1-Benzyl-5-Bromo-1H-Indole → HCID 178456429, compound

HRID 1082869

Reaction equation

HRID 1082869 reaction equation
Brc1ccc2c(ccn2Cc2ccccc2)c1.CC(C)n1ccnc1>C=C[CH2][Pd][Cl].C=C[CH2][Pd][Cl].CC(=O)N(C)C.CC(C)(C)C(=O)[O-].CN(C)c1ccc(P(C2CCCCC2)C2CCCCC2)cc1.[K+]>CC(C)n1cncc1-c1ccc2c(ccn2Cc2ccccc2)c1

Participants

8

Reactant 2

HCID 2857561-Benzyl-5-Bromo-1H-IndoleHCID 101761131H-Imidazole, 1-(1-methylethyl)-

Product 1

HCID 178456429HCID 178456429, compoundYield 9.62%

Reagents, catalysts & solvents 5

HCID 23662159Potassium TrimethylacetateReagentHCID 142458Benzenamine, 4-(dicyclohexylphosphino)-N,N-dimethyl-CatalystHCID 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-78aa4a7b156b475583252f40e3a52ab4
Source dataset
Pd-catalyzed C-H arylation of imidazole with aryl bromide
Original link
View source

Linked notes

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