Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Formylphenylboronic acid | HCID 2734356 | — |
| Reactant | (7-Bromo-pyrrolo[2,1-f][1,2,4]triazin-2-yl)-(4-morpholin-4-yl-phenyl)-amine | HCID 54578326 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86761891 | HCID 86761891 | — |
Reaction Steps
Into a 8-dram vial, Palladium Acetate (0.021 g, 0.000094 mol) and Triphenylphosphine (0.069 g, 0.00026 mol) were added. The mixture was purged under an atmosphere of Nitrogen for 10 minutes. 1,4-Dioxane (7.10 mL) was added and stirred for 10 minutes at room temperature. (7-Bromo-pyrrolo[2,1-f][1,2,4]triazin-2-yl)-(4-morpholin-4-yl-phenyl)-amine (0.35 g, 0.00094 mol), 3-Formylphenyl boronic acid (0.280 g, 0.00187 mol), N,N-Dimethylformamide (14 mL), and 1.50 M of Sodium carbonate in Water (5.61 mL, 8.42 mmol) were added. The reaction was heated at 90° C. for 3 hours. The reaction was partitioned with water and EtOAc. The organic was separated, washed with Brine, and dried over magnesium sulfate. The solid was filtered and washed with EtOAc. The solvent was removed under vacuum. The product was isolated via column chromatography with DCM and Methanol as eluant (0 to 10% MeOH). The collected fractions afforded a solid. The solid was triturated with Et2O and filtered to give 3-[2-(4-Morpholin-4-yl-phenylamino)-pyrrolo[2,1-f][1,2,4]triazin-7-yl]-benzaldehyde as a yellow (0.20 g, 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08471005B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-178aecbe617846bdb290b734aa9ddc3a |
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| Source note | uspto-grants-2013_06 |
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