Piperidine → HCID 178473333, compound

HRID 867281Notes

Reaction equation

HRID 867281 reaction equation
C1CCNCC1.CCOC(=O)N1CCC(=C2c3ccc(Cl)cc3CCc3cc(Br)cnc32)CC1>COc1cccc(OC)c1NC(=O)C(=O)O.CS(C)=O.O=P([O-])([O-])[O-].[Cu][I].[K+].[K+].[K+]>CCOC(=O)N1CCC(=C2c3ccc(Cl)cc3CCc3cc(N4CCCCC4)cnc32)CC1

Participants

7

Reactant 2

HCID 8082PiperidineHCID 10742688Ethyl 4-(3-bromo-8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidine-1-carboxylate

Product 1

HCID 178473333HCID 178473333, compoundYield 50.56%

Reagents, catalysts & solvents 4

HCID 62657Potassium Phosphate, TribasicReagentHCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)CatalystHCID 1188645032-((2,6-Dimethoxyphenyl)amino)-2-oxoacetic acidCatalystHCID 679Dimethyl SulfoxideSolvent2×

Conditions

Temperature
80 °C

Workup

  1. additionThe reaction vials were then cooled to r.t. and diluted with 100 μL of 5% AcOH in DMSO, containing 1,3,5-trimethoxybenzene (0.005M) and were shaken vigorously.
  2. aliquot25 microliter of resulting solution is taken
  3. additionTo the 25 microliter aliquot 700 microliter of MeCN was added prior to UPLC-MS Analysis

Sources & evidence

ORD record
ord-b04ffc62e9d3403599612a4d5f0088af
Source dataset
Figure 4 from Chemistry informer libraries
Original link
View source

Reaction notes

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