HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 63Erstellt: 23. Oktober 2026
4-(N-Boc-amino)piperidine → HCID 178418218, Verbindung
https://huagongshe.com/de/reaction/63
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Edukt | 4,6-Dichloroquinoline | HCID 936075 | — |
| Reagenz | Cesium carbonate | HCID 10796 | — |
| Katalysator | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Katalysator | Palladium (II) acetate | HCID 4144353 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | HCID 178418218 | HCID 178418218 | 5% |
Reaktionsschritte
diacetoxypalladium (5.60 mg, 0.02 mmol) was added in one portion to tert-butyl piperidin-4-ylcarbamate (100 mg, 0.50 mmol), 4,6-dichloroquinoline (89 mg, 0.45 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (28.9 mg, 0.05 mmol) and cesium carbonate (488 mg, 1.50 mmol) in DMA (5 mL). The resulting mixture was stirred at 150 °C for 1 hour. LCMS analysis showed formation of a small amount of the desired product. The mixture was heated for a further 2 hours, after which time LCMS analysis showed loss of this small peak. Abandoned.
Herkunft & Nachweise
| Quelldatensatz | 750 AstraZeneca ELN dataset |
|---|
| ORD ID | ord-af3871564adb47f28d81d03aed7b6196 |
|---|
| Quellennotiz | 750 AstraZeneca ELN dataset |
|---|