HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 386407Erstellt: 26. Oktober 2026
Potassium tert-butoxide → 2-Chloro-5H-pyrrolo[2,3-B]pyrazine
https://huagongshe.com/reaction/386407
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| 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 | — |
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 |
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| Patentnummer | US08372835B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-d8a8fc7882ee4968b2e53b2d95380ef9 |
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| Quellennotiz | uspto-grants-2013_02 |
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