:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06884821B1 |
|---|
| Source dataset | uspto-grants-2005_04 |
|---|
| ORD ID | ord-f5362718a202461cb0d56957affe347a |
|---|
| Source note | uspto-grants-2005_04 |
|---|