HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 563Erstellt: 25. Oktober 2026
tert-Butyl piperazine-1-carboxylate → tert-butyl 4-(1H-indol-7-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/563
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Edukt | 7-Bromoindole | HCID 2757020 | — |
| Reagenz | Sodium t-butoxide | HCID 23676156 | — |
| Katalysator | Palladium (II) acetate | HCID 4144353 | — |
| Katalysator | 2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl | HCID 16217985 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | tert-butyl 4-(1H-indol-7-yl)piperazine-1-carboxylate | HCID 21070951 | 0% |
Reaktionsschritte
2-Dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl (75 mg, 0.16 mmol) and palladium (II) acetate (18.08 mg, 0.08 mmol) were dissoved in toluene (2 mL) at ambient temperature. The mixture was degassed and purged with nitrogen and warmed to 50°C for 20 mins. In a separate vessel, were mixed tert-butyl piperazine-1-carboxylate (300 mg, 1.61 mmol), 7-bromo-1H-indole (316 mg, 1.61 mmol) and sodium-t-butoxide (296 mL, 2.42 mmol) in toluene (3 mL). The mixture was degasssed and purged with nitrogen and warmed to 50°C. The catalyst solution was added to the reaction vessel and the resulting mixture was degassed and purged with nitrogen and heated at 100°C for overnight. UPLC analysis showed virtually no reaction (only 7% conversion to product). Reaction abandoned.
Herkunft & Nachweise
| Quelldatensatz | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-b6527d32ba054a8395bc5ea7808e53a8 |
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| Quellennotiz | 750 AstraZeneca ELN dataset |
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