1-Benzyl-5-Bromo-1H-Indole → HCID 178432947, compound

HRID 1083141Notes

Reaction equation

HRID 1083141 reaction equation
Brc1ccc2c(ccn2Cc2ccccc2)c1.Cc1cn(Cc2ccccc2)c(C)n1>C=C[CH2][Pd][Cl].C=C[CH2][Pd][Cl].CC(=O)N(C)C.CC(C)(C)C(=O)[O-].COc1ccccc1P(c1ccccc1OC)c1ccccc1OC.[K+]>Cc1nc(C)n(Cc2ccccc2)c1-c1ccc2c(ccn2Cc2ccccc2)c1

Participants

8

Reactant 2

HCID 2857561-Benzyl-5-Bromo-1H-IndoleHCID 147449731-Benzyl-2,4-dimethyl-1H-imidazole

Product 1

HCID 178432947HCID 178432947, compoundYield 8.49%

Reagents, catalysts & solvents 5

HCID 23662159Potassium TrimethylacetateReagentHCID 78464Tris(o-methoxyphenyl)phosphineCatalystHCID 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-4788bc96d69e449db758bc14f1fb5ea2
Source dataset
Pd-catalyzed C-H arylation of imidazole with aryl bromide
Original link
View source

Reaction notes

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