HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
[7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl]methanol → 7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehyde
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | [7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl]methanol | HCID 68981956 | — |
| Katalysator | HCID 178418406 | HCID 178418406 | — |
| Lösungsmittel | Methyl, chloro- | HCID 5378701 | — |
| Produkt | 7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehyde | HCID 57893503 | 60% |
Reaktionsschritte
[7-(Dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl]methanol (3.0 g, 8.74 mmol) was dissolved in methylene chlorine (175 mL). Manganese dioxide (8.0 g, 92 mmol) was added and the reaction mixture was stirred at room temperature for 20 h. The slurry was filtered through diatomaceous earth to remove the catalyst, and the filtrate was concentrated to a dark oil. Purification by Biotage chromatography (10-30% ethyl acetate in hexanes) provided 7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehyde (1.78 g, 60%) as a yellow oil: 1H NMR (300 MHz, CDCl3) δ4.89 (4H, s), 7.06-7.12 (2H, m), 7.27-7.38 (10H, m), 7.93 (1H, d, J=5.7 Hz), 8.74 (1H, br s), 9.77 (1H, s).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07608627B2 |
| Quelldatensatz | uspto-grants-2009_10 |
| ORD ID | ord-c1c4f3fb22ea4648afcab6b4086067e5 |
| Quellennotiz | uspto-grants-2009_10 |