HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 60116Erstellt: 26. Oktober 2026
Potassium Carbonate → (3-amino-2,6-difluoro-phenyl)-[5-(2-methyl-pyrimidin-5-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]methanone
https://huagongshe.com/reaction/60116
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 5-Bromo-2-methylpyrimidine | HCID 14387744 | — |
| Edukt | HCID 58368802 | HCID 58368802 | — |
| Katalysator | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | (3-amino-2,6-difluoro-phenyl)-[5-(2-methyl-pyrimidin-5-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]methanone | HCID 58368924 | — |
Reaktionsschritte
In a reaction vial, (3-amino-2,6-difluoro-phenyl)-[5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-methanone is combined with (48, 0.850 g, 2.129 mmol), 5-bromo-2-methyl-pyrimidine (49, 0.737 g, 4.26 mmol), potassium carbonate (0.589 g, 4.26 mmol) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (0.174 g, 0.213 mmol) in 14.20 mL of dioxane and 7.10 mL of water (7.10 mL). The reaction is heated at 100° C. overnight. Upon cooling, the reaction mixture is partitioned between water/brine and ethyl acetate/tetrahydrofuran and then filtered through Celite. The organic layer is separated and concentrated under vacuum. The resulting residue is purified by silica gel column chromatography eluting with 0-10% methanol in dichloromethane to provide the desired compound as a tan solid (50, ˜220 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09440969B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-5416b2e15b9c42a5b1e871eb8154979b |
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| Quellennotiz | uspto-grants-2016_09 |
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