Piperidine → HCID 178481514, compound

HRID 867342Notes

Reaction equation

HRID 867342 reaction equation
C1CCNCC1.CN1C(=O)C[C@@](C)(c2cc(Br)cs2)N/C1=N/C(=O)OC(C)(C)C>CS(C)=O.O=C(O)C(=O)Nc1cc(C(F)(F)F)cc(C(F)(F)F)c1.O=P([O-])([O-])[O-].[Cu][I].[K+].[K+].[K+]>CN1C(=O)C[C@@](C)(c2cc(N3CCCCC3)cs2)N/C1=N/C(=O)OC(C)(C)C

Participants

7

Reactant 2

HCID 8082PiperidineHCID 178481496HCID 178481496, compound

Product 1

HCID 178481514HCID 178481514, compoundYield 0%

Reagents, catalysts & solvents 4

HCID 62657Potassium Phosphate, TribasicReagentHCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)CatalystHCID 1188645142-[3,5-Bis(trifluoromethyl)anilino]-2-oxo-acetic 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-af8231249442440d834de5d07aaf8d2a
Source dataset
Figure 4 from Chemistry informer libraries
Original link
View source

Reaction notes

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