4-Phenylpiperidine → 3-(4-Phenyl-1-piperidinyl)pyridine

HRID 1345884Notes

Reaction equation

HRID 1345884 reaction equation
Ic1cccnc1.c1ccc(C2CCNCC2)cc1>COc1cc(C(c2ccccc2)c2ccccc2)c(N2C=CN(c3c(C(c4ccccc4)c4ccccc4)cc(OC)cc3C(c3ccccc3)c3ccccc3)C2)c(C(c2ccccc2)c2ccccc2)c1.CS(C)=O.O=C([O-])[O-].[Cs+].[Cu][O][Cu]>c1ccc(C2CCN(c3cccnc3)CC2)cc1

Participants

9

Reactant 2

HCID 698734-PhenylpiperidineHCID 707143-Iodopyridine

Product 3

HCID 2519CaffeineHCID 1223802233-(4-Phenyl-1-piperidinyl)pyridineYield 0%HCID 1398883374-(4-Phenylpiperidin-1-yl)pyridineYield 0%

Reagents, catalysts & solvents 4

HCID 14794698CID 14794698ReagentHCID 102190031HCID 102190031, compoundCatalystHCID 178505380HCID 178505380, compoundCatalystHCID 679Dimethyl SulfoxideSolvent5×

Conditions

Temperature
30 °C

Workup

  1. customThe foil sealing tape was removed from the plate.
  2. 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
  3. filtrationThe plates were then centrifuged for 15 to 20 seconds. · Keep liquid
  4. 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.

Sources & evidence

ORD record
ord-a00c02811fb243f5887ff20bc0ed9ad7
Source dataset
High-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions
Original link
View source

Reaction notes

Loading…