HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Potassium tert-butoxide → 2-Chloro-5H-pyrrolo[2,3-B]pyrazine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Edukt | 5-Chloro-3-(triethyl-silanylethynyl)-pyrazin-2-ylamine | HCID 59463522 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Lösungsmittel | Sodium chloride; water | HCID 57417360 | — |
| Produkt | 2-Chloro-5H-pyrrolo[2,3-B]pyrazine | HCID 45789638 | — |
Reaktionsbedingungen
| Temperatur | 80 °C |
|---|
Reaktionsschritte
A solution of potassium tert-butoxide (1 g, 4.5 mM) in N-methylpyrrolidone (3 ml) was heated to 80° C. under nitrogen. A solution of 5-chloro-3-(triethyl-silanylethynyl)-pyrazin-2-ylamine (3) (1.2 g, 4.5 mmol) in N-methylpyrrolidone (10 ml) was added dropwise. The reaction mixture was stirred at 80° C. for a further fifty minutes and then the reaction mixture was allowed to cool to room temperature. Brine (10 ml) was added to the reaction mixture and extracted with ethyl acetate (5×20 ml). The combined organics were washed with brine, dried over magnesium sulfate and concentrated in vacuo to afford the title compound as a solution in N-methylpyrrolidone. MS(ES+): 154
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07795259B2 |
| Quelldatensatz | uspto-grants-2010_09 |
| ORD ID | ord-ca22afe92f4843c3b7c86fc0434c43e7 |
| Quellennotiz | uspto-grants-2010_09 |