HCID 11173122, compound → HCID 178468650, compound

HRID 1084186Notes

Reaction equation

HRID 1084186 reaction equation
CCOC(=O)c1cc(Br)cn1CC.O=[N+]([O-])c1ccc(-n2ccnc2-c2ccccc2)cc1>C=C[CH2][Pd][Cl].C=C[CH2][Pd][Cl].CC(=O)N(C)C.CC(C)(C)C(=O)[O-].[K+].c1ccc(P(c2ccccc2)c2ccccc2)cc1>CCOC(=O)c1cc(-c2cnc(-c3ccccc3)n2-c2ccc([N+](=O)[O-])cc2)cn1CC

Participants

8

Reactant 2

HCID 11173122HCID 11173122, compoundHCID 78918332Ethyl 4-bromo-1-ethyl-1H-pyrrole-2-carboxylate

Product 1

HCID 178468650HCID 178468650, compoundYield 6.91%

Reagents, catalysts & solvents 5

HCID 23662159Potassium TrimethylacetateReagentHCID 11776TriphenylphosphineCatalystHCID 178455864HCID 178455864, compoundCatalystHCID 31374DimethylacetamideSolvent3×HCID 741954,4'-Bis(1,1-dimethylethyl)-1,1'-biphenylInternal standard

Conditions

Temperature
120 °C

Workup

  1. temperatureCool to room temperature
  2. additionNo procedure recorded
  3. aliquotNo procedure recorded
  4. filtrationFilter into HPLC analysis plate · Keep liquid/mobile
  5. washwash filter with 400 microliter of acetonitrile/water (4:1)

Sources & evidence

ORD record
ord-84b3d82b5e2f4f58a583744014fb762f
Source dataset
Pd-catalyzed C-H arylation of imidazole with aryl bromide
Original link
View source

Reaction notes

Loading…