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

HRID 1344945Notes

Reaction equation

HRID 1344945 reaction equation
Ic1cccnc1.c1ccc(C2CCNCC2)cc1>CC(=O)[O][Cu].CS(C)=O.Clc1ccc(-n2cc[n+](-c3ccc(Cl)cc3)c2)cc1.O=C([O-])[O-].[Cl-].[Cs+]>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 159368781,3-Bis(4-chlorophenyl)-1H-imidazol-3-ium chlorideCatalystHCID 178476680HCID 178476680, compoundCatalystHCID 679Dimethyl SulfoxideSolvent5×

Conditions

Temperature
60 °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-108e4442d9e447b582d8dbb7a2e4c93e
Source dataset
High-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions
Original link
View source

Reaction notes

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