Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Cyclobutanecarboxamide | HCID 1274476 | — |
| Edukt | 7-Bromo-6-azaindole | HCID 19696456 | — |
| Katalysator | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Katalysator | Tris(dibenzylideneacetone) dipalladium | HCID 9832798 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | HCID 71061452 | HCID 71061452 | 39,3% |
Reaktionsschritte
To a solution of 7-bromo-1H-pyrrolo[2,3-c]pyridine (500 mg, 2.53 mmol) in toluene were added tris (dibenzylidene acetone) dipalladium (116.20 mg, 0.126 mmol), Xantphos (32.98 mg, 0.057 mmol), cesium carbonate (896 mg, 2.75 mmol), and cyclobutanecarboxamide (251 mg, 2.96 mmol, Intermediate 4). The resulting reaction mixture was heated to 120° C. and stirred for 8 hours. After cooling to room temperature a saturated aqueous sodium bicarbonate solution (20 mL) was added to the reaction mixture and extracted with ethyl acetate (3×50 mL). The combined organic layer was dried over anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by silica gel (100-200) column chromatography to afford N-(1H-pyrrolo[2,3-c]pyridin-7-yl)cyclopropane carboxamide (200 mg, 36% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08980911B2 |
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| Quelldatensatz | uspto-grants-2015_03 |
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| ORD ID | ord-565884b6943b4f10915d60089e539388 |
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| Quellennotiz | uspto-grants-2015_03 |
|---|