3-Bromopyridine → 3-(4-Phenyl-1-piperidinyl)pyridine
Reaktionsgleichung
Brc1cccnc1.c1ccc(C2CCNCC2)cc1>CN1CCCN2CCCN=C12.CS(C)=O.O=C(N[C@@H]1CCCC[C@H]1NC(=O)c1ccccn1)c1ccccn1.O=C1[CH](=Cc2ccccc2)->[Pd]2<-[CH](=Cc3ccccc3)C(=O)[CH](=Cc3ccccc3)->[Pd](<-[CH]1=Cc1ccccc1)<-[CH](=Cc1ccccc1)C(=O)[CH]->2=Cc1ccccc1>c1ccc(C2CCN(c3cccnc3)CC2)cc1Komponenten
9
Edukt 2
Produkt 3
Reagenzien, Katalysatoren, Lösungsmittel 4
Reaktionsbedingungen
- Temperatur
- 60 °C
Aufarbeitung
- customThe foil sealing tape was removed from the plate.
- addition3 μL of a 0.0667 M solution of caffeine in DMSO was added to each reaction well using an SPT Labtech Mosquito® liquid handling robot
- filtrationThe plates were then centrifuged for 15 to 20 seconds. · liquid-Phase beibehalten
- aliquotFollowing centrifugation, 500 nL of the resultant mixture from each well was carefully dispensed into four 384-well analytical plates (Analytical Sales # 38435) using an SPT Labtech Mosquito® liquid handling robot. Each well of these analytical plates contained 30 μL of DMSO with 0.1% acetic acid, pre-dosed by OpenTrons, to facilitate analysis.
Quellen und Nachweise
- ORD-Eintrag
- ord-94c6e4ff0d0a46c39fab748733b48436
- Quelldatensatz
- High-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions
- Originallink
- Quelle ansehen
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