Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | Tert-butyl 4-bromo-2-(5-phenylpyridine-3-carboxamido)benzoate | HCID 58508430 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58508948 | HCID 58508948 | — |
Reaction Steps
Cesium carbonate (0.14 g), aniline (0.030 mL), tris(dibenzylideneacetone)dipalladium(0) (2 mg), palladium(II) acetate (1 mg), and 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (5 mg) were added to a toluene (2.5 mL) solution of tert-butyl 4-bromo-2-(5-phenylpyridine-3-carboxamido)benzoate (0.10 g), followed by heating to reflux under a nitrogen atmosphere for 1 hour and 10 minutes. The reaction mixture was cooled to room temperature, and then ethyl acetate and a 10% aqueous solution of citric acid were added thereto. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 91-80% hexane/ethyl acetate] to obtain tert-butyl 4-anilino-2-(5-phenylpyridine-3-carboxamido)benzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492582B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-52047f9fdc604f7e9d40c30e06dc61c4 |
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| Source note | uspto-grants-2013_07 |
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