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

HRID 1336871Notes

Reaction equation

HRID 1336871 reaction equation
Brc1cccnc1.c1ccc(C2CCNCC2)cc1>CC(C)(C)[O-].CC1=CC(C)=[O]->[Ni]2([O]1)[O]C(C)=CC(C)=[O]->2.COc1cccc(OC)c1NC(=O)C(=O)O.CS(C)=O.[Li+]>c1ccc(C2CCN(c3cccnc3)CC2)cc1

Participants

9

Reactant 2

HCID 122863-BromopyridineHCID 698734-Phenylpiperidine

Product 3

HCID 2519CaffeineHCID 1223802233-(4-Phenyl-1-piperidinyl)pyridineYield 3.328%HCID 1398883374-(4-Phenylpiperidin-1-yl)pyridineYield 3.289%

Reagents, catalysts & solvents 4

HCID 236647642-Propanol, 2-methyl-, lithium salt (1:1)ReagentHCID 1188645032-((2,6-Dimethoxyphenyl)amino)-2-oxoacetic acidCatalystHCID 178427212HCID 178427212, 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-8833eca17cd14f4096e05ca73dffa6f1
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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