Phenylboronic Acid → 7-methyl-6-phenyl-1H-indole-2,3-dione

HRID 539505Notes

Reaction equation

HRID 539505 reaction equation
Br[C:2]1[C:10]([CH3:11])=[C:9]2[C:5]([C:6](=[O:13])[C:7](=[O:12])[NH:8]2)=[CH:4][CH:3]=1.[C:14]1(B(O)O)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C([O-])(O)=O.[Na+]>COCCOC.O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH3:11][C:10]1[C:2]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:3][CH:4]=[C:5]2[C:9]=1[NH:8][C:7](=[O:12])[C:6]2=[O:13]

Participants

7

Reactant 3

HCID 66827Phenylboronic AcidHCID 516892Sodium BicarbonateHCID 112301886-Bromo-7-methyl-1H-indole-2,3-dione

Product 1

HCID 113683787-methyl-6-phenyl-1H-indole-2,3-dioneYield 55.5%

Reagents, catalysts & solvents 3

HCID 178418397HCID 178418397, compoundCatalystHCID 962WaterSolventHCID 80711,2-DimethoxyethaneSolvent

Procedure

6-Bromo-7-methyl-1H-indole-2,3-dione (100 mg, 0.38 mmol) and phenylboronic acid (53 mg, 1.1 eq) were dissolved in 10 mL DME. Pd(PPh3)4 (22 mg, 0.05 eq) were added followed by NaHCO3 (65 mg, 2.0 eq) dissolved in 10 mL water. The mixture was refluxed for 2.5 hr and the organic solvent was removed by evaporation. The mixture was extracted with ethyl acetate and the combined organic layers were dried over Na2SO4 and purified by SiO2 chromatography to give the title compound (50 mg, 51%).

Workup

  1. temperatureThe mixture was refluxed for 2.5 hr
  2. customthe organic solvent was removed by evaporation
  3. extractionThe mixture was extracted with ethyl acetate
  4. dry with materialthe combined organic layers were dried over Na2SO4
  5. custompurified by SiO2 chromatography

Sources & evidence

ORD record
ord-76a6bb61a6d04240844ecda4cc5971be
Source dataset
uspto-grants-2014_10
Patent number
US08871718B2

Reaction notes

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