Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | tert-butyl 4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate | HCID 16217654 | — |
| Reactant | HCID 66797363 | HCID 66797363 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 66797424 | HCID 66797424 | — |
Reaction Steps
A mixture of (6-Bromo-quinoxalin-2-yl)-{(R)-1-[3-(4-methyl-piperazin-1-yl)-phenyl]ethyl}-amine (0.250 g, 1 eq., 0.588 mmol), 1-Boc-4-pyrazole boronic acid pinacol ester (0.190 g, 1.1 eq., 0.647 mmol), caesium carbonate (0.764 g, 4.0 eq., 2.35 mmol) and potassium iodide (0.010 g, 0.1 eq., 0.00588 mmol) in 1,4-dioxane (15 mL) was degassed at RT under vacuum and placed under an atmosphere of nitrogen. The process was repeated twice and Fu's catalyst (Bis(tri-tert-butylphosphine)palladium(0)) (0.015 g, 0.05 eq., 0.029 mmol) was added at room temperature. The reaction mixture was heated at 105° C. in a microwave reactor for 180 minutes. After completion of the reaction (confirmed by TLC), the organic mixture was diluted with ethyl acetate (325 mL) and washed with water (100 mL×3) and brine (100 mL). The organic layer was dried and concentrated under vacuum to give a crude residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716473B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-ebfff6470d4f462cbe6e3f65be972a28 |
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| Source note | uspto-grants-2014_05 |
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