HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → 4-bromo-6-methyl-1H,6H,7H-pyrrolo[2,3-c]pyridin-7-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-Bromo-1,6-dihydro-6-methyl-1-((4-methylphenyl)sulfonyl)-7H-pyrrolo(2,3-c)pyridin-7-one | HCID 89656304 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-bromo-6-methyl-1H,6H,7H-pyrrolo[2,3-c]pyridin-7-one | HCID 57329766 | 108,4% |
Reaktionsbedingungen
| Temperatur | 20 °C |
|---|
Reaktionsschritte
A solution of 4-bromo-6-methyl-1-[(4-methylphenyl)sulfonyl]-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-one (5.81 g, 15.2 mmol) in ethanol (100 mL) was treated with 3.0 M sodium hydroxide in water (50.8 mL, 152 mmol) and stirred at 20° C. for 16 h. The reaction mixture was concentrated in vacuo to remove most of the ethanol. The remaining aqueous layer was neutralized with concentrated HCl to pH ˜7 and extracted with ethyl acetate (2×). The combined organic layers were dried with magnesium sulfate, filtered, and concentrated to give the desired product (3.74 g, quantitative) which was used without further purification. LCMS calculated for C8H8BrN2O (M+H)+: m/z=227.0, 229.0. found: 227.0, 228.9.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09399640B2 |
| Quelldatensatz | uspto-grants-2016_07 |
| ORD ID | ord-6681ac83dd14478d98fc7a54cf5cd8d9 |
| Quellennotiz | uspto-grants-2016_07 |