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

HRID 1336693Notes

Reaction equation

HRID 1336693 reaction equation
Brc1cccnc1.c1ccc(C2CCNCC2)cc1>C1CCC2=NCCCN2CC1.CC(C)(C)C1=CC(=[O]->[Ni]2([O]1)[O]C(=CC(=[O]->2)C(C)(C)C)C(C)(C)C)C(C)(C)C.CNC1CCCCC1NC.CS(C)=O>c1ccc(C2CCN(c3cccnc3)CC2)cc1

Participants

9

Reactant 2

HCID 122863-BromopyridineHCID 698734-Phenylpiperidine

Product 3

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

Reagents, catalysts & solvents 4

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneReagentHCID 5510741-N,2-N-dimethylcyclohexane-1,2-diamineCatalystHCID 178441206HCID 178441206, 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-f433187e3b064a68b01ab4802cc0fdbb
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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